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28. 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]
29. 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]
30. The NAD Hong Y; Zhang Z; Yangzom T; Chen A; Lundberg BC; Fang EF; Siller R; Sullivan GJ; Zeman J; Tzoulis C; Bindoff LA; Liang KX Int J Biol Sci; 2024; 20(4):1194-1217. PubMed ID: 38385069 [TBL] [Abstract][Full Text] [Related]
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36. A family with sudanophilic leucodystrophy. Schenk VW; Stam FC; Batenburg-Plenter AM Acta Neuropathol; 1967 Nov; 9(3):233-43. PubMed ID: 4169518 [No Abstract] [Full Text] [Related]
37. Infantile neuroaxonal dystrophy. Histological and electron microscopical study of two cases. Yagishita S; Kimura S Acta Neuropathol; 1974; 29(2):115-26. PubMed ID: 4446941 [No Abstract] [Full Text] [Related]
38. Gastrointestinal neuromuscular pathology in alpers disease. Kapur RP; Fligner C; Maghsoodi B; Jaffe R Am J Surg Pathol; 2011 May; 35(5):714-22. PubMed ID: 21451360 [TBL] [Abstract][Full Text] [Related]
39. Progressive neuronal degeneration of childhood (Alpers syndrome) with hepatic cirrhosis. Wilson DC; McGibben D; Hicks EM; Allen IV Eur J Pediatr; 1993 Mar; 152(3):260-2. PubMed ID: 8444257 [TBL] [Abstract][Full Text] [Related]
40. 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] [Previous] [Next] [New Search]