These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
26. L-2-hydroxyglutaric aciduria, a defect of metabolite repair. Rzem R; Vincent MF; Van Schaftingen E; Veiga-da-Cunha M J Inherit Metab Dis; 2007 Oct; 30(5):681-9. PubMed ID: 17603759 [TBL] [Abstract][Full Text] [Related]
27. [A 62-year-old man with familial parkinsonism with the onset at 24 years of the age]. Takubo H; Kondo T; Mori H; Miyake T; Suda K; Yokochi M; Imai H; Mizuno Y No To Shinkei; 1996 Jun; 48(6):587-97. PubMed ID: 8703564 [TBL] [Abstract][Full Text] [Related]
28. Abnormality of the alpha-ketoglutarate dehydrogenase complex in fibroblasts from familial Alzheimer's disease. Sheu KF; Cooper AJ; Koike K; Koike M; Lindsay JG; Blass JP Ann Neurol; 1994 Mar; 35(3):312-8. PubMed ID: 8122883 [TBL] [Abstract][Full Text] [Related]
30. Symptomatic and asymptomatic methylenetetrahydrofolate reductase deficiency in two adult brothers. Haworth JC; Dilling LA; Surtees RA; Seargeant LE; Lue-Shing H; Cooper BA; Rosenblatt DS Am J Med Genet; 1993 Mar; 45(5):572-6. PubMed ID: 8456826 [TBL] [Abstract][Full Text] [Related]
31. Juvenile form of dihydropteridine reductase deficiency in 2 Tunisian patients. Larnaout A; Belal S; Miladi N; Kaabachi N; Mebazza A; Dhondt JL; Hentati F Neuropediatrics; 1998 Dec; 29(6):322-3. PubMed ID: 10029353 [TBL] [Abstract][Full Text] [Related]
32. [Glutaric aciduria type 1: clinical presentations, diagnostics and treatment.]. Mikhaĭlova SV; Zakharova EIu; Bobylova MIu; Il'ina ES; Banin AV; Rasskazchikova IV; Baĭdakova GV; Shekhter OV; Briusova IB; Volkova GI; Petrukhin AS Zh Nevrol Psikhiatr Im S S Korsakova; 2007; 107(10):4-12. PubMed ID: 18477973 [TBL] [Abstract][Full Text] [Related]
33. Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduria. Larnaout A; Hentati F; Belal S; Ben Hamida C; Kaabachi N; Ben Hamida M Acta Neuropathol; 1994; 88(4):367-70. PubMed ID: 7839830 [TBL] [Abstract][Full Text] [Related]
35. A defect in pyruvate decarboxylase in a child with an intermittent movement disorder. Blass JP; Avigan J; Uhlendorf BW J Clin Invest; 1970 Mar; 49(3):423-32. PubMed ID: 4313434 [TBL] [Abstract][Full Text] [Related]