Results 131 to 140 of about 26,242 (288)

Comparison of Outcomes Between Primary Laryngotracheal Reconstruction and Partial Cricotracheal Resection in Moderate Grade Pediatric Subglottic Stenosis: A Systematic Review and Meta‐Analysis

open access: yesLaryngoscope Investigative Otolaryngology, Volume 10, Issue 4, August 2025.
ABSTRACT Objective This systematic review and meta‐analysis compare the outcomes of primary laryngotracheal reconstruction (LTR) and partial cricotracheal resection (PCTR) in managing moderate‐grade pediatric subglottic stenosis (severe Grade II and Grade III).
Bigyan Raj Gyawali   +8 more
wiley   +1 more source

Changes in Thyroglossal Duct Cyst Case Volume During the COVID‐19 Pandemic

open access: yesLaryngoscope Investigative Otolaryngology, Volume 10, Issue 4, August 2025.
Patients were more likely to present with an infected thyroglossal duct cyst (TGDC) or sequela of infection after the onset of the COVID‐19 pandemic. Additionally, there was an initial decrease in TGDC incidence with a rebound increase in subsequent years.
Milan P. Fehrenbach   +5 more
wiley   +1 more source

A New Surgical Treatment for Spasmodic Dysphonia.

open access: bronze, 1999
Nobuhiko Isshiki   +2 more
openalex   +2 more sources

Postextubation Laryngospasm in a Patient with Spasmodic Dysphonia [PDF]

open access: bronze, 2005
John F. Capacchione   +2 more
openalex   +1 more source

Contact Urticaria and Related Conditions: Clinical Review

open access: yesContact Dermatitis, Volume 93, Issue 2, Page 87-107, August 2025.
ABSTRACT Contact urticaria (CoU) is an immediate contact reaction occurring within minutes to an hour after exposure to specific proteins or chemicals. CoU is categorised into non‐immunologic (NI‐CoU) and immunologic (I‐CoU) types, with I‐CoU potentially leading to anaphylaxis. Both forms of CoU can be associated with protein contact dermatitis and the
Mojca Bizjak   +15 more
wiley   +1 more source

Nationwide Phenotypic and Genotypic Characterisation of 103 Patients With SH3TC2 Gene‐Related Demyelinating Peripheral Neuropathy

open access: yesEuropean Journal of Neurology, Volume 32, Issue 8, August 2025.
We analysed the clinical, electrophysiological, and genetic features of 103 patients from 89 families with SH3TC2 gene mutations identified in 27 French University Hospitals causing Charcot–Marie‐Tooth type 4C (CMT4C) demyelinating peripheral neuropathy.
Pauline Jaubert   +36 more
wiley   +1 more source

Home - About - Disclaimer - Privacy