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 *

190 related articles for article (PubMed ID: 34658954)

  • 1. Predictors of Comorbid Conditions in Women Who Carry an
    Allen EG; Charen K; Hipp HS; Shubeck L; Amin A; He W; Hunter JE; Shelly KE; Sherman SL
    Front Psychiatry; 2021; 12():715922. PubMed ID: 34658954
    [No Abstract]   [Full Text] [Related]  

  • 2. Clustering of comorbid conditions among women who carry an FMR1 premutation.
    Allen EG; Charen K; Hipp HS; Shubeck L; Amin A; He W; Hunter JE; Sherman SL
    Genet Med; 2020 Apr; 22(4):758-766. PubMed ID: 31896764
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Presence of inclusions positive for polyglycine containing protein, FMRpolyG, indicates that repeat-associated non-AUG translation plays a role in fragile X-associated primary ovarian insufficiency.
    Buijsen RA; Visser JA; Kramer P; Severijnen EA; Gearing M; Charlet-Berguerand N; Sherman SL; Berman RF; Willemsen R; Hukema RK
    Hum Reprod; 2016 Jan; 31(1):158-68. PubMed ID: 26537920
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [FMR1 PREMUTATION CARRIERS - ARE THEY REALLY ASYMPTOMATIC?].
    Elizur S; Berkenstadt M; Ries-Levavi L; Gruber N; Pinhas-Hamiel O; Hassin-Baer S; Raas-Rothschild A; Raanani H; Cukierman-Yaffe T; Orvieto R; Cohen Y; Gabis L
    Harefuah; 2018 Apr; 157(4):241-244. PubMed ID: 29688643
    [TBL] [Abstract][Full Text] [Related]  

  • 5. FMRpolyG accumulates in FMR1 premutation granulosa cells.
    Friedman-Gohas M; Elizur SE; Dratviman-Storobinsky O; Aizer A; Haas J; Raanani H; Orvieto R; Cohen Y
    J Ovarian Res; 2020 Feb; 13(1):22. PubMed ID: 32101156
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fentanyl overdose in a female with the
    El-Deeb M; Adams P; Schneider A; Salcedo-Arellano MJ; Tassone F; Hagerman R
    J Mol Genet (Isleworth); 2018 Nov; 1(1):. PubMed ID: 31032490
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Co-occurring diagnoses among FMR1 premutation allele carriers.
    Hunter JE; Rohr JK; Sherman SL
    Clin Genet; 2010 Apr; 77(4):374-81. PubMed ID: 20059484
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Understanding decreased fertility in women carriers of the FMR1 premutation: a possible mechanism for Fragile X-Associated Primary Ovarian Insufficiency (FXPOI).
    Peprah E
    Reprod Health; 2014 Aug; 11():67. PubMed ID: 25134882
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An explanation of the mechanisms underlying fragile X-associated premature ovarian insufficiency.
    Rose BI; Brown SE
    J Assist Reprod Genet; 2020 Jun; 37(6):1313-1322. PubMed ID: 32377997
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Associated Clinical Disorders Diagnosed by Medical Specialists in 188 FMR1 Premutation Carriers Found in the Last 25 Years in the Spanish Basque Country: A Retrospective Study.
    Merino S; Ibarluzea N; Maortua H; Prieto B; Rouco I; López-Aríztegui MA; Tejada MI
    Genes (Basel); 2016 Oct; 7(10):. PubMed ID: 27775646
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Altered expression of the FMR1 splicing variants landscape in premutation carriers.
    Tseng E; Tang HT; AlOlaby RR; Hickey L; Tassone F
    Biochim Biophys Acta Gene Regul Mech; 2017 Nov; 1860(11):1117-1126. PubMed ID: 28888471
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Clinical implications of somatic allele expansion in female FMR1 premutation carriers.
    Aishworiya R; Hwang YH; Santos E; Hayward B; Usdin K; Durbin-Johnson B; Hagerman R; Tassone F
    Sci Rep; 2023 Apr; 13(1):7050. PubMed ID: 37120588
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Tremor-Ataxia syndrome and primary ovarian insufficiency in an
    Saldarriaga-Gil W; Rodriguez-Guerrero T; Fandiño-Losada A; Ramirez-Cheyne J
    Colomb Med (Cali); 2017 Sep; 48(3):148-151. PubMed ID: 29299012
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Neuropsychological changes in FMR1 premutation carriers and onset of fragile X-associated tremor/ataxia syndrome.
    Famula J; Ferrer E; Hagerman RJ; Tassone F; Schneider A; Rivera SM; Hessl D
    J Neurodev Disord; 2022 Mar; 14(1):23. PubMed ID: 35321639
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A Chinese case of fragile X-associated tremor/ataxia syndrome (FXTAS) with orthostatic tremor:case report and literature review on tremor in FXTAS.
    Zhao C; Liu Y; Wang Y; Li H; Zhang B; Yue Y; Zhang J
    BMC Neurol; 2020 Apr; 20(1):145. PubMed ID: 32312236
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Fragile X-Associated Neuropsychiatric Disorders (FXAND) in Young Fragile X Premutation Carriers.
    Aishworiya R; Protic D; Tang SJ; Schneider A; Tassone F; Hagerman R
    Genes (Basel); 2022 Dec; 13(12):. PubMed ID: 36553666
    [No Abstract]   [Full Text] [Related]  

  • 18. Family history of FXTAS is associated with age-related cognitive-linguistic decline among mothers with the FMR1 premutation.
    Klusek J; Fairchild A; Moser C; Mailick MR; Thurman AJ; Abbeduto L
    J Neurodev Disord; 2022 Jan; 14(1):7. PubMed ID: 35026985
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fragile X premutation in women: recognizing the health challenges beyond primary ovarian insufficiency.
    Hoyos LR; Thakur M
    J Assist Reprod Genet; 2017 Mar; 34(3):315-323. PubMed ID: 27995424
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.