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51 results

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Persistent Mullerian duct syndrome: an update.
Picard JY, Josso N. Picard JY, et al. Reprod Fertil Dev. 2019 Jul;31(7):1240-1245. doi: 10.1071/RD17501. Reprod Fertil Dev. 2019. PMID: 32172781 Review.
Mutations inactivating AMH or AMH receptor type 2 (AMHR2) are responsible for persistent Mullerian duct syndrome (PMDS) in otherwise normally virilised 46,XY males. ...
Mutations inactivating AMH or AMH receptor type 2 (AMHR2) are responsible for persistent Mullerian duct syndrome …
Testicular malignancy in persistent Mullerian duct syndrome: Experience from an apex cancer center with review of literature.
Philips MR, Menon AR, Kumar GR, Malik K, Chandrasekaran S, Ramaswamy T, Narayanaswamy K, Raja A. Philips MR, et al. Urol Oncol. 2023 May;41(5):258.e1-258.e6. doi: 10.1016/j.urolonc.2023.02.008. Epub 2023 Apr 3. Urol Oncol. 2023. PMID: 37019765 Review.
OBJECTIVES: Persistent Mullerian duct syndrome (PMDS) is a rare disorder of sexual differentiation resulting from aberrations in the Mullerian inhibiting factor (MIF) pathway, with consequent failure of regression of fetal Mullerian duct. ...
OBJECTIVES: Persistent Mullerian duct syndrome (PMDS) is a rare disorder of sexual differentiation resulting fro …
AMH and AMH receptor defects in persistent Mullerian duct syndrome.
Josso N, Belville C, di Clemente N, Picard JY. Josso N, et al. Hum Reprod Update. 2005 Jul-Aug;11(4):351-6. doi: 10.1093/humupd/dmi014. Epub 2005 May 5. Hum Reprod Update. 2005. PMID: 15878900 Review.
Similarly, lack of translocation to the surface membrane is responsible for the inactivity of AMHR-II molecules bearing mutations in the extracellular domain. In 15% of cases, the cause of the persistent Mullerian duct syndrome is unknown and could be …
Similarly, lack of translocation to the surface membrane is responsible for the inactivity of AMHR-II molecules bearing mutations in the ext …
The Persistent Mullerian Duct Syndrome: An Update Based Upon a Personal Experience of 157 Cases.
Picard JY, Cate RL, Racine C, Josso N. Picard JY, et al. Sex Dev. 2017;11(3):109-125. doi: 10.1159/000475516. Epub 2017 May 20. Sex Dev. 2017. PMID: 28528332 Free article. Review.
Mutations inactivating AMH or its receptor AMHRII lead to the persistent mullerian duct syndrome (PMDS) in otherwise normally virilized 46,XY males. ...
Mutations inactivating AMH or its receptor AMHRII lead to the persistent mullerian duct syndrome (PMDS) in other …
Radiological Findings in Persistent Mullerian Duct Syndrome: Case Report and Review of Literature.
Alharbi KN, Khushaim AO, Alrasheed M, Akhtar M, Neimatallah M. Alharbi KN, et al. J Radiol Case Rep. 2017 Mar 31;11(3):7-14. doi: 10.3941/jrcr.v11i3.3027. eCollection 2017 Mar. J Radiol Case Rep. 2017. PMID: 28584567 Free PMC article. Review.
These findings reflected a rare autosomal recessive developmental syndrome known as PMDS (persistent Mullerian duct syndrome). The diagnosis was established and confirmed via radiological-mainly MRI-investigation....
These findings reflected a rare autosomal recessive developmental syndrome known as PMDS (persistent Mullerian duct …
Persistent Mullerian duct syndrome.
Muram D. Muram D. J Pediatr Adolesc Gynecol. 1998 May;11(2):101-2. doi: 10.1016/s1083-3188(98)70121-4. J Pediatr Adolesc Gynecol. 1998. PMID: 9593611 Review. No abstract available.
Genetics of anti-Müllerian hormone and its signaling pathway.
Josso N, Picard JY. Josso N, et al. Best Pract Res Clin Endocrinol Metab. 2022 Jan;36(1):101634. doi: 10.1016/j.beem.2022.101634. Epub 2022 Feb 25. Best Pract Res Clin Endocrinol Metab. 2022. PMID: 35249805 Review.
The monogamic relationship between AMH and AMHR2 is supported by molecular studies of the Persistent Mullerian Duct Syndrome, characterized by the presence of Mullerian derivatives in otherwise normally virilized males: mutations of AMH or AMHR2 are cl …
The monogamic relationship between AMH and AMHR2 is supported by molecular studies of the Persistent Mullerian Duct …
AMH and AMHR2 Involvement in Congenital Disorders of Sex Development.
Brunello FG, Rey RA. Brunello FG, et al. Sex Dev. 2022;16(2-3):138-146. doi: 10.1159/000518273. Epub 2021 Aug 31. Sex Dev. 2022. PMID: 34515230 Free article. Review.
Defects in the AMH pathway are the underlying etiology of a subgroup of disorders of sex development (DSD) in 46,XY patients. The condition is known as the persistent mullerian duct syndrome (PMDS), characterized by the existence of a uterus and fallop …
Defects in the AMH pathway are the underlying etiology of a subgroup of disorders of sex development (DSD) in 46,XY patients. The condition …
The persistent mullerian duct syndrome: a rare cause of cryptorchidism.
Josso N, Picard JY, Imbeaud S, Carré-Eusèbe D, Zeller J, Adamsbaum C. Josso N, et al. Eur J Pediatr. 1993;152 Suppl 2:S76-8. doi: 10.1007/BF02125444. Eur J Pediatr. 1993. PMID: 8101816 Review.
The persistent Mullerian duct syndrome is characterized by the retention of Mullerian derivatives in patients otherwise normally virilized. ...The condition is usually discovered at surgery, however preoperative sonography could allow the diagnosis to …
The persistent Mullerian duct syndrome is characterized by the retention of Mullerian derivatives in patients ot …
Anti-Müllerian hormone receptor defect.
di Clemente N, Belville C. di Clemente N, et al. Best Pract Res Clin Endocrinol Metab. 2006 Dec;20(4):599-610. doi: 10.1016/j.beem.2006.09.004. Best Pract Res Clin Endocrinol Metab. 2006. PMID: 17161334 Review.
Like other members of the transforming growth factor beta (TGF-beta) family, AMH signals through two serine/threonine kinase receptors, of which type II is specific, and type I is shared with the bone morphogenetic protein family. Persistent Mullerian duct …
Like other members of the transforming growth factor beta (TGF-beta) family, AMH signals through two serine/threonine kinase receptors, of w …
51 results