References analysis of the Wikipedia article "Müllerian anomalies" in the English version

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Reyes-Muñoz, Enrique; Vitale, Salvatore Giovanni; Alvarado-Rosales, Deisi; Iyune-Cojab, Esther; Vitagliano, Amerigo; Lohmeyer, Franziska Michaela; Guevara-Gómez, Yenara Patricia; Villarreal-Barranca, Alma; Romo-Yañez, José; Montoya-Estrada, Araceli; Morales-Hernández, Fela Vanesa; Aguayo-González, Patricia (2019-10-17). "Müllerian Anomalies Prevalence Diagnosed by Hysteroscopy and Laparoscopy in Mexican Infertile Women: Results from a Cohort Study". Diagnostics. 9 (4): 149. doi:10.3390/diagnostics9040149. ISSN 2075-4418. PMC 6963274. PMID 31627332.

Passos, Itana de Mattos Pinto e; Britto, Renata Lopes (2020-03-01). "Diagnosis and treatment of müllerian malformations". Taiwanese Journal of Obstetrics and Gynecology. 59 (2): 183–188. doi:10.1016/j.tjog.2020.01.003. ISSN 1028-4559. PMID 32127135.

Mullen RD, Behringer RR (2014). "Molecular genetics of Müllerian duct formation, regression and differentiation". Sexual Development. 8 (5): 281–96. doi:10.1159/000364935. PMC 4378544. PMID 25033758.

Chandler TM, Machan LS, Cooperberg PL, Harris AC, Chang SD (December 2009). "Mullerian duct anomalies: from diagnosis to intervention". The British Journal of Radiology. 82 (984): 1034–42. doi:10.1259/bjr/99354802. PMC 3473390. PMID 19433480.

Robbins JB, Broadwell C, Chow LC, Parry JP, Sadowski EA (January 2015). "Müllerian duct anomalies: embryological development, classification, and MRI assessment". Journal of Magnetic Resonance Imaging. 41 (1): 1–12. doi:10.1002/jmri.24771. PMID 25288098. S2CID 45721501.

Fontana L, Gentilin B, Fedele L, Gervasini C, Miozzo M (February 2017). "Genetics of Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome". Clinical Genetics. 91 (2): 233–246. doi:10.1111/cge.12883. PMID 27716927. S2CID 283394.

Aiguo W, Guangren D (2007). "PMID Observer Design of Descriptor Linear Systems". 2007 Chinese Control Conference. IEEE. pp. 161–165. doi:10.1109/chicc.2006.4347343. ISBN 9787811240559. S2CID 72187.

Rasmussen M, Vestergaard EM, Graakjaer J, Petkov Y, Bache I, Fagerberg C, Kibaek M, Svaneby D, Petersen OB, Brasch-Andersen C, Sunde L (November 2016). "17q12 deletion and duplication syndrome in Denmark – A clinical cohort of 38 patients and review of the literature". American Journal of Medical Genetics. Part A. 170 (11): 2934–2942. doi:10.1002/ajmg.a.37848. PMID 27409573. S2CID 20447962.

Williams LS, Demir Eksi D, Shen Y, Lossie AC, Chorich LP, Sullivan ME, Phillips JA, Erman M, Kim HG, Alper OM, Layman LC (July 2017). "Genetic analysis of Mayer–Rokitansky–Kuster–Hauser syndrome in a large cohort of families". Fertility and Sterility. 108 (1): 145–151.e2. doi:10.1016/j.fertnstert.2017.05.017. PMC 5770980. PMID 28600106.

Colvin CW, Abdullatif H (January 2013). "Anatomy of female puberty: The clinical relevance of developmental changes in the reproductive system". Clinical Anatomy. 26 (1): 115–29. doi:10.1002/ca.22164. PMID 22996962. S2CID 46057971.

Heinonen PK (March 2006). "Complete septate uterus with longitudinal vaginal septum". Fertility and Sterility. 85 (3): 700–5. doi:10.1016/j.fertnstert.2005.08.039. PMID 16500341.

Kamio M, Nagata C, Sameshima H, Togami S, Kobayashi H (July 2018). "Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome with septic shock: A case report". The Journal of Obstetrics and Gynaecology Research. 44 (7): 1326–1329. doi:10.1111/jog.13656. PMID 29978541. S2CID 49705192.

de França Neto AH, Nóbrega BV, Clementino Filho J, do Ó TC, de Amorim MM (2014). "Intrapartum diagnosis and treatment of longitudinal vaginal septum". Case Reports in Obstetrics and Gynecology. 2014: 108973. doi:10.1155/2014/108973. PMC 4033546. PMID 24891963.

Pellerito JS, McCarthy SM, Doyle MB, Glickman MG, DeCherney AH (June 1992). "Diagnosis of uterine anomalies: relative accuracy of MR imaging, endovaginal sonography, and hysterosalpingography". Radiology. 183 (3): 795–800. doi:10.1148/radiology.183.3.1584936. PMID 1584936.

Bhagavath B, Ellie G, Griffiths KM, Winter T, Alur-Gupta S, Richardson C, Lindheim SR (June 2017). "Uterine Malformations: An Update of Diagnosis, Management, and Outcomes". Obstetrical & Gynecological Survey. 72 (6): 377–392. doi:10.1097/OGX.0000000000000444. PMID 28661551.

Choussein S, Nasioudis D, Schizas D, Economopoulos KP (June 2017). "Mullerian dysgenesis: a critical review of the literature". Archives of Gynecology and Obstetrics. 295 (6): 1369–1381. doi:10.1007/s00404-017-4372-2. PMID 28434104. S2CID 11461052.

Jasonni VM, La Marca A, Naldi S, Matonti G, D'Anna R (December 2007). "The management of vaginal agenesis: report of 104 cases". Fertility and Sterility. 88 (6): 1653–6. doi:10.1016/j.fertnstert.2007.01.126. hdl:11380/1158599. PMID 17481623.

Reichman DE, Laufer MR (April 2010). "Congenital uterine anomalies affecting reproduction". Best Practice & Research. Clinical Obstetrics & Gynaecology. 24 (2): 193–208. doi:10.1016/j.bpobgyn.2009.09.006. PMID 19897423.

Theodoridis TD, Pappas PD, Grimbizis GF (February 2019). "Surgical management of congenital uterine anomalies (including indications and surgical techniques)". Best Practice & Research. Clinical Obstetrics & Gynaecology. 59: 66–76. doi:10.1016/j.bpobgyn.2019.02.006. PMID 30910446. S2CID 85514424.

Reed CE, Fenton SE (June 2013). "Exposure to diethylstilbestrol during sensitive life stages: a legacy of heritable health effects". Birth Defects Research. Part C, Embryo Today. 99 (2): 134–46. doi:10.1002/bdrc.21035. PMC 3817964. PMID 23897597.

Bromer JG, Wu J, Zhou Y, Taylor HS (July 2009). "Hypermethylation of homeobox A10 by in utero diethylstilbestrol exposure: an epigenetic mechanism for altered developmental programming". Endocrinology. 150 (7): 3376–82. doi:10.1210/en.2009-0071. PMC 2703508. PMID 19299448.

Hoover RN, Hyer M, Pfeiffer RM, Adam E, Bond B, Cheville AL, Colton T, Hartge P, Hatch EE, Herbst AL, Karlan BY, Kaufman R, Noller KL, Palmer JR, Robboy SJ, Saal RC, Strohsnitter W, Titus-Ernstoff L, Troisi R (October 2011). "Adverse health outcomes in women exposed in utero to diethylstilbestrol". The New England Journal of Medicine. 365 (14): 1304–14. doi:10.1056/NEJMoa1013961. PMID 21991952. S2CID 26033585.

D'Aloisio AA, Baird DD, DeRoo LA, Sandler DP (March 2012). "Early-life exposures and early-onset uterine leiomyomata in black women in the Sister Study". Environmental Health Perspectives. 120 (3): 406–12. doi:10.1289/ehp.1103620. PMC 3295338. PMID 22049383.

Chan YY, Jayaprakasan K, Zamora J, Thornton JG, Raine-Fenning N, Coomarasamy A (2011). "The prevalence of congenital uterine anomalies in unselected and high-risk populations: a systematic review". Human Reproduction Update. 17 (6): 761–71. doi:10.1093/humupd/dmr028. PMC 3191936. PMID 21705770.

Shulman LP (June 2008). "Müllerian anomalies". Clinical Obstetrics and Gynecology. 51 (2): 214–22. doi:10.1097/GRF.0b013e31816feba0. PMID 18463453. S2CID 207.

Saravelos SH, Cocksedge KA, Li TC (2008). "Prevalence and diagnosis of congenital uterine anomalies in women with reproductive failure: a critical appraisal". Human Reproduction Update. 14 (5): 415–29. doi:10.1093/humupd/dmn018. PMID 18539641.

Cheroki C, Krepischi-Santos AC, Szuhai K, Brenner V, Kim CA, Otto PA, Rosenberg C (April 2008). "Genomic imbalances associated with mullerian aplasia". Journal of Medical Genetics. 45 (4): 228–32. doi:10.1136/jmg.2007.051839. PMID 18039948. S2CID 37929944.

Sultan C, Biason-Lauber A, Philibert P (January 2009). "Mayer–Rokitansky–Kuster–Hauser syndrome: recent clinical and genetic findings". Gynecological Endocrinology. 25 (1): 8–11. doi:10.1080/09513590802288291. PMID 19165657. S2CID 33461252.

Wang X, Zhang X, Liu S, Li G, Cui L, Qin Y, Chen ZJ (December 2016). "Novel mutations in the TP63 gene are potentially associated with Müllerian duct anomalies". Human Reproduction. 31 (12): 2865–2871. doi:10.1093/humrep/dew259. PMID 27798044.

Biason-Lauber A, Konrad D, Navratil F, Schoenle EJ (August 2004). "A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman". The New England Journal of Medicine. 351 (8): 792–8. doi:10.1056/NEJMoa040533. PMID 15317892.

Rackow BW, Arici A (June 2007). "Reproductive performance of women with müllerian anomalies". Current Opinion in Obstetrics & Gynecology. 19 (3): 229–37. doi:10.1097/GCO.0b013e32814b0649. PMID 17495638. S2CID 5476966.

Goldberg JM, Falcone T (July 1999). "Effect of diethylstilbestrol on reproductive function". Fertility and Sterility. 72 (1): 1–7. doi:10.1016/S0015-0282(99)00153-3. PMID 10428139.

Mittendorf R (June 1995). "Teratogen update: carcinogenesis and teratogenesis associated with exposure to diethylstilbestrol (DES) in utero". Teratology. 51 (6): 435–45. doi:10.1002/tera.1420510609. PMID 7502243.

Raga F, Bauset C, Remohi J, Bonilla-Musoles F, Simón C, Pellicer A (October 1997). "Reproductive impact of congenital Müllerian anomalies". Human Reproduction. 12 (10): 2277–81. doi:10.1093/humrep/12.10.2277. PMID 9402295.

Cahen-Peretz A, Sheiner E, Friger M, Walfisch A (January 2019). "The association between Müllerian anomalies and perinatal outcome". The Journal of Maternal-Fetal & Neonatal Medicine. 32 (1): 51–57. doi:10.1080/14767058.2017.1370703. PMID 28826263. S2CID 22506505.

Breech LL, Laufer MR (March 2009). "Müllerian anomalies". Obstetrics and Gynecology Clinics of North America. 36 (1): 47–68. doi:10.1016/j.ogc.2009.02.002. PMID 19344847.

Fox NS, Roman AS, Stern EM, Gerber RS, Saltzman DH, Rebarber A (June 2014). "Type of congenital uterine anomaly and adverse pregnancy outcomes". The Journal of Maternal-Fetal & Neonatal Medicine. 27 (9): 949–53. doi:10.3109/14767058.2013.847082. PMID 24050215. S2CID 28109172.

Heinonen PK, Kuismanen K, Ashorn R (April 2000). "Assisted reproduction in women with uterine anomalies". European Journal of Obstetrics, Gynecology, and Reproductive Biology. 89 (2): 181–4. doi:10.1016/S0301-2115(99)00198-0. PMID 10725580.

Attia KI, Hug-Koronya M, Ginsburg ES, Hornstein MD (October 2001). "Effects of Mullerian anomalies on in vitro fertilization outcome". Journal of Assisted Reproduction and Genetics. 18 (10): 544–7. doi:10.1023/A:1011950202480. PMC 3455312. PMID 11699126.

Chan YY, Jayaprakasan K, Tan A, Thornton JG, Coomarasamy A, Raine-Fenning NJ (October 2011). "Reproductive outcomes in women with congenital uterine anomalies: a systematic review". Ultrasound in Obstetrics & Gynecology. 38 (4): 371–82. doi:10.1002/uog.10056. PMID 21830244.

Marcus S, al-Shawaf T, Brinsden P (July 1996). "The obstetric outcome of in vitro fertilization and embryo transfer in women with congenital uterine malformation". American Journal of Obstetrics and Gynecology. 175 (1): 85–9. doi:10.1016/S0002-9378(96)70255-7. PMID 8694080.

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Heinonen PK (March 2006). "Complete septate uterus with longitudinal vaginal septum". Fertility and Sterility. 85 (3): 700–5. doi:10.1016/j.fertnstert.2005.08.039. PMID 16500341.

Shulman LP (June 2008). "Müllerian anomalies". Clinical Obstetrics and Gynecology. 51 (2): 214–22. doi:10.1097/GRF.0b013e31816feba0. PMID 18463453. S2CID 207.

Goldberg JM, Falcone T (July 1999). "Effect of diethylstilbestrol on reproductive function". Fertility and Sterility. 72 (1): 1–7. doi:10.1016/S0015-0282(99)00153-3. PMID 10428139.

Breech LL, Laufer MR (March 2009). "Müllerian anomalies". Obstetrics and Gynecology Clinics of North America. 36 (1): 47–68. doi:10.1016/j.ogc.2009.02.002. PMID 19344847.

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Shulman LP (June 2008). "Müllerian anomalies". Clinical Obstetrics and Gynecology. 51 (2): 214–22. doi:10.1097/GRF.0b013e31816feba0. PMID 18463453. S2CID 207.

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Müllerian anomalies (English Wikipedia)

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