285 related articles for article (PubMed ID: 33443313)
1. Fragile X premutation and associated health conditions: A review.
Tassanakijpanich N; Hagerman RJ; Worachotekamjorn J
Clin Genet; 2021 Jun; 99(6):751-760. PubMed ID: 33443313
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. 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]
4. 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]
5. [Triplet expansion cytosine-guanine-guanine: Three cases of OMIM syndrome in the same family].
González-Pérez J; Izquierdo-Álvarez S; Fuertes-Rodrigo C; Monge-Galindo L; Peña-Segura JL; López-Pisón FJ
Med Clin (Barc); 2016 Apr; 146(7):311-5. PubMed ID: 26776484
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Fragile X syndrome and fragile X-associated tremor ataxia syndrome.
Hall DA; Berry-Kravis E
Handb Clin Neurol; 2018; 147():377-391. PubMed ID: 29325626
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on
Tassone F; Protic D; Allen EG; Archibald AD; Baud A; Brown TW; Budimirovic DB; Cohen J; Dufour B; Eiges R; Elvassore N; Gabis LV; Grudzien SJ; Hall DA; Hessl D; Hogan A; Hunter JE; Jin P; Jiraanont P; Klusek J; Kooy RF; Kraan CM; Laterza C; Lee A; Lipworth K; Losh M; Loesch D; Lozano R; Mailick MR; Manolopoulos A; Martinez-Cerdeno V; McLennan Y; Miller RM; Montanaro FAM; Mosconi MW; Potter SN; Raspa M; Rivera SM; Shelly K; Todd PK; Tutak K; Wang JY; Wheeler A; Winarni TI; Zafarullah M; Hagerman RJ
Cells; 2023 Sep; 12(18):. PubMed ID: 37759552
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Mechanisms of Genome Instability in the Fragile X-Related Disorders.
Hayward BE; Usdin K
Genes (Basel); 2021 Oct; 12(10):. PubMed ID: 34681027
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Differential increases of specific FMR1 mRNA isoforms in premutation carriers.
Pretto DI; Eid JS; Yrigollen CM; Tang HT; Loomis EW; Raske C; Durbin-Johnson B; Hagerman PJ; Tassone F
J Med Genet; 2015 Jan; 52(1):42-52. PubMed ID: 25358671
[TBL] [Abstract][Full Text] [Related]
16. CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size.
Ludwig AL; Espinal GM; Pretto DI; Jamal AL; Arque G; Tassone F; Berman RF; Hagerman PJ
Hum Mol Genet; 2014 Jun; 23(12):3228-38. PubMed ID: 24463622
[TBL] [Abstract][Full Text] [Related]
17. [Fragile X syndrome and FMR1-dependent diseases - clinical presentation, epidemiology and molecular background].
Landowska A; Rzońca S; Bal J; Gos M
Dev Period Med; 2018; 22(1):14-21. PubMed ID: 29641417
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]