Results 101 to 110 of about 2,520 (182)

Correlation between three assay systems for anti-Müllerian hormone (AMH) determination [PDF]

, 2012
published_or_final_versio
Anderson, RA, Ho, PC, Li, RHW, Ng, EHY, Wong, BPC, Yeung, WSB   +5 more
core  

Sexually dimorphic expression of secreted frizzled-related (SFRP) genes in the developing mouse Mullerian duct [PDF]

, 2006
In developing male embryos, the female reproductive tract primordia (Müllerian ducts) regress due to the production of testicular anti-Müllerian hormone (AMH).
Bogani, D, Cheeseman, M, Cox, S, Greenfield, A, Siggers, P, Smith, L   +5 more
core   +1 more source

Minimally invasive management of Müllerian anomalies in pediatric patients: A retrospective case series and literature review

Journal of Pediatric Surgery Open
Müllerian anomalies (MA) are structural defects that arise due to alterations in the development of the paramesonephric or Müllerian ducts during the first 16 weeks of gestation. Few cases have been reported on laparoscopic management as a diagnostic and
Mario Riquelme, Juan Pelayo, Irving Cardenas-Medina, Ana Cantu-Zendejas, Alejandro Cendejas-Higuera, Eduardo Olazabal, Mario Palafox   +6 more
doaj   +1 more source

Persistent mullerian duct syndrome: A single-center experience

Journal of Indian Association of Pediatric Surgeons, 2018
Persistent Mullerian duct syndrome (PMDS) is a rare disorder. It is a type of male pseudohermaphroditism, usually presenting as "Hernia Uteri Inguinalis".This study aims to present our experience of PMDS, over a 7-year period.Our center is a tertiary care facility, situated in Tamil Nadu, a southern state of India.This is a retrospective study.
Saravanan Natarajan, Manikandhan Periasamy, Saminathan Rangasamy, Shankar Mohan, Prabakaran Sundararajan   +4 more
openaire   +3 more sources

OSR1 disruption contributes to uterine factor infertility via impaired Müllerian duct development and endometrial receptivity

The Journal of Clinical Investigation, 2023
Three sisters, born from consanguineous parents, manifested a unique Müllerian anomaly characterized by uterine hypoplasia with thin estrogen-unresponsive endometrium and primary amenorrhea, but with spontaneous tubal pregnancies.
Adriana Lofrano-Porto, Sidney Alcântara Pereira, Andrew Dauber, Jordana C.B. Bloom, Audrey N. Fontes, Naomi Asimow, Olívia Laquis de Moraes, Petra Ariadne T. Araujo, Ana Paula Abreu, Michael H. Guo, Silviene F. De Oliveira, Han Liu, Charles Lee, Wendy Kuohung, Michella S. Coelho, Rona S. Carroll, Rulang Jiang, Ursula B. Kaiser   +17 more
doaj   +1 more source

Role of Baseline Antral Follicle Count and Anti-Mullerian Hormone in Prediction of Cumulative Live Birth in the First In Vitro Fertilisation Cycle: A Retrospective Cohort Analysis [PDF]

, 2013
published_or_final_versio
Ho, PC, Lau, EYL, Lee, VCY, Li, RHW, Ng, EHY, Yeung, WSB   +5 more
core   +1 more source

"Sexual differentiation: From genes to gender" [PDF]

, 1998
Amy Wisniewski is Assistant Professor of Biology at Drake University, Des Moines, Iowa. She can be contacted at amy.wisniewski@drake.eduA person's sex can be considered across various levels.
Migeon, Claude J., Wisniewski, Amy B.
core   +2 more sources

Complete transverse vaginal septum complicated by pyocolpos, primary vesicoureteral reflux and ectopic ureter with renal loss: a case report

Urology Case Reports
A transverse vaginal septum is a rare Müllerian anomaly caused by incomplete fusion between the Müllerian ducts and the urogenital sinus. It can obstruct menstrual flow, leading to hematocolpos, hydrocolpos, or pyocolpos.
Izadora Gabriela Coutinho, Paulo Acácio Egger, Ailton Fernandes Junior, Angelo Cezar Bolognese Junior, Abikeilla Ariane Bomfim Gomes Bernardi, Amanda Yumi Ono Valderrama   +5 more
doaj   +1 more source

A Case of Mayer–Rokitansky–Küster–Hauser Syndrome with a Fused Pancake-shaped Pelvic Kidney

Advanced Biomedical Research, 2019
Mayer–Rokitansky–Küster–Hauser (MRKH) Syndrome is a female reproductive system disorder. It is characterized by a defect in the Müllerian ducts development, and it causes the absence of the uterus in variable degrees in upper vaginal hypoplasia.
Ali Reza Eftekhari Moghadam, Ghasem Saki, Mahin Taheri Moghadam, Seyed Mohamad Hossein Mohseni, Vajieh Heidari, Mohammad Hossein Jamshidi   +5 more
doaj   +1 more source

An unusual diagnosis of a bicornuate unicollis uterus [PDF]

, 2008
We present a case of an unusual diagnosis of a bicornuate unicollis uterus mimicking a uterus didelphys with blind hemivagina. Few cases of a bicornuate uterus have been reported with the primary symptom of a paracervical pyocolpos.
Foidart, Jean-Michel, Nisolle, Michelle, Panayotidis, Costas   +2 more
core   +1 more source