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24. Early onset hereditary spinocerebellar ataxia: an autosomal recessive disorder distinct from Friedreich's ataxia. Kumar D; Blank CE Indian Pediatr; 1989 Oct; 26(10):1014-9. PubMed ID: 2630444 [TBL] [Abstract][Full Text] [Related]
25. Pseudodominant Friedreich's ataxia with phenotypic heterogeneity. Panas M; Kalfakis N; Vassilopoulos D Acta Neurol Scand; 2007 May; 115(5):364-6. PubMed ID: 17489949 [TBL] [Abstract][Full Text] [Related]
26. Clinical and genetic abnormalities in patients with Friedreich's ataxia. Dürr A; Cossee M; Agid Y; Campuzano V; Mignard C; Penet C; Mandel JL; Brice A; Koenig M N Engl J Med; 1996 Oct; 335(16):1169-75. PubMed ID: 8815938 [TBL] [Abstract][Full Text] [Related]
27. [Genetic tests: how far should we go? A case of late-onset Friedreich's disease]. Ruolt I; Tranchant C; Warter JM Rev Neurol (Paris); 2000 Dec; 156(12):1148-50. PubMed ID: 11139731 [TBL] [Abstract][Full Text] [Related]
28. Friedreich's ataxia in the elderly. Abyad A; Kligman E J Int Med Res; 1995; 23(1):74-84. PubMed ID: 7774761 [TBL] [Abstract][Full Text] [Related]
29. Late onset recessive ataxia with Friedreich's disease phenotype. De Michele G; Filla A; Barbieri F; Perretti A; Santoro L; Trombetta L; Santorelli F; Campanella G J Neurol Neurosurg Psychiatry; 1989 Dec; 52(12):1398-401. PubMed ID: 2614435 [TBL] [Abstract][Full Text] [Related]
30. Friedreich's ataxia presenting with pure sensory ataxia: a long-term follow-up study of two patients. Berciano J; Combarros O; Calleja J; Polo JM; Pascual J; Leno C J Neurol; 1993; 240(3):177-80. PubMed ID: 8482991 [TBL] [Abstract][Full Text] [Related]
31. A family with pseudodominant Friedreich's ataxia showing marked variation of phenotype between affected siblings. Webb S; Doudney K; Pook M; Chamberlain S; Hutchinson M J Neurol Neurosurg Psychiatry; 1999 Aug; 67(2):217-9. PubMed ID: 10406994 [TBL] [Abstract][Full Text] [Related]
32. Early-Onset Friedreich's Ataxia With Oculomotor Apraxia. Saghazadeh A; Hafizi S; Hosseini F; Ashrafi MR; Rezaei N Acta Med Iran; 2017 Feb; 55(2):128-130. PubMed ID: 28282710 [TBL] [Abstract][Full Text] [Related]
34. Friedreich's ataxia and frataxin: molecular genetics, evolution and pathogenesis (Review). Palau F Int J Mol Med; 2001 Jun; 7(6):581-9. PubMed ID: 11351269 [TBL] [Abstract][Full Text] [Related]
35. Mutation detection in an equivocal case of Friedreich's ataxia. Potter NT; Miller CA; Anderson IJ Pediatr Neurol; 2000 May; 22(5):413-5. PubMed ID: 10913738 [TBL] [Abstract][Full Text] [Related]
36. Friedreich's ataxia: clinical heterogeneity in two sisters. Armani M; Zortea M; Pastorello E; Lombardi S; Tonello S; Zuliani L; Rigoni MT; Trevisan CP Neurol Sci; 2006 Jun; 27(2):140-2. PubMed ID: 16816915 [TBL] [Abstract][Full Text] [Related]
37. Molecular analysis of Friedreich's ataxia locus in the Indian population. Mukerji M; Choudhry S; Saleem Q; Padma MV; Maheshwari MC; Jain S Acta Neurol Scand; 2000 Oct; 102(4):227-9. PubMed ID: 11071107 [TBL] [Abstract][Full Text] [Related]
38. Marked variation in the cardiomyopathy associated with Friedreich's ataxia. Dutka DP; Donnelly JE; Nihoyannopoulos P; Oakley CM; Nunez DJ Heart; 1999 Feb; 81(2):141-7. PubMed ID: 9922348 [TBL] [Abstract][Full Text] [Related]