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Ischemic thalamic infarction in children: clinical presentation, etiology, and outcome

Pediatric neurology, 1995-07, Vol.13 (1), p.46-49

1995

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Magnetic Resonance Brain Images in Schizophrenic and Normal Subjects: Influence of Diagnosis and Education

Schizophrenia bulletin, 1988, Vol.14 (1), p.21-37

1988

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Pelizaeus-Merzbacher Disease: Tight Linkage to Proteolipid Protein Gene Exon Variant

Proceedings of the National Academy of Sciences - PNAS, 1989-12, Vol.86 (23), p.9427-9430

1989

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Hypoxic-ischemic encephalopathy in areas of primary myelination: a neuroimaging and PET study

Pediatric neurology, 1996-02, Vol.14 (2), p.108-116

1996

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Megalencephaly: Types, clinical syndromes, and management

Pediatric Neurology, 1986-11, Vol.2 (6), p.321-328

DeMyer, William

1986

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Pointers and Pitfalls in the Neurologic Examination

Seminars in neurology, 1998, Vol.18 (2), p.161-168

DeMyer, William

1998

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Infantile Autism

Neurologic clinics, 1984-02, Vol.2 (1), p.139-153

1984

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From swelling to sclerosis: acute change in mesial hippocampus after prolonged febrile seizure

Seizure (London, England), 2003-06, Vol.12 (4), p.237-240

2003

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Vermian Hypoplasia and Arrested Cerebral Myelination in Two Sisters: Variant of Joubert's Syndrome or a New Syndrome?

Journal of child neurology, 2003-11, Vol.18 (11), p.755-762

2003

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Classification of cerebral malformations

Birth defects original article series, 1971-02, Vol.7 (1), p.78

DeMyer, W

1971

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Aberrant peripheral nerve fibres in the medulla oblongata of man

Journal of neurology, neurosurgery and psychiatry, 1965-04, Vol.28 (2), p.121-123

Demyer, William

1965

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A 46 CHROMOSOME CEBOCEPHALY, WITH REMARKS ON THE RELATION OF 13-15 TRISOMY TO HOLOPROSENCEPHALY (ARHINENCEPHALY)

Annales paediatrici. International review of pediatrics, 1964, Vol.203, p.169

DEMYER, W

1964

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Girl with signs of Pelizaeus-Merzbacher disease heterozygous for a mutation in exon 2 of the proteolipid protein gene

American journal of medical genetics, 1995-02, Vol.55 (4), p.397-401

1995

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THE FACE PREDICTS THE BRAIN: DIAGNOSTIC SIGNIFICANCE OF MEDIAN FACIAL ANOMALIES FOR HOLOPROSENCEPHALY (ARHINENCEPHALY)

Pediatrics (Evanston), 1964-08, Vol.34 (2), p.256-263

1964

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Clinical Findings in Pelizaeus-Merzbacher Disease

Journal of child neurology, 2004-05, Vol.19 (5), p.328-331

2004

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Development of axonal pathways after neurosurgical lesions in the septum of the fetal rat: fornix ventralis, commissure of the fornix ventralis, corpus callosum and anterior commissure

Research publications - Association for Research in Nervous and Mental Disease, 1973, Vol.51, p.269

DeMyer, W E

1973

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Usefulness of BAER studies in the early diagnosis of Pelizaeus-Merzbacher disease

Neurology, 1983-07, Vol.33 (7), p.955-955

1983

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Prognosis in autism: a follow-up study

Journal of Autism and Childhood Schizophrenia, 1973-07, Vol.3 (3), p.199-246

1973

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EEG ABNORMALITIES IN EARLY CHILDHOOD SCHIZOPHRENIA : A DOUBLE-BLIND STUDY OF PSYCHIATRICALLY DISTURBED AND NORMAL CHILDREN DURING PROMAZINE SEDATION

The American journal of psychiatry, 1964-04, Vol.120 (10), p.950-958

1964

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Roentogenology of the Brachmann-de Lange syndrome

Radiology, 1967-01, Vol.88 (1), p.101

1967

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Axoplasmic flow rates during nerve regeneration

Experimental neurology, 1960-12, Vol.2 (6), p.627-637

1960

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Imitation in autistic, early schizophrenic, and non-psychotic subnormal children

Journal of Autism and Childhood Schizophrenia, 1972-09, Vol.2 (3), p.264-287

1972

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The median cleft face syndrome. Differential diagnosis of cranium bifidum occultum, hypertelorism, and median cleft nose, lip, and palate

Neurology, 1967-10, Vol.17 (10), p.961-961

DeMyer, W

1967

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Peripheral motor and sensory neuropathy of early childhood, simulating Werdnig-Hoffmann disease

Neuropediatrics, 1976-05, Vol.7 (2), p.182-195

1976

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Alobar holoprosencephaly (arhinencephaly) with median cleft lip and palate: clinical, electroencephalographic and nosologic considerations

Confinia neurologica, 1963, Vol.23, p.1

1963

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Ischemic thalamic infarction in children: clinical presentation, etiology, and outcome

Magnetic Resonance Brain Images in Schizophrenic and Normal Subjects: Influence of Diagnosis and Education

Pelizaeus-Merzbacher Disease: Tight Linkage to Proteolipid Protein Gene Exon Variant

Hypoxic-ischemic encephalopathy in areas of primary myelination: a neuroimaging and PET study

Megalencephaly: Types, clinical syndromes, and management

Pointers and Pitfalls in the Neurologic Examination

Infantile Autism

From swelling to sclerosis: acute change in mesial hippocampus after prolonged febrile seizure

Vermian Hypoplasia and Arrested Cerebral Myelination in Two Sisters: Variant of Joubert's Syndrome or a New Syndrome?

Classification of cerebral malformations

Aberrant peripheral nerve fibres in the medulla oblongata of man

A 46 CHROMOSOME CEBOCEPHALY, WITH REMARKS ON THE RELATION OF 13-15 TRISOMY TO HOLOPROSENCEPHALY (ARHINENCEPHALY)

Girl with signs of Pelizaeus-Merzbacher disease heterozygous for a mutation in exon 2 of the proteolipid protein gene

THE FACE PREDICTS THE BRAIN: DIAGNOSTIC SIGNIFICANCE OF MEDIAN FACIAL ANOMALIES FOR HOLOPROSENCEPHALY (ARHINENCEPHALY)

Clinical Findings in Pelizaeus-Merzbacher Disease

Development of axonal pathways after neurosurgical lesions in the septum of the fetal rat: fornix ventralis, commissure of the fornix ventralis, corpus callosum and anterior commissure

Usefulness of BAER studies in the early diagnosis of Pelizaeus-Merzbacher disease

Prognosis in autism: a follow-up study

EEG ABNORMALITIES IN EARLY CHILDHOOD SCHIZOPHRENIA : A DOUBLE-BLIND STUDY OF PSYCHIATRICALLY DISTURBED AND NORMAL CHILDREN DURING PROMAZINE SEDATION

Roentogenology of the Brachmann-de Lange syndrome

Axoplasmic flow rates during nerve regeneration

Imitation in autistic, early schizophrenic, and non-psychotic subnormal children

The median cleft face syndrome. Differential diagnosis of cranium bifidum occultum, hypertelorism, and median cleft nose, lip, and palate

Peripheral motor and sensory neuropathy of early childhood, simulating Werdnig-Hoffmann disease

Alobar holoprosencephaly (arhinencephaly) with median cleft lip and palate: clinical, electroencephalographic and nosologic considerations

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