312 related articles for article (PubMed ID: 18363164)
21. Cognitive decline, neuromotor and behavioural disturbances in a mouse model for fragile-X-associated tremor/ataxia syndrome (FXTAS).
Van Dam D; Errijgers V; Kooy RF; Willemsen R; Mientjes E; Oostra BA; De Deyn PP
Behav Brain Res; 2005 Jul; 162(2):233-9. PubMed ID: 15876460
[TBL] [Abstract][Full Text] [Related]
22. Motor and mental dysfunction in mother-daughter transmitted FXTAS.
Rodriguez-Revenga L; Pagonabarraga J; Gómez-Anson B; López-Mourelo O; Madrigal I; Xunclà M; Kulisevsky J; Milà M
Neurology; 2010 Oct; 75(15):1370-6. PubMed ID: 20938029
[TBL] [Abstract][Full Text] [Related]
23. Parkinsonism, dysautonomia, and intranuclear inclusions in a fragile X carrier: a clinical-pathological study.
Louis E; Moskowitz C; Friez M; Amaya M; Vonsattel JP
Mov Disord; 2006 Mar; 21(3):420-5. PubMed ID: 16250026
[TBL] [Abstract][Full Text] [Related]
24. Fragile X-associated tremor/ataxia syndrome--an older face of the fragile X gene.
Hagerman PJ; Hagerman RJ
Nat Clin Pract Neurol; 2007 Feb; 3(2):107-12. PubMed ID: 17279084
[TBL] [Abstract][Full Text] [Related]
25. A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changes.
Loesch DZ; Cook M; Litewka L; Gould E; Churchyard A; Tassone F; Slater HR; Storey E
J Med Genet; 2008 Mar; 45(3):179-81. PubMed ID: 18057083
[TBL] [Abstract][Full Text] [Related]
26. Penetrance of marked cognitive impairment in older male carriers of the FMR1 gene premutation.
Sévin M; Kutalik Z; Bergman S; Vercelletto M; Renou P; Lamy E; Vingerhoets FJ; Di Virgilio G; Boisseau P; Bezieau S; Pasquier L; Rival JM; Beckmann JS; Damier P; Jacquemont S
J Med Genet; 2009 Dec; 46(12):818-24. PubMed ID: 19542082
[TBL] [Abstract][Full Text] [Related]
27. Fragile X-premutation tremor/ataxia syndrome (FXTAS) in a young woman: clinical, genetics, MRI and 1H-MR spectroscopy correlates.
Sarac H; Henigsberg N; Markeljević J; Pavlisa G; Hof PR; Simić G
Coll Antropol; 2011 Jan; 35 Suppl 1():327-32. PubMed ID: 21648356
[TBL] [Abstract][Full Text] [Related]
28. [Fragile X-associated tremor/ataxia syndrome].
Han WW; Zhang L; Jiang H; Tang BS
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Feb; 28(1):52-5. PubMed ID: 21287510
[TBL] [Abstract][Full Text] [Related]
29. Argonaute-2-dependent rescue of a Drosophila model of FXTAS by FRAXE premutation repeat.
Sofola OA; Jin P; Botas J; Nelson DL
Hum Mol Genet; 2007 Oct; 16(19):2326-32. PubMed ID: 17635840
[TBL] [Abstract][Full Text] [Related]
30. [Neurodevelopmental (fragile X syndrome) and neurodegenerative (tremor/ataxia syndrome) disorders associated to the 'growth' of a gene].
Castro-Volio I; Cuenca-Berger P
Rev Neurol; 2005 Apr 1-15; 40(7):431-7. PubMed ID: 15849678
[TBL] [Abstract][Full Text] [Related]
31. Screening for FXTAS in 95 Spanish patients negative for Huntington disease.
Rodriguez-Revenga L; Santos MM; Sánchez A; Pujol M; Gómez-Anson B; Badenas C; Jiménez D; Madrigal I; Milà M
Genet Test; 2008 Mar; 12(1):135-8. PubMed ID: 18373410
[TBL] [Abstract][Full Text] [Related]
32. Mapping self-reports of working memory deficits to executive dysfunction in Fragile X Mental Retardation 1 (FMR1) gene premutation carriers asymptomatic for FXTAS.
Kogan CS; Cornish KM
Brain Cogn; 2010 Aug; 73(3):236-43. PubMed ID: 20573435
[TBL] [Abstract][Full Text] [Related]
33. The fragile X-associated tremor ataxia syndrome (FXTAS) in Indonesia.
Winarni TI; Mundhofir FE; Ediati A; Belladona M; Nillesen WM; Yntema HG; Hamel BC; Faradz SM; Hagerman RJ
Clin Genet; 2013 Mar; 83(3):263-8. PubMed ID: 22568721
[TBL] [Abstract][Full Text] [Related]
34. A fragile balance: FMR1 expression levels.
Oostra BA; Willemsen R
Hum Mol Genet; 2003 Oct; 12 Spec No 2():R249-57. PubMed ID: 12952862
[TBL] [Abstract][Full Text] [Related]
35. The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy.
Moore CJ; Daly EM; Tassone F; Tysoe C; Schmitz N; Ng V; Chitnis X; McGuire P; Suckling J; Davies KE; Hagerman RJ; Hagerman PJ; Murphy KC; Murphy DG
Brain; 2004 Dec; 127(Pt 12):2672-81. PubMed ID: 15483045
[TBL] [Abstract][Full Text] [Related]
36. [Triplet expansion cytosine-guanine-guanine: Three cases of OMIM syndrome in the same family].
González-Pérez J; Izquierdo-Álvarez S; Fuertes-Rodrigo C; Monge-Galindo L; Peña-Segura JL; López-Pisón FJ
Med Clin (Barc); 2016 Apr; 146(7):311-5. PubMed ID: 26776484
[TBL] [Abstract][Full Text] [Related]
37. Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism.
Pešić M; Dragašević Mišković N; Marjanović A; Dobričić V; Maksimović N; Svetel M; Perović D; Novaković I; Cirković S; Stanković I; Kostić V
Neurol Res; 2021 Apr; 43(4):321-326. PubMed ID: 33403926
[No Abstract] [Full Text] [Related]
38. Newborn, carrier, and early childhood screening recommendations for fragile X.
Abrams L; Cronister A; Brown WT; Tassone F; Sherman SL; Finucane B; McConkie-Rosell A; Hagerman R; Kaufmann WE; Picker J; Coffey S; Skinner D; Johnson V; Miller R; Berry-Kravis E
Pediatrics; 2012 Dec; 130(6):1126-35. PubMed ID: 23129072
[TBL] [Abstract][Full Text] [Related]
39. FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia.
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 A
Neurology; 2005 Jan; 64(1):145-7. PubMed ID: 15642922
[TBL] [Abstract][Full Text] [Related]
40. Screening for premutation in the FMR1 gene in male patients suspected of spinocerebellar ataxia.
Rajkiewicz M; Sułek-Piatkowska A; Krysa W; Zdzienicka E; Szirkowiec W; Zaremba J
Neurol Neurochir Pol; 2008; 42(6):497-504. PubMed ID: 19235102
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
