|1.||Rall, Katharina: 2 articles (08/2013 - 03/2011)|
|2.||Aniuliene, R: 1 article (11/2015)|
|3.||Aniulis, P: 1 article (11/2015)|
|4.||Latha, Kharka: 1 article (03/2015)|
|5.||Muralidhar, Pai V: 1 article (03/2015)|
|6.||Pandya, Kartikey A: 1 article (03/2015)|
|7.||Koga, Hiroyuki: 1 article (03/2015)|
|8.||Jayaram, Nambiar: 1 article (03/2015)|
|9.||Teitelbaum, Daniel H: 1 article (03/2015)|
|10.||Okawada, Manabu: 1 article (03/2015)|
|1.||Androgen-Insensitivity Syndrome (Testicular Feminization)
05/01/2014 - "A total of 38 patients (33 with Mayer-Rokitansky-Kuster-Hauser syndrome and five with complete androgen insensitivity syndrome) were included in the present study. "
07/01/2007 - "Twenty-six women were recruited into a prospective observational study: 18 had Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH) and 8 had Complete Androgen Insensitivity Syndrome (CAIS). "
05/01/2014 - "Transvestibular vaginoplasty with autologous buccal micromucosa is an effective and feasible approach for patients with Mayer-Rokitansky-Kuster-Hauser syndrome and complete androgen insensitivity syndrome. "
11/01/2013 - "Indications for reconstruction included the following: Mayer Rokitansky Kuster Hauser syndrome (29 patients), isolated vaginal agenesis (2 patients), androgen insensitivity syndrome (2 patients), and (1) history of gynecologic-oncologic surgery. "
03/01/2011 - "Congenital vaginal agenesis occurs in Mayer-Rokitansky-Kuster-Hauser syndrome patients and in androgen insensitivity syndrome. "
|2.||Polycystic Ovary Syndrome (Syndrome, Stein-Leventhal)
08/01/2013 - "[A questionnaire for the assessment of women's perception of their own femininity: a study on women with Mayer-Rokitansky-Kuster-Hauser-syndrome and women with polycystic ovary syndrome]."
06/01/2009 - "The purpose of this study was to assess self-reported depressive and anxiety symptoms in adolescents with polycystic ovary syndrome (PCOS) and those with the rare Mayer-Rokitansky-Kuster-Hauser Syndrome (MRKHS), compared with healthy adolescents. "
08/01/2013 - "Women with Mayer-Rokitansky-Kuster-Hauser syndrome (MRKHS) or polycystic ovary syndrome (PCOS) experience substantial changes in female body characteristics. "
12/01/2013 - "Uterine adenomyosis which developed from hypoplastic uterus in postmenopausal woman with mayer-rokitansky-kuster-hauser syndrome: a case report."
10/01/2009 - "We present here a case of endometrioma in a patient with Rokitansky-Kuster-Hauser syndrome. "
10/01/2009 - "Endometriosis in Rokitansky-Kuster-Hauser syndrome has been reported only once previously. "
10/01/2009 - "Endometriosis in a patient with Rokitansky-Kuster-Hauser syndrome."
09/01/2008 - "An incidental coexistence of Mayer-Rokitansky-Kuster-Hauser syndrome with pelvic ectopic kidney and perirenal endometrioma."
|4.||Leiomyoma (Uterine Fibroids)
03/01/2015 - "Mayer-Rokitansky-Kuster-Hauser syndrome with multiple leiomyomas."
03/01/2013 - "Large leiomyoma in a woman with Mayer-Rokitansky-Kuster-Hauser syndrome."
04/01/2003 - "Multiple fibroids in a postmenopausal woman with Mayer Rokitansky Kuster Hauser syndrome."
05/01/1999 - "We report the discovery of a leiomyoma which developed from a fibrous myometrial band in a woman with Rokitansky-Kuster-Hauser syndrome. "
05/01/1999 - "[Uterine leiomyoma in a patient with Rokitansky-Kuster-Hauser syndrome. "
08/01/2009 - "Congenital absence of uterus and vagina, the Mayer-Rokitansky-Küster-Hauser Syndrome (MRKHS), results from defective müllerian duct development during female embryogenesis; it is the second most common cause of primary amenorrhea. "
09/01/2007 - "Fourth case of uterine aplasia, ovarian dysgenesis, amenorrhea and impuberism: a variant of Mayer-Rokitansky-Kuster-Hauser syndrome."
07/01/2007 - "Congenital absence of uterus and vagina, Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome, is mullerian agenesis and is the second most frequent cause of primary amenorrhea. "
10/01/2001 - "[Mayer-Rokitansky-Kuster-Hauser syndrome: a cause of primary amenorrhea in adolescents]."
05/01/1997 - "Mayer-Rokitansky-Kuster-Hauser syndrome is an unusual müllerian-duct anomaly that is a cause of primary amenorrhea. "
|1.||Familial duodenal atresia
|5.||Hereditary renal agenesis