Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 131

1.

Recurrent aberrations identified by array-CGH in patients with Mayer-Rokitansky-Küster-Hauser syndrome.

Ledig S, Schippert C, Strick R, Beckmann MW, Oppelt PG, Wieacker P.

Fertil Steril. 2011 Apr;95(5):1589-94. doi: 10.1016/j.fertnstert.2010.07.1062. Epub 2010 Aug 24.

PMID:
20797712
2.

Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports.

Bernardini L, Gimelli S, Gervasini C, Carella M, Baban A, Frontino G, Barbano G, Divizia MT, Fedele L, Novelli A, Béna F, Lalatta F, Miozzo M, Dallapiccola B.

Orphanet J Rare Dis. 2009 Nov 4;4:25. doi: 10.1186/1750-1172-4-25.

3.

Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.

Chen MJ, Wei SY, Yang WS, Wu TT, Li HY, Ho HN, Yang YS, Chen PL.

Hum Reprod. 2015 Jul;30(7):1732-42. doi: 10.1093/humrep/dev095. Epub 2015 Apr 29.

PMID:
25924657
4.

Frame shift mutation of LHX1 is associated with Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome.

Ledig S, Brucker S, Barresi G, Schomburg J, Rall K, Wieacker P.

Hum Reprod. 2012 Sep;27(9):2872-5. doi: 10.1093/humrep/des206. Epub 2012 Jun 26.

PMID:
22740494
5.

Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci.

Morcel K, Watrin T, Pasquier L, Rochard L, Le Caignec C, Dubourg C, Loget P, Paniel BJ, Odent S, David V, Pellerin I, Bendavid C, Guerrier D.

Orphanet J Rare Dis. 2011 Mar 15;6:9. doi: 10.1186/1750-1172-6-9.

6.

DNA copy number variations are important in the complex genetic architecture of müllerian disorders.

McGowan R, Tydeman G, Shapiro D, Craig T, Morrison N, Logan S, Balen AH, Ahmed SF, Deeny M, Tolmie J, Tobias ES.

Fertil Steril. 2015 Apr;103(4):1021-1030.e1. doi: 10.1016/j.fertnstert.2015.01.008. Epub 2015 Feb 20.

PMID:
25707337
7.

The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome without and with associated features: two separate entities?

Strübbe EH, Cremers CW, Willemsen WN, Rolland R, Thijn CJ.

Clin Dysmorphol. 1994 Jul;3(3):192-9.

PMID:
7981853
8.

SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome.

Gervasini C, Grati FR, Lalatta F, Tabano S, Gentilin B, Colapietro P, De Toffol S, Frontino G, Motta F, Maitz S, Bernardini L, Dallapiccola B, Fedele L, Larizza L, Miozzo M.

Genet Med. 2010 Oct;12(10):634-40. doi: 10.1097/GIM.0b013e3181ed6185.

PMID:
20847698
9.

Leiomyomas in both uterine remnants in a woman with the Mayer-Rokitansky-Küster-Hauser syndrome.

Lamarca M, Navarro R, Ballesteros ME, García-Aguirre S, Conte MP, Duque JA.

Fertil Steril. 2009 Mar;91(3):931.e13-5. doi: 10.1016/j.fertnstert.2008.08.132. Epub 2008 Oct 18.

PMID:
18930201
10.

A complex microdeletion 17q12 phenotype in a patient with recurrent de novo membranous nephropathy.

Hinkes B, Hilgers KF, Bolz HJ, Goppelt-Struebe M, Amann K, Nagl S, Bergmann C, Rascher W, Eckardt KU, Jacobi J.

BMC Nephrol. 2012 May 14;13:27. doi: 10.1186/1471-2369-13-27.

11.

Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-Küster-Hauser Syndrome in Chinese Han.

Ma W, Li Y, Wang M, Li H, Su T, Li Y, Wang S.

PLoS One. 2015 Jun 15;10(6):e0130202. doi: 10.1371/journal.pone.0130202. eCollection 2015.

12.

Mayer-Rokitansky-Küster-Hauser syndrome associated with thrombocytopenia-absent radius syndrome.

Griesinger G, Dafopoulos K, Schultze-Mosgau A, Schroder A, Felberbaum R, Diedrich K.

Fertil Steril. 2005 Feb;83(2):452-4.

PMID:
15705390
13.

Mayer-Rokitansky-Küster-Hauser syndrome: a review of 245 consecutive cases managed by a multidisciplinary approach with vaginal dilators.

Edmonds DK, Rose GL, Lipton MG, Quek J.

Fertil Steril. 2012 Mar;97(3):686-90. doi: 10.1016/j.fertnstert.2011.12.038. Epub 2012 Jan 21.

PMID:
22265001
14.

Impact of human papillomavirus infection on the neovaginal and vulval tissues of women who underwent surgical treatment for Mayer-Rokitansky-Kuster-Hauser syndrome.

Frega A, Scirpa P, Sopracordevole F, Biamonti A, Bianchi P, De Sanctis L, Lorenzon L, Pacchiarotti A, French D, Moscarini M.

Fertil Steril. 2011 Oct;96(4):969-73. doi: 10.1016/j.fertnstert.2011.07.1099. Epub 2011 Aug 5.

PMID:
21820652
15.

[Mayer-Rokitansky-Küster-Hauser syndrome. A case report and a review of the medical literature on its treatment].

Alvarez Navarro M, Cabrera Carranco E, Hetnández Estrada AI, Aguirre Osete X.

Ginecol Obstet Mex. 2012 Jul;80(7):473-9. Review. Spanish.

PMID:
22916641
16.

Sexuality after sigmoid vaginoplasty in patients with Mayer-Rokitansky-Küster-Hauser syndrome.

Carrard C, Chevret-Measson M, Lunel A, Raudrant D.

Fertil Steril. 2012 Mar;97(3):691-6. doi: 10.1016/j.fertnstert.2011.12.015. Epub 2012 Jan 14.

PMID:
22245530
17.

Bilateral ovarian agenesis and the presence of the testis-specific protein 1-Y-linked gene: two new features of Mayer-Rokitansky-Küster-Hauser syndrome.

Plevraki E, Kita M, Goulis DG, Hatzisevastou-Loukidou H, Lambropoulos AF, Avramides A.

Fertil Steril. 2004 Mar;81(3):689-92.

PMID:
15037423
18.

A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients.

Rall K, Barresi G, Walter M, Poths S, Haebig K, Schaeferhoff K, Schoenfisch B, Riess O, Wallwiener D, Bonin M, Brucker S.

Orphanet J Rare Dis. 2011 May 28;6:32. doi: 10.1186/1750-1172-6-32.

19.

Inguinal ovary as a rare diagnostic sign of Mayer-Rokitansky-Küster-Hauser syndrome.

Demirel F, Kara O, Esen I.

J Pediatr Endocrinol Metab. 2012;25(3-4):383-6.

PMID:
22768675
20.

Sexuality after laparoscopic peritoneal vaginoplasty in women with Mayer-Rokitansky-Kuster-Hauser syndrome.

Liu X, Liu M, Hua K, Li B, Guo SW.

J Minim Invasive Gynecol. 2009 Nov-Dec;16(6):720-9. doi: 10.1016/j.jmig.2009.07.018.

PMID:
19896598

Supplemental Content

Support Center