BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

320 related articles for article (PubMed ID: 24028275)

  • 1. FXTAS in an unmethylated mosaic male with fragile X syndrome from Chile.
    Santa MarĂ­a L; Pugin A; Alliende MA; Aliaga S; Curotto B; Aravena T; Tang HT; Mendoza-Morales G; Hagerman R; Tassone F
    Clin Genet; 2014 Oct; 86(4):378-82. PubMed ID: 24028275
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program.
    Jarmolowicz AI; Baker EK; Bartlett E; Francis D; Ling L; Gamage D; Delatycki MB; Godler DE
    Am J Med Genet A; 2021 May; 185(5):1498-1503. PubMed ID: 33544979
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Partially methylated alleles, microdeletion, and tissue mosaicism in a fragile X male with tremor and ataxia at 30 years of age: A case report.
    Hwang YT; Aliaga SM; Arpone M; Francis D; Li X; Chong B; Slater HR; Rogers C; Bretherton L; Hunter M; Heard R; Godler DE
    Am J Med Genet A; 2016 Dec; 170(12):3327-3332. PubMed ID: 27696642
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fragile X-associated tremor/ataxia syndrome: influence of the FMR1 gene on motor fiber tracts in males with normal and premutation alleles.
    Wang JY; Hessl D; Schneider A; Tassone F; Hagerman RJ; Rivera SM
    JAMA Neurol; 2013 Aug; 70(8):1022-9. PubMed ID: 23753897
    [TBL] [Abstract][Full Text] [Related]  

  • 5. High functioning male with fragile X syndrome and fragile X-associated tremor/ataxia syndrome.
    Basuta K; Schneider A; Gane L; Polussa J; Woodruff B; Pretto D; Hagerman R; Tassone F
    Am J Med Genet A; 2015 Sep; 167A(9):2154-61. PubMed ID: 25920745
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Unmethylated Mosaic Full Mutation Males without Fragile X Syndrome.
    Tak Y; Schneider A; Santos E; Randol JL; Tassone F; Hagerman P; Hagerman RJ
    Genes (Basel); 2024 Mar; 15(3):. PubMed ID: 38540390
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Fragile X-associated tremor ataxia syndrome in FMR1 gray zone allele carriers.
    Hall D; Tassone F; Klepitskaya O; Leehey M
    Mov Disord; 2012 Feb; 27(2):296-300. PubMed ID: 22161987
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS): Pathophysiology and Clinical Implications.
    Cabal-Herrera AM; Tassanakijpanich N; Salcedo-Arellano MJ; Hagerman RJ
    Int J Mol Sci; 2020 Jun; 21(12):. PubMed ID: 32575683
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A methylation PCR method determines
    Hadd AG; Filipovic-Sadic S; Zhou L; Williams A; Latham GJ; Berry-Kravis E; Hall DA
    Clin Epigenetics; 2016; 8():130. PubMed ID: 27980694
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Unstable mutations in the FMR1 gene and the phenotypes.
    Loesch D; Hagerman R
    Adv Exp Med Biol; 2012; 769():78-114. PubMed ID: 23560306
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The spectrum of tremor among carriers of the FMR1 premutation with or without the fragile X-associated tremor/ataxia syndrome (FXTAS).
    Fay-Karmon T; Hassin-Baer S
    Parkinsonism Relat Disord; 2019 Aug; 65():32-38. PubMed ID: 31126791
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Preliminary evidence of an effect of cerebellar volume on postural sway in FMR1 premutation males.
    Birch RC; Hocking DR; Cornish KM; Menant JC; Georgiou-Karistianis N; Godler DE; Wen W; Hackett A; Rogers C; Trollor JN
    Genes Brain Behav; 2015 Mar; 14(3):251-9. PubMed ID: 25689687
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Methadone use in a male with the FMRI premutation and FXTAS.
    Muzar Z; Lozano R; Schneider A; Adams PE; Faradz SM; Tassone F; Hagerman RJ
    Am J Med Genet A; 2015 Jun; 167(6):1354-9. PubMed ID: 25900641
    [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. Volumetric brain changes in females with fragile X-associated tremor/ataxia syndrome (FXTAS).
    Adams JS; Adams PE; Nguyen D; Brunberg JA; Tassone F; Zhang W; Koldewyn K; Rivera SM; Grigsby J; Zhang L; DeCarli C; Hagerman PJ; Hagerman RJ
    Neurology; 2007 Aug; 69(9):851-9. PubMed ID: 17724287
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Parkinsonism in fragile X-associated tremor/ataxia syndrome (FXTAS): revisited.
    Niu YQ; Yang JC; Hall DA; Leehey MA; Tassone F; Olichney JM; Hagerman RJ; Zhang L
    Parkinsonism Relat Disord; 2014 Apr; 20(4):456-9. PubMed ID: 24491663
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 16.