118 related articles for article (PubMed ID: 15657320)
1. Premutation alleles and fragile X-associated tremor/ataxia syndrome.
Toft M; Farrer M
JAMA; 2005 Jan; 293(3):296; author reply 296-7. PubMed ID: 15657320
[No Abstract] [Full Text] [Related]
2. Premutation alleles associated with Parkinson disease and essential tremor.
Deng H; Le W; Jankovic J
JAMA; 2004 Oct; 292(14):1685-6. PubMed ID: 15479932
[No Abstract] [Full Text] [Related]
3. Identification of FXTAS presenting with SCA 12 like phenotype in India.
Faruq M; Srivastava AK; Suroliya V; Kumar D; Garg A; Shukla G; Behari M
Parkinsonism Relat Disord; 2014 Oct; 20(10):1089-93. PubMed ID: 25085749
[TBL] [Abstract][Full Text] [Related]
4. Screening for FMR-1 premutations in 122 older Flemish males presenting with ataxia.
Van Esch H; Dom R; Bex D; Salden I; Caeckebeke J; Wibail A; Borghgraef M; Legius E; Fryns JP; Matthijs G
Eur J Hum Genet; 2005 Jan; 13(1):121-3. PubMed ID: 15483640
[TBL] [Abstract][Full Text] [Related]
5. Screen for expanded FMR1 alleles in patients with essential tremor.
Garcia Arocena D; Louis ED; Tassone F; Gilliam TC; Ottman R; Jacquemont S; Hagerman PJ
Mov Disord; 2004 Aug; 19(8):930-3. PubMed ID: 15300658
[TBL] [Abstract][Full Text] [Related]
6. Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome.
Tassone F; Hagerman RJ; Garcia-Arocena D; Khandjian EW; Greco CM; Hagerman PJ
J Med Genet; 2004 Apr; 41(4):e43. PubMed ID: 15060119
[No Abstract] [Full Text] [Related]
7. The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group.
Kamm C; Healy DG; Quinn NP; Wüllner U; Moller JC; Schols L; Geser F; Burk K; Børglum AD; Pellecchia MT; Tolosa E; del Sorbo F; Nilsson C; Bandmann O; Sharma M; Mayer P; Gasteiger M; Haworth A; Ozawa T; Lees AJ; Short J; Giunti P; Holinski-Feder E; Illig T; Wichmann HE; Wenning GK; Wood NW; Gasser T;
Brain; 2005 Aug; 128(Pt 8):1855-60. PubMed ID: 15947063
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. Fragile X-associated tremor/ataxia syndrome (FXTAS).
Hagerman PJ; Hagerman RJ
Ment Retard Dev Disabil Res Rev; 2004; 10(1):25-30. PubMed ID: 14994285
[TBL] [Abstract][Full Text] [Related]
10. Familial essential tremor is not associated with SCA-12 mutation in southern Italy.
Nicoletti G; Annesi G; Carrideo S; Tomaino C; Di Costanzo A; Zappia M; Quattrone A
Mov Disord; 2002 Jul; 17(4):837-8. PubMed ID: 12210890
[TBL] [Abstract][Full Text] [Related]
11. Screening for FXTAS.
Jacquemont S
Eur J Hum Genet; 2005 Jan; 13(1):2-3. PubMed ID: 15494737
[No Abstract] [Full Text] [Related]
12. FXTAS, SCA10, and SCA17 in American patients with movement disorders.
Seixas AI; Maurer MH; Lin M; Callahan C; Ahuja A; Matsuura T; Ross CA; Hisama FM; Silveira I; Margolis RL
Am J Med Genet A; 2005 Jul; 136(1):87-9. PubMed ID: 15889413
[No Abstract] [Full Text] [Related]
13. Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort.
Tan EK; Zhao Y; Puong KY; Law HY; Chan LL; Yew K; Tan C; Shen H; Chandran VR; Teoh ML; Yih Y; Pavanni R; Wong MC; Ng IS
Neurology; 2004 Jul; 63(2):362-3. PubMed ID: 15277639
[TBL] [Abstract][Full Text] [Related]
14. [Fragile X-associated tremor/ataxia syndrome].
Lisik M
Neurol Neurochir Pol; 2005; 39(3):226-9. PubMed ID: 15981162
[TBL] [Abstract][Full Text] [Related]
15. Should we screen for FMR1 premutations in female subjects presenting with ataxia?
Van Esch H; Matthijs G; Fryns JP
Ann Neurol; 2005 Jun; 57(6):932-3. PubMed ID: 15929044
[No Abstract] [Full Text] [Related]
16. FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy.
Biancalana V; Toft M; Le Ber I; Tison F; Scherrer E; Thibodeau S; Mandel JL; Brice A; Farrer MJ; Dürr A
Arch Neurol; 2005 Jun; 62(6):962-6. PubMed ID: 15956167
[TBL] [Abstract][Full Text] [Related]
17. Premutations in the FMR1 gene are uncommon in men undergoing genetic testing for spinocerebellar ataxia.
Adams SA; Steenblock KJ; Thibodeau SN; Lindor NM
J Neurogenet; 2008; 22(1):77-92. PubMed ID: 18363164
[TBL] [Abstract][Full Text] [Related]
18. A case of fragile X premutation tremor/ataxia syndrome with evidence of mitochondrial dysfunction.
Rizzo G; Pizza F; Scaglione C; Tonon C; Lodi R; Barbiroli B; Ambrosetto P; Martinelli P
Mov Disord; 2006 Sep; 21(9):1541-2. PubMed ID: 16830323
[No Abstract] [Full Text] [Related]
19. 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]
20. Genetic cerebellar ataxias.
Storey E
Semin Neurol; 2014 Jul; 34(3):280-92. PubMed ID: 25192506
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]