Results 191 to 200 of about 1,653,711 (317)

Syndrome of the Month: An Update on Smith‐Kingsmore Syndrome: Characterization of Developmental Milestones and a Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Smith‐Kingsmore syndrome (SKS) is a rare autosomal dominant condition characterized by neurodevelopmental differences, macrocephaly/megalencephaly, describable facial features, sleep–wake abnormalities, hyperphagia, and overgrowth. SKS is caused by pathogenic gain‐of‐function variants in MTOR which lead to hyperactivation of the mTOR pathway ...
Carolyn R. Raski, Carlos E. Prada
wiley   +1 more source

Psychiatric Comorbidities and Treatment Modalities in Children With Osteogenesis Imperfecta: A Systematic Review of Mental Health

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT To evaluate the prevalence of psychiatric signs and symptoms and describe psychotherapeutic and psychopharmacological interventions among children with osteogenesis imperfecta (OI). PRISMA guidelines were followed, and the study was registered in PROSPERO (CRD42024588284). Studies (n = 1419) were identified across five databases.
Julia M. Morales   +13 more
wiley   +1 more source

Health research in the Syrian conflict: opportunities for equitable and multidisciplinary collaboration. [PDF]

open access: yesJ Public Health (Oxf), 2022
Ekzayez A   +6 more
europepmc   +1 more source

A collaborative engineering platform for supporting design optimisation of advanced aero engine sub-systems [PDF]

open access: yes, 2011
Bosco, P.   +4 more
core  

Guiding Principles for a Successful Multidisciplinary Research Collaboration [PDF]

open access: yesFuture Science OA, 2015
Lustig, Lindsay C   +7 more
openaire   +2 more sources

Facilitating Genetic Testing for Perinatal Demise: Development of a Multidisciplinary Workflow

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Genetic contributors to perinatal demise are common but frequently undiagnosed due to clinical and logistical barriers. We aimed to improve access to genetic for intrauterine fetal demise (IUFD), stillbirth, and early neonatal death by developing a multidisciplinary workflow.
Mackenzie Mosera   +15 more
wiley   +1 more source

Application of multidisciplinary collaborative H2H nutrition management model in patients with liver failure

open access: yesHuli yanjiu
ObjectiveTo explore the effectiveness of multidisciplinary collaborative H2H nutrition management model in patients with liver failure.MethodsA total of 91 patients with liver failure hospitalized in an infectious diseases department of an infectious ...
CHEN Xinyue   +4 more
doaj  

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