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 *

503 related articles for article (PubMed ID: 33757613)

  • 1. 'Essential Tremor' Phenotype in FMR1 Premutation/Gray Zone Sibling Series: Exploring Possible Genetic Modifiers.
    Loesch DZ; Duffy DL; Martin NG; Tassone F; Atkinson A; Storey E
    Twin Res Hum Genet; 2021 Apr; 24(2):95-102. PubMed ID: 33757613
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 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. 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]  

  • 8. The Spectrum of Neurological and White Matter Changes and Premutation Status Categories of Older Male Carriers of the
    Loesch DZ; Trost N; Bui MQ; Hammersley E; Lay ST; Annesley SJ; Sanislav O; Allan CY; Tassone F; Chen ZP; Ngoei KRW; Kemp BE; Francis D; Fisher PR; Storey E
    Front Genet; 2018; 9():531. PubMed ID: 30483310
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Carriage of One or Two FMR1 Premutation Alleles Seems to Have No Effect on Illness Severity in a FXTAS Female with an Autozygous FMR1 Premutation Allele.
    Rodriguez-Revenga L; Pagonabarraga J; Gómez-Anson B; López-Mourelo O; Izquierdo S; Alvarez-Mora MI; Granell E; Madrigal I; Milà M
    Cerebellum; 2016 Oct; 15(5):570-7. PubMed ID: 27315125
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Differential Progression of Motor Dysfunction Between Male and Female Fragile X Premutation Carriers Reveals Novel Aspects of Sex-Specific Neural Involvement.
    Loesch DZ; Tassone F; Atkinson A; Stimpson P; Trost N; Pountney DL; Storey E
    Front Mol Biosci; 2020; 7():577246. PubMed ID: 33511153
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fragile X-associated tremor/ataxia syndrome (FXTAS) in grey zone carriers.
    Liu Y; Winarni TI; Zhang L; Tassone F; Hagerman RJ
    Clin Genet; 2013 Jul; 84(1):74-7. PubMed ID: 23009394
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fragile X-associated tremor/ataxia syndrome: An under-recognised cause of tremor and ataxia.
    Kalus S; King J; Lui E; Gaillard F
    J Clin Neurosci; 2016 Jan; 23():162-164. PubMed ID: 26439425
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Gait and Functional Mobility Deficits in Fragile X-Associated Tremor/Ataxia Syndrome.
    O'Keefe JA; Robertson-Dick EE; Hall DA; Berry-Kravis E
    Cerebellum; 2016 Aug; 15(4):475-82. PubMed ID: 26298472
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Fragile x-associated tremor ataxia syndrome: the expanding clinical picture, pathophysiology, epidemiology, and update on treatment.
    Hall DA; O'keefe JA
    Tremor Other Hyperkinet Mov (N Y); 2012; 2():. PubMed ID: 23439567
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Neuropsychological findings from older premutation carrier males and their noncarrier siblings from families with fragile X syndrome.
    Allen EG; Hunter JE; Rusin M; Juncos J; Novak G; Hamilton D; Shubeck L; Charen K; Sherman SL
    Neuropsychology; 2011 May; 25(3):404-411. PubMed ID: 21443343
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical phenotypes of a juvenile sibling pair carrying the fragile X premutation.
    Basuta K; Narcisa V; Chavez A; Kumar M; Gane L; Hagerman R; Tassone F
    Am J Med Genet A; 2011 Mar; 155A(3):519-25. PubMed ID: 21344625
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 26.