Results 191 to 200 of about 28,820 (229)

Morphometric Analysis of the Radial Artery in a Select White South African Donor Cohort

open access: yesAnatomia, Histologia, Embryologia, Volume 55, Issue 3, May 2026.
ABSTRACT The radial artery is a vital access point for various cardiovascular and neurological interventions yet detailed morphometric studies in African populations are limited. This study aimed to investigate the radial artery dimensions in thirty adult body donors housed in the Department of Clinical Anatomy, University of KwaZulu‐Natal, Durban ...
Aleisha J. Singh   +2 more
wiley   +1 more source

Retinal Pigment Epitheliopathy due to Sub‐Optimal Recycling of Vitamin A (RESORVA): A Novel RDH11 ‐Related Phenotype

open access: yesClinical Genetics, Volume 109, Issue 5, Page 972-977, May 2026.
RDH11 is a minor isoenzyme that catalyses the oxidation of 11‐cis‐retinol to 11‐cis‐retinal in the retinal pigment epithelium, alongside RDH5 and RDH10. Biallelic null variants in RDH11 lead to upregulation of RDH5 and RDH10 (transcriptional adaptation), maintaining 11‐cis‐retinal bioavailability, but still causing Retinal Pigment Epitheliopathy due to
Kirk A. J. Stephenson   +11 more
wiley   +1 more source

Holding a wing horizontal: Roles for muscles of the pectoral girdle other than the main two flight muscles

open access: yesJournal of Anatomy, Volume 248, Issue 5, Page 830-842, May 2026.
This report explores which muscles of the pectoral girdle are employed to allow birds to hold their wings horizontally with a level aerofoil surface during a glide. Abstract Whilst many birds glide briefly with wings held horizontally, some species maintain this posture for extended periods during soaring.
D. Charles Deeming, María Clelia Mosto
wiley   +1 more source

Isolated Kidney Transplant in Primary Hyperoxaluria‐1 Enabled by Small Interfering RNA (siRNA) Therapy. Is It Time for Change? Case Report and Review of the Literature

open access: yesPediatric Transplantation, Volume 30, Issue 5, May 2026.
ABSTRACT Background Primary hyperoxaluria type 1 (PH1) is a rare genetic disorder characterized by excessive oxalate production that leads to nephrocalcinosis or nephrolithiasis and progressive kidney failure, associated with systemic oxalosis that is not reversed by dialysis. Pharmacological treatment is limited.
Shameer M. Habeeb   +8 more
wiley   +1 more source

Easily missed fracture: distal radius and concomitant proximal ulna. [PDF]

open access: yesBMJ Case Rep, 2016
Seewoonarain S, Shakokani M, Pryke S.
europepmc   +1 more source

Anatomy of the woodchuck (Marmota monax) / [PDF]

open access: yes, 2005
Bezuidenhout, A. J. (Abraham Johannes), 1942-   +1 more
core   +2 more sources

Intramedullary compression device for proximal ulna fracture. [PDF]

open access: yesSingapore Med J, 2015
Hong CC   +4 more
europepmc   +1 more source

A Comprehensive X-ray Dataset for Pediatric Ulna and Radius Fractures Analysis. [PDF]

open access: yesSci Data
Tang S   +7 more
europepmc   +1 more source

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