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25. Comparison of lactate and pyruvate during endotoxic shock. Holtzman S; Balderman SC Surg Gynecol Obstet; 1977 Nov; 145(5):677-81. PubMed ID: 198913 [TBL] [Abstract][Full Text] [Related]
26. Diffuse leukodystrophy with a large-scale mitochondrial DNA deletion. Nakai A; Goto Y; Fujisawa K; Shigematsu Y; Kikawa Y; Konishi Y; Nonaka I; Sudo M Lancet; 1994 Jun; 343(8910):1397-8. PubMed ID: 7910887 [TBL] [Abstract][Full Text] [Related]
27. Familial progressive poliodystrophy with cirrhosis of the liver. Wefring KW; Lamvik JO Acta Paediatr Scand; 1967 May; 56(3):295-300. PubMed ID: 6033104 [No Abstract] [Full Text] [Related]
28. [An autopsy case of sudanophilic leukodystrophy with depositions of lipid granules in general organs and peripheral neuropathy]. Hirase T; Araki S; Eto M; Takahashi K; Ide M Rinsho Shinkeigaku; 1984 Jan; 24(1):56-64. PubMed ID: 6088147 [No Abstract] [Full Text] [Related]
29. Phenotypic and genotypic variability in Alpers syndrome. Sofou K; Moslemi AR; Kollberg G; Bjarnadóttir I; Oldfors A; Nennesmo I; Holme E; Tulinius M; Darin N Eur J Paediatr Neurol; 2012 Jul; 16(4):379-89. PubMed ID: 22237560 [TBL] [Abstract][Full Text] [Related]
30. Proof of progression over time: finally fulminant brain, muscle, and liver affection in Alpers syndrome associated with the A467T POLG1 mutation. Boes M; Bauer J; Urbach H; Elger CE; Frank S; Baron M; Zsurka G; Kunz WS; Kornblum C Seizure; 2009 Apr; 18(3):232-4. PubMed ID: 18783964 [TBL] [Abstract][Full Text] [Related]
31. A mutation in mitochondrial DNA-encoded cytochrome c oxidase II gene in a child with Alpers-Huttenlocher-like disease. Uusimaa J; Finnilä S; Vainionpää L; Kärppä M; Herva R; Rantala H; Hassinen IE; Majamaa K Pediatrics; 2003 Mar; 111(3):e262-8. PubMed ID: 12612282 [TBL] [Abstract][Full Text] [Related]
32. POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion. Naviaux RK; Nguyen KV Ann Neurol; 2004 May; 55(5):706-12. PubMed ID: 15122711 [TBL] [Abstract][Full Text] [Related]
33. Muscle pyruvate oxidation following denervation and reinnervation. Evans OB Muscle Nerve; 1983 Oct; 6(8):557-60. PubMed ID: 6689053 [TBL] [Abstract][Full Text] [Related]
34. [Early mitochondrial encephalomyopathy due to complex IV deficiency consistent with Alpers-Huttenlocher syndrome: report of two cases]. Castro-Gago M; González-Conde V; Fernández-Seara MJ; Rodrigo-Sáez E; Fernández-Cebrián S; Alonso-Martín A; Campos Y; Arenas J; Eirís-Puñal J Rev Neurol; 1999 Nov 16-30; 29(10):912-7. PubMed ID: 10637838 [TBL] [Abstract][Full Text] [Related]
35. Progressive cerebral degeneration of childhood with liver disease (Alpers Huttenlocher disease) with cytochrome oxidase deficiency presenting with epilepsia partialis continua as the first clinical manifestation. Wörle H; Köhler B; Schlote W; Winkler P; Bastanier CK Clin Neuropathol; 1998; 17(2):63-8. PubMed ID: 9561326 [TBL] [Abstract][Full Text] [Related]