Results 101 to 110 of about 21,237 (225)
Soft-tissue mineralization in Werner syndrome.
Werner syndrome is a rare autosomal recessive disorder characterized by clinical signs of premature aging, short stature, scleroderma-like skin changes, endocrine abnormalities, cataracts, and an increased incidence of malignancies.
Bonomo, Lorenzo +2 more
core
Essential role of limiting telomeres in the pathogenesis of Werner syndrome
Mutational inactivation of the gene WRN causes Werner syndrome, an autosomal recessive disease characterized by premature aging, elevated genomic instability and increased cancer incidence.
Cabrera, Noelia G +17 more
core +1 more source
Subterranean environments contribute to three‐quarters of classified ecosystem services
ABSTRACT Beneath the Earth's surface lies a network of interconnected caves, voids, and systems of fissures forming in rocks of sedimentary, igneous, or metamorphic origin. Although largely inaccessible to humans, this hidden realm supports and regulates services critical to ecological health and human well‐being.
Stefano Mammola +30 more
wiley +1 more source
Intracerebral calcification in Werner syndrome
We present two siblings with Werner syndrome; one of them with intracerebral calcification. Case 1, a 22-year old female was admitted to our clinic due to -diabetes mellitus and thinning in both wrists and ankles, and graying hair. Further investigations
Tamer Tetiker, Murat Sert
core
A pesar de que la asociación entre útero didelfo, hemivagina obstruida y agenesia renal homolateral (síndrome de Herlyn-Werner-Wünderlich) ha sido reportada en la literatura ginecológica, no es familiar al especialista en diagnóstico por imágenes, en ...
Jorge Ahualli +4 more
doaj
WRN regulates pathway choice between classical and alternative non-homologous end joining
Werner Syndrome is an accelerated aging disorder marked by genome instability, large deletions and telomere fusions, hallmarks of aberrant DNA repair.
Raghavendra A. Shamanna +5 more
doaj +1 more source
Parent/caregiver needs during pediatric genome‐wide sequencing: A scoping literature review
Abstract The integration of genome‐wide sequencing (GWS) including whole‐exome and whole‐genome sequencing, has transformed pediatric diagnostics, yet the needs of parents and caregivers during this process remain insufficiently explored. This scoping review aims to synthesize current knowledge on parental and caregiver needs across the GWS process in ...
Priyanka Murali, Joon‐Ho Yu
wiley +1 more source
Herlyn-Werner-Wünderlich syndrome: case report
Introduction: The Herlyn-Werner-Wünderlich (HWW) syndrome is the association of three urogenital anatomic alterations of low incidence. Müllerian alterations are rare and are usually incidental findings; consequently, they are underdiagnosed and their ...
Andrés Felipe Figueroa-Blanco +1 more
doaj +1 more source
Guidelines for Essential Trauma Care: Second Edition (2026)
Injury is a major cause of death and disability globally, with the highest burden in low‐ and middle‐income countries (LMICs). Strengthening the organization and planning for trauma care (care of the injured) can improve care and lower mortality. In 2004, the International Association for Trauma Surgery and Intensive Care (IATSIC) and the World Health ...
Charles Mock +41 more
wiley +1 more source
Read the free Plain Language Summary for this article on the Journal blog. Abstract Most terrestrial plant species form symbioses with arbuscular mycorrhizal fungi (AMF). However, the below‐ground carbon (C) allocation of plants and the nutritional and growth benefits provided by AMF within this symbiosis vary greatly across species and environments ...
Hengjun Zhao +3 more
wiley +1 more source

