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48. Gender variability in presentation with Alpers' syndrome: a report of eight patients from the UAE. Mohamed K; Fathallah W; Ahmed E J Inherit Metab Dis; 2011 Apr; 34(2):439-41. PubMed ID: 21305355 [TBL] [Abstract][Full Text] [Related]
49. 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]
50. Pelizaeusmerzbacher disease "infantile acute type"; report of a family. Nisenbaum C; Sandbank U; Kohn R Ann Paediatr; 1965; 204(6):365-76. PubMed ID: 5898404 [No Abstract] [Full Text] [Related]
51. Studies on arylsulfatase-A activity in metachromatic leucodystrophy. Komiya K; Arima M Paediatr Univ Tokyo; 1970 Dec; 18():99-104. PubMed ID: 5535257 [No Abstract] [Full Text] [Related]
52. Progressive neuronal degeneration of childhood: prenatal diagnosis by MRI. de Laveaucoupet J; Roffi F; Audibert F; Guis F; Lacroix C; Villeneuve N; Landrieu P; Labrune P Prenat Diagn; 2005 Apr; 25(4):307-10. PubMed ID: 15852481 [TBL] [Abstract][Full Text] [Related]
53. [A case of simple form of sudanophilic leukodystrophy of a child which showed a marked loss of cerebral white matter and fatty liver]. Hayashi K; Taguchi K; Tsutsumi A; Ogawa K; Fujita H; Hiramoto A; Taki T No To Shinkei; 1985 Oct; 37(10):957-63. PubMed ID: 4074573 [TBL] [Abstract][Full Text] [Related]
55. Friedreich ataxia and low pyruvate carboxylase activity in liver and fibroblasts. Dijkstra UJ; Willems JL; Joosten EM; Gabreëls FJ Ann Neurol; 1983 Mar; 13(3):325-7. PubMed ID: 6847147 [TBL] [Abstract][Full Text] [Related]
56. 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]
57. [On diffuse round cell sclerosis Krabbe type)(clinical and genetic notes)]. van Bogaert L; de Barsy T Arch Fr Pediatr; 1967 Dec; 24(10):1123-9. PubMed ID: 5590821 [No Abstract] [Full Text] [Related]
58. Delineating selective vulnerability of inhibitory interneurons in Alpers' syndrome. Smith LA; Erskine D; Blain A; Taylor RW; McFarland R; Lax NZ Neuropathol Appl Neurobiol; 2022 Oct; 48(6):e12833. PubMed ID: 35790454 [TBL] [Abstract][Full Text] [Related]
59. 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]
60. Progressive poliodystrophy (Alpers' disease) with a defect in cytochrome aa3 in muscle: a report of two unrelated patients. Prick MJ; Gabreëls FJ; Trijbels JM; Janssen AJ; le Coultre R; van Dam K; Jaspar HH; Ebels EJ; Op de Coul AA Clin Neurol Neurosurg; 1983; 85(1):57-70. PubMed ID: 6303665 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]