Hans Zellweger

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Hans Zellweger is affiliated with the following schools: American University, American University of Beirut, University of Iowa, University of Pennsylvania

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Hans Zellweger

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Hans Zellweger's Degrees

Doctorate Medicine University of Pennsylvania

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According to Wikipedia, Hans Ulrich Zellweger was a Swiss-American pediatrician known for his research on Zellweger syndrome. Zellweger trained in Zurich, Hamburg, Rome and Berlin and received his doctorate in Zurich in 1934, where he worked until 1950. In the 1950s he was appointed Professor at the American University in Beirut and from 1959 until his retirement in 1977, he was Professor of Paediatrics at the University of Iowa. There he performed research on neuromuscular disorders and genetic diseases and is known for his research on Zellweger syndrome which is named after him.

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Hans Zellweger'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

A FAMILIAL SYNDROME OF MULTIPLE CONGENITAL DEFECTS. (1964) (226)
Newborn screening for Duchenne muscular dystrophy. (1975) (150)
ELECTRON MICROSCOPY OF TWO CEREBRAL, BIOPSIES IN GARGOYLISM (1965) (130)
Congenital nonprogressive myopathy (1965) (102)
Experimental myopathy after microarterial embolization; comparison with childhood x-linked pseudohypertrophic muscular dystrophy. (1970) (99)
Human cytogenetics, I. (1968) (98)
Mathematical Tables for Research Workers in Human Genetics (1962) (81)
Blood-serotonin deficiency in Down's syndrome. (1965) (80)
Cardiac Manifestations of the Mucopolysaccharidoses (1975) (74)
Ribosomal protein synthesis in Duchenne muscular dystrophy. (1971) (71)
Is lysergic-acid diethylamide a teratogen? (1967) (70)
The Cerebro‐Hepato‐Renal (Zellweger) Syndrome And Other Peroxisomal Disorders (1987) (68)
Myotonic Dystrophy and its Differential Diagnosis (1973) (61)
Muscular form of glycogenosis, type II (Pompe) (1967) (60)
Glycogenosis. IV. A new cause of infantile hypotonia. (1972) (57)
PARENTAL CONSANGUINITY IN PYCNODYSOSTOSIS (1976) (57)
Psychometric Studies in Muscular Dystrophy Type Ilia (Duchenne) (1967) (56)
Mucopolysaccharidosis VI (Maroteaux-Lamy's disease). (1970) (56)
Early Verbal Disability in Children with Duchenne Muscular Dystrophy (1978) (55)
Severe congenital muscular dystrophy. (1967) (55)
Satellite association and translocation mongolism. (1966) (50)
Myopathy in Marinesco-Sjogren syndrome. (1987) (49)
Type IV glycogenosis (amylopectinosis). Light and electron microscopic observations. (1970) (49)
Morquio-Ullrich's disease (1961) (44)
Central nervous system manifestations in childhood muscular dystrophy (CMD). I. Psychometric and electroencephalographic findings. (1965) (44)
A mild form of muscular glycogenosis in two brothers with alpha-1, 4-glucosidase deficiency. (1965) (41)
Glycogen disease of skeletal muscle; report of two cases and review of literature. (1955) (41)
FIBROBLAST CULTURES IN DUCHENNE MUSCULAR DYSTROPHY (1977) (41)
Centronuclear myopathy: disease entity or a syndrome? Light- and electron-microscopic study of two cases and review of the literature. (1972) (41)
Two cases of multiple malformations with an autosomal chromosomal aberration- partial trisomy D? (1962) (39)
Familial Occurrence of Ivemark Syndrome with Splenic Hypoplasia and Asplenia in Sibs (1973) (39)
A new approach for carrier detection in Duchenne muscular dystrophy (1971) (35)
Familial Prader-Willi syndrome with apparently normal chromosomes. (1987) (34)
Chromosomal mosaicism and mongolism. (1963) (33)
An unusual translocation in a case of Mongolism. (1963) (33)
Comparative studies of infants with mosaic and complete triploidy: an analysis of 55 cases. (1982) (32)
Pathology of muscular hypotonia in the Prader-Willi syndrome. Light and electron microscopic study. (1969) (31)
Increased collagen synthesis in arthrogryposis multiplex congenita. (1970) (30)
Frequency of cerebral infarction in patients with inherited neuromuscular diseases. (1987) (30)
Partial trisomy 14q -- and parental translocation of No. 14 chromosome. Report of a case and review of the literature. (1977) (29)
Lipid abnormalities in a variant of the Hurler syndrome. (1968) (28)
Benign Congenital Muscular Dystrophy (1967) (27)
Early onset of myotonic dystrophy in infants. (1973) (27)
Creatine phospholinase in normal neonates and young infants. (1971) (27)
FAMILIAL MOSAICISM ATTRIBUTABLE TO A NEW GENE. (1965) (24)
Prenatal determination of fetal sex and chromosomal complement. (1970) (24)
TRISOMY 18. REPORT OF A CASE AND DISCUSSION OF THE SYNDROME. (1964) (23)
The syndrome of the metacentric microchromosome. (1970) (23)
Congenital muscular dystrophy: light and electron microscopic observations. (1969) (23)
Letter: Parental consanguinity in pycnodysostosis. (1976) (22)
PROTEIN SYNTHESIS IN MUSCLE CULTURES FROM PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY (1976) (21)
FOUR COMMON EYE SIGNS IN MONGOLISM. (1965) (21)
Double trisomy and double trisomic mosaicism. (1967) (21)
Teratogenic effect of anticonvulsant drugs. (1976) (21)
A possible role for electron microscopy in detection of carriers of Duchenne type muscular dystrophy1 (1973) (21)
The cavum veli interpositi and its differentiation from cavum vergae. (1959) (20)
Ocular findings in Morquio-Ullrich's disease. With report of two cases. (1960) (20)
The role of collagen in the pathogenesis of idiopathic clubfoot. Biochemical and electron microscopic correlations. (1974) (20)
The Marshall syndrome: report of a new family. (1974) (20)
Anticonvulsants During Pregnancy: A Danger to the Developing Fetus? (1974) (20)
Is lysergide a teratogen? (1967) (19)
The Problem of Trisomy 22 (1976) (19)
Gargoylism and Morquio's disease. (1952) (18)
THE DIAGNOSTIC SIGNIFICANCE OF SERUM ENZYMES AND ELECTROCARDIOGRAM IN VARIOUS MUSCULAR DYSTROPHIES (1972) (17)
[The floppy infant syndrome]. (1972) (17)
CRI-DU-CHAT WITH CHROMOSOMAL MOSAICISM (1966) (17)
The floppy infant: a practical approach. (1983) (17)
Genetics in Neurology (1983) (17)
Spinal muscular atrophy with autosomal dominant inheritance (1972) (17)
Satellite association (SA) in familial mosaicism. (1966) (16)
Two cases of non-mongoloid trisomy G. (1962) (16)
PHOCOMELIA AND TRISOMY E. (1965) (16)
DUCHENNE MUSCULAR DYSTROPHY IN YOUNG GIRLS? (1974) (15)
FAMILIAL MOTOR NEURON DISEASE, NON‐CHAMORRO TYPE: REPORT OF KINSHIP (1971) (15)
[Glycogen storage disorders]. (1956) (15)
Differential Diagnosis in Prader-Willi Syndrome (1988) (15)
Trisomy 22. (1975) (14)
Congenital muscular hypertrophy (1959) (14)
[Mongolism--Down's syndrome]. (1965) (13)
FAMILIAL AGGREGATES OF THE 21‐TRISOMY SYNDROME * (1969) (13)
Observations on the electrocardiogram in Duchenne's progressive muscular dystrophy. (1971) (13)
The Marinesco-Sjögren syndrome described a quarter of a century before Marinesco. (1985) (12)
Effect of oral contraceptive pills on the level of creatine phosphokinase with regard to carrier detection in Duchenne muscular dystrophy. (1974) (12)
Muscular hypotonia in infancy; diagnosis and differentiation. (1962) (12)
Cleidocranial dysostosis with osteopetrosis. (1954) (12)
Chromosomes of Man (1959) (12)
Fibroblast cultures in Duchenne muscular dystrophy. Alterations in synthesis and secretion of collagen and noncollagen proteins. (1977) (11)
Genetic aspects of mental retardation. (1963) (10)
Utilization of capillary blood for serum enzyme analysis. (1970) (10)
Autosomal cytogenetics. (1961) (9)
Effect of coenzyme Q on serum levels of creatine phosphokinase in preclinical muscular dystrophy. (1974) (9)
The short arm deletion syndrome of chromosome 4 (4p- syndrome). (1975) (9)
The Prader-Willi syndrome. (1984) (8)
ATAXIA TELANGIECTASIA. REPORT OF TWO CASES. (1963) (8)
Can women with the Prader-Labhart-Willi syndrome (PLWS) reproduce? Does the deletion (15)(q 11-13) occur in individuals not affected with PLWS? (1988) (8)
Autosomal recessive generalized myotonia (1980) (8)
THE CHROMOSOMAL CONSTITUTION OF THE STURGE-WEBER SYNDROME (1961) (8)
Encephalopathy in Salmonella infections. (1960) (8)
Basic Science Review : Familial Mongolism (1964) (8)
Pertussis encephalopathy. (1959) (7)
FAMILIAL AGGREGATES OF THE 21‐TRISOMY SYNDROME * (1968) (7)
The floppy infant syndrome in muscular glycogenosis. (1972) (7)
Peroxisomes and peroxisomal disorders. (1988) (7)
Peroxisomopathies: New Developments (1989) (7)
[MODERN PROBLEMS OF MONGOLISM. MONGOLISM, PARAMONGOLISM AND MONGOLOID STIGMATIZATION IN THEIR CLINICAL AND CYTOGENETIC ASPECTS]. (1964) (7)
GENETIC ASPECTS OF ACHONDROPLASIA. (1965) (7)
Is routine prenatal karyotyping indicated in pregnancies of very young women? (1973) (7)
Hurler's disease in infancy and early childhood. (1957) (6)
FAMILIAL MONGOLISM AND EUGENIC COUNSELLING (1962) (6)
Malignant tumors in early life. (1955) (6)
Harriet Lane Handbook: A Manual for Pediatric House Officers, ed. 5, edited by Jerry A. Winkelstein, M.D. and Herbert M. Swick, M.D. Chicago: Year Book Medical Publishers (35 East Wacker Drive), 1969, 264 pp., $4.25 (1969) (5)
Letter: Screening of the newborn for duchenne muscular dystrophy. (1975) (5)
Hurler's disease and neurofibromatosis in a family. (1957) (5)
[Hodgkin's disease in children; a clinical study]. (1957) (5)
About a new gene as a cause of increased satellite association (1965) (5)
Muscle ribosomal protein synthesis in normal pregnancy: implication for carrier detection in Duchenne muscular dystrophy (1974) (5)
Morquio-Ullrich's disease. Report of 2 cases. (1961) (5)
Familial chromosomal aberrations. I. (1966) (4)
Fetal face syndrome with acral dysostosis. (1974) (4)
GENETIC ASPECTS OF NEUROLOGICAL DISEASE. (1965) (4)
NEWS IN CYTOGENETICS. (1963) (4)
Aminoaciduria and mental retardation. II. Phenylpyruvic oligophrenia, phenylketonuria (PKU). (1961) (4)
FAMILIAL MONGOLISM. HISTORY AND PRESENT STATUS. (1964) (4)
Is Down's syndrome a modern disease? (1968) (4)
New Tasks: Prevention of Handicap * : Presidential Address to the American Academy for Cerebral Palsy, 1975 (1976) (3)
Mongolism Preventable by Amniocentesis (1971) (3)
Biochemical abnormalities of muscle ribosomes during attacks of hyperkalemic periodic paralysis. (1973) (3)
Amino-aciduria and mental retardation. (1961) (3)
The Myth of Nonmongoloid Trisomy G (1981) (3)
Partial trisomy 14 q and parental translocation of No . 14 chromosome Report of a case and review of the literature (3)
Screening for Duchenne Muscular Dystrophy (1980) (3)
Protein synthesis in muscle cultures from patients with myotonic dystrophy. Influence of A23187 ionophore and calcium: preliminary investigation. (1977) (3)
AUTOSOMAL AND SEX CHROMOSOMAL ANEUPLOIDY: AN EXHIBIT. (1963) (3)
Familial chromosomal aberrations. II. (1966) (3)
[The nervous regulation of homeostasis and its pathology]. (1959) (2)
Prenatal genetics and cytogenetics. (1971) (2)
Newer aspects of mongolism. (1962) (2)
Secondary renal hyperchloremic acidosis complicated by impairment of other tubular functions. (1955) (2)
[A familial skeletal disorder with multilocular, aseptic bone necrosis, and with osteochondritis dissecans in particular]. (1951) (2)
Labial pits--cleft lip and-or palate syndrome. A report of five new families. (1970) (2)
CHROMOSOMAL ABERRATIONS AND THEIR SIGNIFICANCE FOR OPHTHALMO-OTORHINOLARYNGOLOGY. (1965) (2)
General aspects of muscular hypotonia. (1961) (2)
[Congenital Toxoplasma encephalitis and its differntial diagnosis]. (1960) (2)
Human cytogenetics II. (1968) (1)
The metacarpal index in spontaneous pneumothorax. (1982) (1)
[The floppy infant syndrome]. (1972) (1)
MODERN MEDICAL PROBLEMS (1975) (1)
[On the problem of convulsive disorders in child]. (1953) (1)
[Agenesis of the corpus callosum]. (1952) (1)
Familial congenital nonprogressive myopathy (1964) (1)
Genetic counseling in medical practice. I. (1969) (1)
[Duchenne's muscular dystrophy: also in girls?]. (1984) (1)
Modern trends in poliomyelitis with special consideration of the outbreak in Lebanon in 1952. (1953) (1)
Chromosomal aneuploidy, mosaicism and eugenics. (1969) (1)
[Electrocardiogram in poliomyelitis]. (1950) (1)
Trisomy 22. (1975) (1)
Smallpox vaccination and pregnancy. (1957) (1)
Enzyme deficiency diseases. I. Galactosemia. (1958) (1)
TERATOGENIC EFFECT OF ANTICONVULSANT DRUGS (1977) (1)
Clinical aspects of poliomyelitis. (1953) (1)
Sporadic Duchenne muscular dystrophy in females; genetic counseling of women with pelvifemoral muscular dystrophy. (1980) (1)
Partial trisomy 13: the myth of nonmongoloid trisomy G. (1981) (1)
Indications for chromosomal analysis in mongolism. (1966) (1)
Enzyme deficiency diseases. II. Phenylketonuria. (1958) (1)
Twenty years-iowa muscle clinic: Reminiscences and prospects (1982) (1)
[Penicillin therapy in scarlet fever]. (1950) (0)
Cleidocranial Dysostosis with Osteopetrosis (1954) (0)
[Not Available]. (1945) (0)
Il Mongolismo, Auxopatia, Somatopsichica, Cariotipica, by Enrico Aldeghi and Amelia Maderna, with the collaboration of Aureliano Rovescalli and Nardo Calvi. Torino, Italy: Edizioni Minerva Medica, 1968, 418 pp. (price approximately $18.00). In Italian (1969) (0)
Convulsions in childhood. (1958) (0)
Indications for chromosomal analysis in mongolism. (1966) (0)
[Infantile cortical hyperostosis and its differential diagnosis]. (1954) (0)
Down's Anomaly (1966) (0)
[Clinical aspects and pathogenesis of pertussis encephalopathy]. (1950) (0)
[Not Available]. (1946) (0)
[Narcolepsy and epilepsy; a case of narcolepsy with spikes and waves in the electroencephalogram]. (1956) (0)
A STUDY OF THE EARLY DEVELOPMENT OF MONGOLS, by Valerie A. Cowie, M.D., Ph.D., D.P.M.: New York: Pergamon Press, 1970, 109 pp., $8.00 (1970) (0)
[Critical study of biological tests in diagnosis of spasmophilic states in the child. Resistance test to induced hypercalcemia; Fünfgeld's test]. (1951) (0)
Book Review: Progress in Medical Genetics. Volume VIII (1973) (0)
Prenatal Genetics with Particular Reference to Neurological Disease (1974) (0)
[Heterogeneity of muscular dystrophy]. (1972) (0)
[Differential diagnosis of malignant lymphomas in childhood; a statistical-clinical study with case reports]. (1956) (0)
Letter to the Editor (1972) (0)
About different forms of childhood muscle hypotension. (1946) (0)
Epidemiology of Mental Retardation, by Rick Heber, Ph.D. Springfield, Illinois: Charles C Thomas, 1970, 119 pp., $8.75 (1971) (0)
[Williams syndrome]. (1986) (0)
Kohlenhydratstörungen im Kindesalter (Postgraduate Courses in Pediatrics) Vol. 19 (1967) (0)
Subject Index Vol. 16, 1977 (1977) (0)
Contributions to the Epidemiology of Anterior Poliomyelitis. (1942) (0)
[Disorders of the autonomic nervous system in poliomyelitis; disorders as a result of lesions in the autonomic centers of the brain stem]. (1950) (0)
[Not Available]. (1947) (0)
[Determination of mercury excretion in urine and its significance in diagnosis of acrodynia]. (1951) (0)
The essential muscle hypotension in degenerative children. (1946) (0)
Prenatal genetics. (1984) (0)
Chromosomal aberrations. (1961) (0)
[Not Available]. (1949) (0)
[Charcot-Marie-Tooth disease with early onset. Presentation of a family]. (1971) (0)
Aminoaciduria and mental retardation. I. (1961) (0)
Plasma androgen and cytogenetic studies of a patient with Morgagni's syndrome. (1971) (0)
The clinical diagnosis of inclusion body encephalitis (Dawson). (1958) (0)
On Type-Differentiation in Diphtheria. (1946) (0)
Intestinal parasitism in lebanon; a statistical analysis of 1000 children. (1955) (0)
STATE UNIVERSITY OF IOWA COLLEGE OF MEDICINE: CLINICAL PATHOLOGICAL CONFERENCE. (1963) (0)
Genetic counseling for Huntington's disease in Iowa. (1979) (0)
On a sporadic case of constitutional, infantile Panmyelopathy Fanconi. (1946) (0)
[Periodic hypopotassemic paralysis with hyperelectrolytemia in a case of dystrophia adiposogenitalis]. (1952) (0)
Citogenética Humana: Normal y Pathologia, by Salvator Armendares Sagrera. Mexico: Editorial Interamericana, S.A., 1968, 255 pp., no price given (1969) (0)
[Not Available]. (1946) (0)
Book Review: Advances in Human Genetics (1973) (0)
[Neurovegetative disorders in poliomyelitis; trophic disorders]. (1950) (0)
[On electrolyte regulation disorder in salmonellosis]. (1960) (0)
[Herter's infantilism and sprue; catamnestic study of 22 cases of celiac disease]. (1950) (0)
Mild Exanthematic Lymphocytic Meningitis in Zurich. (1948) (0)
[Not Available]. (1946) (0)
Down's Syndrome (Mongolism), Annals of the New York Academy of Sciences, vol. 171, article 2, edited by Virginia Apgar, M.D. New York: The National Foundation–March of Dimes, 1970, pp. 303–688, $24.50 (1971) (0)
[The assessment of the subarachnoid spaces in the encephalogram of infants]. (1949) (0)
[Critical study of biological and diagnostic tests in spasmophilic states in children. I. Induced calciuria]. (1951) (0)
Letters to the editor (1982) (0)
Problems of childhood tuberculosis. (1957) (0)
Trisomy 21 with borderline mental retardation. (1968) (0)
Partial trisomy 14q andparental translocation ofNo.14chromosome Report ofa caseandreview oftheliterature (1977) (0)
[Spasmophilic states of childhood]. (1951) (0)
Intestinal Bilharzia in Gabon due to Schistosoma intercalatum. (1940) (0)
[Not Available]. (1947) (0)
Genetic counseling in medical practice. II. (1969) (0)
[The intraventricular cistern and its clinical significance]. (1951) (0)
[On pseudohypoparathyroidism and hypoparathyroid cretinism]. (1951) (0)
[A case of craniostenosis with multiple epiphyseal abnormalities and luxations]. (1952) (0)
Congenital muscular dystrophy : light and electron microscopic observations RESULTS LIGHT MICROSCOPIC OBSERVATIONS (0)
Genetic Counselling, by Alan Carruth Stevenson and B. C. Davidson, with assistance from Michael W. Oakes. Philadelphia: J. B. Lippincott Company, 1970, 355 pp., no price given (1971) (0)
[Not Available]. (1948) (0)
[Periodic abdominal pain]. (1953) (0)
Re: Dermoid tumors (1963) (0)
[Prenatal sex determination and cytogenetics]. (1971) (0)
[Feer's disease and mercury]. (1950) (0)
Effect ofCoenzymeQ onSerumLevels ofCreatine Phosphokinase in Preclinical Muscular Dystrophy*t (treatment/bioenergetics) (1974) (0)
[Critical study of biological tests in diagnosis of spasmophilic states in the child. Induced hypocalcemia; Klotz and Barbier test]. (1951) (0)
[Not Available]. (1945) (0)
A quick review of prenatal screening for chromosomal abnormalities. (1976) (0)
[Antismallpox vaccination in pregnancy]. (1957) (0)
[Chronic hypocalcemia and tetany of cerebral origin]. (1953) (0)
[Not Available]. (1946) (0)
[Pathology of the septum pellucidum in the pneumoencephalogram]. (1952) (0)
On Anterior Poliomyelitis (in Switzerland) in 1944. (1945) (0)
Trisomy E-trisomy G mosaicism. A report of two cases. (1971) (0)
About bone changes in dystrophia musculorum progressiva. (1946) (0)
‘Modern Medical Problems’ (1976) (0)
Muscle disorders in childhood. Victor Dubowitz, 282 pp, illus, WB Saunders Co, Philadelphia, PA, 1978. $24.50 (1979) (0)
Down's syndrome and institutionalization. (1972) (0)
An abortive form of Pompe's disease (1965) (0)
Book Review: Perspectives in Cytogenetics. The Next Decade (1973) (0)
Prognosis of palsies from cranial nerve involvement in poliomyelitis. (1952) (0)
Congenital broncho-esophageal fistula in an adult. (1956) (0)
For the therapy of enterocolitis. (1946) (0)
[Not Available]. (1946) (0)
Myotonic dystrophy of the neonate-inheritance and environment. (1975) (0)
About polio and its treatment. (1947) (0)
[Cyclencephalia and congenital single lateral ventricle]. (1952) (0)
Letter: Marshall syndrome: eulogy or resurrection? (1975) (0)

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