Victor Dubowitz

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Victor Dubowitz is affiliated with the following schools: University of Sheffield, University of Cape Town, Imperial College London, Royal Postgraduate Medical School

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Why Is Victor Dubowitz Influential?

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According to Wikipedia, Victor Dubowitz, FRCP, Hon FRCPCH is a British neurologist and professor emeritus at Imperial College London. He is principally known along with his wife Lilly Dubowitz for developing two clinical tests, the Dubowitz Score to estimate gestational age and the other for the systematic neurological examination of the newborn.

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Victor Dubowitz's Published Works

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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Clinical assessment of gestational age in the newborn infant. (1970) (1914)
Muscle biopsy: A modern approach (1973) (1280)
Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.213.3 (1990) (556)
Muscle disorders in childhood. (1977) (428)
Final report of the Medical Research Council/Royal College of Obstetricians and Gynaecologists Multicentre Randomised Trial of Cervical Cerclage (1993) (404)
Ultrasound imaging in the diagnosis of muscle disease. (1982) (358)
Genomic variation and gene conversion in spinal muscular atrophy: implications for disease process and clinical phenotype. (1997) (321)
Genetic homogeneity between acute and chronic forms of spinal muscular atrophy (1990) (313)
Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy. (1999) (302)
Quantitation of muscle function in children: A prospective study in duchenne muscular dystrophy (1982) (286)
Optimality score for the neurologic examination of the infant at 12 and 18 months of age. (1999) (244)
Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy. (1995) (239)
A new approach to the neurological assessment of the preterm and full-term newborn infant (1980) (230)
Phenotypic spectrum associated with mutations in the fukutin‐related protein gene (2003) (216)
PREDICTIVE VALUE OF CRANIAL ULTRASOUND IN THE NEWBORN BABY: A REAPPRAISAL (1985) (202)
Muscle disorders in childhood. (1977) (199)
DERMATOMYOSITIS, POLYMYOSITIS, AND COXSACKIE-B-VIRUS INFECTION (1987) (180)
Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletion. (1994) (175)
Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal (1995) (174)
A Clinician's View of Neuromuscular Diseases (1978) (165)
Very severe spinal muscular atrophy (SMA type 0): an expanding clinical phenotype. (1999) (161)
An optimality score for the neurologic examination of the term newborn. (1998) (160)
Demyelinating Peripheral Neuropathy in Merosin-Deficient Congenital Muscular Dystrophy (1995) (157)
DETECTION OF PATHOLOGICAL CHANGE IN DYSTROPHIC MUSCLE WITH B-SCAN ULTRASOUND IMAGING (1980) (156)
Real‐time ultrasound imaging of muscles (1988) (156)
Reciprocal Relationship of Phosphorylase and Oxidative Enzymes in Skeletal Muscle (1960) (155)
Enzyme histochemistry of skeletal muscle. (1965) (150)
Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores (2002) (148)
INFANTILE MUSCULAR ATROPHY. A PROSPECTIVE STUDY WITH PARTICULAR REFERENCE TO A SLOWLY PROGRESSIVE VARIETY. (1964) (142)
INCREASED EXPRESSION OF HLA ABC CLASS I ANTIGENS BY MUSCLE FIBRES IN DUCHENNE MUSCULAR DYSTROPHY, INFLAMMATORY MYOPATHY, AND OTHER NEUROMUSCULAR DISORDERS (1985) (140)
Chaos in the classification of SMA: A possible resolution (1995) (140)
Cross‐innervated mammalian skeletal muscle: histochemical, physiological and biochemical observations (1967) (138)
Persistence of enteroviral RNA in chronic fatigue syndrome is associated with the abnormal production of equal amounts of positive and negative strands of enteroviral RNA. (1990) (136)
A role for collagen in the pathogenesis of muscular dystrophy? (1980) (131)
The Structure and Function of Muscle (1974) (129)
The infant cry. A spectrographic and auditory analysis (1970) (129)
CYCLOSPORIN IN JUVENILE DERMATOMYOSITIS (1989) (128)
Nature of the mononuclear infiltrate and the mechanism of muscle damage in juvenile dermatomyositis and Duchenne muscular dystrophy (1990) (127)
Cerebral structure and intraventricular haemorrhage in the neonate: a real-time ultrasound study. (1981) (125)
Intellect and Behaviour in Duchenne Muscular Dystrophy (1981) (125)
Neurological, electrophysiological and MRI abnormalities in infants with extensive cystic leukomalacia. (1987) (124)
The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studies. (1995) (120)
Muscle Biopsy: A Practical Approach (2020) (119)
The natural history of type I (severe) spinal muscular atrophy (1994) (117)
A mutation in the dystrophin gene selectively affecting dystrophin expression in the heart. (1995) (117)
Hemorrhagic periventricular leukomalacia in the neonate: a real-time ultrasound study. (1983) (115)
A comparative histochemical study of oxidative enzyme and phosphorylase activity in skeletal muscle (2004) (114)
Prednisone for Duchenne muscular dystrophy (2005) (113)
Night-time nasal ventilation in neuromuscular disease (1990) (111)
Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging (1999) (110)
Measurements of muscle strength and performance in children with normal and diseased muscle. (1976) (107)
Chaos in classification of the spinal muscular atrophies of childhood (1991) (106)
Expression of laminin subunits in congenital muscular dystrophy (1995) (105)
Continuous EEG monitoring of neonatal seizures: diagnostic and prognostic considerations. (1989) (105)
Nemaline myopathy: report of a fatal case, with histochemical and electron microscopic studies. (1967) (105)
Expression of class I and class II MHC antigens in neuromuscular diseases (1989) (104)
Clinical and EEG response to anticonvulsants in neonatal seizures. (1989) (103)
Intravenous immunoglobulin in juvenile dermatomyositis--four year review of nine cases. (1995) (102)
Hearing threshold in preterm and term infants by auditory brainstem response. (1985) (101)
Correlation of neurologic assessment in the preterm newborn infant with outcome at 1 year. (1984) (100)
Exon skipping and translation in patients with frameshift deletions in the dystrophin gene. (1993) (100)
Developmental and neurological progress of preterm infants with intraventricular haemorrhage and ventricular dilatation. (1982) (100)
Paramyotonia congenita: The R1448P Na+ channel mutation in adult human skeletal muscle (1996) (97)
22nd ENMC Sponsored Workshop on Congenital Muscular Dystrophy held in Baarn, The Netherlands, 14–16 May 1993 (1994) (97)
Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy. (2002) (97)
Final report of the Medical Research Council/Royal College of Obstetricians and Gynaecologists multicentre randomised trial of cervical cerclage. MRC/RCOG Working Party on Cervical Cerclage. (1993) (94)
Continuous 4-channel EEG monitoring: a guide to interpretation, with normal values, in preterm infants. (1987) (94)
Nuclear magnetic resonance imaging of the brain in children (1982) (94)
Oxidative enzymes and phosphorylase in central-core disease of muscle. (1960) (93)
Familial Low Birthweight Dwarfism with an Unusual Facies and a Skin Eruption (1965) (93)
Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle α-actin (ACTA1) gene (2001) (93)
Intellectual Impairment in Muscular Dystrophy (1965) (92)
Pathology of experimentally re-innervated skeletal muscle. (1967) (89)
Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy (1999) (88)
Congenital centronuclear (myotubular) myopathy. A clinical, pathological and genetic study in eight children. (1985) (87)
Gene deletions in spinal muscular atrophy. (1996) (87)
Neurological and neurobehavioural differences between preterm infants at term and full-term newborn infants. (1982) (86)
Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin α2 chain (1997) (85)
Feeding problems in merosin-deficient congenital muscular dystrophy (1997) (85)
Measurement of quadriceps muscle thickness and subcutaneous tissue thickness in normal children by real‐time ultrasound imaging (1988) (85)
Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathy. (1995) (84)
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy. (1989) (84)
The central nervous system in Duchenne muscular dystrophy. (1969) (84)
THE "FLOPPY" infant. (1959) (84)
Creatine kinase isoenzymes in neuromuscular diseases (1976) (84)
Subclinical cardiomyopathy in Becker muscular dystrophy (1992) (83)
Prednisone in Duchenne dystrophy (1991) (82)
Duchenne muscular dystrophy, 2nd edn.: Alan E. H. Emery. Oxford Monographs on Medical Genetics No. 24. Published 1993 by Oxford University Press, Oxford. ISBN 019 262370 2, 384 pp. Price £45 (1993) (82)
Effect of exercise in Duchenne muscular dystrophy. (1981) (81)
Neurologic signs in neonatal intraventricular hemorrhage: a correlation with real-time ultrasound. (1981) (80)
Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsy (1996) (80)
Failure of “Dystrophic” Neurones to Support Functional Regeneration of Normal or Dystrophic Muscle in Culture (1973) (79)
Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42. (2000) (78)
Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency (1997) (77)
Management of Children with Non‐organic (Hysterical) Disorders of Motor Function (1976) (77)
Histological and Histochemical Stains and Reactions (2020) (75)
An effective, low-dosage, intermittent schedule of prednisolone in the long-term treatment of early cases of Duchenne dystrophy (2002) (75)
Enzymic activity of normal and dystrophic human muscle: A histochemical study (1961) (75)
Rigid Spine Syndrome: A Muscle Syndrome in Search of a Name (1973) (75)
Ultrastructural changes in diseased muscle (2007) (73)
Sleep studies and supportive ventilatory treatment in patients with congenital muscle disorders. (1996) (73)
Peripheral Neuropathy in Cockayne's Syndrome (1970) (72)
Element analysis of skeletal muscle in duchenne muscular dystrophy using x‐ray fluorescence spectrometry (1980) (71)
The Development of Visual Function in Normal and Neurologically Abnormal Preterm and Fullterm Infants (1982) (70)
Mutations in MYH7 cause Multi-minicore Disease (MmD) with variable cardiac involvement (2012) (70)
Dystrophin in frameshift deletion patients with Becker muscular dystrophy. (1992) (70)
Ramblings in the history of spinal muscular atrophy (2009) (69)
Dystrophin-related protein, utrophin, in normal and dystrophic human fetal skeletal muscle (2004) (68)
Proceedings of the 27th ENMC sponsored workshop on congenital muscular dystrophy 22–24 April 1994, The Netherlands (1995) (68)
Phenotypic heterogeneity of spinal muscular atrophy mapping to chromosome 5q11.2‐13.3 (SMA 5q) (1990) (68)
Scoliosis in Spinal Muscular Atrophy: Review of 63 Cases (1989) (68)
Responses of muscles of patients with Duchenne muscular dystrophy to chronic electrical stimulation. (1986) (68)
A balanced de novo X/autosome translocation in a girl with manifestations of Lowe syndrome. (1986) (67)
Therapeutic possibilities of chronic low frequency electrical stimulation in children with Duchenne muscular dystrophy (1990) (67)
Prevention of Rapidly Progressive Scoliosis in Duchenne Muscular Dystrophy by Prolongation of Walking with Orthoses (1988) (67)
Dystrophin and nebulin in the muscular dystrophies (1988) (66)
Lipoma of the Cauda Equina* (1965) (66)
Collagen types in neuromuscular diseases (1982) (66)
Abnormalities in α-, β- and γ-sarcoglycan in patients with limb-girdle muscular dystrophy (1996) (65)
Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin status. (1995) (65)
PROLONGATIÓN OF WALKING IN DUCHENNE MUSCULAR DYSTROPHY WITH LIGHTWEIGHT ORTHOSES; REVIEW OF 57 CASES (1985) (64)
Congenital myotonic dystrophy: respiratory function at birth determines survival. (1989) (64)
Myopathy with unique ultrastructural feature in marchinesco‐sjögren syndrome (1988) (64)
Predictive value of early continuous electroencephalogram monitoring in ventilated preterm infants with intraventricular hemorrhage. (1988) (63)
Assessment of quadriceps femoris muscle atrophy and hypertrophy in neuromuscular disease in children (1988) (63)
Prevention of deformity in Duchenne muscular dystrophy. A prospective study of passive stretching and splintage. (1981) (63)
THE EFFECT OF PETHIDINE ON THE NEONATAL EEG (1992) (61)
Central core disease of muscle: clinical, histochemical and electron microscopic studies of an affected mother and child. (1970) (61)
Steroids in Duchenne muscular dystrophy; Pilot study of a new low-dosage schedule (1993) (61)
Effects of chronic low frequency electrical stimulation on normal human tibialis anterior muscle. (1985) (60)
Minicore myopathy in children: a clinical and histopathological study of 19 cases (2000) (58)
Electron-microscopic X-ray microanalysis of normal and diseased human muscle (1977) (58)
Remission of clinical signs in early duchenne muscular dystrophy on intermittent low-dosage prednisolone therapy. (2002) (58)
Carrier detection in Duchenne muscular dystrophy (1970) (57)
Effects of posture and spinal bracing on respiratory function in neuromuscular disease. (1986) (57)
Chloroquine‐induced cytosomes with curvilinear profiles in muscle (1979) (56)
Visual Function in the Preterm and Fullterm Newborn Infant (1980) (54)
An X‐linked disease of the nervous system with disordered copper metabolism and features differing from Menkes disease (1981) (53)
Prenatal prediction of spinal muscular atrophy. (1992) (53)
Colonic Perforation after Exchange Transfusion (1968) (52)
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental ability (1992) (52)
Low serum thyroxine concentrations and neural maturation in preterm infants. (1986) (52)
Progressive muscular dystrophy of the Duchenne type in females and its mode of inheritance. (1960) (51)
41st ENMC international workshop on congenital muscular dystrophy 8–10 March 1996, Naarden, The Netherlands (1996) (50)
Ultrasound Imaging and Directed Needle Biopsy in the Diagnosis of Selective Involvement in Muscle Disease (1987) (50)
Characterisation of dystrophin in carriers of Duchenne muscular dystrophy (1991) (50)
Echocardiographic assessment of left ventricular function in Duchenne's muscular dystrophy. (1978) (49)
Diagnostic advantage of needle muscle biopsy and ultrasound imaging in the detection of focal pathology in a girl with limb girdle dystrophy (1985) (49)
Myopathic changes in a muscular dystrophy carrier (1963) (49)
Enzymatic Maturation of Skeletal Muscle (1963) (47)
A randomized controlled trial of early surgery in duchenne muscular dystrophy (1992) (46)
Morphological studies on normal and diseased human muscle in culture. (1971) (46)
A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysis (1995) (46)
Use of liposomes in treating type II glycogenosis. (1976) (46)
Dystrophin-related protein, utrophin, in normal and dystrophic human fetal skeletal muscle (1993) (45)
Treatment of dermatomyositis in childhood. (1976) (45)
Increased calcium-activated neutral protease activity in muscles of dystrophic hamsters and mice (1979) (45)
Sequential study of central and peripheral nervous system involvement in an infant with merosin-deficient congenital muscular dystrophy (1996) (45)
Nerve Conduction Velocity—An Index of Neurological Maturity of the Newborn Infant (1968) (45)
Laminin α2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy (1998) (44)
50th ENMC International Workshop: congenital muscular dystrophy. 28 February 1997 to 2 March 1997, Naarden, The Netherlands. (1997) (44)
A syndrome with juvenile cataract, cerebellar atrophy, mental retardation and myopathy. (1987) (43)
68th ENMC international workshop (5th international workshop): On congenital muscular dystrophy, 9-11 April 1999, Naarden, The Netherlands. (1999) (42)
Management of muscular dystrophy. Pharmacological and physical aspects. (1980) (41)
Motor nerve conduction velocity in spinal muscular atrophy of childhood. (1976) (41)
Immunocytochemical localisation of complement components C8 and C9 in human diseased muscle the role of complement in muscle fibre damage (1987) (41)
Fatal rhabdomyolysis complicating general anaesthesia in a child with Becker muscular dystrophy (1991) (41)
Enhancement of resolution in two‐dimensional gel electrophoresis and simultaneous resolution of acidic and basic proteins (1982) (41)
Continuous four-channel EEG monitoring in the evaluation of echodense ultrasound lesions and cystic leucomalacia. (1987) (40)
218th ENMC International Workshop: Revisiting the consensus on standards of care in SMA Naarden, The Netherlands, 19–21 February 2016 (2017) (40)
Dominantly inherited peroneal muscular atrophy (hereditary motor and sensory neuropathy type I) in infancy and childhood (1981) (40)
X-linked myotubular myopathy--a long-term follow-up study. (1998) (40)
A severe clinical and pathological variant of central core disease with possible autosomal recessive inheritance (1998) (40)
Early presentation of X-linked Emery–Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophy (1998) (40)
Change in Enzyme Pattern after Cross-innervation of Fast and Slow Skeletal Muscle (1967) (39)
ANTENATAL DIAGNOSIS OF DUCHENNE MUSCULAR DYSTROPHY (1979) (39)
Epilepsy in Duchenne and Becker muscular dystrophies. (1997) (39)
Linkage analysis of spinal muscular atrophy. (1992) (38)
Drug treatment of juvenile dermatomyositis. (1983) (38)
Prenatal diagnosis in congenital muscular dystrophy (1995) (37)
Respiratory muscle training in Duchenne muscular dystrophy. (1989) (37)
Central core disease of muscle with focal wasting. (1965) (37)
Cardiac transplantation in Becker muscular dystrophy (1992) (37)
Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy. (1997) (36)
Diagnostic needle muscle biopsy. A practical and reliable alternative to open biopsy. (1984) (35)
Definition of pathological changes seen in muscle biopsies (2007) (35)
The abnormal expression of utrophin in Duchenne and Becker muscular dystrophy is age related (1997) (35)
Cerebral ventricular dilation in congenital myotonic dystrophy. (1987) (35)
INVOLVEMENT OF THE NERVOUS SYSTEM IN MUSCULAR DYSTROPHIES IN MAN (1979) (34)
Monoclonal antibodies detect a spectrin-like protein in normal and dystrophic human skeletal muscle. (1984) (34)
The muscular dystrophies. (1992) (34)
Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2. (1995) (33)
Chronic graft versus host disease presenting with polymyositis. (1983) (33)
Early onset autosomal dominant myopathy with rigidity of the spine: a possible role for laminin β1? (1997) (33)
Needle muscle biopsy for carrier detection in Duchenne muscular dystrophy Part. 1. Light microscopy — Histology, histochemistry and quantitation (1981) (33)
Histochemical studies on normal and diseased human and chick muscle in tissue culture. (1972) (33)
The role of Coxsackie B viruses in the pathogenesis of myocarditis, dilated cardiomyopathy and inflammatory muscle disease. (1987) (32)
Mutations in the laminin alpha2-chain gene in two children with early-onset muscular dystrophy. (2000) (32)
Prolongation of ambulation in Duchenne muscular dystrophy by appropriate orthoses. (1982) (32)
Expression of laminin chains in skin in merosin-deficient congenital muscular dystrophy. (1997) (32)
Duchenne's Muscular Dystrophy and the Xg Blood Groups: a Search for Linkage (1965) (31)
Postnatal maturation of peripheral nerves in preterm and full-term infants. (1971) (31)
Fetal Movements in Utero (1977) (31)
75th European Neuromuscular Centre International Workshop: 2nd Workshop on the Treatment of Muscular Dystrophy 10–12 December, 1999, Naarden, The Netherlands (2000) (31)
Developing and Diseased Muscle. A Histochemical Study (1968) (30)
Manifesting carriers of Xp21 muscular dystrophy; Lack of correlation between dystrophin expression and clinical weakness (1993) (30)
Cognitive abilities in children with congenital muscular dystrophy: correlation with brain MRI and merosin status (1999) (30)
Nocturnal hypoventilation in children with nonprogressive neuromuscular disease. (1989) (30)
Clinical spectrum and diagnostic difficulties of infantile ponto-cerebellar hypoplasia type 1. (1999) (29)
The Procedure of Muscle Biopsy (2020) (29)
Visual function in the newborn: A study of preterm and full-term infants (1980) (29)
Therapeutic trial of isaxonine in duchenne muscular dystrophy (1988) (29)
Polymyositis—an immunofluorescence study on the distribution of collagen types (1980) (29)
Expression of utrophin (dystrophin–related protein) during regeneration and maturation of skeletal muscle in canine X–linked muscular dystrophy (1994) (29)
Spinal muscular atrophy in childhood (1973) (28)
The Neurological Assessment of the Preterm & Full-Term Newborn Infant (1999) (28)
Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophy (1995) (28)
The Duchenne Dystrophy Story: From Phenotype to Gene and Potential Treatment (1989) (28)
Enzyme histochemistry of skeletal muscle. 3. Neurogenic muscular atrophies. (1966) (28)
DIFFERENTIATION OF DISEASED HUMAN MUSCLE IN CULTURE (1969) (28)
An early onset muscular dystrophy with diaphragmatic involvement, early respiratory failure and secondary alpha2 laminin deficiency unlinked to the LAMA2 locus on 6q22. (1998) (28)
Expression of dystrophin-associated glycoproteins and utrophin in carriers of Duchenne muscular dystrophy (1994) (27)
ORIGINAL ARTICLESINFLUENZAL ENCEPHALITIS (1958) (27)
Lobulated fibers in neuromuscular diseases (1985) (27)
The muscular dystrophies--clarity or chaos? (1997) (27)
Olivopontocerebellar hypoplasia with anterior horn cell involvement (SMA) does not localize to chromosome 5q (1995) (27)
Characterisation of novel point mutations in the survival motor neuron gene SMN, in three patients with SMA (2001) (27)
Neuromuscular disorders in childhood. Old dogmas, new concepts. (1975) (27)
Enzyme Histochemistry of Developing Human Muscle (1966) (26)
Growth of diseased human muscle in combined cultures with normal mouse embryonic spinal cord (1975) (26)
Myopathic Changes in Muscular Dystrophy Carriers (1963) (25)
UNEXPLAINED INHERITANCE OF THE XG GROUPS IN TWO FAMILIES. (1964) (25)
Large in-frame deletions of the rod-shaped domain of the dystrophin gene resulting in severe phenotype. (2003) (25)
Maternal mosaicism for a second mutational event in a type I spinal muscular atrophy family. (1998) (25)
Reversible changes in cerebral activity associated with acidosis in preterm neonates (1994) (25)
Early onset, autosomal recessive muscular dystrophy with Emergy-Dreifuss phenotype and normal emerin expression (1998) (24)
The female carrier of Duchenne muscular dystrophy. (1982) (24)
Brain magnetic resonance imaging abnormalities in merosin-positive congenital muscular dystrophy. (2000) (24)
Altered binding of Ricinus communis I lectin by muscle membranes in Duchenne muscular dystrophy (1984) (23)
Cytochemical studies of lectin binding by diseased human muscle (1982) (23)
A Colour Atlas of Muscle Disorders in Childhood (1988) (23)
Infantile muscular atrophy--a broad spectrum. (1967) (22)
Recent advances in neuromuscular disorders. (1971) (22)
Quantitative electromyography: carrier detection in Duchenne type muscular dystrophy using a new automatic technique (1972) (22)
The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy. (1987) (22)
Use of nerve conduction velocity to determine gestational age in infants at risk and in very-low-birth-weight infants. (1983) (22)
Prenatal diagnosis in merosin-deficient congenital muscular dystrophy (1997) (22)
Deficiency of the 50 kDa dystrophin-associated glycoprotein and abnormal expression of utrophin in two South Asian cousins with variable expression of severe childhood autosomal recessive muscular dystrophy (1994) (21)
High resolution magnetic resonance imaging of the brain in the dy/dy mouse with merosin-deficient congenital muscular dystrophy (2000) (21)
5‐Hydroxyindoles in the Cerebrospinal Fluid of Infants with Down's Syndrome and Muscle Hypotonia (1969) (21)
Enigmatic conflict of clinical and molecular diagnosis in Duchenne/Becker muscular dystrophy (2006) (21)
Lectin binding in human skeletal muscle: a comparison of 15 different lectins (2005) (21)
Minor neurological and perceptuo-motor deficits in children with congenital muscular dystrophy: correlation with brain MRI changes. (1995) (20)
Fifty year follow-up of a patient with central core disease shows slow but definite progression (1998) (20)
Analysis of skin fibroblast proteins in Duchenne muscular dystrophy: 2. Isoelectric focusing under dissociating conditions (1982) (20)
CHROMOSOME 15 IN PRADER‐WILLI SYNDROME (1985) (20)
Myonuclear calcium in carriers of Duchenne muscular dystrophy An X-ray microanalysis study (1979) (20)
The screening of Duchenne muscular dystrophy patients for submicroscopic deletions. (1986) (20)
The role of immunocytochemistry and linkage analysis in the prenatal diagnosis of merosin-deficient congenital muscular dystrophy (1997) (20)
Assessment of Gestational Age in Newborn Infants: Nerve Conduction Velocity versus Maturity Score (1972) (19)
Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle muscular dystrophy. (1996) (19)
Tests of skeletal muscle function in children. (1978) (19)
C-reactive protein in childhood dermatomyositis (1982) (18)
Slow Nerve Conduction Velocity in Cretins (1971) (18)
Juvenile dermatomyositis: serial studies of circulating autoantibodies to a 56kD nuclear protein. (1994) (18)
The “New” Myopathies (1969) (18)
The history of a genetic disease: Duchenne muscular dystrophy or Meryon's disease (1996) (18)
Therapeutic possibilities in muscular dystrophy: the hope versus the hype (2002) (18)
5‐Hydroxyindoles in Hydrocephalus. A Comparative Study of Cerebrospinal Fluid and Blood Levels (1970) (18)
BENIGN INFANTILE SPINAL MUSCULAR ATROPHY (1974) (18)
LYMPHOCYTE CAPPING IN DUCHENNE MUSCULAR DYSTROPHY (1979) (18)
Auditory brainstem responses in neurologically abnormal infants. (1983) (18)
In vivo sodium channel structure/function studies: consecutive Arg1448 changes to Cys, His, and Pro at the extracellular surface of IVS4. (1995) (18)
Analysis of skin fibroblast proteins in Duchenne muscular dystrophy: 1. Sodium dodecyl sulphate polyacrylamide gel electrophoresis (1982) (18)
C4 complement allotypes in juvenile dermatomyositis. (1988) (18)
Expression of HLA Class I Antigens in Skeletal Muscle Is a Diagnostic Marker in Juvenile Dermatomyositis (1997) (18)
Changes in center of gravity in boys with duchenne muscular dystrophy (1988) (18)
Binding of Ricinus communis I lectin to the muscle cell plasma membrane in diseased muscle (1984) (17)
Muscle biopsy--technical and diagnostic aspects. (1974) (17)
Linkage studies in Duchenne and Becker muscular dystrophies. (1986) (17)
A NEW SYSTEM FOR COTSIDE DISPLAY AND ANALYSIS OF THE PRETERM NEONATAL ELECTROENCEPHALOGRAM (1991) (17)
Ultrastructure of muscle in infantile spinal muscular atrophy. (1971) (17)
What Is Muscular Dystrophy? Forty Years of Progressive Ignorance (2000) (17)
Renal haemodynamics of cyclosporin A nephrotoxicity in children with juvenile dermatomyositis. (1991) (17)
VIRILISATION AND MALFORMATION OF A FEMALE INFANT (1962) (16)
Acute Dermatomyositis Presenting with Pulmonary Manifestations (1964) (16)
The application of direct tissue isoelectric focusing to the study of human skeletal muscle (1981) (16)
Erythrocyte-ghost Ca2+-stimulated Mg2+-dependent adenosine triphosphatase in Duchenne muscular dystrophy. (1982) (16)
Improvements of isoelectric focusing in agarose for direct tissue isoelectric focusing (1982) (16)
Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele. (1995) (16)
Comprar Muscle Biopsy: A Practical Approach, 4th Edition | Caroline A. Sewry | 9780702043406 | Saunders (2013) (16)
X;autosome translocations in females with Duchenne or Becker muscular dystrophy (1986) (16)
Duchenne muscular dystrophy presenting with failure to thrive. (1995) (16)
A Syndrome of Benign Congenital Hypotonia, Gross Obesity, Delayed Intellectual Development, Retarded Bone Age, and Unusual Facies (1967) (16)
Experimental regeneration in canine muscular dystrophy—2. Expression of myosin heavy chain isoforms (1994) (16)
Experimental regeneration in canine muscular dystrophy—1. Immunocytochemical evaluation of dystrophin and β-spectrin expression (1992) (15)
An Unusual Case of Neonatal Myasthenia (1987) (15)
Identification of regenerated dystrophic minced muscle transplanted in normal mice (1975) (15)
Evaluation and Differential Diagnosis of the Hypotonic Infant (1985) (15)
Congenital muscular dystrophy: An expanding clinical syndrome (2000) (15)
DNA deletions in mild and severe Becker muscular dystrophy (1987) (15)
The Floppy Infant—A Practical Approach to Classification (1968) (15)
Gestational age of the newborn : a clinical manual (1977) (15)
Congenital Clubfoot with Central Core Disease of Muscle (1968) (15)
ABSENCE OF DYSTROPHIN IN BECKER MUSCULAR DYSTROPHY (1989) (15)
SERUM ENZYMES IN DIAGNOSIS OF TETANUS. (1964) (15)
Abnormal expression of utrophin in Duchenne and Becker muscular dystrophy is age related (1997) (15)
Activity of creatine kinase in sera from healthy women, carriers of Duchenne muscular dystrophy and cord blood, determined by the "European" recommended method with NAC-EDTA activation. (1981) (15)
Screening for Duchenne muscular dystrophy. (1976) (15)
Carrier detection in Duchenne muscular dystrophy. A comparative study of electron microscopy, light microscopy and serum enzymes. (1970) (15)
MUSCLE TRANSPLANTATION BETWEEN NORMAL AND DYSTROPHIC MICE. 1. HISTOLOGICAL STUDIES (1975) (15)
Characterisation of dystrophin in fetuses at risk for Duchenne muscular dystrophy (1992) (15)
PRENATAL DIAGNOSIS IN DUCHENNE MUSCULAR DYSTROPHY: SALVAGE OF NORMAL MALE FETUS (1978) (15)
A novel procedure for pattern analysis of features present on freeze-fractured plasma membranes. (1985) (14)
Correlation of single fibre EMG and muscle histochemistry using an open biopsy recording technique (1977) (14)
Distribution of dystrophin, nebulin and Ricinus communis I (RCA I)-binding glycoprotein in tissues of normal and mdx mice (1989) (14)
Sialic acid storage disease. (1990) (14)
Therapeutic efforts in Duchenne muscular dystrophy; the need for a common language between basic scientists and clinicians (2004) (14)
Late infantile metachromatic leucodystrophy. Effect of low vitamin A diet. (1971) (13)
Progressive Muscular Dystrophy (1964) (13)
Muscle transplantation and regeneration in the dystrophic hamster. Part 2. Histochemical studies. (1974) (13)
Early white matter changes on brain magnetic resonance imaging in a newborn affected by merosin-deficient congenital muscular dystrophy (2001) (13)
Characterization of genetic deletions in Becker muscular dystrophy using monoclonal antibodies against a deletion-prone region of dystrophin. (1995) (13)
Hereditary Proximal Spinal Muscular Atrophy (1966) (13)
Laminin alpha 2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy. (1998) (13)
Protein degradation in skin fibroblasts from patients with Duchenne muscular dystrophy. (1980) (12)
Muscle transplantation and regeneration in the dystrophic hamster. Part 1. Histological studies. (1974) (12)
Special Centennial Workshop – 101st ENMC International Workshop: Therapeutic Possibilities in Duchenne Muscular Dystrophy, 30th November–2nd December 2001, Naarden, The Netherlands (2002) (12)
Responses of diseased muscle to electrical and mechanical intervention. (1988) (12)
ALLOPURINOL IN DUCHENNE MUSCULAR DYSTROPHY (1977) (12)
DETECTING THE DUCHENNE CARRIER BY ULTRASOUND AND COMPUTERISED TOMOGRAPHY (1983) (12)
Autoradiographic studies of RNA and DNA synthesis during myogenesis in cultures of human, chick and rat muscle. (1972) (11)
Prevention of deformities. (1977) (11)
Dystrophin abnormalities in polymyositis and dermatomyositis (1991) (11)
Calmodulin‐binding profiles for nebulin and dystrophin in human skeletal muscle (1988) (11)
Auditory brain stem responses in infants with posthaemorrhagic ventricular dilatation. (1989) (11)
Muscular dystrophies and allied disorders I: Duchenne and Becker muscular dystrophy (2007) (10)
Neurological fragility in the newborn: Influence of medication in labour. (1975) (10)
Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? (2002) (10)
Congenital muscular dystrophy: the importance of early diagnosis and orthopaedic management in the long-term prognosis. (1979) (10)
Notechis scutatus venom increases the yield of proliferating muscle cells from biopsies of normal and dystrophic canine muscle—A possible source for myoblast transfer studies (1993) (10)
Current Concepts in Childhood Spinal Muscular Atrophy (1989) (10)
Concomitance of basophilia, ribonucleic acid and acid phosphatase activity in regenerating muscle fibres (1977) (10)
Assessment of gestational age. (1971) (10)
Lectin blotting of human muscle Identification of a high molecular weight glycoprotein which is absent or altered in Duchenne muscular dystrophy (1985) (10)
Molecular studies of spinal muscular atrophy (1991) (10)
A comparison of neurological function in growth-retarded and appropriate-sized full-term newborn infants in two ethnic groups. (1982) (10)
Deformities in Duchenne dystrophy (2010) (9)
Diaphragmatic spinal muscular atrophy with bulbar weakness. (2000) (9)
Cell surface abnormality in clones of skin fibroblasts from a carrier of Duchenne muscular dystrophy. (1985) (9)
Neonatal arthrogryposis and absent limb muscles: a muscle developmental gene defect? (2001) (9)
Muscular Dystrophy and Related Disorders (1965) (9)
Hypoxanthine‐guanine phosphoribosyltransferase activity of blood and muscle in duchenne dystrophy (1979) (9)
CARRIER DETECTION AND GENETIC COUNSELLING IN DUCHENNE DYSTROPHY (1975) (9)
Subcellular fractionation studies on hepatic tissue from a patient with Pompe's disease (type II glycogen-storage disease). (1980) (9)
Mental retardation, unusual facies, and abnormal nails associated with a group-G ring chromosome. A case report on two unrelated cases. (1971) (9)
Steroids in Duchenne dystrophy (2013) (9)
Illustrated Guide to Malformations of the Central Nervous System at Birth (1984) (9)
Rapid assessment of gestational age at birth. (1976) (9)
A de novo X;13 translocation with abnormal phenotype. (1986) (8)
Continuous muscle fibre activity (Isaacs' syndrome) in infancy: A report of two cases (1994) (8)
A comparative study of in vitro proliferative responses to mitogens and immunoglobulin production in patients with inflammatory muscle disease. (1989) (8)
Erythrocyte ghost Na+, K+-adenosine triphosphatase in Duchenne muscular dystrophy (1980) (8)
Myoblast transfer in muscular dystrophy: Panacea or pie in the sky? (1992) (8)
Isoenzyme studies in the identification of transplanted muscle in the mouse. (1974) (8)
A linkage study of Emery-Dreifuss muscular dystrophy (1986) (8)
Absence of alpha‐sarcoglycan and novel missense mutations in the alpha‐sarcoglycan gene in a young British girl with muscular dystrophy (1997) (8)
Management of children: pharmacological and physical. (1989) (8)
MUSCULAR DYSTROPHY — WHERE IS THE LESION? (1971) (8)
Nonprogressive Neurogenic Muscular Atrophy with ‘Voluntary Fasciculation’ (1964) (7)
Functional properties of muscles transplanted between normal and dystrophic mice (1976) (7)
Recent Advances in Neuromuscular Disorders in Childhood (1991) (7)
What's in a name? Muscular dystrophy revisited. (1998) (7)
Ultrasound Imaging in the Diagnosis of Muscle Disease (1981) (7)
REGENERATION AND INNERVATION OF NORMAL AND DYSTROPHIC MUSCLE CULTURED WITH NORMAL AND DYSTROPHIC SPINAL CORD (1975) (7)
Effects of Electrical Stimulation on Normal and Diseased Human Muscle (1986) (7)
The Value of Guided Needle Muscle Biopsy (1988) (7)
Analysis of neuromuscular disease. (1977) (7)
Duchenne muscular dystrophy: 45Ca exchange in cultured skin fibroblasts and the effect of calcium ionophore A23187. (1979) (7)
Linkage of emery-dreifuss muscular dystrophy to the red/green cone pigment (RGCP) genes, proximal to factor VIII (1992) (7)
Congenital symmetrical weakness of the upper limbs resembling brachial plexus palsy: A possible sequel of drug toxicity in first trimester of pregnancy? (1995) (7)
DNA DELETION IN BOY WITH BECKER MUSCULAR DYSTROPHY (1986) (7)
Current and future therapy in muscular dystrophy; need for a common language between basic scientists and clinicians. (2004) (6)
The Reflexes in Progressive Muscular Dystrophy (1964) (6)
Erythrocyte membrane studies in duchenne muscular dystrophy (1980) (6)
A simplified method of specimen preparation for X-ray microanalysis of muscle and blood cells (1975) (6)
Quantitative morphological studies on transplanted muscle in the hamster. (1974) (6)
BRAIN ULTRASOUND IN PRETERM INFANTS (1981) (6)
Increased calcium in dystrophic muscle. (1980) (6)
Needle biopsy of skeletal muscle. (1984) (6)
"Catch-up" growth in steroid dependent dermatomyositis treated with cyclosporin-A. (1992) (6)
A new muscle journal for the nineties (1991) (6)
NEUROLOGICAL ASSESSMENT OF THE NEWBORN INFANT (1982) (6)
Visual function in children with merosin-deficient and merosin-positive congenital muscular dystrophy. (1998) (6)
Duchenne muscular dystrophy: studies of cell motility in vitro. (1985) (5)
Analysis of Genetic Muscle Disorders by Two-Dimensional Electrophoresis (1985) (5)
MUSCLE TRANSPLANTATION BETWEEN NORMAL AND DYSTROPHIC MICE. 2. HISTOCHEMICAL STUDIES (1975) (5)
Ion channel disorders (2002) (5)
HYPERMETHIONINÆMIA IN ACUTE TYROSINOSIS (1966) (5)
Muscular dystrophies and allied disorders V: Facioscapulohumeral, myotonic and oculopharyngeal muscular dystrophy (2007) (5)
The role of histochemistry in muscle disease. (1970) (5)
Enzyme histochemistry of skeletal muscle Part III Neurogenic muscular atrophies (5)
Ocular Involvement in Juvenile Rheumatoid Arthritis (Still's Disease) (1964) (5)
227th ENMC International Workshop: Finalizing a plan to guarantee quality in translational research for neuromuscular diseases Heemskerk, Netherlands, 10–11 February 2017 (2017) (5)
Diagnostic criteria for neuromuscular disorders Edited by Alan E. H. Emery. Published 1994, European Neuromuscular Centre, Baarn, The Netherlands. ISBN 90 261 0719 6, 72 pp (1994) (4)
Clinical assessment newborn infant of gestational age in the (1970) (4)
Rotation-mediated aggregation of skin fibroblasts in dochenne muscular dystrophy Effects of monensin (1983) (4)
Infantile axonal neuropathy in two siblings (1994) (4)
No evidence of association between apolipoprotein E genotype and phenotypic severity in childhood onset proximal spinal muscular atrophy (1999) (4)
Analytical subcellular fractionation and enzymic analysis of dystrophic mouse skeletal muscle [proceedings]. (1978) (4)
A short history of the World Muscle Society (2005) (4)
Binding of Ricinus communis I lectin to developing dystrophic muscle in human fetus (1988) (4)
Progressive neurological disorder associated with obstructive jaundice and vitamin E deficiency. (1982) (4)
Studies of the extracellular matrix in diseased human muscle. (1984) (4)
5‐HFAA in Cerebrospinal Fluid (1970) (4)
Duchenne muscular dystrophy: early diagnosis, and screening. (1976) (4)
The protein defect in congenital muscular dystrophy. (1996) (4)
Third International Congress of Histochemistry and Cytochemistry (1968) (4)
Muscular dystrophies and allied disorders II: Limb-girdle muscular dystrophies (2007) (4)
ANALYSIS OF CULTURED SKIN FIBROBLASTS FROM PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY USING ELECTROPHORETIC TECHNIQUES (1981) (4)
Dermatoglyphics of leukaemic children. (1969) (3)
Morphological studies on transplanted muscle between normal and dystrophic animals. (1973) (3)
Comparison of γ-glutamyl transpeptidase activity in tissues of normal and dystrophic hamsters and mice (1977) (3)
Hypotonia in infancy. (1976) (3)
Refinement of the laminin a2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy (3)
Muscle biopsy: A modern approach (Major problems in neurology, vol. 2), by V. Dubowitz and M. H. Brooke, with a contribution by H. E. Neville, × +475 pages, 677 illustrations, 5 tables, Saunders, London, 1973, £7.50 (1975) (3)
MOLECULAR ANALYSIS OF CHILDHOOD-ONSET SPINAL MUSCULAR-ATROPHY (1995) (3)
Becker muscular dystrophy: an unusual presentation. (1994) (3)
A Tribute and Toast on the Occasion of the Retirement of Professor Shaul Harel, MD (2010) (3)
Metabolic myopathies I: Glycogenoses (2007) (3)
Polyacrylamide-gel-electrophoretic analysis of cultured skin fibroblasts from patients with Duchenne muscular dystrophy. (1981) (3)
Utrophin euphoria (1997) (3)
Letter: Genetic miscounselling in muscular dystrophy. (1976) (3)
Treatment of muscular dystrophy (1963) (3)
Normal and diseased muscle in tissue culture. (1973) (3)
Asymmetrical Moro Response in Neurologically Normal Infants (1965) (3)
Metabolic myopathies II: Lipid related disorders and mitochondrial myopathies (2007) (3)
Regeneration of muscles transplanted between normal and dystrophic mice: a quantitative study of early transplants. (1977) (3)
Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy? (1999) (3)
Transferring myoblasts in Duchenne dystrophy. (1992) (3)
Dystrophin and Duchenne dystrophy (2015) (3)
Some Clinical Observations on Childhood Muscular Dystrophy (1963) (3)
New developments in congenital muscular dystrophy (1996) (3)
Investigation of Neuromuscular Disorders (1983) (3)
Effect of pentobarbitone sodium on serum creatine kinase of normal and dystrophic hamsters. (1977) (2)
Spinal Muscular Atrophy Revisited (2019) (2)
Dystrophia myotonica in infancy and childhood. (1972) (2)
Unnatural natural history of Duchenne muscular dystrophy (2015) (2)
214th ENMC International Workshop: Establishing an international consortium for gene discovery and clinical research for Congenital Muscle Disease, Heemskerk, the Netherlands, 6–18 October 2015 (2019) (2)
Hypoxanthine--guanine phosphoribosyltransferase activity in blood and skeletal muscles of normal and dystrophic mice. (1978) (2)
Muscle cramps and coffee (2011) (2)
Histochemical Techniques in the Analysis of Neuromuscular Disease — Some Recent Trends (1975) (2)
Tissue Culture in the Study of Neuromuscular Diseases (1977) (2)
Proceedings: Genetics of wheezy children assessed by exercise-induced bronchial lability. (1974) (2)
The History of a Genetic Disease: Duchenne Muscular Dystrophy or Meryon's Disease (1995) (2)
Duchenne muscular dystrophy: Ringo to the rescue? (2016) (2)
Neuromuscular disorders: Gene location (1991) (2)
Forty years of neuromuscular disease: a historical perspective. (1999) (2)
An epidemic of gastroenteritis due to an uncommon variant of Escherichia coli 0.128 (1962) (2)
Commentary from the Editor (2007) (2)
Enzymehistochemistry ofskeletal muscle (1965) (2)
Letter 7 (2010) (2)
Acute Monocytic Leukaemia with Response to Methotrexate (1964) (2)
Ramblings of a Peripatetic Paediatrician (2005) (2)
Hereditary Motor and Sensory Neuropathy Type I in Infancy and Childhood: A Clinical, Electrodiagnostic, Genetic and Muscle Biopsy Study (1979) (2)
Prognostic factors in dermatomyositis. (1984) (2)
Electron Microscopic X-Ray Analysis as a Potential Tool in the Localization and Quantitation of Intracellular Elements (1976) (2)
Neurological Assessment of the Newborn (1977) (2)
Muscular dystrophies and allied disorders III: Congenital muscular dystrophies (2007) (2)
The myopathies. (1960) (2)
Sixty Years of Spinal Muscular Atrophy: A Personal Odyssey (2017) (1)
Responses ofmuscles ofpatients withDuchenne muscular dystrophy tochronic electrical stimulation (1986) (1)
THE EFFECT OF INOTROPIC THERAPY ON THE VERY PRETERM NEONATAL ELECTROENCEPHALOGRAM (EEG) (1994) (1)
ASPECTS OF HIGH RESOLUTION TWO DIMENSIONAL GEL ELECTROPHORESIS : ATTEMPTS TO INCREASE RESOLUTION (1983) (1)
[Membrane changes in Duchenne/Becker muscular dystrophy: lectin binding and localization of dystrophin]. (1989) (1)
Management of muscular dystrophy in 1977. (1977) (1)
Myosin isoforms in congenital muscular dystrophy (1992) (1)
Early onset X-linked Emery-Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophy (1997) (1)
Commentary from the Editor (2008) (1)
Commentary from the Editor (2016) (1)
Two novel microsatellite markers for prenatal prediction of spinal muscular atrophy (SMA) (1993) (1)
Nemaline myopathy: A tale of two cultures (2009) (1)
DERMATOLOGICAL NON-DISEASE: A LOUSY DIAGNOSIS? (1981) (1)
Closed spinal dysraphism. (1998) (1)
Symposium on Muscular Dystrophy (1976) (1)
Very severe spinal muscular atrophy (SMA an expanding clinical phenotype type 0) (1999) (1)
HISTOLOGICAL CHANGES IN MUSCULAR-DYSTROPHY CARRIERS (1963) (1)
Comprar Neurological Assessment of the Preterm and Fullterm Newborn Infant | Dorian J. Pritchard | 9781898683155 | Wiley (2007) (1)
NERVE CONDUCTION VELOCITIES IN PREMATURE AND FULL‐TERM INFANTS (1965) (1)
Effect of Nasal Ventilation on Nocturnal Hypoxia in Neuromuscular Patients (1991) (1)
Erythrocyte membrane (Ca2+ + Mg2+)-activated adenosine triphosphatase in Duchenne muscular dystrophy (1981) (1)
Management of Meningitis (1964) (1)
A new journal in paediatric neurology for the next millennium (1997) (1)
An Introduction to Paediatric Neurology (1982) (1)
Fasciculation of the eyelids: an additional clue to clinical diagnosis in spinal muscular atrophy. (1984) (1)
Ultrasound imaging in of muscle disease the diagnosis (1982) (1)
Growth of human muscle in tissue culture (1976) (1)
Neurological assessment of gestational age in newborn. (1969) (1)
DERMATOGLYPHICS OF LEUKÆMIC CHILDREN (1969) (1)
Neuromuscular Disorders at 30 (2020) (1)
Fools rush in where angels fear to tread (2021) (1)
Clinical myology at the crossroads; the gospel truth (2010) (1)
Letters to the editor (1984) (1)
QUANTITATIVE STUDIES OF MUSCLES TRANSPLANTED BETWEEN NORMAL AND DYSTROPHIC MICE (1976) (1)
Treatment ofdermatomyositis inchildhood (1976) (1)
ISOENZYME STUDIES I N THE IDENTIFICATION OF TRANSPLANTED MUSCLE I N THE MOUSE (2012) (0)
Clinical presentation in merosin-positive congenital muscular dystrophy (1997) (0)
Diagnostic advances in neuromuscular disorders. (1972) (0)
Welcome to the World Muscle Society Congress in Brighton (2015) (0)
Response (2013) (0)
A family with a dystrophin gene mutation specifically affecting dystrophin expression in the heart (1994) (0)
Effects ofpostureandspinal bracing on respiratory function inneuromuscular disease (2011) (0)
Binding of Five Lectins to the Muscle Cell Plasma Membrane in Duchenne Dystrophy (1988) (0)
Professor Dubowitz comments (1976) (0)
Lowserum thyroxine concentrations andneural maturation inpreterminfants (2011) (0)
Commentary from the Editor (2012) (0)
Neuromuscular Disorders Affecting the Lower Extremities (1992) (0)
Commentary (1985) (0)
How to Read a Biopsy (2020) (0)
Commentary from the editor (1996) (0)
Plasma Digoxin Concentration in Children with Heart Failure (1973) (0)
Current concerns in the therapy of neuromuscular disorders (2011) (0)
Commentary from the editor (1992) (0)
Erythrocyte membrane (Ca/+ + Mg/+)-activated adenosine triphosphatase in Duchenne muscular dystrophy. (1981) (0)
Parmyotonia Congenita : The R M 8 P Na ’ Channel Mutagon in Adult Human Skeletal Muscle (0)
Volume contentsVolume contents (2000) (0)
Letter to the editor (1976) (0)
Muscular dystrophy and other muscle disorders (1989) (0)
Commentary from the editor (1994) (0)
Becker muscular dystrophy . in families with Duchenne or analysis to genetic counselling The application of linkage (0)
Neonatal Anatomy (1973) (0)
X-ray microanalysis of mast cells in rat's muscle (1975) (0)
GENERAL DISCUSSION (1979) (0)
THERAPEUTIC INNOVATIONS IN THE NEUROMUSCULAR DISORDERS (2006) (0)
Anita Harding (1952 – 1995) (1995) (0)
Abstracts for the Jubilaeum Congresses (2000) (0)
Welcome to the World Muscle Society Congress in Granada (2016) (0)
352 Therapeutic possibilities in muscular dystrophies (1999) (0)
[Current status of research on muscular dystrophy]. (1979) (0)
Happy birthday, world muscle society (1996) (0)
Commentary from the Editor (2014) (0)
5-Hydroxyindoles in mongolism and hydrocephalus. (1969) (0)
Film review: The Dubowitz assessment of newborn gestational age (1978) (0)
Enzymehistochemistry ofskeletal muscle PartIIINeurogenic muscular atrophies (1966) (0)
Neuromuscular disorders: Gene location (1991) (0)
Ultrastructural Localisation Of Ricinus Communis-I Lectin To Skeletal Muscle From Foetuses At High Risk For Duchenne Muscular Dystrophy (1987) (0)
Genetic counselling (1992) (0)
Clinical Casebook (2006) (0)
The Incidence of Minor Retinal Abnormalities in Premature Infants and their Relationship to Retinopathy of Prematurity (1974) (0)
Muscular dystrophies and allied disorders IV: Emery–Dreifuss muscular dystrophies and Bethlem myopathy (2007) (0)
Richard H.T. Edwards PhD, FRCP (1939–2009) (2010) (0)
Neuromuscular disorders: Gene location (1991) (0)
The World Wide Web (WWW): For better or for worse (2019) (0)
Editorial comment (1997) (0)
The Journal: a crisis of space and time (2002) (0)
Nerve conduction velocity-an index of neurological maturity of the newborn. (1968) (0)
Commentary from the Editor (2018) (0)
EJPN 2001: Referees consultedEJPN 2001: Referees consulted (2002) (0)
Neuromuscular disorders: Gene location (1991) (0)
Sleep studies andsupportive ventilatory treatment inpatients withcongenital muscle disorders (1996) (0)
XII CONGRESS OF MEDITERRANEAN SOCIETY OF MYOLOGY Naples, Italy - May 18-20, 2015 Program (Summary) (2015) (0)
Sialic acidstorage disease (1989) (0)
Third International Congress of Histochemistry and Cytochemistry: August 18–22, 1968, New York, N.Y. (1968) (0)
ELECTROPHORETIC ANALYSIS OF TISSUES IN DUCHENNE MUSCULAR DYSTROPHY (1983) (0)
Drugtreatment ofjuvenile dermatomyositis (1983) (0)
Commentary from the Editor (2017) (0)
Commentary from the Editor (2005) (0)
Preface to the Fifth Edition (2021) (0)
Clinical andEEG response toanticonvulsants inneonatal seizures (1989) (0)
Myotonia Congenita with “Delayed Myotonia.” (1960) (0)
Selected proceedings of Strasbourg meeting (1993) (0)
Early diagnosis of muscular dystrophy. (1976) (0)
Subclinical cardiomyopathy in Becker muscular dystrophy Table S Echocardiographic values in patients with Becker muscular dystrophy and controls FS mVcFc (2004) (0)
EJPN 2000: Referees consulted (2001) (0)
An early-onset autosomal recessive muscular dystrophy with distal wasting and rigidity of the spine (1997) (0)
Commentary from the Editor (1977) (0)
Editorial board (1988) (0)
The clinical phenotype in congenital muscular dystrophy (1996) (0)
Myopathic changes inamuscular dystrophy carrier (1963) (0)
Classification of Neuromuscular Disorders (2020) (0)
Commentary from the Editor (2015) (0)
Editorial (1994) (0)
Sensory Ganglio-neuropathy in Infantile Spinal Muscular Atrophy (1982) (0)
Anepidemic ofgastroenteritis duetoan uncommon variant ofEscherichia coli 0.128 (1962) (0)
Collagen synthesis in Duchenne muscular dystrophy (1981) (0)
Letters to the editor (0)
Commentary from the Editor (2011) (0)
Dystrophic central core disease or muscular dystrophy with central cores? A possible new autosomal recessive disorder with central core disease (1997) (0)
Muscular dystrophy and other inherited diseases of skeletal muscle in animals, annals of the New York Academy of Sciences (Ed. J. B. Harris), 317: 1–716, published by the New York Academy of Sciences, New York, NY, 1979, US$ 80.00 (1981) (0)
Index of Keywords (2002) (0)
Letters to the editor (1982) (0)
Commentary from the Editor (2009) (0)
RESPIRATORY FUNCTION IN CHILDREN WITH NEUROMUSCULAR DISORDERS (1975) (0)
Key word indexKey word index (2001) (0)
Critical Review Ahead of Publication (2019) (0)
Neonatal Neurology edited by Mary Coleman, University Park Press, 1981. £41.95 (xv + 417 pages) ISBN 0 8391 1584 9 (1983) (0)
Editorial commentEditorial comment/Referees consulted (2000) (0)
Genedeletions inspinal muscular atrophy (2017) (0)
Commentary from the Editor (2019) (0)
New approaches to nerve and muscle disorders: Basic and applied contributions. Edited by A. D. Kidman, J. K. Tomkins, R. A. Westerman, 418 pp, excerpta medica, Amsterdam, The Netherlands, 1981. $63.75 (1982) (0)
Personal Point of View Steroids in Duchenne dystrophy (2013) (0)
298 Mutations in the lamin a2 chain gene in children with merosin-deficient CMD and cortical dysplasia (1999) (0)
Normal visual function in children with pure congenital muscular dystrophy (1997) (0)
Muscle Glycogenosis (1966) (0)
Commentary from the Editor (2020) (0)
Editorial comment/Referees consulted (2000) (0)
Clinical phenotype in limb girdle dystrophies with defects in α, β & γ sarcoglycans (1996) (0)
Forthcoming meetingsForthcoming meetings (2002) (0)
Mutations in the LAMA2 gene in patients with muscular dystrophy due to partial merosin deficiency (1997) (0)
Commentary from the editor (1995) (0)
DUBOWITZ : Muscular Dystrophy and Related Disorders clinical types (0)
Commentary from the Editor (2004) (0)
BOOK REVIEWS (1993) (0)
D N A deletions in mild and severe Becker muscular dystrophy (0)
Meryon's disease (1993) (0)
Neurobehavioural Teratology edited by Joseph Yanai, Elsevier Science Publishers BV, 1984. US$ 134.50/Dfl 350.00 (xxi + 454 pages) ISBN 0 444 80516 8 (1985) (0)
Neonatal neurology: Mary Coleman (ed.) University Park Press, Baltimore, MD, 1981, 400 pages, US-$65.00 (1982) (0)
Computerised neonatal EEG monitoring and analysis (1990) (0)
Commentary from the Editor (2013) (0)
Neuromuscular Disorders: Recent Advances and Special Emphasis on Spinal Deformities (1992) (0)
Refinement ofthelaminin a2chainlocus to humanchromosome 6q2insevereandmild merosin deficient congenital muscular dystrophy (2011) (0)
How primitive is the Moro reflex? (1997) (0)
Recent Advances in Neuromuscular Disorders ; Therapeutic Prospects for the Future (1999) (0)
Morphological studies on transplanted muscle between normal and dystrophic animals. (1973) (0)
Alan E H Emery and Marcia L H Emery, The history of a genetic disease: Duchenne muscular dystrophy or Meryon's disease , London, Royal Society of Medicine Press, 1995, pp. xvi, 248, illus., £20.00, $40.00 (1-85315-249-8). (1996) (0)
Commentary from the editor (1993) (0)
Veterinary Myology (2007) (0)
Commentary from the editor (1997) (0)
Paediatric Neurology (1985) (0)
Ultrasound Imaging and Needle Biopsy in Detecting Selective Pathology within the Quadriceps Muscles (1986) (0)
The myopathies. (1968) (0)
Genetic counselling. (1992) (0)
Multiple transcripts in the exons 47–53 region of the dystrophin gene: does this influence dystrophin expression in normal and dystrophic tissues? (1997) (0)
Neonatal Neurology (1981) (0)
A Modern Approach to Muscle Disease (1974) (0)
The Infant of Inappropriate Size (2008) (0)
Editorial board (1987) (0)
Muscle transplantation in normal and dystrophic animals. (1973) (0)
297 Early presentation of autosomal dominant Emery-Dreifuss muscular dystrophy (1999) (0)
A Study of Visual Function in the Newborn by the Brazelton Behavioural Scale and Fantz Box Method (1979) (0)
Erratum to “Clinical casebook: Enigmatic conflict of clinical and molecular diagnosis in Duchenne/Becker muscular dystrophy” [Neuromuscular Disorders 16 (2006) 813] (2007) (0)
Diagnostic mousetrap. (1977) (0)
World Muscle Society (WMS) (1996) (0)
Erythrocyte-ghost Ca 2 +-stimulated Mg 2 +-dependent adenosine triphosphatase in Duchenne muscular dystrophy (2005) (0)

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