397 related articles for article (PubMed ID: 18310677)
1. Anti-Mullerian hormone indicates early ovarian decline in fragile X mental retardation (FMR1) premutation carriers: a preliminary study.
Rohr J; Allen EG; Charen K; Giles J; He W; Dominguez C; Sherman SL
Hum Reprod; 2008 May; 23(5):1220-5. PubMed ID: 18310677
[TBL] [Abstract][Full Text] [Related]
2. Correlation of triple repeats on the FMR1 (fragile X) gene to ovarian reserve: a new infertility test?
Gleicher N; Weghofer A; Oktay K; Barad DH
Acta Obstet Gynecol Scand; 2009; 88(9):1024-30. PubMed ID: 19642041
[TBL] [Abstract][Full Text] [Related]
3. A pilot study of premature ovarian senescence: II. Different genotype and phenotype for genetic and autoimmune etiologies.
Gleicher N; Weghofer A; Barad DH
Fertil Steril; 2009 May; 91(5):1707-11. PubMed ID: 18384784
[TBL] [Abstract][Full Text] [Related]
4. Reproductive health of adolescent girls who carry the FMR1 premutation: expected phenotype based on current knowledge of fragile x-associated primary ovarian insufficiency.
De Caro JJ; Dominguez C; Sherman SL
Ann N Y Acad Sci; 2008; 1135():99-111. PubMed ID: 18574214
[TBL] [Abstract][Full Text] [Related]
5. Premature ovarian failure and fragile X female premutation carriers: no evidence for a skewed X-chromosome inactivation pattern.
Rodriguez-Revenga L; Madrigal I; Badenas C; Xunclà M; Jiménez L; Milà M
Menopause; 2009; 16(5):944-9. PubMed ID: 19373114
[TBL] [Abstract][Full Text] [Related]
6. Diminished ovarian reserve is not observed in infertility patients with high normal CGG repeats on the fragile X mental retardation 1 (FMR1) gene.
Schufreider A; McQueen DB; Lee SM; Allon R; Uhler ML; Davie J; Feinberg EC
Hum Reprod; 2015 Nov; 30(11):2686-92. PubMed ID: 26345686
[TBL] [Abstract][Full Text] [Related]
7. The relationship between the number of CGG repeats and serum level of anti-Müllerian hormone in women without FMR1 premutation.
Choe SA; Kim KC; Lee JY; Kim CH; Hwang D; Jee BC
Eur J Obstet Gynecol Reprod Biol; 2013 Jul; 169(2):275-8. PubMed ID: 23731704
[TBL] [Abstract][Full Text] [Related]
8. Analysis of the molecular parameters that could predict the risk of manifesting premature ovarian failure in female premutation carriers of fragile X syndrome.
Tejada MI; García-Alegría E; Bilbao A; Martínez-Bouzas C; Beristain E; Poch M; Ramos-Arroyo MA; López B; Fernandez Carvajal I; Ribate MP; Ramos F
Menopause; 2008; 15(5):945-9. PubMed ID: 18427356
[TBL] [Abstract][Full Text] [Related]
9. [Abnormal function of ovaries in women carriers of premutation in the FMR1 gene].
Lisik MZ
Wiad Lek; 2007; 60(5-6):265-9. PubMed ID: 17966892
[TBL] [Abstract][Full Text] [Related]
10. Prevalence and instability of fragile X alleles: implications for offering fragile X prenatal diagnosis.
Cronister A; Teicher J; Rohlfs EM; Donnenfeld A; Hallam S
Obstet Gynecol; 2008 Mar; 111(3):596-601. PubMed ID: 18310361
[TBL] [Abstract][Full Text] [Related]
11. Very early premature ovarian failure in two sisters compound heterozygous for the FMR1 premutation.
Van Esch H; Buekenhout L; Race V; Matthijs G
Eur J Med Genet; 2009; 52(1):37-40. PubMed ID: 19041959
[TBL] [Abstract][Full Text] [Related]
12. A pilot study of premature ovarian senescence: I. Correlation of triple CGG repeats on the FMR1 gene to ovarian reserve parameters FSH and anti-Müllerian hormone.
Gleicher N; Weghofer A; Barad DH
Fertil Steril; 2009 May; 91(5):1700-6. PubMed ID: 18384775
[TBL] [Abstract][Full Text] [Related]
13. Association of FMR1 repeat size with ovarian dysfunction.
Sullivan AK; Marcus M; Epstein MP; Allen EG; Anido AE; Paquin JJ; Yadav-Shah M; Sherman SL
Hum Reprod; 2005 Feb; 20(2):402-12. PubMed ID: 15608041
[TBL] [Abstract][Full Text] [Related]
14. Penetrance of marked cognitive impairment in older male carriers of the FMR1 gene premutation.
Sévin M; Kutalik Z; Bergman S; Vercelletto M; Renou P; Lamy E; Vingerhoets FJ; Di Virgilio G; Boisseau P; Bezieau S; Pasquier L; Rival JM; Beckmann JS; Damier P; Jacquemont S
J Med Genet; 2009 Dec; 46(12):818-24. PubMed ID: 19542082
[TBL] [Abstract][Full Text] [Related]
15. Ovarian dysfunction and FMR1 alleles in a large Italian family with POF and FRAXA disorders: case report.
Miano MG; Laperuta C; Chiurazzi P; D'Urso M; Ursini MV
BMC Med Genet; 2007 Apr; 8():18. PubMed ID: 17428316
[TBL] [Abstract][Full Text] [Related]
16. Examination of reproductive aging milestones among women who carry the FMR1 premutation.
Allen EG; Sullivan AK; Marcus M; Small C; Dominguez C; Epstein MP; Charen K; He W; Taylor KC; Sherman SL
Hum Reprod; 2007 Aug; 22(8):2142-52. PubMed ID: 17588953
[TBL] [Abstract][Full Text] [Related]
17. Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation.
Bodega B; Bione S; Dalprà L; Toniolo D; Ornaghi F; Vegetti W; Ginelli E; Marozzi A
Hum Reprod; 2006 Apr; 21(4):952-7. PubMed ID: 16361284
[TBL] [Abstract][Full Text] [Related]
18. Increased frequency of occult fragile X-associated primary ovarian insufficiency in infertile women with evidence of impaired ovarian function.
Karimov CB; Moragianni VA; Cronister A; Srouji S; Petrozza J; Racowsky C; Ginsburg E; Thornton KL; Welt CK
Hum Reprod; 2011 Aug; 26(8):2077-83. PubMed ID: 21646280
[TBL] [Abstract][Full Text] [Related]
19. Premature ovarian failure in the fragile X syndrome.
Sherman SL
Am J Med Genet; 2000; 97(3):189-94. PubMed ID: 11449487
[TBL] [Abstract][Full Text] [Related]
20. AMH in women with diminished ovarian reserve: potential differences by FMR1 CGG repeat level.
Pastore LM; McMurry TL; Williams CD; Baker VL; Young SL
J Assist Reprod Genet; 2014 Oct; 31(10):1295-301. PubMed ID: 24938362
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]