Results 281 to 290 of about 2,185,996 (384)
Androgyny in adolescent psychiatric patients and in delinquents. [PDF]
Audrey Henderson, P. I. Dugard
openalex +1 more source
Complications in Endoscopic Sinus Surgery: A TriNetX Network Analysis
Abstract Background The potential complications of endoscopic sinus surgery (ESS) remain a critical surgical consideration. This study aims to examine complication rates and identify trends in ESS‐related complications. Methods The TriNetX network was queried for patients undergoing ESS between 2005 and 2024.
Jakob L. Fischer+8 more
wiley +1 more source
The impact of the COVID-19 pandemic on the lives of the 2004 Pelotas (Brazil) birth cohort adolescents. [PDF]
Matijasevich A+5 more
europepmc +1 more source
ASSESSMENT OF DISADVANTAGED ADOLESCENTS: A DIFFERENT APPROACH TO RESEARCH AND EVALUATION MEASURES1 [PDF]
Norman E. Freeberg
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Neutrophil‐to‐lymphocyte ratio (NLR) and monocyte‐to‐lymphocyte ratio (MLR) were investigated as potential markers. A total of 3545 subjects were included in the analysis retrospectively. Adult men and women with impaired glucose metabolism were assessed. NLR and MLR may help assess inflammation in individuals with impaired glucose metabolism. Abstract
Ayed A. Dera+11 more
wiley +1 more source
The Highly Creative and the Highly Intelligent Adolescent: Some Exploratory Findings [PDF]
Philip W. Jackson, William T. Gruhn
openalex +1 more source
Autosomal Recessive Cerebellar Ataxias: Translating Genes to Therapies
Autosomal recessive cerebellar ataxias are disabling neurodegenerative genetic conditions affecting balance and coordination. Advancements in genomic testing have improved diagnosis, leading to a new focus on the development of targeted precision therapeutics addressing cellular, biochemical, and genetic disease mechanisms with a resulting emphasis on ...
Brent L. Fogel+10 more
wiley +1 more source
Experience of adolescents/young adults with chronic kidney disease and of their families during transition of care. [PDF]
Roveri JR+5 more
europepmc +1 more source
Objective A growing body of evidence indicates a strong genetic overlap between developmental and epileptic encephalopathies (DEEs) and movement disorders. De novo loss‐of‐function variants in NUS1 have been recently identified in DEE cases. Herein, we report a large cohort of cases with pathogenic NUS1 variants and describe their clinical presentation
Sarah M. Brooker+79 more
wiley +1 more source