Results 91 to 100 of about 107,401 (218)
Abstract Objective Dravet syndrome (DS) is a rare early‐onset developmental and epileptic encephalopathy with persistent delays between seizure onset and diagnosis. The DS'coverED study aimed to characterize current diagnostic timelines by examining each step and its duration, identifying residual barriers, and actionable solutions to optimize the ...
Loucas Christodoulou +9 more
wiley +1 more source
Abstract Background The prevalence of insulin dysregulation (ID) has not been investigated in sport horses. Stall‐side insulin assays offer convenience but need further validation. Objectives To determine the prevalence of and risk factors for ID in a sport horse population using an oral sugar test (OST) and assess agreement between stall‐side and ...
Kimberly L. Hallowell +7 more
wiley +1 more source
Prevalence of risk factors for primary postpartum hemorrhage in a university hospital. [PDF]
Betti T +5 more
europepmc +1 more source
O objetivo do estudo foi comparar as características dos enfermeiros de um hospital universitário, selecionados antes e depois do ano de 2004. Estudo descritivo, exploratório, realizado em um hospital universitário da região centro-oeste, com 81 ...
Thatianny Tanferri de Brito Paranaguá +4 more
doaj +2 more sources
ABSTRACT Background The socio‐economic burden of increasingly prevalent non‐communicable diseases (NCDs) in low‐income countries is substantial and widely recognised. This study aimed to fill the remaining evidence gap for type 2 diabetes (T2DM) and hypertension (HTN) patients in selected health facilities across two provinces in Mozambique.
Maria Verykiou +9 more
wiley +1 more source
A EQUIPE INTERPROFISSIONAL NO HOSPITAL UNIVERSITÁRIO
Cid Veloso
doaj +1 more source
Demographic, Clinical, and Serological Characteristics of Antiphospholipid Syndrome Patients From the Anticoagulation Clinic of Hospital Universitario San Vicente Fundación, Medellín, Colombia. [PDF]
Álvarez-López S +5 more
europepmc +1 more source
ABSTRACT Wilms Tumour (WT), the most common kidney cancer in children, presents features of altered kidney development and frequently exhibits molecular alterations at the 11p15.5 imprinted locus, affecting the IGF2 and H19 genes, which contribute to tumour growth and predisposition.
Abu Saadat +14 more
wiley +1 more source
Abstract Objective The aim of the present study was to evaluate the association between intertwin birth weight discordance and fetal and neonatal outcomes in twin pregnancies, and to assess its relationship with mode of delivery. Methods This retrospective cohort study included twin pregnancies delivered at a tertiary referral center.
Ana Martínez‐Zarco +8 more
wiley +1 more source
Distal 1q43q44 deletions lead to a consistent neurodevelopmental phenotype characterized by microcephaly, corpus callosum abnormalities, and developmental delay. Despite differences in genomic architecture, overlapping deletions affecting dosage‐sensitive genes such as AKT3, HNRNPU, and ZBTB18 define the core phenotype.
Ma. Guadalupe Domínguez‐Quezada +6 more
wiley +1 more source

