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7. Alpers progressive infantile neuronal poliodystrophy: an acute neonatal form with findings of the fetal akinesia syndrome. Frydman M; Jager-Roman E; de Vries L; Stoltenburg-Didinger G; Nussinovitch M; Sirota L Am J Med Genet; 1993 Aug; 47(1):31-6. PubMed ID: 8368248 [TBL] [Abstract][Full Text] [Related]
8. Status epilepticus in children with Alpers' disease caused by POLG1 mutations: EEG and MRI features. Wolf NI; Rahman S; Schmitt B; Taanman JW; Duncan AJ; Harting I; Wohlrab G; Ebinger F; Rating D; Bast T Epilepsia; 2009 Jun; 50(6):1596-607. PubMed ID: 19054397 [TBL] [Abstract][Full Text] [Related]
9. Progressive infantile poliodystrophy. Association with disturbed pyruvate oxidation in muscle and liver. Prick MJ; Gabreëls FJ; Renier WO; Trijbels JM; Sengers RC; Slooff JL Arch Neurol; 1981 Dec; 38(12):767-72. PubMed ID: 7316843 [TBL] [Abstract][Full Text] [Related]
10. Mitochondrial DNA depletion in Alpers syndrome. Tesarova M; Mayr JA; Wenchich L; Hansikova H; Elleder M; Blahova K; Sperl W; Zeman J Neuropediatrics; 2004 Aug; 35(4):217-23. PubMed ID: 15328560 [TBL] [Abstract][Full Text] [Related]
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12. 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]
13. 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]