Results 171 to 180 of about 38,746 (286)

Reproxalap ‐ A Novel Treatment Option for Allergic Conjunctivitis – A Comprehensive Narrative Review

Health Science Reports, Volume 9, Issue 6, June 2026.
ABSTRACT Background and Aims Allergic conjunctivitis is a prevalent, immune‐mediated hypersensitivity disorder of the ocular surface affecting 10%–20% of the global population. Current therapeutic options, while effective to some extent, are often limited by side effects and inconsistent efficacy.
Sanila Mughal, Roshanay Ejaz Awan, Hur Abbas, Zahra Sania, Ashna Habib, Syeda Kaneez Sakina, Amina Mahmud, Mohammed Mahmmoud Fadelallah Eljack   +7 more
wiley   +1 more source

Modeling ventricular tachycardia in genetic long QT syndrome using engineered cardiac tissues. [PDF]

Bioact Mater
Zhuang RZ, Doufexi G, Yehya M, Morsink MAJ, Liao X, Ben-Johny M, Vunjak-Novakovic G.   +6 more
europepmc   +1 more source

Sexually Dimorphic Regulation of MiR‐29a/c‐3p in Human Endothelial Cells: Cell Functions and Transcriptome

Journal of Cellular Physiology, Volume 241, Issue 6, June 2026.
ABSTRACT Preeclampsia (PE) is a major cause of maternal and fetal morbidity and mortality during pregnancy. PE is characterized by widespread endothelial dysfunction in mothers and fetuses. The etiology of PE remains elusive, but the dysregulation of microRNAs (miRNAs) in endothelial cells may contribute to the pathogenesis of PE. We have reported that
Si‐yan Zhang, Colman I. Freel, Chi Zhou, Jing Zheng   +3 more
wiley   +1 more source

Perinatal management of congenital long QT syndrome: A case of maternal and fetal manifestations. [PDF]

HeartRhythm Case Rep
da Silva Lopes M, Dias J, Ferreira I, Silva CM, Ramalho AR, Rosmaninho-Salgado J, Amaral ME, Andrade H, Martins P, Pires A.   +9 more
europepmc   +1 more source

Digital genetic counseling services for cascade cardiogenetic testing

Journal of Genetic Counseling, Volume 35, Issue 3, June 2026.
Abstract Digital interventions are potentially promising to improve accessibility and efficiency of genetic counseling services. However, current literature on user perspectives toward digital tools for cascade testing is limited. Therefore, this focus‐group study aimed to gain insights into the attitude and perspectives of probands, at‐risk relatives (
Marlies N. van Lingen, Sietske A. L. van Till, Noor A. A. Giesbertz, Tessa C. Beinema, Margreet G. E. M. Ausems, Randy Klaassen, Martina C. Cornel, Lieke M. van den Heuvel, J. Peter van Tintelen   +8 more
wiley   +1 more source

Overlap of Congenital Deafness and Long QT Syndrome With Distinct Genetic Basis: A Diagnostic Challenge. [PDF]

JACC Case Rep
Pirah R, Ali A, Qadir F, Mumtaz Z, Alam M, Mohsin M.   +5 more
europepmc   +1 more source

Reticulated Platelets and an Optimal Model for Differentiating Thrombocytopenia Etiologies

eJHaem, Volume 7, Issue 3, June 2026.
ABSTRACT Objectives This study aimed to investigate the clinical value of reticulated platelets (RtcPLT) percentage derived from an automated hematology analyzer in differentiating thrombocytopenia due to peripheral etiology from decreased bone marrow production (BME). In addition, a secondary objective was to establish specific reference intervals for
Tung Thanh Tran, Quyen Ngoc Truong, Hong Phuoc Mac, Thang Thanh Phan, Tai Chau Quach, Son Truong Nguyen   +5 more
wiley   +1 more source

T‐Cell Acute Lymphoblastic Leukemia in a Young Patient With Andersen–Tawil Syndrome Successfully and Safely Treated With Intensive Chemotherapy Including Potential Precipitating Drugs: A Case Report After 3.5 Years of Follow‐up

eJHaem, Volume 7, Issue 3, June 2026.
ABSTRACT Andersen–Tawil syndrome (ATS) is a rare, hereditary channelopathy characterized by periodic paralysis, cardiac arrhythmias, and sometimes developmental anomalies. No association with hematologic malignancies has previously been reported. We describe the case of a 27‐year‐old man with genetically confirmed Type 1 ATS who developed T‐cell acute ...
Ramy Rahmé, Paule Moussounda Bamba, Thi Thuy Duong Do, Anthony Behin, Estelle Gandjbakhch, Claude Gardin, Thorsten Braun   +6 more
wiley   +1 more source

Fetal Long QT Syndrome: Case Series and Literature Review With Focus on Multidisciplinary Care Coordination. [PDF]

Case Rep Cardiol
Samples S, Cherny S, Chandler S, Wakai RT, Strasburger JF, Patel S.   +5 more
europepmc   +1 more source

Clarithromycin-Induced Long QT Syndrome: A Case Report

Long QT syndrome develops for a number of reasons. The number of non-antiarrhythmic drugs reported to induce QT interval prolongation with or without torsade de pointes continues to increase.
Coskun, S, Cetin, M, Özen, S, Yildirimer, M, Tanriverdi, S   +4 more
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