Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Cerebellar Ataxia and FMR1[original query] |
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Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort. Neurology 2004 Jul 63 (2): 362-3. Tan E K, Zhao Y, Puong K Y, Law H Y, Chan L L, Yew K, Tan C, Shen H, Chandran V R, Teoh M L, Yih Y, Pavanni R, Wong M C, Ng I |
FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy. Archives of neurology 2005 Jun 62 (6): 962-6. Biancalana Valérie, Toft Mathias, Le Ber Isabelle, Tison François, Scherrer Elisabeth, Thibodeau Stephen, Mandel Jean Louis, Brice Alexis, Farrer Matthew J, Dürr Alexand |
FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia. Neurology 2005 Jan 64 (1): 145-7. Brussino A, Gellera C, Saluto A, Mariotti C, Arduino C, Castellotti B, Camerlingo M, de Angelis V, Orsi L, Tosca P, Migone N, Taroni F, Brusco |
Frequency of FMR1 premutation in individuals with ataxia and/or tremor and/or parkinsonism. Genetics and molecular research : GMR 2008 7 (1): 74-84. Reis A H O, Ferreira A C S, Gomes K B, Aguiar M J B, Fonseca C G, Cardoso F E, Pardini V C, Carvalho M R |
Penetrance of marked cognitive impairment in older male carriers of the FMR1 gene premutation. Journal of medical genetics 2009 Jun . Sevin M, Kutalik Z, Bergmann S, Vercelletto M, Renou P, Lamy E, Vingerhoets F, Di-Virgilio G, Boisseau P, Bezieau S, Pasquier L, Rival JM, Beckmann J, Damier P, Jacquemont S |
FXTAS: new insights and the need for revised diagnostic criteria. Neurology 2012 Oct . Apartis E, Blancher A, Meissner WG, Guyant-Maréchal L, Maltête D, De Broucker T, Legrand AP, Bouzenada H, Tran Thanh H, Sallansonnet-Froment M, Wang A, Tison F, Roué-Jagot C, Sedel F, Charles P, Whalen S, Héron D, Thobois S, Poisson A, Lesca G, Ouvrard-Hernandez AM, Fraix V, Palfi S, Habert MO, Gaymard B, Dussaule JC, Pollak P, Vidailhet M, Durr A, Barbot JC, Gourlet V, Brice A, Anheim M |
Skewed X Inactivation in Women Carrying the FMR1 Premutation and Its Relation with Fragile-X-Associated Tremor/Ataxia Syndrome. Neuro-degenerative diseases 2015 Nov . Alvarez-Mora Maria Isabel, Rodriguez-Revenga Laia, Feliu Aina, Badenas Celia, Madrigal Irene, Milà Montserr |
Men with FMR1 premutation alleles of less than 71 CGG repeats have low risk of being affected with fragile X-associated tremor/ataxia syndrome (FXTAS). Journal of medical genetics 2021 Jul . Martin Ellenore M, Zhu Ying, Kraan Claudine M, Kumar Kishore R, Godler David E, Field Micha |
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- Page last updated:Apr 29, 2024
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