Results 271 to 280 of about 214,536 (370)

The contribution of age and sex hormones to female neuromuscular function across the adult lifespan

open access: yesThe Journal of Physiology, EarlyView.
Abstract figure legend This study mapped the age‐related trajectory of neuromuscular deterioration in 88 healthy females aged 18–80 years old. An accelerated reduction in neuromuscular function, primarily of peripheral muscular origin, coincided with the age of menopause onset.
Steven J. O'Bryan   +4 more
wiley   +1 more source

FSH receptor N680S genotype-guided gonadotropin choice increases cumulative pregnancy and live birth rates after <i>in vitro</i> fertilization. [PDF]

open access: yesFront Endocrinol (Lausanne)
Hjelmér I   +8 more
europepmc   +1 more source

Pancreatic Neuroendocrine Tumor Leading to a Diagnosis of Multiple Endocrine Neoplasia Type 1

open access: yesDEN Open, Volume 6, Issue 1, April 2026.
ABSTRACT Pancreatic neuroendocrine neoplasms are rare but occasionally encountered. They are generally highly vascularized solid tumors, often round in shape with clear boundaries, defined contours, and a homogeneous internal structure. However, they can also present with atypical features, such as cystic degeneration, hemorrhage, calcification, and ...
Noriyuki Hirakawa   +9 more
wiley   +1 more source

Higher FSH Level Is Associated With Increased Risk of Incident Hip Fracture in Older Adults, Independent of Sex Hormones.

open access: yesJ Clin Endocrinol Metab
Koh EH   +13 more
europepmc   +1 more source

Effects of Lead Exposure on 1573 Male Workers' Sex Hormones in China. [PDF]

open access: yesToxics
Wang P   +15 more
europepmc   +1 more source

PRODUCTION, METABOLISM OF FSH AND LH IN PUBERTY DISORDERS [PDF]

open access: bronze, 1975
Noel K. Maclaren   +2 more
openalex   +1 more source

Next Generation Sequencing Allows Identification of a Novel Mutation in the TfR2 Gene and Outperforms the Conventional Diagnostic Techniques

open access: yeseJHaem, Volume 6, Issue 4, August 2025.
ABSTRACT Introduction Type 3 hereditary hemochromatosis (HH) is a rare genetic disease due to mutations in the transferrin receptor 2 (TFR2) gene. Methods and Results Here, we describe the case of an Italian patient presenting with hyperferritinemia and hepatic iron accumulation, not evidenced by magnetic resonance imaging, that was subsequently ...
Miriam Longo   +9 more
wiley   +1 more source

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