Stirling Carpenter
#137,582
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Stirling Carpentermedical Degrees
Medical
#2417
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#2841
Historical Rank
Neurology
#230
World Rank
#308
Historical Rank

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Why Is Stirling Carpenter Influential?
(Suggest an Edit or Addition)Stirling Carpenter's Published Works
Number of citations in a given year to any of this author's works
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
- Neurologic sequelae of domoic acid intoxication due to the ingestion of contaminated mussels. (1990) (523)
- Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy (1998) (479)
- Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage. (2012) (414)
- Proximal axonal enlargement in motor neuron disease (1968) (376)
- The syndrome of systemic carnitine deficiency (1975) (369)
- Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination (1996) (367)
- Expression of immunoreactive major histocompatibility complex products in human skeletal muscles (1988) (301)
- Progressive myoclonus epilepsies: specific causes and diagnosis. (1986) (295)
- Periventricular and subcortical nodular heterotopia. A study of 33 patients. (1995) (277)
- Pathology of Skeletal Muscle (1984) (256)
- Myopathy with thick filament (myosin) loss following prolonged paralysis with vecuronium during steroid treatment (1991) (246)
- Dystrophin is expressed in mdx skeletal muscle fibers after normal myoblast implantation. (1989) (233)
- Small‐caliber skeletal muscle fibers do not suffer necrosis in mdx mouse dystrophy (1988) (231)
- Inclusion body myositis (1978) (230)
- Dystrophin-deficient mdx muscle fibers are preferentially vulnerable to necrosis induced by experimental lengthening contractions (1990) (219)
- Duchenne muscular dystrophy: plasma membrane loss initiates muscle cell necrosis unless it is repaired. (1979) (216)
- ELECTRON MICROSCOPIC STUDIES ON THE VASCULAR PERMEABILITY AND THE MECHANISM OF DEMYELINATION IN EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS. (1965) (212)
- Kufs' disease: a critical reappraisal. (1988) (210)
- Temporal lobe epilepsy caused by domoic acid intoxication: Evidence for glutamate receptor–mediated excitotoxicity in humans (1995) (208)
- Myoclonus epilepsy and ragged-red fibres (MERRF). 1. A clinical, pathological, biochemical, magnetic resonance spectrographic and positron emission tomographic study. (1989) (196)
- Relationship between atrophy of the amygdala and ictal fear in temporal lobe epilepsy. (1994) (181)
- Subacute necrotizing encephalomyelopathy. A review and a study of two families. (1971) (178)
- The childhood type of dermatomyositis (1976) (176)
- Experimental ischemic myopathy. (1974) (171)
- Neurofibrillary axonal swellings and amyotrophic lateral sclerosis (1984) (165)
- Localization and Quantitation of the Chromosome 6-Encoded Dystrophin-Related Protein in Normal and Pathological Human Muscle (1993) (146)
- Small-caliber skeletal muscle fibers do not suffer deleterious consequences of dystrophic gene expression. (1986) (144)
- Mitochondrial dysfunction in multiple symmetrical lipomatosis (1991) (139)
- The Kearns-Shy syndrome. A multisystem disease with mitochondrial abnormality demonstrated in skeletal muscle and skin. (1973) (134)
- Creutzfeldt‐Jakob disease presenting as isolated aphasia (1989) (133)
- Experimental core-like lesions and nemaline rods. A correlative morphological and physiological study. (1972) (130)
- In vivo muscle magnetic resonance spectroscopy in the clinical investigation of mitochondria1 disease (1991) (129)
- Glucocorticoid excess induces preferential depletion of myosin in denervated skeletal muscle fibers (1987) (128)
- Sweat gland duct cells in Lafora disease (1981) (127)
- The ultrastructural characteristics of the abnormal cytosomes in Batten-Kufs' disease. (1977) (122)
- Specific involvement of muscle, nerve, and skin in late infantile and juvenile amaurotic idiocy (1972) (120)
- Cardiac myxoma (1976) (118)
- Chronic inflammatory demyelinating polyneuropathy (CIDP) in diabetics (1996) (118)
- Injury of neck as cause of vertebral artery thrombosis. (1961) (116)
- Loss and renewal of thick myofilaments in glucocorticoid‐treated rat soleus after denervation and reinnervation (1992) (115)
- Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis. (2013) (107)
- Late‐onset mitochondrial myopathy (1995) (103)
- Glycogen branching enzyme deficiency in adult polyglucosan body disease (1993) (100)
- Myopathy caused by a deficiency of Ca2+‐adenosine triphosphatase in sarcoplasmic reticulum (Brody's disease) (1986) (100)
- A new concept of childhood nemaline myopathy. (1971) (92)
- Giant axonal neuropathy. A clinically and morphologically distinct neurological disease. (1974) (89)
- Identification of retinoyl complexes as the autofluorescent component of the neuronal storage material in Batten disease (1977) (89)
- 'Onion bulb' formations in the central and peripheral nervous system in association with multiple sclerosis and hypertrophic polyneuropathy. (1977) (88)
- Lectin histochemistry of human skeletal muscle. (1981) (86)
- Action myoclonus-renal failure syndrome: characterization of a unique cerebro-renal disorder. (2004) (85)
- A pathologic basis for Kleine-Levin syndrome. (1982) (81)
- Combined central and peripheral myelinopathy (1987) (77)
- The neurotoxins 2,5‐hexanedione and acrylamide promote aggregation of intermediate filaments in cultured fibroblasts (1983) (77)
- Hereditary motor and sensory neuropathy with agenesis of the corpus callosum (2003) (76)
- Lafora disease. (2016) (72)
- Clinical spectrum of mitochondrial DNA mutation at base pair 8344 (1991) (67)
- Type I muscle fibre atrophy and central nuclei. A rare familial neuromuscular disease. (1970) (65)
- An ultrastructural study of an acute fatal case of the Guillain-Barré syndrome. (1972) (63)
- The adult form of acid maltase (α‐1,4‐glucosidase) deficiency (1977) (60)
- Lafora's disease (1974) (59)
- Time Course of Cerebral Blood Flow and Histological Outcome After Focal Cerebral Ischemia in Rats (1992) (58)
- A type of juvenile cerebromacular degeneration characterized by granular osmiophilic deposits. (1973) (58)
- Familial inclusion body myositis among Kurdish-Iranian Jews. (1991) (58)
- Diffuse craniospinal seeding from a benign fourth ventricle choroid plexus papilloma. Case report. (1998) (57)
- Familial infantile cerebellar atrophy associated with retinal degeneration. (1966) (54)
- Segmental Necrosis and Its Demarcation in Experimental Micropuncture Injury of Skeletal Muscle Fibers (1989) (54)
- Age-Related Conversion of Dystrophin-Negative to -Positive Fiber Segments of Skeletal but not Cardiac Muscle Fibers in Heterozygote mdx Mice (1990) (53)
- Pathology of the inflammatory myopathies. (1993) (52)
- Dystrophin is localized to the plasma membrane of human skeletal muscle fibers by electron‐microscopic cytochemical study (1990) (52)
- Necrosis of capillaries in denervation atrophy of human skeletal muscle (1982) (52)
- Conspicuous accumulation of a single-stranded DNA binding protein in skeletal muscle fibers in inclusion body myositis. (1994) (52)
- The motor unit profile of the rat soleus in experimental myopathy and reinnervation (1974) (52)
- Familial myopathy with changes resembling inclusion body myositis and periventricular leucoencephalopathy. A new syndrome. (1988) (52)
- The effect of muscle hyper- and hypoactivity upon fibre diameters of intact and regenerating nerves. (1973) (50)
- THE EFFECT OF VINCRISTINE ON SKELETAL MUSCLE IN THE RAT: A Correlative Histochemical, Ultrastructural and Chemical Study (1972) (49)
- Experimental mitochondrial myopathy produced by in vivo uncoupling of oxidative phosphorylation (1975) (47)
- Fatal infantile glycogen storage disease (1981) (46)
- SANDO: Two novel mutations in POLG1 gene (2006) (45)
- The clinical consequences of X-chromosome inactivation: Duchenne muscular dystrophy in one of monozygotic twins (1987) (45)
- Genetic locus heterogeneity in Lafora's progressive myoclonus epilepsy (1999) (41)
- Vacuolar myelopathy in transgenic mice expressing human immunodeficiency virus type 1 proteins under the regulation of the myelin basic protein gene promoter (1996) (40)
- The major inflammatory myopathies of unknown cause. (1981) (40)
- Hexosaminidase-A deficiency presenting as atypical juvenile-onset spinal muscular atrophy. (1985) (39)
- Juvenile dystonic lipidosis (1977) (39)
- Action myoclonus-renal failure syndrome: a previously unrecognized neurological disorder unmasked by advances in nephrology. (1986) (38)
- Progressive dystonia with bilateral putaminal hypodensities. (1987) (38)
- Infantile myotonic dystrophy (1973) (37)
- Glucocorticoids and immunosup pressants do not change the prevalence of necrosis and regeneration in mdx skeletal muscles (1991) (37)
- Adult onset motor neuronopathy in the juvenile type of hexosaminidase A and B deficiency (1988) (37)
- Morphological diagnosis and misdiagnosis in Batten-Kufs disease. (1988) (37)
- Major Alteration of the Pathological Phenotype in Gamma Irradiated mdx Soleus Muscles (1991) (36)
- Pathological involvement of primary sensory neurons in Werdnig-Hoffmann disease (1978) (36)
- Letter to the editor: Subtypes of the histochemical type I muscle fibers. (1975) (34)
- Virus‐like filaments and phospholipid accumulation in skeletal muscle (1970) (34)
- Metabolic and Histological Reversibility of Thiamine Deficiency (1983) (34)
- Inclusion Body Myositis, a Review (1996) (34)
- Simulation of Brain Death from Fulminant De-efferentation (2003) (34)
- Vacuolation of Muscle Fibers Near Sarcolemmal Breaks Represents T-Tubule Dilatation Secondary to Enhanced Sodium Pump Activity (1988) (33)
- Immunocytochemical studies of intermediate filament aggregates and their relationship to microtubules in cultured skin fibroblasts from patients with giant axonal neuropathy. (1983) (32)
- CENTRAL NERVOUS SYSTEM EFFECTS OF LASER RADIATION. (1965) (32)
- In vivo magnetic resonance spectroscopy of brain and muscle in a type of mitochondrial encephalomyopathy (MERRF) (1991) (32)
- Neurofilament subunit–related proteins in neuronal intranuclear inclusions (1984) (32)
- Kufs disease: clinical features and forms. (1988) (31)
- Neurological sequelae of domoic acid intoxication. (1990) (31)
- A peculiar polysaccharide accumulation in muscle in a case of cardioskeletal myopathy (1969) (30)
- Cylindrical spirals in human skeletal muscle (1979) (30)
- The Pathological Diagnosis of Specific Inflammatory Myopathies (1991) (29)
- Subacute skeletal myopathy induced by 2,4‐dichlorophenoxyacetate in rats and guinea pigs (1978) (29)
- Muscle pain associated with tubular aggregates and structures resembling cylindrical spirals (1989) (29)
- Prevention of skeletal muscle fiber necrosis in hamster dystrophy (1982) (28)
- Correlative multidisciplinary approach to the study of mitochondrial encephalomyopathies. (1991) (27)
- Three familial midline malformtion syndromes of the central nervous system: agenesis of the corpus callosum and anterior horn-cell disease; agenesis of cerebellar vermis; and atrophy of the cerebellar vermis. (1975) (25)
- Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs disease) (2016) (25)
- The Ramsay Hunt syndrome is no longer a useful diagnostic category (1989) (24)
- Congenital inflammatory myopathy (1990) (24)
- Hereditary sensory neuropathy (1985) (24)
- Hypophysectomy mitigates skeletal muscle fiber damage in hamster dystrophy (1985) (23)
- A hypothesis for the pathogenesis of amyotrophic lateral sclerosis. (1988) (23)
- The Newfoundland aggregate of neuronal ceroid-lipofuscinosis. (1988) (22)
- Rud syndrome: congenital ichthyosis, hypogonadism, mental retardation, retinitis pigmentosa and hypertrophic polyneuropathy. (1982) (21)
- Inhibition of myosatellite cell proliferation by gamma irradiation does not prevent the age-related increase of the number of dystrophin-positive fibers in soleus muscles of mdx female heterozygote mice. (1991) (21)
- Adult-onset leukodystrophy with axonal spheroids (2010) (21)
- Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features (2018) (20)
- New observations in reducing body myopathy (1985) (20)
- Metachromatic leukodystrophy: Multiple nonfunctional and pseudodeficiency alleles in a pedigree: Problems with diagnosis and counseling (1993) (20)
- Ultrastructural findings in lafora disease (1981) (20)
- Lysosomal storage in human skeletal muscle. (1986) (20)
- Syndrome of systemic carnitine deficiency: Clinical, morphologic, biochemical, and pathophysiologic features (2011) (20)
- Multiple peripheral nerve entrapments. An unusual phenotypical variant of the Hunter syndrome (mucopolysaccharidosis II) in a family. (1974) (20)
- Prenatal axonal dystrophy and osteopetrosis. (1973) (19)
- A histochemical study of oxidative enzymes in the nervous system of vitamin E‐deficient rats (1965) (19)
- Reserpine induced alteration of physiological properties and histochemical fiber types in rat skeletal muscle (1975) (18)
- Myopathy with trabecular muscle fibers (1999) (18)
- Skeletal Muscle Pathology (1984) (17)
- Sweat gland vacuoles in Unverricht‐Lundborg disease (1994) (16)
- Myopathy with hexagonally cross‐linked tubular arrays: A new autosomal dominant or sporadic congenital myopathy (1999) (16)
- An experimental morphometric study of neutral lipid accumulation in skeletal muscles (1981) (16)
- Reinnervation is followed by necrosis in previously denervated skeletal muscles of dystrophic hamsters (1983) (15)
- Histopathological evidence of Fabry disease in a female patient with left ventricular noncompaction. (2014) (15)
- Familial myopathy with conspicuous depletion of mitochondria in muscle fibers: a morphologically distinct disease (1995) (14)
- Mitochondrial Encephalomyopathies: A Solution to the Enigma of the Ramsay Hunt Syndrome (1987) (13)
- Cerebral Vein Thrombosis due to Hereditary Antithrombin III Deficiency (1993) (12)
- The human neuropathology of encephalopathic mussel toxin poisoning. (1990) (12)
- Progressive myoclonus epilepsy in young adults with neuropathologic features of Alzheimer's disease (1997) (11)
- Skin biopsy for diagnosis of hereditary neurologic metabolic disease. (1987) (11)
- Calcium paradox in skeletal muscles: Physiologic and microscopic observations (1986) (11)
- Antiepileptic drug myopathy (1994) (10)
- “Killer” cell activity in Duchenne muscular dystrophy (1986) (9)
- The Pathology of the Andermann Syndrome (1994) (8)
- Subacute enlarging cerebral hematoma from amyloid angiopathy: case report. (1995) (8)
- Morphological Diagnostic and Pathological Considerations (2011) (7)
- Atypical inclusion body progressive myoclonus epilepsy (1986) (6)
- 10 – Resin Histology and Electron Microscopy in Inflammatory Myopathies (1988) (6)
- The effects of muscle hyper- and hypoactivity upon fiber diameters of intact and regenerating nerves. (1973) (5)
- Primary Bilateral Thalamic Astrocytoma Presenting With Head Tremor, Ataxia, and Dementia (2010) (5)
- Familial multiple peripheral nerve entrapments--an unusual manifestation of a peripheral neuropathy. (1973) (5)
- Variant Creutzfeldt–Jakob disease: the first confirmed case from Portugal shows early onset, long duration and unusual pathology (2009) (5)
- A novel type of familial proximal axonal dystrophy: three cases and a review of the axonal dystrophies. (2012) (4)
- Type 2 GM1 gangliosidosis and neuronal ceroid lipofuscinosis (1982) (4)
- Calcium-induced damage of skeletal muscle fibers is markedly reduced by calcium channel blockers (2004) (4)
- ADULT POLYGLUCOSAN BODY AXONOPATHY - A DISTINCT CHRONIC NEUROLOGICAL DISEASE (1978) (4)
- Maturational arrest. (1976) (4)
- Effects of lidocaine on the lysosomes of cultured skin fibroblasts. (1982) (3)
- Muscle Biopsy for Diagnosis of Neuromuscular and Metabolic Diseases (2015) (3)
- Virus like filaments and phospholipid accumulations in a case of chronic myopathy. (1971) (3)
- Sporadic Creutzfeldt-Jakob Disease Causing a 2-Years Slowly Progressive Isolated Dementia (2009) (3)
- The motor unit profile in two experimental chronic myopathies (1975) (3)
- Regeneration of skeletal muscle fibers after necrosis. (1990) (2)
- PERIPHERAL NERVE PATHOLOGY IN THE SYNDROME OF AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY (1985) (2)
- Teaching NeuroImages: Neuropathy caused by Mycobacterium leprae (2011) (2)
- Granulomatous infectious disease in an immunosuppressed patient: a case report with radiological and pathological correlation. (2009) (2)
- A distinctive type of infantile inflammatory myopathy with abnormal myonuclei (1996) (2)
- Neuroaxonal dystrophy and osteopetrosis (1978) (2)
- Histopathological evidence of Fabry disease in a female patient with left ventricular noncompaction (2014) (2)
- The Ultrastructure of Demyelination in a Case of Acute Guillain-Barré Syndrome (1970) (2)
- A chronic myopathy with coated vesicles and tubular masses (1992) (2)
- Cortical Metabolic Dysfunction in a Mitochondrial Encephalomyopathy (MERRF) Demonstrated by Positron Emission Tomography (1987) (2)
- In Memoriam: Morrison H. Finlayson, M.B. Ch.B., F.R.C.P. (C) (1929-1982) (1983) (1)
- Retinitis pigmentosa in Lafora disease: Expanding findings of progressive myoclonic epilepsy (2016) (1)
- Letters to the editor (1991) (1)
- George Karpati O.C., C.Q., M.D., FRCPC, FRS (C) 1934–2009 (2009) (1)
- Variant Creutzfeldt-Jakob [corrected] disease: the second case in Portugal and in the same geographical region. (2008) (1)
- Case report SANDO: Two novel mutations in POLG1 gene (2006) (0)
- Jakob-Creutzfeldt Disease Presenting as Isolated Aphasia (1987) (0)
- Infantile neuroaxonal dystrophy with urinary oligosaccharide excretion not due to defective α-N- acetylgalactosaminidase activity (1994) (0)
- LUXOL FAST BLUE DISTINGUISHES LIPOFUSCIN FROM THE STORAGE DEPOSITS OF TYPICAL LATE INFANTILE AND JUVENILE BATTENʼS DISEASE: 260 (1990) (0)
- Mitochondrial myopathy in primary biliary cirrhosis an antibody mediated mitochondrial cytopathy (1988) (0)
- Expression of immunoreactive major histocompatibility complex determinants in normal and pathological human muscles (1987) (0)
- THE CURVILINEAR BODIES OF LATE INFANTILE BATTENʼS DISEASE-ISOLATION AND CHEMICAL AND ULTRASTRUCTURAL CHARACTERIZATION: 90 (1976) (0)
- Tracer and marker techniques in the microscopic study of skeletal muscles. (1981) (0)
- Late-onset seizures and dementia in MELAS syndrome (1992) (0)
- Experimental vincristine myopathy--a histochemical, ultrastructural and biochemical study. (1971) (0)
- [Myositis with inclusion bodies]. (1989) (0)
- Prominent T-Tubule Dilatation in Muscle Fibers Near Sarcolemmal Breaks: An In Vitro Model (1987) (0)
- 144. Lectin Cytochemistry of Spinal Cord and Roots. (1982) (0)
- 145 HOW NECROSIS IS DEMARCATED IN SKELETAL MUSCLE FIBERS AFTER EXPERIMENTAL MICROPUNCTURE INJURY (1984) (0)
- Central and peripheral demyelinization (1988) (0)
- Familial Adult-onset Motor Neuronopathy Due to a β-Locus Hexosaminidase Mutation (1987) (0)
- Familial Inclusion Body Myopathy with Periventricular Leukodystrophy: A Newly Recognized Syndrome (1987) (0)
- Focal myositis with neurogenic atrophy: A case report. (2018) (0)
- Nervous Tissue, Non-Neural Components of (2003) (0)
- Central nervous system Ä ^ effects of laser radiation 1 copy ~ WPW COPY DDC r ? f ^ r ? nnnr ? (0)
- Histology and histopathology of the nervous system. Edited by Webb Haymaker and Raymond Adams, 2 vol, 2,597 pp, illus, Charles C. Thomas, Springfield, Illinois, 1982. $295.00 (1983) (0)
- Unusual Evolution and Computerized Tomographic Appearance of a Gliosarcoma (1994) (0)
- Neuroaxonal dystrohpy and osteopetrosis. (1978) (0)
- Autosomal dominant Kufs` disease: Clinical heterogeneity in nine families, and exclusion of linkage to CLN1 and CLN3 markers in a large American kindred (1994) (0)
- What happens to capillaries in de nervated muscles (1980) (0)
- Expression of Immunoreactive Class 1 Major Histocompatibility Complex (MHC) Determinants in Pathologic Human Skeletal Muscle Fibers (1987) (0)
- Primary bilateral thalamic astrocytoma presenting with head tremor, ataxia, and dementia. (2010) (0)
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