Results 191 to 200 of about 52,798 (289)

Unclassified complex urogenital anomaly in a 3-year-old girl: Diagnostic and surgical challenges. [PDF]

Urol Case Rep
Manghi I, Gargano T, Ruspi F, Maffi M, Libri M, Domini M.   +5 more
europepmc   +1 more source

The Edmonton Obesity Staging System Clinical Support Tool: A Structured EOSS‐Domain‐Based Tool for Primary Care

Clinical Obesity, Volume 16, Issue 4, August 2026.
ABSTRACT Although body mass index (BMI) is widely used to diagnose obesity, it is an imprecise measure of health. The Edmonton Obesity Staging System (EOSS) assesses the health impacts of elevated BMI based on medical, mental and functional complications and has been shown to predict mortality more accurately than BMI alone. This study aimed to develop
Annalena Philipp, Christel Moll, Arya M. Sharma, Christine Joisten   +3 more
wiley   +1 more source

Nrf2 Levels in Human Semen and Spermatozoa: Association with F₂-Isoprostanes as Markers of Lipid Peroxidation. [PDF]

Int J Mol Sci
Moretti E, Signorini C, Liguori L, Leoni E, Collodel G.   +4 more
europepmc   +1 more source

Germline TP53 Mutations Causing Diamond–Blackfan Anemia: A French Report

Pediatric Blood &Cancer, Volume 73, Issue 7, July 2026.
ABSTRACT Diamond–Blackfan anemia is a rare congenital erythroblastopenia typically caused by mutations in ribosomal protein genes. Recently, gain‐of‐function mutations in TP53 have been identified as a novel cause of Diamond–Blackfan anemia. We report two French patients who both harbored a heterozygous TP53 deletion (NM_000546.5: c.1077delA; p ...
Rafael Moisan, Lydie Da Costa, Ludivine David Nguyen, Heloise Chosseler, Audrey Riquet, Benedicte Bruno, Melissa Barbati   +6 more
wiley   +1 more source

Associated Urogenital Injuries Following Pelvic Trauma in Pediatrics: A 15-Year Single-Center Retrospective Study. [PDF]

Cureus
Van Wagoner C, Shumway T, Saroyan A, Saleh L, Hasan S, Chrumka A, Saleh E.   +6 more
europepmc   +1 more source

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12 ‐Related Developmental Disorders

American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1619-1650, July 2026.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source

From environment to organs: individual and combined effects of MPs and PFAS on urinary system health. [PDF]

Front Physiol
Li D, Wang T, Zhang W, Li M, Du W, Wang J.   +5 more
europepmc   +1 more source

A Hoxa13:Cre mouse strain for conditional gene manipulation in developing limb, hindgut, and urogenital system. [PDF]

Genesis, 2015
Scotti M, Kherdjemil Y, Roux M, Kmita M.
europepmc   +1 more source

A contribution to the anatomy of two rare cetacean species: The hourglass dolphin (Cephalorhynchus cruciger) and the spectacled porpoise (Phocoena dioptrica)

The Anatomical Record, Volume 309, Issue 7, Page 1797-1820, July 2026.
Abstract The anatomical description of the hourglass dolphin (Cephalorhynchus cruciger) and the spectacled porpoise (Phocoena dioptrica) remains largely unexplored, due to limited specimen availability and preservation challenges. This study employed digital imaging techniques, conventional histology, and computed tomography to provide visualization of
Jean‐Marie Graïc, Tommaso Gerussi, Bruno Cozzi, Rebecca M. Boys, Brian Chin Wing Kot, Matthew R. Perrott, Kane Fleury, Tabris Yik To Chung, Henry Chun Lok Tsui, Emma Burns, Trudi Webster, Stuart Hunter, Emma L. Betty, Odette Howarth, Carolina Loch, Sophie White, Steve Dawson, William Rayment, Ros Cole, Derek Cox, Tom Waterhouse, Hannah Hendriks, Anton van Helden, Muriel Johnstone, Ramari Oliphant Stewart, R. Ewan Fordyce, Karen A. Stockin   +26 more
wiley   +1 more source