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Items: 7

1.
2.

Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical management.

Anheim M, Fleury M, Monga B, Laugel V, Chaigne D, Rodier G, Ginglinger E, Boulay C, Courtois S, Drouot N, Fritsch M, Delaunoy JP, Stoppa-Lyonnet D, Tranchant C, Koenig M.

Neurogenetics. 2010 Feb;11(1):1-12. doi: 10.1007/s10048-009-0196-y.

PMID:
19440741
3.

Autosomal recessive cerebellar ataxias.

Palau F, Espinós C.

Orphanet J Rare Dis. 2006 Nov 17;1:47. Review.

4.

Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families.

Mariotti C, Gellera C, Rimoldi M, Mineri R, Uziel G, Zorzi G, Pareyson D, Piccolo G, Gambi D, Piacentini S, Squitieri F, Capra R, Castellotti B, Di Donato S.

Neurol Sci. 2004 Jul;25(3):130-7.

PMID:
15300460
5.

Friedreich's Ataxia: disease mechanisms, antioxidant and Coenzyme Q10 therapy.

Cooper JM, Schapira AH.

Biofactors. 2003;18(1-4):163-71. Review.

PMID:
14695932
6.

A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia.

Cellini E, Piacentini S, Nacmias B, Forleo P, Tedde A, Bagnoli S, Ciantelli M, Sorbi S.

Arch Neurol. 2002 Dec;59(12):1952-3.

PMID:
12470185
7.

The complex clinical and genetic classification of inherited ataxias. II. Autosomal recessive ataxias.

Di Donato S, Gellera C, Mariotti C.

Neurol Sci. 2001 Jun;22(3):219-28. Review.

PMID:
11731874

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