144 related articles for article (PubMed ID: 33749916)
1. Autosomal-Recessive Cerebellar Ataxias and Movement Disorders With Elevated Alpha-Fetoprotein.
Teive HAG; Camargo CHF; Munhoz RP
Mov Disord; 2021 Mar; 36(3):789. PubMed ID: 33749916
[No Abstract] [Full Text] [Related]
2. Reply to: "Autosomal-Recessive Cerebellar Ataxias With Elevated Alpha-Fetoprotein: Uncommon Diseases, Common Biomarker".
Renaud M; Tranchant C; Koenig M; Anheim M
Mov Disord; 2021 Mar; 36(3):789-790. PubMed ID: 33749920
[No Abstract] [Full Text] [Related]
3. Autosomal Recessive Cerebellar Ataxias With Elevated Alpha-Fetoprotein: Uncommon Diseases, Common Biomarker.
Renaud M; Tranchant C; Koenig M; Anheim M
Mov Disord; 2020 Dec; 35(12):2139-2149. PubMed ID: 33044027
[TBL] [Abstract][Full Text] [Related]
4. ARV1 Gene: A Novel Cause of Autosomal Recessive Cerebellar Ataxia with Elevated Alpha Fetoprotein.
Kamate M; Basavanagowda T
Cerebellum; 2024 Jun; 23(3):1239-1244. PubMed ID: 37749428
[TBL] [Abstract][Full Text] [Related]
5. Alpha-fetoprotein as a biomarker for recessive ataxias.
Braga-Neto P; Dutra LA; Pedroso JL; Barsottini OG
Arq Neuropsiquiatr; 2010 Dec; 68(6):953-5. PubMed ID: 21243258
[No Abstract] [Full Text] [Related]
6. The Classification of Autosomal Recessive Cerebellar Ataxias: a Consensus Statement from the Society for Research on the Cerebellum and Ataxias Task Force.
Beaudin M; Matilla-Dueñas A; Soong BW; Pedroso JL; Barsottini OG; Mitoma H; Tsuji S; Schmahmann JD; Manto M; Rouleau GA; Klein C; Dupre N
Cerebellum; 2019 Dec; 18(6):1098-1125. PubMed ID: 31267374
[TBL] [Abstract][Full Text] [Related]
7. The genetic nomenclature of recessive cerebellar ataxias.
Rossi M; Anheim M; Durr A; Klein C; Koenig M; Synofzik M; Marras C; van de Warrenburg BP;
Mov Disord; 2018 Jul; 33(7):1056-1076. PubMed ID: 29756227
[TBL] [Abstract][Full Text] [Related]
8. Autosomal recessive cerebellar ataxias.
Palau F; Espinós C
Orphanet J Rare Dis; 2006 Nov; 1():47. PubMed ID: 17112370
[TBL] [Abstract][Full Text] [Related]
9. Progressive Ataxia with Elevated Alpha-Fetoprotein: Diagnostic Issues and Review of the Literature.
Paucar M; Taylor AMR; Hadjivassiliou M; Fogel BL; Svenningsson P
Tremor Other Hyperkinet Mov (N Y); 2019; 9():. PubMed ID: 31656689
[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. The autosomal recessive cerebellar ataxias.
Anheim M; Tranchant C; Koenig M
N Engl J Med; 2012 Feb; 366(7):636-46. PubMed ID: 22335741
[No Abstract] [Full Text] [Related]
12. 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]
13. Autosomal recessive cerebellar ataxias: the current state of affairs.
Vermeer S; van de Warrenburg BP; Willemsen MA; Cluitmans M; Scheffer H; Kremer BP; Knoers NV
J Med Genet; 2011 Oct; 48(10):651-9. PubMed ID: 21856962
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. [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]
16. Clinical features and molecular genetics of autosomal recessive cerebellar ataxias.
Fogel BL; Perlman S
Lancet Neurol; 2007 Mar; 6(3):245-57. PubMed ID: 17303531
[TBL] [Abstract][Full Text] [Related]
17. [Autosomal recessive cerebellar ataxias].
Tranchant C; Anheim M
Presse Med; 2009 Dec; 38(12):1852-9. PubMed ID: 19442480
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [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]
20. Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2.
Moreira MC; Klur S; Watanabe M; Németh AH; Le Ber I; Moniz JC; Tranchant C; Aubourg P; Tazir M; Schöls L; Pandolfo M; Schulz JB; Pouget J; Calvas P; Shizuka-Ikeda M; Shoji M; Tanaka M; Izatt L; Shaw CE; M'Zahem A; Dunne E; Bomont P; Benhassine T; Bouslam N; Stevanin G; Brice A; Guimarães J; Mendonça P; Barbot C; Coutinho P; Sequeiros J; Dürr A; Warter JM; Koenig M
Nat Genet; 2004 Mar; 36(3):225-7. PubMed ID: 14770181
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
