Results 181 to 190 of about 55,459 (294)

Swallowing and Communication in Cockayne Syndrome: Clinical Characteristics and Management

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cockayne syndrome (CS) is an ultrarare genetic disorder associated with genes encoding proteins involved in DNA repair. The clinical course of CS involves neurodevelopmental and neurodegenerative features, including swallowing and communication impairments.
Abigail M. Spoden, Katlyn E. McGrattan, Peter B. Kang   +2 more
wiley   +1 more source

Technostress in the Era of Generative Artificial Intelligence: Mental Health Implications in Medical Education. [PDF]

Psychiatry Investig
Um YJ.
europepmc   +1 more source

Relative Exchangeable Copper Confirms Wilson Disease and Supports Reclassification of the ATP7B p.Met665Ile Variant With Conflicting Pathogenicity Evidence

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Wilson disease (WD) is an autosomal recessive disorder of copper metabolism caused by ATP7B mutations. Diagnosis is usually straightforward in symptomatic patients, but can be challenging in children and adolescents with mild liver disease, borderline urinary copper excretion, or inconclusive genetic findings.
Emanuele Nicastro, Caterina Zuccoli, Roberto Marozzi, Antonino Barletta, Lisa Licini, Paola Tebaldi, Valeria Casotti, Mariangela Stinco, Lidia Pezzani, Maria Iascone, Lorenzo D'Antiga   +10 more
wiley   +1 more source

Association between psychoeducational factors and perceived academic stress in medical students: a gender-based analysis. [PDF]

BMC Med Educ
Lagares-Franco C, Viñolo Gil MJ, O Ferrall González C, López Ruiz H, García-Campanario I.   +4 more
europepmc   +1 more source

When I Receive Too Much Social Support: The Effect of Social Support Overload on Users’ Life Burnout and Discontinuance in Fitness Apps [PDF]

Ruihan Li, Shuang Wang, Tailai Wu
openalex   +1 more source

Electrocardiographic and Skin Manifestations of Turner Syndrome: Association With Cardiovascular Disease

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Congenital heart disease (CHD) and dermatologic conditions such as lymphedema and acquired melanocytic nevi (AMN) are common in Turner Syndrome (TS). We hypothesized that abnormalities of cranial neural crest cell derivatives drive the skin and heart manifestations of TS. We conducted joint cardiac and skin examinations of volunteers at a 2023
Sarah Elsaim, Brett Vernier, Van Thi Thanh Truong, Riya T. Patel, Matthew Brown, Martin Chacon Portillo, Megan Rogge, David Rodriguez‐Buritica, Siddharth K. Prakash   +8 more
wiley   +1 more source

Malnutrition and fluid overload as independent predictors of mortality in dialysis patients: A multicenter cohort study in Colombia. [PDF]

Sci Prog
Vargas-Correa V, Orellana-Cáceres JJ, Vargas-Alvarado E, Gómez-Jordan S, Tuta-Quintero E.   +4 more
europepmc   +1 more source

Implementing Indigenous Data Sovereignty in Australia: A Five‐Phase Framework for Indigenous Data Governance

Australian Journal of Social Issues, EarlyView.
ABSTRACT This article presents the development of a five‐phase Indigenous Data Governance (IDGov) Framework in Australia, focusing on partnerships between the Aboriginal Community Controlled Health Organisation (ACCHO) sector and non‐Indigenous health entities.
Jacob Prehn, Michael A. Guerzoni, Maggie Walter, Gawaian Bodkin‐Andrews, Bobby Maher   +4 more
wiley   +1 more source

Social media distrust and turn to artificial intelligence among generation Z: a qualitative model linking digital minimalism and financial discipline with social policy recommendations. [PDF]

Front Artif Intell
Ökten B.
europepmc   +1 more source

“Too much to handle”: Impact of mobile social networking sites on information overload, depressive symptoms, and well-being

, 2019
Jörg Matthes, Kathrin Karsay, Desirée Schmuck, Anja Stević   +3 more
openalex   +2 more sources