113 related articles for article (PubMed ID: 15929093)
1. Premutations in the FMR1 gene as a modifying factor in Parkin-associated Parkinson's disease?
Hedrich K; Pramstaller PP; Stübke K; Hiller A; Kabakci K; Purmann S; Kasten M; Scaglione C; Schwinger E; Volkmann J; Kostic V; Vieregge P; Martinelli P; Abbruzzese G; Klein C; Zühlke C
Mov Disord; 2005 Aug; 20(8):1060-2. PubMed ID: 15929093
[TBL] [Abstract][Full Text] [Related]
2. Parkinsonism, FXTAS, and FMR1 premutations.
Toft M; Aasly J; Bisceglio G; Adler CH; Uitti RJ; Krygowska-Wajs A; Lynch T; Wszolek ZK; Farrer MJ
Mov Disord; 2005 Feb; 20(2):230-3. PubMed ID: 15390127
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Compound heterozygosity at the FMR1 gene.
Hegde MR; Fawkner M; Chong B; McGaughran J; Gilbert D; Love DR
Genet Test; 2001; 5(2):135-8. PubMed ID: 11551100
[TBL] [Abstract][Full Text] [Related]
5. A neuropsychological investigation of male premutation carriers of fragile X syndrome.
Moore CJ; Daly EM; Schmitz N; Tassone F; Tysoe C; Hagerman RJ; Hagerman PJ; Morris RG; Murphy KC; Murphy DG
Neuropsychologia; 2004; 42(14):1934-47. PubMed ID: 15381024
[TBL] [Abstract][Full Text] [Related]
6. Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers.
Kenneson A; Zhang F; Hagedorn CH; Warren ST
Hum Mol Genet; 2001 Jul; 10(14):1449-54. PubMed ID: 11448936
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. Magnetic resonance imaging study in older fragile X premutation male carriers.
Loesch DZ; Litewka L; Brotchie P; Huggins RM; Tassone F; Cook M
Ann Neurol; 2005 Aug; 58(2):326-30. PubMed ID: 16049924
[TBL] [Abstract][Full Text] [Related]
11. Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population.
Patsalis PC; Sismani C; Stylianou S; Ioannou P; Joseph G; Manoli P; Holden JJ; Hettinger JA
Am J Med Genet; 1999 May; 84(3):217-20. PubMed ID: 10331595
[TBL] [Abstract][Full Text] [Related]
12. No association between FMR1 premutations and multiple system atrophy.
Yabe I; Soma H; Takei A; Fujik N; Sasaki H
J Neurol; 2004 Nov; 251(11):1411-2. PubMed ID: 15592742
[No Abstract] [Full Text] [Related]
13. Molecular predictors of cognitive involvement in female carriers of fragile X syndrome.
Taylor AK; Safanda JF; Fall MZ; Quince C; Lang KA; Hull CE; Carpenter I; Staley LW; Hagerman RJ
JAMA; 1994 Feb; 271(7):507-14. PubMed ID: 8301764
[TBL] [Abstract][Full Text] [Related]
14. Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population.
Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; Levine RA; Brunberg JA; Zhang L; Jardini T; Gane LW; Harris SW; Herman K; Grigsby J; Greco CM; Berry-Kravis E; Tassone F; Hagerman PJ
JAMA; 2004 Jan; 291(4):460-9. PubMed ID: 14747503
[TBL] [Abstract][Full Text] [Related]
15. Reduced FMR1 mRNA translation efficiency in fragile X patients with premutations.
Primerano B; Tassone F; Hagerman RJ; Hagerman P; Amaldi F; Bagni C
RNA; 2002 Dec; 8(12):1482-8. PubMed ID: 12515381
[TBL] [Abstract][Full Text] [Related]
16. Screen for excess FMR1 premutation alleles among males with parkinsonism.
Kraff J; Tang HT; Cilia R; Canesi M; Pezzoli G; Goldwurm S; Hagerman PJ; Tassone F
Arch Neurol; 2007 Jul; 64(7):1002-6. PubMed ID: 17620491
[TBL] [Abstract][Full Text] [Related]
17. Analysis of FMR1 gene expression in female premutation carriers using robust segmented linear regression models.
García-Alegría E; Ibáñez B; Mínguez M; Poch M; Valiente A; Sanz-Parra A; Martinez-Bouzas C; Beristain E; Tejada MI
RNA; 2007 May; 13(5):756-62. PubMed ID: 17449730
[TBL] [Abstract][Full Text] [Related]
18. Reverse mutations in the fragile X syndrome.
Brown WT; Houck GE; Ding X; Zhong N; Nolin S; Glicksman A; Dobkin C; Jenkins EC
Am J Med Genet; 1996 Aug; 64(2):287-92. PubMed ID: 8844067
[TBL] [Abstract][Full Text] [Related]
19. Fragile X gene premutation in multiple system atrophy.
Garland EM; Vnencak-Jones CL; Biaggioni I; Davis TL; Montine TJ; Robertson D
J Neurol Sci; 2004 Dec; 227(1):115-8. PubMed ID: 15546601
[TBL] [Abstract][Full Text] [Related]
20. Fragile X premutations are not a major cause of early menopause.
Kenneson A; Cramer DW; Warren ST
Am J Hum Genet; 1997 Dec; 61(6):1362-9. PubMed ID: 9399905
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
