Results 231 to 240 of about 96,778 (277)

Genome characterization of the SARS-CoV-2 omicron in Cameroon. [PDF]

open access: yesBMC Infect Dis
Monamele CG   +10 more
europepmc   +1 more source

Pathogenic or Likely Pathogenic GRN Variants Are Found in 0.1% of Parkinson's Disease Patients

open access: yesMovement Disorders, Volume 41, Issue 4, Page 1020-1027, April 2026.
Abstract Background Parkinsonism may be observed in multiple neurodegenerative diseases, including GRN‐associated frontotemporal dementia (FTD‐GRN), complicating the differential diagnosis of Parkinson's disease (PD). Objectives To investigate the presence of GRN variants in a large group of PD patients.
Christian A. Ganoza   +31 more
wiley   +1 more source

A Narrative Review on the Recent Insights Into the Pathogenicity and Potential Role of Middle East Respiratory Syndrome Coronavirus (MERS-CoV) in the Emergence of "Disease X". [PDF]

open access: yesHealth Sci Rep
Ahmed Z   +14 more
europepmc   +1 more source

VPS13A Deficiency Leads to Impaired Lipid Distribution and Alteration of Mitochondrial Calcium Homeostasis in Fibroblasts of VPS13A Disease Patients

open access: yesMovement Disorders, Volume 41, Issue 4, Page 856-869, April 2026.
Abstract Background Membrane contact sites are crucial for the exchange of ions or lipids and thus are critical for the function and maintenance of organelles. VPS13A is a membrane‐residing, bridge‐like protein connecting two membranes to enable bulk lipid transfer. Loss‐of‐function mutations in the VPS13A gene cause VPS13A disease.
Dajana Grossmann   +10 more
wiley   +1 more source

Estimating the transmissibility of the 2025 chikungunya fever outbreak in Foshan, China: a modelling study. [PDF]

open access: yesInfect Dis Poverty
Zhao Y   +10 more
europepmc   +1 more source

International Registry of NKX2‐1‐Related Disorders: Clinical, Genetic, and Imaging Perspectives

open access: yesMovement Disorders, Volume 41, Issue 4, Page 889-900, April 2026.
Abstract Background NKX2‐1–related disorders result from heterozygous variants in NKX2‐1, a gene crucial for brain, lung, and thyroid development. Although movement disorders, hypothyroidism, and neonatal respiratory distress are recognized, the full phenotype and genotype–phenotype relationships remain incompletely defined.
Laia Nou‐Fontanet   +47 more
wiley   +1 more source

A systematic review to guide measles exposure periods for contact tracing. [PDF]

open access: yesEBioMedicine
Wellham HF   +7 more
europepmc   +1 more source

Transmissibility of Clade IIb Monkeypox Virus in Young Rabbits. [PDF]

open access: yesMicroorganisms
Chen Z   +9 more
europepmc   +1 more source

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