Familial Schizencephaly

Author:

Robinson Richard O.

Publisher

Wiley

Subject

Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health

Reference10 articles.

1. Turricephalie hereditaire, microencephalie familiale avec lissencephalie: rapport d'un syndrome malformatif avec les dysraphies cerebromedullaires;Alberca-Serrano;Journal of the Neurological Sciences,1964

2. Multiple acyl CoA dehydrogenase deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty degeneration of the cerebral cortex in two new-born brothers. II: Morphology and pathogenesis;Böhm;European Journal of Pediatrics,1982

3. The Lissencephaly syndrome;Dieker;Birth Defects, Original Article Series, V,1969

4. Neuropathological considerations in cerebrohepato-renal syndrome (Zellweger's syndrome);Liu;Acta Neuropathologica,1976

5. Computed tomography of the brain in the Smith-Lemli-Opitz syndrome;Marion;Journal of Child Neurology,1987

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1. Developmental Disorders;Atlas of Clinical Neurology;2019

2. Specialized Neurological Studies;Volpe's Neurology of the Newborn;2018

3. Neuronal Migration;Volpe's Neurology of the Newborn;2018

4. Schizencephaly;Atlas of Genetic Diagnosis and Counseling;2017

5. Telencephalic Flexure and Malformations of the Lateral Cerebral (Sylvian) Fissure;Pediatric Neurology;2016-10

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