Results 91 to 100 of about 107,401 (218)

From first seizure to specific antiseizure medication in Dravet syndrome: Quantifying delays in the DS'coverED study

open access: yesEpilepsia Open, EarlyView.
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

Prevalence of insulin dysregulation in a sport horse population as determined by traditional and stall‐side testing

open access: yesEquine Veterinary Journal, EarlyView.
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]

open access: yesRev Bras Enferm, 2023
Betti T   +5 more
europepmc   +1 more source

Enfermeiros de um hospital universitário: evidências do processo de seleção [Nurses at a university hospital: evidence from the selection process] [Enfermeros de un hospital universitario: evidencias del proceso de selección]

open access: yesRevista Enfermagem UERJ, 2012
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

Exploring the Socio‐Economic Toll of Non‐Communicable Diseases in Low‐Resource Settings: Novel Evidence From Mozambique

open access: yesThe International Journal of Health Planning and Management, EarlyView.
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

open access: yesRevista Brasileira de Educação Médica, 2021
Cid Veloso
doaj   +1 more source

DNA Methylation and Transcriptomic Profiles of Wilms Tumour Reveal New Deregulated Genes and Epigenetic Processes Relevant for Tumour Stratification and Management

open access: yesInternational Journal of Cancer, EarlyView.
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

Intertwin birth weight discordance, mode of delivery, and fetal and neonatal outcomes in twin pregnancies

open access: yesInternational Journal of Gynecology &Obstetrics, EarlyView.
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

Clinical and Cytogenomic Characterization of Three Patients With Distal 1q43q44 Deletion: Twin Sisters With a de novo Deletion and a Patient With der(1)t(1;21)(q43;q22.3)mat

open access: yesJournal of Clinical Laboratory Analysis, EarlyView.
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

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