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24. Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32. Brkanac Z; Fernandez M; Matsushita M; Lipe H; Wolff J; Bird TD; Raskind WH Am J Med Genet; 2002 May; 114(4):450-7. PubMed ID: 11992570 [TBL] [Abstract][Full Text] [Related]
25. [Should the term Pierre Marie's heredo-ataxia still be used?]. Trouillas P; Robert JM; Aimard G Lyon Med; 1972 Jun; 227(11):1105-16. PubMed ID: 5080072 [No Abstract] [Full Text] [Related]
26. Morphological changes of olivopontocerebellar atrophy in computed tomography and comments on its pathogenesis. Huang YP; Plaitakis A Adv Neurol; 1984; 41():39-85. PubMed ID: 6496229 [No Abstract] [Full Text] [Related]
31. Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes? Schöls L; Amoiridis G; Büttner T; Przuntek H; Epplen JT; Riess O Ann Neurol; 1997 Dec; 42(6):924-32. PubMed ID: 9403486 [TBL] [Abstract][Full Text] [Related]
32. [A polygraphic study on nocturnal sleep of patients with spino-cerebellar degeneration--a comparative study of Marie's ataxia and OPCA (author's transl)]. Kazukawa S Seishin Shinkeigaku Zasshi; 1982; 84(3):135-61. PubMed ID: 7111513 [No Abstract] [Full Text] [Related]
33. An interesting case of Roussy-Levy syndrome inherited as autosomal dominant with diabetes mellitus. Garg SC; Singh N; Singh H; Thapar A J Assoc Physicians India; 1983 Jul; 31(7):467-8. PubMed ID: 6654813 [No Abstract] [Full Text] [Related]
36. [Spinocerebellar ataxia type 7: clinical and molecular genetic analysis of a Mexican family]. Rolón Lacarriere O; Rasmussen Almaraz A; Hernández Cruz H; Carranza del Río J; González Cruz M; Gutiérrez Moctezuma J Rev Neurol; 2004 Apr 16-30; 38(8):736-40. PubMed ID: 15122543 [TBL] [Abstract][Full Text] [Related]
37. An apology and an introduction to the olivopontocerebellar atrophies. Duvoisin RC Adv Neurol; 1984; 41():5-12. PubMed ID: 6496230 [TBL] [Abstract][Full Text] [Related]
38. The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1. Benomar A; Krols L; Stevanin G; Cancel G; LeGuern E; David G; Ouhabi H; Martin JJ; Dürr A; Zaim A Nat Genet; 1995 May; 10(1):84-8. PubMed ID: 7647798 [TBL] [Abstract][Full Text] [Related]
39. A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34. Thiffault I; Rioux MF; Tetreault M; Jarry J; Loiselle L; Poirier J; Gros-Louis F; Mathieu J; Vanasse M; Rouleau GA; Bouchard JP; Lesage J; Brais B Brain; 2006 Sep; 129(Pt 9):2332-40. PubMed ID: 16672289 [TBL] [Abstract][Full Text] [Related]