Results 171 to 180 of about 1,152,871 (332)
Visual Recovery Reflects Cortical MeCP2 Sensitivity in Rett Syndrome
ABSTRACT Objective Rett syndrome (RTT) is a devastating neurodevelopmental disorder with developmental regression affecting motor, sensory, and cognitive functions. Sensory disruptions contribute to the complex behavioral and cognitive difficulties and represent an important target for therapeutic interventions.
Alex Joseph Simon +12 more
wiley +1 more source
ENDOSURGICAL APPROACH IN TREATMENT OF POLYPUS AND EARLY CANCER OF STOMACH
Tatiana V. Bochkova
openalex +2 more sources
Cell-specific Processing of Chromogranin A in Endocrine Cells of the Rat Stomach [PDF]
Per Norlén +9 more
openalex +1 more source
ABSTRACT Objective Cognitive impairment, fatigue, and depression are common in multiple sclerosis (MS), potentially due to disruption of regional functional connectivity caused by white matter (WM) lesions. We explored whether WM lesions functionally connected to specific brain regions contribute to these MS‐related manifestations.
Alessandro Franceschini +7 more
wiley +1 more source
Impact of high sodium intake on stomach cancer burden in China: A comprehensive analysis from 1990 to 2021. [PDF]
Zhan Z +7 more
europepmc +1 more source
A chief source of cancer and repair in stomachs [PDF]
Megan D. Radyk, Jason C. Mills
openalex +1 more source
ABSTRACT Objective Epilepsy is increasingly associated with immune dysregulation and inflammation. The T cell receptor (TCR), a key mediator of adaptive immunity, shows repertoire alterations in various immune‐mediated diseases. The unique TCR sequence serves as a molecular barcode for T cells, and clonal expansion accompanied by reduced overall TCR ...
Yong‐Won Shin +12 more
wiley +1 more source
The effects of the heavy metals cadmium and lead on six metabolic and immune-related enzymes in the loach <i>(Misgurnus anguillicaudatus)</i>. [PDF]
Wang Q +6 more
europepmc +1 more source
SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas +18 more
wiley +1 more source

