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10. Brain MR imaging findings in two patients with Alpers' syndrome. Smith JK; Mah JK; Castillo M Clin Imaging; 1996; 20(4):235-7. PubMed ID: 8959359 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Alpers' syndrome presenting with seizures and multiple stroke-like episodes in a 17-year-old male. Montine TJ; Powers JM; Vogel FS; Radtke RA Clin Neuropathol; 1995; 14(6):322-6. PubMed ID: 8605737 [TBL] [Abstract][Full Text] [Related]
13. Alpers syndrome: an unusual etiology of failure to thrive. Mangalat N; Tatevian N; Bhattacharjee M; Rhoads JM Ultrastruct Pathol; 2012 Aug; 36(4):219-21. PubMed ID: 22849523 [No Abstract] [Full Text] [Related]
15. [Contribution to the question of diffuse infantile cerebral sclerosis with primary dystrophy of the suprarenal gland]. Riedel H Psychiatr Neurol Med Psychol (Leipz); 1968 Feb; 20(2):67-73. PubMed ID: 5304006 [No Abstract] [Full Text] [Related]
16. [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]
17. 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]
18. Early childhood hepatocerebral degeneration misdiagnosed as valproate hepatotoxicity. Bicknese AR; May W; Hickey WF; Dodson WE Ann Neurol; 1992 Dec; 32(6):767-75. PubMed ID: 1471867 [TBL] [Abstract][Full Text] [Related]
19. Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase-gammaA. Ferrari G; Lamantea E; Donati A; Filosto M; Briem E; Carrara F; Parini R; Simonati A; Santer R; Zeviani M Brain; 2005 Apr; 128(Pt 4):723-31. PubMed ID: 15689359 [TBL] [Abstract][Full Text] [Related]