Results 171 to 180 of about 74,702 (247)

Neuro‐Behçet's Disease and Psychiatric Disorders: From a Case Report to a Systematic Review

open access: yesBrain and Behavior, Volume 16, Issue 7, July 2026.
ABSTRACT Background Behçet's disease is a chronic, relapsing systemic vasculitis that can affect multiple organ systems. Neurological involvement, known as neuro‐Behçet's disease, occurs in a subset of patients, while psychiatric manifestations—termed neuro‐psycho Behçet's disease—remain poorly characterized.
Jorge Renau   +5 more
wiley   +1 more source

Exploring Genetic Contributions to Prostate Cancer Risk in an Asian Population‐Based Study

open access: yesCancer Medicine, Volume 15, Issue 7, July 2026.
ABSTRACT Background Genetic susceptibility to prostate cancer (PCa) varies across populations, yet East Asian men remain underrepresented in genome‐wide association studies (GWAS). This study aimed to identify genetic variants associated with PCa in a Taiwanese cohort and to explore their potential biological relevance using integrative annotation ...
Jiun‐Hung Geng   +8 more
wiley   +1 more source

Quantitative Control of Transposable Elements: From Genome Plasticity to Immune Regulatory Circuits

open access: yesCell Biochemistry and Function, Volume 44, Issue 7, July 2026.
ABSTRACT Transposable elements (TEs) constitute nearly half of the human genome and are increasingly recognized as context‐dependent regulators of genome function rather than passive repetitive DNA. This Review synthesizes classical and recent evidence on TE biology, including TE classification, mechanisms of mobilization, host restriction pathways ...
Irving Jesús Reyes‐Barragán
wiley   +1 more source

Seronegative Morvan Syndrome Presenting With Agrypnia Excitata and Peripheral Nerve Hyperexcitability: A Phenotype‐Supported Diagnostic and Therapeutic Approach in a Resource‐Limited Setting

open access: yesClinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT We report a 63‐year‐old Palestinian man with seronegative Morvan syndrome presenting with the complete clinical triad: continuous neuromyotonia with visible myokymia, severe insomnia consistent with agrypnia excitata phenotype (2–3 h/night; Insomnia Severity Index [ISI] 24/28, validated Arabic version), tachycardia (118 bpm), profuse ...
Hatem Mousa Taha, Khaled Hatem Taha
wiley   +1 more source

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