Results 291 to 300 of about 52,618 (383)

Mechanics of blunting of actin–myosin interaction dynamics by the actinopathy‐causing mutation E334Q in cytoskeletal γ‐actin

The Journal of Physiology, Volume 604, Issue 1, Page 317-335, 1 January 2026.
Abstract figure legend Residue E334 is located in a region of the cytoskeletal γ‐actin monomer that is fundamental for the interaction with myosin. In humans, its mutation p.E334Q has been found to lead to several phenotypic alterations mostly affecting cerebral cortex development and muscle tone, and generically classified under the group of rare ...
Irene Pertici, Valentina Buonfiglio, Johannes N. Greve, Elena Battirossi, Duccio Fanelli, Dietmar J. Manstein, Pasquale Bianco   +6 more
wiley   +1 more source

Role of Ocular Pathology in Understanding Glaucoma. [PDF]

Ocul Oncol Pathol
Bouhenni RA, Edward DP.
europepmc   +1 more source

A New Method for Revision of Encapsulated Blebs after Trabeculectomy: Combination of Standard Bleb Needling with Transconjunctival Scleral Flap Sutures Prevents Early Postoperative Hypotony

, 2016
Panagiotis Laspas, Philipp David Culmann, Franz H. Grus, Verena Prokosch‐Willing, Alicia Poplawksi, Norbert Pfeiffer, Esther M. Hoffmann   +6 more
openalex   +2 more sources

Drug‐Induced Fuchs Syndrome With Isolated Oral Involvement: A Rare Case Report

Case Reports in Dermatological Medicine, Volume 2026, Issue 1, 2026.
Stevens–Johnson syndrome (SJS) is a rare, potentially life‐threatening mucocutaneous disorder characterized by epidermal necrosis and mucosal bullous lesions involving less than 10% of the total body surface area. The majority of cases are aggravated by delayed hypersensitivity reactions to medications.
Salina Paudel, Manoj Kumar Bhatt, Shiv Kumar Chaudhary, Sandhya Silwal, Abinash Parajuli, Pramod Kumar Kafle, Pedro Rodriguez Jimenez   +6 more
wiley   +1 more source

Prevalence, Geometry, and Hemodynamics of Small and Medium-Sized Intracranial Aneurysms With and Without Blebs in the Chinese Han Population. [PDF]

J Cent Nerv Syst Dis
Cui X, Zhao Y, Wang L, Jin Y, Yang Z, Li Y, Zhao Z, Zhang H, Wei K, Sun Z, Huai P, Chen L, Yang X.   +12 more
europepmc   +1 more source

Clinical Spectrum of Hemolytic Anemia in Loxoscelism: Report of Two Cases Highlighting Variable Severity and Management

Case Reports in Hematology, Volume 2026, Issue 1, 2026.
Loxoscelism can cause local as well as systemic manifestations. Hematologic complications of brown recluse spider venom can be life‐threatening. Here, we present two cases of loxoscelism‐mediated hemolysis that highlight the variable clinical presentations and treatment options available based on severity and pathophysiology of hemolysis.
Anas Al-Sadi, Aakriti Adhikari, Israa Jawarneh, Elrazi Ali, Anuj Shrestha, Yoshito Nishimura   +5 more
wiley   +1 more source

Integrating Laplace's law with patient-specific hemodynamics to predict rupture risk in unruptured intracranial aneurysms: A systematic review of a biophysical and computational framework. [PDF]

Surg Pract Sci
Khan MM, Shah N, Chaurasia B.
europepmc   +1 more source

A Case of Refractory Childhood Glaucoma Associated With Sturge–Weber Syndrome Treated With Baerveldt Glaucoma Implant

Case Reports in Ophthalmological Medicine, Volume 2026, Issue 1, 2026.
We reported the clinical course of refractory childhood glaucoma associated with Sturge–Weber syndrome (SWS) treated with Baerveldt glaucoma implant (BGI). The patient was a 14‐year‐old male diagnosed with SWS after birth. He had previously undergone four trabeculotomies for glaucoma and vitrectomy for submacular hemorrhage from a diffuse choroidal ...
Wakako Imamura, Akira Matsuda, Akira Hirota, Kohei Kuroda, Yorihisa Kitagawa, Tadashiro Saeki, Tomoka Kambe, Shutaro Yamamoto, Satoru Yamagami, Cristiano Giusti   +9 more
wiley   +1 more source

Factors Affecting Bleb Morphology and Postoperative Intraocular Pressure in Inferotemporal PreserFlo MicroShunt Implantation. [PDF]

Transl Vis Sci Technol
Nakakura S, Asaoka R, Terao E, Fujisawa Y, Oogi S, Ueda K.   +5 more
europepmc   +1 more source

Pulmonary Involvement in Proteus Syndrome: Clinical and Imaging Correlates in a Rare Case

Case Reports in Radiology, Volume 2026, Issue 1, 2026.
Proteus syndrome is an uncommon, sporadic disorder characterized by progressive and heterogeneous overgrowth of tissues, resulting in distorted and asymmetric development. In most individuals, Proteus syndrome has minimal to no manifestations at birth but progresses during childhood and adolescence.
Cody Reid Johnson, Syed Muhammad Awais Bukhari, Amit Gupta, Atsushi Komemushi   +3 more
wiley   +1 more source