Results 111 to 120 of about 60,759 (242)

An Unusual Presentation of Herpes Zoster [PDF]

open access: yes, 2020
Cristiano, Peter   +3 more
core   +2 more sources

Herpesvirus genome integration in whole‐genome sequences of dementia and control cohorts

open access: yesAlzheimer's &Dementia, Volume 22, Issue 3, March 2026.
Abstract INTRODUCTION The infectious hypothesis suggests that microbes like herpesviruses may play a role in the pathogenesis of Alzheimer's disease (AD) and other related dementias through methods that may include viral genome integration. The occurrence of herpesvirus genome integration in dementia patients has not been thoroughly characterized ...
Stacey L. Piotrowski   +27 more
wiley   +1 more source

Herpes Zoster in Children and Adolescents: Case Series Of 8 Patients

open access: yesNational Journal of Community Medicine, 2013
Herpes zoster can occur at any age but is rare in childhood and adolescents. Zoster can occur at any time after primary varicella infection or varicella vaccination. Recent studies have shown its increasing incidence in children.
Pragya A Nair, Pankil H Patel
doaj  

Can we refute a role for infections in Alzheimer's disease pathogenesis?

open access: yesAlzheimer's &Dementia, Volume 22, Issue 3, March 2026.
Abstract While a growing body of literature suggests a role for infections in Alzheimer's disease (AD), microbial contributions to AD remains a contentious topic, in part due to challenges in reconciling the positive evidence with studies reporting null findings.
Zena K. Chatila   +6 more
wiley   +1 more source

American College of Rheumatology Guidance Statement for Diagnosis and Management of VEXAS Developed by the International VEXAS Working Group Expert Panel

open access: yesArthritis &Rheumatology, Volume 78, Issue 3, Page 509-522, March 2026.
Objective Vacuoles E1 enzyme X‐linked autoinflammatory somatic syndrome (VEXAS) is a recently identified rare genetic disorder associated with somatic mutations in the UBA1 gene. VEXAS presents with a combination of inflammatory and hematologic manifestations, leading to increased morbidity and mortality.
Arsene Mekinian   +111 more
wiley   +1 more source

The Differential Diagnosis of Coma in the ICU: Hyperacute Postoperative Guillain‐Barré Syndrome—A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Guillain‐Barré syndrome (GBS) is a rare, immune‐mediated neurological disorder that can be challenging to diagnose in postoperative patients due to atypical manifestations and overlapping conditions. This case report highlights the diagnostic and therapeutic challenges of GBS following vascular surgery. We present the case of a 56‐year‐old man
Miron Tiganas   +3 more
wiley   +1 more source

Ervaringen met intraveneus toegediend acyclovir bij ernstige herpesvirus infecties [PDF]

open access: yes, 1981
Contains fulltext : 4333.pdf (publisher's version ) (Open ...
Meer, J.W.M. van der, Versteeg, J.
core  

An Optimized Protocol for the Generation of iPSC Lines from Lymphoblastoid Cell Lines Using the Non‐integrative Sendai Virus

open access: yesCurrent Protocols, Volume 6, Issue 3, March 2026.
Abstract The choice of cell source for generating induced pluripotent stem cells (iPSCs) is influenced by several factors, including accessibility, reprogramming efficiency, and the invasiveness of the cell collection procedure. Traditional sources such as skin fibroblasts or peripheral blood mononuclear cells often require invasive sampling, which can
Laurie Martineau   +4 more
wiley   +1 more source

Multifocal Vasculopathy Due to Varicella-Zoster Virus (VZV): Serial Analysis of VZV DNA and Intrathecal Synthesis of VZV Antibody in Cerebrospinal Fluid [PDF]

open access: yes, 2017
Recognition of multifocal vasculopathy due to varicella-zoster virus (VZV) is often problematic. We describe a human immunodeficiency virus—infected patient who had progressive central nervous system disease for >3 months.
Bossart, Walter   +6 more
core  

Clinical, biological and cytometric characteristics of two patients with a homozygous A91V PRF1 mutation

open access: yesClinical &Translational Immunology, Volume 15, Issue 3, 2026.
Familial haemophagocytic lymphohistiocytosis (FHL) is a rare, inherited granzyme–perforin system defect that predisposes individuals to haemophagocytic lymphohistiocytosis. This article presents two original case reports of FHL type 2, along with a comprehensive literature review. Together, these elements aim to enhance the current understanding of FHL
Nicolas Perrard   +12 more
wiley   +1 more source

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