Results 231 to 240 of about 52,618 (383)

Angina Bullosa Hemorrhagica: A Rare Case Involving the Ventral Tongue

open access: yesClinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Angina bullosa hemorrhagica (ABH) is a rare benign condition characterized by the sudden onset of hemorrhagic blisters in the oral mucosa, often triggered by minor trauma. We report a case of ABH in a 55‐year‐old woman with a history of asthma managed with inhaled corticosteroids who presented with a painful blister on the ventral tongue, an ...
Fatemeh Khajehzadeh
wiley   +1 more source

XEN‑45 implantation for refractory secondary glaucoma. [PDF]

open access: yesBMC Ophthalmol
Lv K   +6 more
europepmc   +1 more source

Prenatal Identification of a Novel ITGB4 Gene Mutation Associated With Junctional Epidermolysis Bullosa: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 1, January 2026.
Ultrasonographic characteristics of fetal junctional epidermolysis bullosa associated with ITGB4 gene mutation. ABSTRACT Homozygous or compound heterozygous mutations in the ITGB4 gene are associated with the pathogenesis of junctional epidermolysis bullosa, characterized by increased fragility of the skin and mucous membranes.
Qi Xu   +7 more
wiley   +1 more source

Blue rubber bleb nevus syndrome.

open access: diamond, 1987
染田 幸子   +5 more
openalex   +1 more source

Membrane bleb: A seesaw game of two small GTPases

open access: yesSmall GTPases, 2017
Junichi Ikenouchi, Kana Aoki
semanticscholar   +1 more source

Pneumomediastinum and Pneumothorax as Rare Complications of Ruptured Pulmonary Hydatid Cyst: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Ruptured hydatid cyst should be considered when encountering spontaneous pneumothorax and pneumomediastinum, especially in young patients in regions with high prevalence of hydatid cyst. Awareness of atypical signs ensures instant diagnosis, guiding appropriate surgical and medical treatment to prevent serious complications.
Farzaneh Akbari   +5 more
wiley   +1 more source

Dual AAV gene therapy achieves recovery of hearing and auditory processing in a DFNB16 mouse model

open access: yesClinical and Translational Medicine, Volume 16, Issue 1, January 2026.
DFNB16 is among the most prevalent forms of congenital deafness, caused by mutations in the Stereocilin gene. Although no treatment currently exists, gene therapy represents a promising curative approach. Here, we demonstrate that AAV‐mediated gene delivery in a DFNB16 mouse model restored both peripheral hearing and central auditory processing ...
Sepideh Iranfar   +12 more
wiley   +1 more source

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