Results 41 to 50 of about 8,597 (215)

Mutations of gonadotropins and gonadotropin receptors: elucidating the physiology and pathophysiology of pituitary-gonadal function [PDF]

open access: yes, 2000
The recent unraveling of structures of genes for the gonadotropin subunits and gonadotropin receptors has provided reproductive endocrinologists with new tools to study normal and pathological functions of the hypothalamic ...
Huhtaniemi, I.T., Themmen, A.P.N. (Axel)
core   +2 more sources

Epidemiology of hypospadias in China: A nationwide surveillance‐based study, 2010–2020

open access: yesAndrology, Volume 14, Issue 3, Page 880-889, March 2026.
Abstract Background The prevalence of hypospadias varied internationally. However, epidemiological data on hypospadias in contemporary China remain limited. Objectives We aim to examine the epidemiological characteristics of hypospadias in Chinese population.
Chen Zhiyu   +7 more
wiley   +1 more source

Persistent Müllerian duct syndrome: A surgical surprise and management during laparoscopic transabdominal pre-peritoneal repair

open access: yesJournal of Minimal Access Surgery, 2023
Persistent Müllerian duct syndrome is an intersex disorder which occurs due to the failure of regression of Müllerian structures in genotypical and phenotypical males.
K Ganesh Shenoy   +2 more
doaj   +1 more source

Development of Free Testosterone Chemiluminescence Detection Kit and Its Clinical Application

open access: yesJournal of Analytical Methods in Chemistry, Volume 2026, Issue 1, 2026.
Background Free testosterone (FT), the bioactive form comprising 1%–2% of total testosterone, directly enters cells. Unlike total testosterone, FT levels are less affected by sex hormone–binding globulin and better reflect biological activity. Accurate serum FT measurement is crucial for diagnosing conditions like male hypogonadism, PCOS, metabolic ...
Shuang Han   +6 more
wiley   +1 more source

A Case with late onset of ambiguous genitalia

open access: yesInternational Journal of Reproductive BioMedicine, 2017
Background: Ambiguous genitalia is an uncommon situation that happensbetween 1 and 2 per every 1000 live births and falls under the umbrella diagnosisof disorders of sexual development.
Soraya Saleh Gargari   +3 more
doaj   +2 more sources

Prevalence and Characteristics of Prostatic Utricles: A Retrospective MRI Study in Middle‐Aged to Elderly Men

open access: yesThe Prostate, Volume 85, Issue 11, Page 1000-1004, August 2025.
ABSTRACT Background Congenital urological malformations encompass a wide range of anomalies affecting the urinary tract and reproductive organs. MRI has emerged as a diagnostic tool in identifying these conditions. Prostatic utricle is an enlarged diverticulum in the posterior urethra, which results from incomplete degradation of the Müllerian ducts or
Tomer Bashi   +6 more
wiley   +1 more source

Gonadal dysgenesis and tumors: genetic and clinical features [PDF]

open access: yes, 2005
Gonadal dysgenesis comprises a clinical spectrum of anomalies in patients with female, ambiguous or male phenotype, absent or impaired puberty and karyotype with or without Y chromosome and/or chromosome markers.
Bianco, Bianca Alves Vieira   +2 more
core   +3 more sources

Adrenal Insufficiency Associated Cardiomyopathy, From Molecule to Clinic: A Comprehensive Review

open access: yesHealth Science Reports, Volume 8, Issue 5, May 2025.
ABSTRACT Background and Aim Adrenal insufficiency (AI), the lack of glucocorticoids (GCs) production or function with or without a lack of mineralocorticoids (MCs) and adrenal androgens, can result in uncommon but life‐threatening complications like shock, circulatory failure, syncope, arrhythmias, dilated cardiomyopathy (DCM), and congestive heart ...
Narges Bazgir   +4 more
wiley   +1 more source

Persistent Müllerian duct syndrome of mixed anatomical variant (combined male and female type) with mixed germ cell tumor of left intra-abdominal testis

open access: yesIndian Journal of Pathology and Microbiology, 2016
Persistent Müllerian duct syndrome (PMDS) is a rare form of internal male pseudohermaphroditism characterized by retention of Müllerian duct derivatives in a phenotypically and karyotypically male patient.
Manisha Mohapatra   +1 more
doaj   +1 more source

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