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9. Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation. Shih VE; Efron ML; Moser HW Am J Dis Child; 1969 Jan; 117(1):83-92. PubMed ID: 5782534 [No Abstract] [Full Text] [Related]
10. Hypomyelination and reversible white matter attenuation in 3-phosphoglycerate dehydrogenase deficiency. de Koning TJ; Jaeken J; Pineda M; Van Maldergem L; Poll-The BT; van der Knaap MS Neuropediatrics; 2000 Dec; 31(6):287-92. PubMed ID: 11508546 [TBL] [Abstract][Full Text] [Related]
12. Defects in amino acid catabolism and the urea cycle. Hoffmann GF; Kölker S Handb Clin Neurol; 2013; 113():1755-73. PubMed ID: 23622399 [TBL] [Abstract][Full Text] [Related]
13. Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency. Hoffmann GF; Athanassopoulos S; Burlina AB; Duran M; de Klerk JB; Lehnert W; Leonard JV; Monavari AA; Müller E; Muntau AC; Naughten ER; Plecko-Starting B; Superti-Furga A; Zschocke J; Christensen E Neuropediatrics; 1996 Jun; 27(3):115-23. PubMed ID: 8837070 [TBL] [Abstract][Full Text] [Related]
14. [Macrocephaly and dystonic cerebral palsy in a child with type I glutaric aciduria]. Plöchl E; Christensen E; Colombo JP; Weiss-Wichert P; Wenger E Padiatr Padol; 1991; 26(2):97-101. PubMed ID: 1945471 [TBL] [Abstract][Full Text] [Related]