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Mucolipidosis type IV: clinical spectrum and natural history

Pediatrics (Evanston), 1987-06, Vol.79 (6), p.953-959

1987

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Glutaric aciduria type I: Enzymatic and neuroradiologic investigations of two kindreds

The Journal of pediatrics, 1989-06, Vol.114 (6), p.983-989

1989

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Familial Association of Neuropsychological Traits in Patients With Generalized and Partial Seizure Disorders

Journal of clinical and experimental neuropsychology, 2002-05, Vol.24 (3), p.311-326

2002

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Striatal degeneration and spongy myelinopathy in glutaric acidemia

Journal of the neurological sciences, 1992-02, Vol.107 (2), p.199-204

1992

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Cardio‐facio cutaneous syndrome: neurological manifestations

Clinical genetics, 1990-11, Vol.38 (5), p.382-386

1990

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Linguistic development of a child with a congenital, localised l.h. lesion

Cognitive neuropsychology, 1992-02, Vol.9 (1), p.1-32

1992

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Developmental Right-Hemisphere Syndrome: Clinical Spectrum of the Nonverbal Learning Disability

Journal of learning disabilities, 1995-02, Vol.28 (2), p.80-86

1995

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Heat in Workplaces Such as a Neighborhood Bakery or a Glass Factory Can Promote Aging of the Eye Lens

Open longevity science, 2008-10, Vol.2 (1), p.58-65

2008

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Cognitive and Behavioural Development of Israeli Males with Fragile X and Down Syndrome

International journal of behavioral development, 1999-06, Vol.23 (2), p.519-531

1999

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Glutaric aciduria type I: clinical heterogeneity and neuroradiologic features

Neurology, 1987-10, Vol.37 (10), p.1654-1654

1987

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Complex partial status epilepticus

Archives of neurology (Chicago), 1983-02, Vol.40 (2), p.90-92

1983

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Linguistic Development of a Child with a Congenital, Localised L. H. Lesion

Cognitive neuropsychology, 1992-02, Vol.9 (1), p.1-32

1992

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Reply from the Authors

Neurology, 1990-01, Vol.40 (1), p.188

1990

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Variability of clinical presentation in fumarate hydratase deficiency

The Journal of pediatrics, 1992-11, Vol.121 (5), p.752-754

1992

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Familial intracranial arachnoid cysts

Child's nervous system, 1991-04, Vol.7 (2), p.100-102

1991

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Acute Spinal Cord Diseases in Childhood

Developmental medicine and child neurology, 1982-08, Vol.24 (4), p.395-396

1982

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Clinical Spectrum of Mucolipidosis Type IV

Pediatrics (Evanston), 1988-04, Vol.81 (4), p.602-603

1988

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Holocarboxylase Synthetase Deficiency: A Treatable Metabolic Disorder Masquerading as Cerebral Palsy

Journal of child neurology, 1994-04, Vol.9 (2), p.170-172

1994

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BIOTINIDASE DEFICIENCY ASSOCIATED WITH SEVERE COMBINED IMMUNODEFICIENCY

The Lancet (British edition), 1989-07, Vol.334 (8656), p.228-229

1989

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Attention deficit disorder: Association with familial-genetic factors

Pediatric neurology, 1991-07, Vol.7 (4), p.258-261

1991

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Opercular sign: Significance beyond cerebral dysgenesis

Annals of neurology, 1990-02, Vol.27 (2), p.213-214

1990

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Neurobehavioral profile of children with persistent hyperinsulinemic hypoglycemia of infancy

Developmental neuropsychology, 1994-01, Vol.10 (2), p.153-163

1994

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Developmental Dyscalculia

Cortex, 1988-12, Vol.24 (4), p.555-561

1988

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Oculomotor apraxia: The presenting sign of Gaucher disease

Pediatric neurology, 1989-03, Vol.5 (2), p.128-129

1989

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Echocardiographic and Doppler findings in the Williams syndrome

The American journal of cardiology, 1989-03, Vol.63 (9), p.633-635

1989

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Mucolipidosis type IV: clinical spectrum and natural history

Glutaric aciduria type I: Enzymatic and neuroradiologic investigations of two kindreds

Familial Association of Neuropsychological Traits in Patients With Generalized and Partial Seizure Disorders

Striatal degeneration and spongy myelinopathy in glutaric acidemia

Cardio‐facio cutaneous syndrome: neurological manifestations

Linguistic development of a child with a congenital, localised l.h. lesion

Developmental Right-Hemisphere Syndrome: Clinical Spectrum of the Nonverbal Learning Disability

Heat in Workplaces Such as a Neighborhood Bakery or a Glass Factory Can Promote Aging of the Eye Lens

Cognitive and Behavioural Development of Israeli Males with Fragile X and Down Syndrome

Glutaric aciduria type I: clinical heterogeneity and neuroradiologic features

Complex partial status epilepticus

Linguistic Development of a Child with a Congenital, Localised L. H. Lesion

Reply from the Authors

Variability of clinical presentation in fumarate hydratase deficiency

Familial intracranial arachnoid cysts

Acute Spinal Cord Diseases in Childhood

Clinical Spectrum of Mucolipidosis Type IV

Holocarboxylase Synthetase Deficiency: A Treatable Metabolic Disorder Masquerading as Cerebral Palsy

BIOTINIDASE DEFICIENCY ASSOCIATED WITH SEVERE COMBINED IMMUNODEFICIENCY

Attention deficit disorder: Association with familial-genetic factors

Opercular sign: Significance beyond cerebral dysgenesis

Neurobehavioral profile of children with persistent hyperinsulinemic hypoglycemia of infancy

Developmental Dyscalculia

Oculomotor apraxia: The presenting sign of Gaucher disease

Echocardiographic and Doppler findings in the Williams syndrome

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