Author:
Elpeleg Orly N.,Costeff Hanan,Joseph Adina,Shental Yitzhak,Weitz Raphael,Gibson K. Michael
Subject
Clinical Neurology,Developmental Neuroscience,Pediatrics, Perinatology, and Child Health
Reference18 articles.
1. Die komlizierle, hereditar-familiare optikusatrophie des kindesalters. Ein bisher nicht beschriebener symptomkoraplex;Behr;Ktinische Monatsblatter für Augenheilkunde.,1909
2. A familial syndrome of infantile optic atrophy, movement disorder, and spastic paraplegia;Costeff;Neurology,1989
3. 3-methylglutaconic aciduria in “optic atrophy plus”;Costeff;Annals of Neurology,1993
4. 3-methylglutaconic aciduria with persistent metabolic acidosis and “uncoupling episodes”;Elpeleg;Journal of Inherited Metabolic Diseases,1990
5. Familial benign hypotonia of childhood due to isolated 3-methylcrotonyl-CoA carboxylase deficiency;Elpeleg;Journal of Pediatrics,1992
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