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ICD-10 codes for surveillance of non-fatal abusive head trauma in Aotearoa New Zealand: a retrospective cohort study

Abstract: Objectives To assess the validity of an International Classification of Diseases (ICD) code based definition of non-fatal head trauma caused by child abuse (abusive head…

Date: 2023-06-05

Hybrid Palliation for Hypoplastic Left Heart Syndrome: Role of Echocardiography

Abstract: Hypoplastic left heart syndrome is a spectrum of complex congenital cardiac defects. Although in borderline cases, biventricular repair is a viable option, in the…

Date: 2023-06-04

NeoCheck: A New Checklist to Assess Performance during Newborn Life Support—A Validation Study

Abstract: Background: The aim of this study was to design and validate a new checklist and standardized scenario for assessing providers’ performance during Newborn Life Support…

Date: 2023-06-04

Prevalence of Active Primitive Reflexes and Craniosacral Blocks in Apparently Healthy Children and Relationships with Neurodevelopment Disturbances

Abstract: Background: In healthy children, the frequency of the anomalous persistence of primitive reflexes (PRs) and craniosacral blocks (CBs) is unknown, as well as their impact…

Date: 2023-06-04

Mental Health and Health-Related Quality of Life of Children and Youth during the First Year of the COVID-19 Pandemic: Results from a Cross-Sectional Survey in Saskatchewan, Canada

Abstract: For children and youth, the COVID-19 pandemic surfaced at a critical time in their development. Children have experienced extended disruptions to routines including…

Date: 2023-06-03

School and Bicultural Factors as Mediators between Immigrant Mothers’ Acculturative Stress and Adolescents’ Depression in Korea

Abstract: In Korea, marriages between Korean men and foreign women have surged since the late 1990s, resulting in public interest in the psychosocial adjustment of their children.…

Date: 2023-06-03

Autosomal Dominant Hypocalcemia Type 1 and Neonatal Focal Seizures

Abstract: Autosomal dominant hypocalcemia type 1 (ADH1) is a rare form of hypoparathyroidism that is characterized by gain-of-function mutations in the CASR gene, which provides…

Date: 2023-06-03