556 related articles for article (PubMed ID: 16193447)
1. [Autosomal recessive cerebellar ataxias. Their classification, genetic features and pathophysiology].
Espinós-Armero C; González-Cabo P; Palau-Martínez F
Rev Neurol; 2005 Oct 1-15; 41(7):409-22. PubMed ID: 16193447
[TBL] [Abstract][Full Text] [Related]
2. Autosomal recessive cerebellar ataxias.
Palau F; Espinós C
Orphanet J Rare Dis; 2006 Nov; 1():47. PubMed ID: 17112370
[TBL] [Abstract][Full Text] [Related]
3. [Autosomal recessive cerebellar ataxias].
Anheim M
Rev Neurol (Paris); 2011 May; 167(5):372-84. PubMed ID: 21087783
[TBL] [Abstract][Full Text] [Related]
4. 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. PubMed ID: 19440741
[TBL] [Abstract][Full Text] [Related]
5. [Recent advance in genetic study of hereditary autosomal recessive cerebellar ataxia].
Guan WJ; Wang JL; Tang BS
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Dec; 29(6):673-6. PubMed ID: 23225047
[TBL] [Abstract][Full Text] [Related]
6. Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.
Hamza W; Ali Pacha L; Hamadouche T; Muller J; Drouot N; Ferrat F; Makri S; Chaouch M; Tazir M; Koenig M; Benhassine T
BMC Med Genet; 2015 Jun; 16():36. PubMed ID: 26068213
[TBL] [Abstract][Full Text] [Related]
7. Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies.
Le Ber I; Moreira MC; Rivaud-Péchoux S; Chamayou C; Ochsner F; Kuntzer T; Tardieu M; Saïd G; Habert MO; Demarquay G; Tannier C; Beis JM; Brice A; Koenig M; Dürr A
Brain; 2003 Dec; 126(Pt 12):2761-72. PubMed ID: 14506070
[TBL] [Abstract][Full Text] [Related]
8. Recessive ataxias.
Synofzik M; Németh AH
Handb Clin Neurol; 2018; 155():73-89. PubMed ID: 29891078
[TBL] [Abstract][Full Text] [Related]
9. Rare forms of autosomal recessive neurodegenerative ataxia.
Koenig M
Semin Pediatr Neurol; 2003 Sep; 10(3):183-92. PubMed ID: 14653406
[TBL] [Abstract][Full Text] [Related]
10. Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.
Gros-Louis F; Dupré N; Dion P; Fox MA; Laurent S; Verreault S; Sanes JR; Bouchard JP; Rouleau GA
Nat Genet; 2007 Jan; 39(1):80-5. PubMed ID: 17159980
[TBL] [Abstract][Full Text] [Related]
11. Current and Promising Therapies in Autosomal Recessive Ataxias.
Picher-Martel V; Dupre N
CNS Neurol Disord Drug Targets; 2018; 17(3):161-171. PubMed ID: 29676235
[TBL] [Abstract][Full Text] [Related]
12. [Autosomal recessive cerebellar ataxias with oculomotor apraxia].
Le Ber I; Rivaud-Péchoux S; Brice A; Dürr A
Rev Neurol (Paris); 2006 Feb; 162(2):177-84. PubMed ID: 16518257
[TBL] [Abstract][Full Text] [Related]
13. Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients.
Anheim M; Monga B; Fleury M; Charles P; Barbot C; Salih M; Delaunoy JP; Fritsch M; Arning L; Synofzik M; Schöls L; Sequeiros J; Goizet C; Marelli C; Le Ber I; Koht J; Gazulla J; De Bleecker J; Mukhtar M; Drouot N; Ali-Pacha L; Benhassine T; Chbicheb M; M'Zahem A; Hamri A; Chabrol B; Pouget J; Murphy R; Watanabe M; Coutinho P; Tazir M; Durr A; Brice A; Tranchant C; Koenig M
Brain; 2009 Oct; 132(Pt 10):2688-98. PubMed ID: 19696032
[TBL] [Abstract][Full Text] [Related]
14. New autosomal recessive cerebellar ataxias with oculomotor apraxia.
Le Ber I; Brice A; Dürr A
Curr Neurol Neurosci Rep; 2005 Sep; 5(5):411-7. PubMed ID: 16131425
[TBL] [Abstract][Full Text] [Related]
15. [Therapeutic developments in chronic ataxias].
Buompadre MC
Medicina (B Aires); 2013; 73 Suppl 1():49-54. PubMed ID: 24072051
[TBL] [Abstract][Full Text] [Related]
16. Atypical presentation of ataxia-oculomotor apraxia type 1.
Shahwan A; Byrd PJ; Taylor AM; Nestor T; Ryan S; King MD
Dev Med Child Neurol; 2006 Jun; 48(6):529-32. PubMed ID: 16700949
[TBL] [Abstract][Full Text] [Related]
17. Distinct phenotypes within autosomal recessive ataxias not linked to already known loci.
Bouhlal Y; El-Euch-Fayeche G; Amouri R; Hentati F
Acta Myol; 2005 Oct; 24(2):155-61. PubMed ID: 16550933
[TBL] [Abstract][Full Text] [Related]
18. Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration.
Wolf NI; Koenig M
Handb Clin Neurol; 2013; 113():1869-78. PubMed ID: 23622410
[TBL] [Abstract][Full Text] [Related]
19. Peripheral nerve involvement in hereditary cerebellar and multisystem degenerative disorders.
Berciano J; García A; Infante J
Handb Clin Neurol; 2013; 115():907-32. PubMed ID: 23931821
[TBL] [Abstract][Full Text] [Related]
20. SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.
Nanetti L; Cavalieri S; Pensato V; Erbetta A; Pareyson D; Panzeri M; Zorzi G; Antozzi C; Moroni I; Gellera C; Brusco A; Mariotti C
Orphanet J Rare Dis; 2013 Aug; 8():123. PubMed ID: 23941260
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]