Human Epilepsy Genetics--Neuronal Migration Disorders Study | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Human Epilepsy Genetics--Neuronal Migration Disorders Study	Choristoma, Cognition Disorders, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Malformations of Cortical Development, Group I, Malformations of Cortical Development, Group II, Malformations of Cortical Development, Group III, Musculoskeletal Abnormalities, Neurologic Manifestations, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, brain disorder, central nervous system disorder, central nervous system malformation, cerebral cortical dysplasia, cognitive disorder, epilepsy, lissencephaly spectrum disorders, microcephaly, musculoskeletal system disorder, nervous system disorder, polymicrogyria, psychiatric disorder, schizencephaly, visual epilepsy	Recruiting	Not stated	2023-09-21		NCT00041600

3 results · Page 1 of 1

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Organizations	Linked trials
Harvard University Faculty of Medicine	4
Howard Hughes Medical Institute	3
National Institute of Neurological Disorders and Stroke (NINDS)	370

1 results · Page 1 of 1

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Research sites	City	Country	Linked trials
Boston Children's Hospital, Walsh Laboratory	Boston	United States	1