H. Zellweger

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TRISOMY 18. REPORT OF A CASE AND DISCUSSION OF THE SYNDROME.

C. Hawtrey, H. Zellweger, K. Beck, 1964, Archives of internal medicine.

Newborn screening for Duchenne muscular dystrophy.

H. Zellweger, A. Antonik, Hans Zellweger, 1975, Pediatrics.

Teratogenic effect of anticonvulsant drugs.

V. Ionasescu, H. Zellweger, M. Waziri, 1976, American journal of diseases of children.

Magnetic resonance imaging of children with Duchenne muscular dystrophy

Wilbur L. Smith, J. Ehrhardt, E. Franken, 2006, Pediatric Radiology.

Familial Prader-Willi syndrome with apparently normal chromosomes.

D. Ledbetter, I. Hansmann, M. Lubinsky, 1987, American journal of medical genetics.

Cardiac Manifestations of the Mucopolysaccharidoses

R. Kerber, R. Schieken, H. Zellweger, 1975, Circulation.

Chromosomes of Man

H. Zellweger, J. Simpson, 1959 .

DETECTION of CARRIERS and GENETIC COUNSELING IN DUCHENNE MUSCULAR DYSTROPHY BY RIBOSOMAL PROTEIN SYNTHESIS

V. Ionasescu, H. Zellweger, L. Burmeister, 1976, Acta neurologica Scandinavica.

A possible role for electron microscopy in detection of carriers of Duchenne type muscular dystrophy1

A. Afifi, R. Bergman, H. Zellweger, 1973, Journal of neurology, neurosurgery, and psychiatry.

Twenty years-iowa muscle clinic: Reminiscences and prospects

V. Ionasescu, H. Zellweger, J. Simpson, 1982, European Journal of Pediatrics.

Experimental myopathy after microarterial embolization; comparison with childhood x-linked pseudohypertrophic muscular dystrophy.

W. Engel, H. Zellweger, P. Hathaway, 1970, Archives of neurology.

Congenital muscular dystrophy: light and electron microscopic observations.

A. Afifi, W. Mccormick, H. Zellweger, 1969, Journal of neurology, neurosurgery, and psychiatry.

Severe congenital muscular dystrophy.

A. Afifi, W. Mergner, W. Mccormick, 1967, American journal of diseases of children.

Benign Congenital Muscular Dystrophy

A. Afifi, W. Mergner, W. Mccormick, 1967, Clinical pediatrics.

Enzyme deficiency diseases. II. Phenylketonuria.

H. Zellweger, 1958, Journal of the American Dietetic Association.

New Tasks: Prevention of Handicap * : Presidential Address to the American Academy for Cerebral Palsy, 1975

H. Zellweger, Hans Zellweger, 1976, Developmental medicine and child neurology.

Effect of oral contraceptive pills on the level of creatine phosphokinase with regard to carrier detection in Duchenne muscular dystrophy.

M. K. Nielsen, H. Zellweger, L. Burmeister, 1974, Clinica chimica acta; international journal of clinical chemistry.

Screening for Duchenne Muscular Dystrophy

H. Zellweger, 1980, Developmental medicine and child neurology.

ELECTRON MICROSCOPY OF TWO CEREBRAL, BIOPSIES IN GARGOYLISM

R. Terry, H. Zellweger, F. Aleu, 1965, Journal of neuropathology and experimental neurology.

DUCHENNE MUSCULAR DYSTROPHY IN YOUNG GIRLS?

V. Ionasescu, H. Zellweger, 1974, Acta neurologica Scandinavica.

Prenatal Genetics with Particular Reference to Neurological Disease

H. Zellweger, 1974 .

THE DIAGNOSTIC SIGNIFICANCE OF SERUM ENZYMES AND ELECTROCARDIOGRAM IN VARIOUS MUSCULAR DYSTROPHIES

R. Durnin, H. Zellweger, J. Simpson, 1972, Acta neurologica Scandinavica.

General aspects of muscular hypotonia.

H. Zellweger, 1961, American journal of physical medicine.

Amino-aciduria and mental retardation.

H. Zellweger, 1961, Clinical chemistry.

Enzyme deficiency diseases. I. Galactosemia.

H. Zellweger, 1958, Journal of the American Dietetic Association.

Anticonvulsants During Pregnancy: A Danger to the Developing Fetus?

H. Zellweger, 1974, Clinical pediatrics.

Central nervous system manifestations in childhood muscular dystrophy (CMD). I. Psychometric and electroencephalographic findings.

E. Niedermeyer, H. Zellweger, 1965, Annales paediatrici. International review of pediatrics.

The short arm deletion syndrome of chromosome 4 (4p- syndrome).

J. Bardach, H. Zellweger, J. Bordwell, 1975, Archives of otolaryngology.

Blood-serotonin deficiency in Down's syndrome.

H. Zellweger, J. Tu, Hans Zellweger, 1965, Lancet.

Secondary renal hyperchloremic acidosis complicated by impairment of other tubular functions.

A. Acra, H. Zellweger, F. Farah, 1955, Helvetica paediatrica acta.

Encephalopathy in Salmonella infections.

H. Zellweger, H. Idriss, 1960, A.M.A. journal of diseases of children.

Peroxisomopathies: New Developments

H. Zellweger, 1989, Developmental medicine and child neurology.

Myotonic Dystrophy and its Differential Diagnosis

V. Ionasescu, H. Zellweger, 1973, Acta neurologica Scandinavica. Supplementum.

Ocular findings in Morquio-Ullrich's disease. With report of two cases.

G. V. von Noorden, I. Ponseti, H. Zellweger, 1960, Archives of ophthalmology.

Morquio-Ullrich's disease

I. Ponseti, V. Pedrini, H. Zellweger, 1961 .

The role of collagen in the pathogenesis of idiopathic clubfoot. Biochemical and electron microscopic correlations.

V. Ionasescu, I. Ponseti, H. Zellweger, 1974, Helvetica paediatrica acta.

Human cytogenetics, I.

H. Zellweger, 1968, Journal of the Iowa Medical Society.

Mathematical Tables for Research Workers in Human Genetics

H. Zellweger, 1962 .

Basic Science Review : Familial Mongolism

H. Zellweger, 1964 .

FAMILIAL MONGOLISM. HISTORY AND PRESENT STATUS.

H. Zellweger, 1964, Clinical pediatrics.

FAMILIAL MONGOLISM AND EUGENIC COUNSELLING

H. Zellweger, 1962 .

PHOCOMELIA AND TRISOMY E.

H. Zellweger, D. Huff, G. Abbo, 1965, Acta geneticae medicae et gemellologiae.

Genetic aspects of mental retardation.

H. Zellweger, 1963, Archives of internal medicine.

Chromosomal mosaicism and mongolism.

H. Zellweger, G. Abbo, 1963, Lancet.

An unusual translocation in a case of Mongolism.

H. Zellweger, K. Mikamo, G. Abbo, 1963, The Journal of pediatrics.

Partial trisomy 14q -- and parental translocation of No. 14 chromosome. Report of a case and review of the literature.

H. Zellweger, J. Simpson, 1977, Journal of medical genetics.

A FAMILIAL SYNDROME OF MULTIPLE CONGENITAL DEFECTS.

P. Bowen, H. Zellweger, R. Lindenberg, 1964, Bulletin of the Johns Hopkins Hospital.

The Cerebro‐Hepato‐Renal (Zellweger) Syndrome And Other Peroxisomal Disorders

H. Zellweger, H. Zellweger, 1987, Developmental medicine and child neurology.

Is lysergic-acid diethylamide a teratogen?

J. Mcdonald, H. Zellweger, G. Abbo, 1967, Lancet.

Comparative studies of infants with mosaic and complete triploidy: an analysis of 55 cases.

W. Blackburn, W. Wertelecki, H. Zellweger, 1982, Birth defects original article series.

Congenital nonprogressive myopathy

A. Afifi, H. Zellweger, James W. Smith, 1965, Neurology.

The Problem of Trisomy 22

V. Ionasescu, H. Zellweger, L. Burmeister, 1976, Clinical pediatrics.

Two cases of multiple malformations with an autosomal chromosomal aberration- partial trisomy D?

H. Zellweger, K. Mikamo, G. Abbo, 1962, Helvetica paediatrica acta.

Mucopolysaccharidosis VI (Maroteaux-Lamy's disease).

V. McKusick, H. Wiedemann, J. Spranger, 1970, Helvetica paediatrica acta.

Trisomy 22.

V. Ionasescu, H. Zellweger, J. Simpson, 1975, Journal de genetique humaine.

A case of trisomy 18 mosaicism with peculiar features

L. Pavone, H. Zellweger, G. Abbo, 2004, Humangenetik.

Malignant tumors in early life.

H. Zellweger, S. Firzli, F. Hamaoui, 1955, Le Journal medical libanais. The Lebanese medical journal.

FOUR COMMON EYE SIGNS IN MONGOLISM.

G. Solomons, H. Zellweger, P. G. Jahnke, 1965, American journal of diseases of children.

The syndrome of the metacentric microchromosome.

H. Zellweger, G. Abbo, 1970, Helvetica paediatrica acta.

Peroxisomes and peroxisomal disorders.

H. Zellweger, 1988, The Alabama journal of medical sciences.

GENETIC ASPECTS OF NEUROLOGICAL DISEASE.

H. Zellweger, 1965, Archives of internal medicine.

Ribosomal protein synthesis in Duchenne muscular dystrophy.

V. Ionasescu, H. Zellweger, T. Conway, 1971, Archives of biochemistry and biophysics.

A new approach for carrier detection in Duchenne muscular dystrophy

V. Ionasescu, H. Zellweger, T. Conway, 1971, Neurology.

FIBROBLAST CULTURES IN DUCHENNE MUSCULAR DYSTROPHY

V. Ionasescu, H. Zellweger, L. Burmeister, 1977 .

PROTEIN SYNTHESIS IN MUSCLE CULTURES FROM PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY

V. Ionasescu, P. Cancilla, H. Zellweger, 1976, Acta neurologica Scandinavica.

Muscle ribosomal protein synthesis in normal pregnancy: implication for carrier detection in Duchenne muscular dystrophy

V. Ionasescu, H. Zellweger, T. Conway, 1974, Journal of medical genetics.

Biochemical abnormalities of muscle ribosomes during attacks of hyperkalemic periodic paralysis.

V. Ionasescu, S. Schochet, H. Zellweger, 1973, Journal of the neurological sciences.

Increased collagen synthesis in arthrogryposis multiplex congenita.

L. Filer, V. Ionasescu, H. Zellweger, 1970, Archives of neurology.

Satellite association and translocation mongolism.

H. Zellweger, R. Cuany, G. Abbo, 1966, Journal of medical genetics.

Muscular form of glycogenosis, type II (Pompe)

A. Afifi, J. Smith, H. Zellweger, 1967, Neurology.

A mild form of muscular glycogenosis in two brothers with alpha-1, 4-glucosidase deficiency.

B. Brown, W. Mccormick, H. Zellweger, 1965, Annales paediatrici. International review of pediatrics.

Glycogen disease of skeletal muscle; report of two cases and review of literature.

H. Zellweger, A. Dark, G. Abu-Haidar, 1955, Pediatrics.

Glycogenosis. IV. A new cause of infantile hypotonia.

V. Ionasescu, W. Mccormick, S. Schochet, 1972, The Journal of pediatrics.

Centronuclear myopathy: disease entity or a syndrome? Light- and electron-microscopic study of two cases and review of the literature.

V. Ionasescu, W. Mccormick, S. Schochet, 1972, Journal of the neurological sciences.

[The floppy infant syndrome].

H. Zellweger, 1972, Pediatria Polska.

Early onset of myotonic dystrophy in infants.

V. Ionasescu, H. Zellweger, 1973, American journal of diseases of children.

Report of a new kindred

V. Ionasescu, W. Mccormick, H. Zellweger, 2006 .

Muscular hypotonia in infancy; diagnosis and differentiation.

J. Smith, H. Zellweger, M. Cusminsky, 1962, Revue canadienne de biologie.

Differential Diagnosis in Prader-Willi Syndrome

H. Zellweger, 1988 .

Familial Occurrence of Ivemark Syndrome with Splenic Hypoplasia and Asplenia in Sibs

H. Zellweger, J. Simpson, 1973, Journal of medical genetics.

Double trisomy and double trisomic mosaicism.

H. Zellweger, G. Abbo, 1967, American journal of diseases of children.

FAMILIAL MOTOR NEURON DISEASE, NON‐CHAMORRO TYPE: REPORT OF KINSHIP

H. Zellweger, J. Nelson, L. D. Amick, 1971, Acta neurologica Scandinavica.

Zellweger : Familial Aggregates of 2 1 Trisomy 787 rier

H. Zellweger, 2006 .

FAMILIAL AGGREGATES OF THE 21‐TRISOMY SYNDROME *

H. Zellweger, 1968 .

Lipid abnormalities in a variant of the Hurler syndrome.

J. A. Cifonelli, R. Matalon, H. Zellweger, 1968, Proceedings of the National Academy of Sciences of the United States of America.

Pathology of muscular hypotonia in the Prader-Willi syndrome. Light and electron microscopic study.

A. Afifi, H. Zellweger, 1969, Journal of the neurological sciences.

Gargoylism and Morquio's disease.

H. Zellweger, S. Firzli, L. Giaccai, 1952, A.M.A. American journal of diseases of children.

Morquio-Ullrich's disease. Report of 2 cases.

G. V. von Noorden, I. Ponseti, V. Pedrini, 1961, Jornal de Pediatria.

The cavum veli interpositi and its differentiation from cavum vergae.

H ZELLWEGER, E F VAN EPPS, H. Zellweger, 1959, The American journal of roentgenology, radium therapy, and nuclear medicine.

Cleidocranial Dysostosis with Osteopetrosis

H. Zellweger, L. Giaccai, M. Salaam, 1954 .

Prenatal determination of fetal sex and chromosomal complement.

H. Zellweger, G. Abbo, 1970, Lancet.

Early Verbal Disability in Children with Duchenne Muscular Dystrophy

N. Karagan, H. Zellweger, Hans Zellweger, 1978, Developmental medicine and child neurology.

Genetics in Neurology

V. Ionasescu, H. Zellweger, 1983 .

Is lysergide a teratogen?

J. Mcdonald, H. Zellweger, G. Abbo, 1967, Lancet.

Psychometric Studies in Muscular Dystrophy Type Ilia (Duchenne)

J. Hanson, H. Zellweger, 1967, Developmental medicine and child neurology.

Myopathy in Marinesco-Sjogren syndrome.

F. Bastian, W. Wertelecki, H. Zellweger, 1987, European neurology.

Autosomal recessive generalized myotonia

R. Schieken, L. Pavone, V. Ionasescu, 1980, Muscle & nerve.

PARENTAL CONSANGUINITY IN PYCNODYSOSTOSIS

J. Seibert, H. Zellweger, M. Waziri, 1976, The Lancet.

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

H. Zellweger, 1969 .

Chromosomal aneuploidy, mosaicism and eugenics.

H. Zellweger, 1969, Acta geneticae medicae et gemellologiae.

CRI-DU-CHAT WITH CHROMOSOMAL MOSAICISM

H. Zellweger, 1966 .

[MODERN PROBLEMS OF MONGOLISM. MONGOLISM, PARAMONGOLISM AND MONGOLOID STIGMATIZATION IN THEIR CLINICAL AND CYTOGENETIC ASPECTS].

H. Zellweger, G. Abbo, 1964, Deutsche medizinische Wochenschrift.

Satellite association (SA) in familial mosaicism.

H. Zellweger, R. Cuany, G. Abbo, 1966, Helvetica paediatrica acta.

Familial chromosomal aberrations. II.

H. Zellweger, 1966, Annales paediatrici. International review of pediatrics.

The Myth of Nonmongoloid Trisomy G

S. Patil, H. Zellweger, 1981 .

Newer aspects of mongolism.

E. Witschi, H. Zellweger, K. Mikamo, 1962, Postgraduate medicine.

Lysergic acid diethylamide (LSD-25) and chromosome breaks

H. Zellweger, G. Abbo, A. Norris, 2004, Humangenetik.

[On the problem of convulsive disorders in child].

H. Zellweger, 1953, Deutsche medizinische Wochenschrift.

[Glycogen storage disorders].

H. Zellweger, 1956, Deutsche medizinische Wochenschrift.

Blepharo-cheilo-dontic (BCD) syndrome.

E. Zackai, M. Warburg, B. Prahl-Andersen, 2009, American journal of medical genetics.

Creatine phospholinase in normal neonates and young infants.

J. Bodensteiner, H. Zellweger, 1971, The Journal of laboratory and clinical medicine.

Effect of coenzyme Q on serum levels of creatine phosphokinase in preclinical muscular dystrophy.

G. Littarru, K. Folkers, R. Nakamura, 1974, Proceedings of the National Academy of Sciences of the United States of America.

Frequency of cerebral infarction in patients with inherited neuromuscular diseases.

H. Adams, J. Biller, V. Ionasescu, 1987, Stroke.

The Marshall syndrome: report of a new family.

J. Smith, H. Zellweger, P. Grützner, 1974, The Journal of pediatrics.

FAMILIAL AGGREGATES OF THE 21‐TRISOMY SYNDROME *

H. Zellweger, 1969 .

Spinal muscular atrophy with autosomal dominant inheritance

V. Ionasescu, W. Mccormick, H. Zellweger, 1972, Neurology.

Mosaic mongolism with normal chromosomal complement in the white blood cells

H. Zellweger, G. Abbo, M. Kay Nielsen, 2004, Humangenetik.

Leadership by Soft Skills

H. Zellweger, 2004 .

Can women with the Prader-Labhart-Willi syndrome (PLWS) reproduce? Does the deletion (15)(q 11-13) occur in individuals not affected with PLWS?

H. Zellweger, 1988, American journal of medical genetics.

Type IV glycogenosis (amylopectinosis). Light and electron microscopic observations.

W. Mccormick, S. Schochet, H. Zellweger, 1970, Archives of pathology.

Letter: Parental consanguinity in pycnodysostosis.

J. Seibert, H. Zellweger, M. Waziri, 1976, Lancet.

Labial pits--cleft lip and-or palate syndrome. A report of five new families.

H. Zellweger, F. Mcconnel, R. A. Lawrence, 1970, A M A Archives of Otolaryngology.

The Prader-Willi syndrome.

H. Zellweger, 1984, JAMA.

Autosomal cytogenetics.

H. Zellweger, K. Mikamo, 1961, Helvetica paediatrica acta.

Two cases of non-mongoloid trisomy G.

H. Zellweger, K. Mikamo, G. Abbo, 1962, Annales paediatrici. International review of pediatrics.

Smallpox vaccination and pregnancy.

H. Zellweger, 1957, Helvetica paediatrica acta.

FAMILIAL MOSAICISM ATTRIBUTABLE TO A NEW GENE.

H. Zellweger, G. Abbo, 1965, Lancet.

Is Down's syndrome a modern disease?

H. Zellweger, 1968, Lancet.

Utilization of capillary blood for serum enzyme analysis.

J. Bodensteiner, H. Zellweger, 1970, Helvetica paediatrica acta.