Results 81 to 90 of about 4,112 (210)
Diagnostic Implications and Correlates of Plasma Adenosine Deaminase 2 Activity and ADA2 Variants
Arthritis &Rheumatology, Volume 78, Issue 3, Page 734-742, March 2026.Objective Deficiency of adenosine deaminase 2 (DADA2) is a monogenic autoinflammatory disease manifested as polyarteritis nodosa, stroke, and bone marrow failure. Leveraging an international cohort of 200 DADA2 cases, we aimed to characterize the diagnostic utility of a plasma ADA2 enzyme activity assay and understand the implications of residual ADA2 ...
Jian Yue +55 more
wiley +1 more source
The Current Situation and Development of Endoscopic Ear Surgery in China
World Journal of Otorhinolaryngology - Head and Neck Surgery, Volume 12, Issue 1, Page 136-143, February 2026.ABSTRACT Endoscopic ear surgery has been widely performed in China since 2015 due to the development and rapid popularization of endoscopic technology. Due to the relative shortness of the auditory meatus, only a fixed endoscope is required in many cases, rather than a motion similar to a nasal endoscope, and uncontrollable bleeding is virtually non ...
Meng‐Wen Shi, Ge Yin, Yu Sun
wiley +1 more source
Impact of Acute Versus Chronic Unilateral Hearing Loss on Head Movement in a Novel Binaural Task
The Laryngoscope, Volume 136, Issue 1, Page 434-442, January 2026.Individuals with single‐sided deafness (SSD) may develop adaptive listening strategies with head movement patterns to optimize monaural localization and speech‐in‐noise understanding. Granular understanding of adaptive behaviors may better inform rehabilitation for SSD.
Madison V. Epperson +4 more
wiley +1 more source
The pathophysiology of labyrinthitis
, 2010 Labyrinthitis is an inflammatory response within the membranous inner ear structures in response to infection. It is a generally short-lived minor illness that has the potential to cause temporary or permanent disablement in terms of hearing loss.
Mildenhall, Joanne
core +1 more source
Molecular Genetics &Genomic Medicine, Volume 14, Issue 1, January 2026.This study reports a rare case of bone marrow failure syndrome type 1 (BMFS1) caused by a novel de novo splicing mutation (c.1502+1G>A) in the SRP72 gene. The 6‐year‐old patient presented with aplastic anemia and pancytopenia. Genetic analysis identified the mutation, which was absent in both parents, confirming its de novo origin.
Wang Xiangwen +3 more
wiley +1 more source
The diagnostic labyrinth [PDF]
Internal and Emergency Medicine, 2006 1. Kaleya RN, Boley SJ. Acute mesenteric ischemia. Crit Care Med 1995; 11: 479-512. 2. Acosta S, Bjorck M. Acute thrombo-embolic occlusion of the superior mesenteric artery: a prospective study in a well defined population. Eur J Vasc Endovasc Surg 2003; 26: 179-83. 3. Mamode N, Pickford I, Leiberman P.
openaire +2 more sources
Mastoidites agudas na criança.
Acta Médica Portuguesa, 1998 We retrospectively studied seventeen cases of acute mastoiditis admitted to the Paediatric Ward of S. Francisco Xavier Hospital during 8 years and 8 months. Seven patients were admitted in 1995. We found no reason for this increase.
A Serrão Neto +7 more
doaj +1 more source
Otolaryngology–Head and Neck Surgery, Volume 174, Issue 1, Page 239-245, January 2026.Abstract Objective To evaluate outcomes of surgically treated acute mastoiditis (AM) in pediatric patients using the Pediatric Health Information System (PHIS). Study Design Retrospective cohort study. Setting Pediatric tertiary care centers participating in the PHIS. Methods Children aged 0 to 18 years with AM treated from January 1, 2016, to December
Shachi Srivatsa +7 more
wiley +1 more source
, 2016 Purpose: To determine histopathological findings in the cochlea of human temporal bones with serous ...
Tsuprun, Vladimir +5 more
core +1 more source