Results 51 to 60 of about 113,258 (161)

Human biomarker navigator

open access: yesiMeta, EarlyView.
The Human Biomarker Navigator integrates the disease continuum, biomarker dynamics, cross‐organ biomarker networks, biomarker classification, and technology‐driven paradigms. It maps how biomarkers link multi‐system physiology and pathology across the nervous, respiratory, endocrine, circulatory, immune, digestive, urinary, reproductive, and ...
Meng‐Yao Li   +29 more
wiley   +1 more source

Persistent Müllerian Duct Syndrome: Understanding the Challenges

open access: yesCase Reports in Urology, 2022
Persistent Müllerian duct syndrome (PMDS) is a rare autosomal recessive condition defined by the presence of Müllerian duct-derived structures in an otherwise normally masculinized phenotypical and genotypical (46,XY) male.
Irene Chua, Naeem Samnakay
doaj   +1 more source

Lactation, Childrearing, and Gender Justice

open access: yesJournal of Applied Philosophy, EarlyView.
ABSTRACT In this article, I discuss the significance of early infant feeding choices for the goal of gender justice. Focusing on human lactation practices, I identify Exclusive Gestational Nursing (EGN) as the norm in advanced industrial societies, which creates the expectation and permission for gestators, and only gestators, to nurse children, and ...
Jenny Brown
wiley   +1 more source

Persistent Mullerian Duct Syndrome with Transverse Testicular Ectopia [PDF]

open access: yes, 2016
Persistent Mullerian duct syndrome (PMDS) is a rare form of male pseudohermaphroditism characterized by the presence of Mullerian duct structures in a normal male with 46, XY karyotype.
Kumar, P. Naresh, Venugopala, Kandgal
core  

MR assessment of Müllerian duct anomalies: Does it help?

open access: yesThe Egyptian Journal of Radiology and Nuclear Medicine, 2014
Purpose: To evaluate the role of magnetic resonance imaging in diagnosis of Müllerian duct anomalies. Patients and methods: A prospective study included 48 female patients suspected to have Müllerian duct anomalies. All patients underwent trans-abdominal
Nadia F. El Ameen   +2 more
doaj   +1 more source

A Uterus‐Preserving Laparoscopic Technique for Cervicovaginal Agenesis With Functional Uterine Remnants

open access: yesBJOG: An International Journal of Obstetrics &Gynaecology, EarlyView.
ABSTRACT Background Cervicovaginal agenesis with functional uterine remnants is a rare Müllerian anomaly that may cause obstructed menstrual flow, pelvic pain, haematometra, haematosalpinx and endometriosis. Uterus‐preserving reconstruction is challenging because it requires both neovaginal creation and durable uterine drainage.
Kiper Aslan   +3 more
wiley   +1 more source

Giant mullerian duct cyst: a case report [PDF]

open access: yes, 1991
27歳男, 本邦20例目であり, 本邦最大の大きさ.ミュラー管嚢胞への精管異所開口は本邦2例目A case of giant mullerian duct cyst is reported. The patient was a 27-year-old male, complaining of microscopic hematuria. A giant cystic abdominal mass was palpable.
稲土, 博右   +4 more
core  

Persistent Mullerian Duct Syndrome in Adult Men Diagnosed Using Laparoscopy

open access: yes, 2011
Persistent mullerian duct syndrome is a rare disease that occurs in men with a completely normal phenotype and is characterized by the presence of mullerian duct structures.
Adil Ahmet Esen   +7 more
core   +1 more source

The mechanisms underlying the effects of AMH on Mullerian duct regression in male mice [PDF]

open access: yes, 2018
Anti-Mullerian hormone (AMH) produced in the developing testis induces the regression of the Mullerian duct, which develops into the oviducts, uterus and upper vagina. In our true hermaphrodite mouse with an ovary on one side and a testis on the other (O/
Anzu YAMAMOTO   +19 more
core   +1 more source

Partial Mullerian Duct Retention in Smad4 Conditional Mutant Male Mice

open access: yes, 2016
International audienceMullerian duct regression is a complex process which involves the AMH signalling pathway. We have previously demonstrated that besides AMH and its specific type II receptor (AMHRII), BMPR-IA and Smad5 are two essential factors ...
Petit, Fabrice   +2 more
core   +1 more source

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