Myoclonic absence epilepsy with photosensitivity and a gain of function mutation in glutamate dehydrogenase-Reference-Cited by-同舟云学术

Myoclonic absence epilepsy with photosensitivity and a gain of function mutation in glutamate dehydrogenase

Published:2008-10 Issue:7 Volume:17 Page:658-664
ISSN:1059-1311
Container-title:Seizure
language:en
Short-container-title:Seizure

Author:

Bahi-Buisson Nadia,El Sabbagh Sandra,Soufflet Christine,Escande Fabienne,Boddaert Nathalie,Valayannopoulos Vassili,Bellané-Chantelot Christine,Lascelles Karine,Dulac Olivier,Plouin Perrine,de Lonlay Pascale

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology,General Medicine

Reference19 articles.

1. Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene;Stanley;N Engl J Med,1998

2. Hyperinsulinism/hyperammonemia syndrome: insights into the regulatory role of glutamate dehydrogenase in ammonia metabolism;Stanley;Mol Genet Metab,2004

3. Facial appearance in persistent hyperinsulinemic hypoglycemia;de Lonlay;Am J Med Genet,2002

4. Central nervous system hyperexcitability associated with glutamate dehydrogenase gain of function mutations;Raizen;J Pediatr,2005

5. Hyperinsulinemic hypoglycemia in children;de Lonlay;Ann Endocrinol (Paris),2004

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