246 related articles for article (PubMed ID: 26075712)
21. 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. PubMed ID: 22768675
[TBL] [Abstract][Full Text] [Related]
22. Clinical characteristics of 1,055 Chinese patients with Mayer-Rokitansky-Küster-Hauser syndrome: a nationwide multicentric study.
Chen N; Pan H; Luo G; Wang P; Xie Z; Hua K; Luo X; Huang X; Liu Q; Sun L; Hu W; Tao G; Zhao S; Wu N; Zhu L
Fertil Steril; 2021 Aug; 116(2):558-565. PubMed ID: 33745726
[TBL] [Abstract][Full Text] [Related]
23. Mayer-Rokitansky-Küster-Hauser syndrome as an interdisciplinary problem.
Liszewska-Kapłon M; Strózik M; Kotarski Ł; Bagłaj M; Hirnle L
Adv Clin Exp Med; 2020 Apr; 29(4):505-511. PubMed ID: 32348039
[TBL] [Abstract][Full Text] [Related]
24. Search for altered imprinting marks in Mayer-Rokitansky-Küster-Hauser patients.
Eggermann T; Ledig S; Begemann M; Elbracht M; Kurth I; Wieacker P
Mol Genet Genomic Med; 2018 Nov; 6(6):1225-1228. PubMed ID: 30099855
[TBL] [Abstract][Full Text] [Related]
25. Syndrome Mayer-Rokitansky-Küster-Hauser - uterine and vaginal agenesis: current knowledge and therapeutic options.
Chmel R; Pastor Z; Mužík M; Brtnický T; Nováčková M
Ceska Gynekol; 2019; 84(5):386-392. PubMed ID: 31826637
[TBL] [Abstract][Full Text] [Related]
26. Heterozygous ZNHIT3 variants within the 17q12 recurrent deletion region are associated with Mayer-Rokitansky-Kuster Hauser (MRKH) syndrome.
Brakta S; Du Q; Chorich LP; Hawkins ZA; Sullivan ME; Ko EK; Kim HG; Knight J; Taylor HS; Friez M; Phillips JA; Layman LC
Mol Cell Endocrinol; 2024 Aug; 589():112237. PubMed ID: 38599276
[TBL] [Abstract][Full Text] [Related]
27. Mayer-Rokitansky-Kuster-Hauser syndrome: complications, diagnosis and possible treatment options: a review.
Bombard DS; Mousa SA
Gynecol Endocrinol; 2014 Sep; 30(9):618-23. PubMed ID: 24948340
[TBL] [Abstract][Full Text] [Related]
28. A life course perspective on Mayer-Rokitansky-Küster-Hauser syndrome: women's experiences and negotiations of living with an underdeveloped uterus and vagina.
Jensen AH; Herlin MK; Vogel I; Lou S
Disabil Rehabil; 2024 Mar; 46(6):1130-1140. PubMed ID: 36987844
[TBL] [Abstract][Full Text] [Related]
29. HOXA10 and HOXA13 sequence variations in human female genital malformations including congenital absence of the uterus and vagina.
Ekici AB; Strissel PL; Oppelt PG; Renner SP; Brucker S; Beckmann MW; Strick R
Gene; 2013 Apr; 518(2):267-72. PubMed ID: 23376215
[TBL] [Abstract][Full Text] [Related]
30. Discordant Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome in identical twins - a case report and implications for reproduction in MRKH women.
Milsom SR; Ogilvie CM; Jefferies C; Cree L
Gynecol Endocrinol; 2015; 31(9):684-7. PubMed ID: 26291808
[TBL] [Abstract][Full Text] [Related]
31. Genetics of agenesis/hypoplasia of the uterus and vagina: narrowing down the number of candidate genes for Mayer-Rokitansky-Küster-Hauser Syndrome.
Mikhael S; Dugar S; Morton M; Chorich LP; Tam KB; Lossie AC; Kim HG; Knight J; Taylor HS; Mukherjee S; Capra JA; Phillips JA; Friez M; Layman LC
Hum Genet; 2021 Apr; 140(4):667-680. PubMed ID: 33469725
[TBL] [Abstract][Full Text] [Related]
32. Coexistence of Mayer-Rokitansky-Küster-Hauser Syndrome and Turner Syndrome: A Case Report.
Białka A; Gawlik A; Drosdzol-Cop A; Wilk K; Małecka-Tendera E; Skrzypulec-Plinta V
J Pediatr Adolesc Gynecol; 2016 Apr; 29(2):e35-8. PubMed ID: 26524664
[TBL] [Abstract][Full Text] [Related]
33. Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive update.
Herlin MK; Petersen MB; Brännström M
Orphanet J Rare Dis; 2020 Aug; 15(1):214. PubMed ID: 32819397
[TBL] [Abstract][Full Text] [Related]
34. 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; 6():9. PubMed ID: 21406098
[TBL] [Abstract][Full Text] [Related]
35. Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina).
Burel A; Mouchel T; Odent S; Tiker F; Knebelmann B; Pellerin I; Guerrier D
J Negat Results Biomed; 2006 Mar; 5():4. PubMed ID: 16556301
[TBL] [Abstract][Full Text] [Related]
36. A Case Report of Familial Mayer-Rokitansky-Küster-Hauser Syndrome as Part of the Phenotypic Spectrum of the 2q37 Deletion.
Daum H; Kremer E; Frumkin A; Meiner V; Diamant H; Harel I; Bauman D
J Pediatr Adolesc Gynecol; 2024 Feb; 37(1):95-97. PubMed ID: 37734585
[TBL] [Abstract][Full Text] [Related]
37. Vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association with Mayer-Rokitansky-Küster-Hauser syndrome in co-occurrence: two case reports and a review of the literature.
Bjørsum-Meyer T; Herlin M; Qvist N; Petersen MB
J Med Case Rep; 2016 Dec; 10(1):374. PubMed ID: 28003020
[TBL] [Abstract][Full Text] [Related]
38. Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a historical perspective.
Patnaik SS; Brazile B; Dandolu V; Ryan PL; Liao J
Gene; 2015 Jan; 555(1):33-40. PubMed ID: 25260227
[TBL] [Abstract][Full Text] [Related]
39. Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a case report.
Dell'Edera D; Allegretti A; Ventura M; Mercuri L; Mitidieri A; Cuscianna G; Epifania AA; Morizio E; Alfonsi M; Guanciali-Franchi P
J Med Case Rep; 2021 Apr; 15(1):208. PubMed ID: 33883018
[TBL] [Abstract][Full Text] [Related]
40. Rare variant of atypical Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome with breast malformation: case report and review of literature.
Mahey R; Ramaswamy A; Cheluvaraju R; Manchanda S; Bhatla N
Clin Dysmorphol; 2022 Jul; 31(3):141-144. PubMed ID: 35165209
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]