Neurological, cardiological, and oculomotor progression in 104 patients with Friedreich ataxia during long-term follow-up

Autor: Pascale Ribai, Alain Mallet, Marie-Laure Tanguy, Anne-Sophie Béraud, Michèle Schmitt, Alexandra Durr, Perrine Charles, Françoise Pousset, Michel Koenig, Alexis Brice, Sophie Rivaud-Péchoux, Franchesca Gasparini, Isabelle Le Ber

Publikováno v: Archives of Neurology-Chigago
Archives of Neurology-Chigago-, American Medical Association, 2007, 64 (4), pp.558-64. ⟨10.1001/archneur.64.4.558⟩
Archives of Neurology-Chigago-, 2007, 64 (4), pp.558-64. ⟨10.1001/archneur.64.4.558⟩

BACKGROUND: Friedreich ataxia (FA) is the most frequent autosomal recessive cerebellar ataxia. Although the phenotype is well known, disease progression has not been evaluated in a prospective manner. OBJECTIVE: To perform a long-term prospective fol

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40cca0763597016a49acd2f51431ee54
https://hal.archives-ouvertes.fr/hal-00166262