These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

395 related articles for article (PubMed ID: 20573435)

  • 1. 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]  

  • 2. [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]  

  • 3. Investigation of memory, executive functions, and anatomic correlates in asymptomatic FMR1 premutation carriers.
    Hippolyte L; Battistella G; Perrin AG; Fornari E; Cornish KM; Beckmann JS; Niederhauser J; Vingerhoets FJ; Draganski B; Maeder P; Jacquemont S
    Neurobiol Aging; 2014 Aug; 35(8):1939-46. PubMed ID: 24612675
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Tremor/ataxia syndrome and fragile X premutation: diagnostic caveats.
    Loesch DZ; Litewka L; Churchyard A; Gould E; Tassone F; Cook M
    J Clin Neurosci; 2007 Mar; 14(3):245-8. PubMed ID: 17194594
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. An fMRI study of the prefrontal activity during the performance of a working memory task in premutation carriers of the fragile X mental retardation 1 gene with and without fragile X-associated tremor/ataxia syndrome (FXTAS).
    Hashimoto R; Backer KC; Tassone F; Hagerman RJ; Rivera SM
    J Psychiatr Res; 2011 Jan; 45(1):36-43. PubMed ID: 20537351
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Age- and CGG repeat-related slowing of manual movement in fragile X carriers: A prodrome of fragile X-associated tremor ataxia syndrome?
    Shickman R; Famula J; Tassone F; Leehey M; Ferrer E; Rivera SM; Hessl D
    Mov Disord; 2018 Apr; 33(4):628-636. PubMed ID: 29389022
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Selective spatial processing deficits in an at-risk subgroup of the fragile X premutation.
    Hocking DR; Kogan CS; Cornish KM
    Brain Cogn; 2012 Jun; 79(1):39-44. PubMed ID: 22417865
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Prenatal carrier testing for fragile X: counseling issues and challenges.
    Musci TJ; Moyer K
    Obstet Gynecol Clin North Am; 2010 Mar; 37(1):61-70, Table of Contents. PubMed ID: 20494258
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The emerging fragile X premutation phenotype: evidence from the domain of social cognition.
    Cornish K; Kogan C; Turk J; Manly T; James N; Mills A; Dalton A
    Brain Cogn; 2005 Feb; 57(1):53-60. PubMed ID: 15629215
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization and Early Detection of Balance Deficits in Fragile X Premutation Carriers With and Without Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS).
    O'Keefe JA; Robertson-Dick E; Dunn EJ; Li Y; Deng Y; Fiutko AN; Berry-Kravis E; Hall DA
    Cerebellum; 2015 Dec; 14(6):650-62. PubMed ID: 25763861
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Progressive ataxia and cognitive deficits caused by premutation in the fragile-X-mental retardation gene].
    Roks G; Sistermans EA; de Vries LB; Nijssen PC
    Ned Tijdschr Geneeskd; 2005 Oct; 149(43):2418-22. PubMed ID: 16277133
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Static and dynamic postural control deficits in aging fragile X mental retardation 1 (FMR1) gene premutation carriers.
    Wang Z; Khemani P; Schmitt LM; Lui S; Mosconi MW
    J Neurodev Disord; 2019 Jan; 11(1):2. PubMed ID: 30665341
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Brain structure in asymptomatic FMR1 premutation carriers at risk for fragile X-associated tremor/ataxia syndrome.
    Battistella G; Niederhauser J; Fornari E; Hippolyte L; Gronchi Perrin A; Lesca G; Forzano F; Hagmann P; Vingerhoets FJ; Draganski B; Maeder P; Jacquemont S
    Neurobiol Aging; 2013 Jun; 34(6):1700-7. PubMed ID: 23298734
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Fragile X-associated tremor/ataxia phenotype in a male carrier of unmethylated full mutation in the FMR1 gene.
    Loesch DZ; Sherwell S; Kinsella G; Tassone F; Taylor A; Amor D; Sung S; Evans A
    Clin Genet; 2012 Jul; 82(1):88-92. PubMed ID: 21476992
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 20.