Results 71 to 80 of about 7,402 (242)
The Rhesus Factor and Disease Prevention [PDF]
, 2004 First published by the Wellcome Trust Centre for the History of Medicine at UCL, 2004. ©The Trustee of the Wellcome Trust, London, 2004. All volumes are freely available online at: www.history.qmul.ac.uk/research/modbiomed/wellcome_witnesses/Annotated ...
Christie, DA, Tansey, EM, Zallen, DT
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Major structural congenital anomalies and causal pathways in people with cerebral palsy
Developmental Medicine &Child Neurology, Volume 67, Issue 3, Page 374-381, March 2025.Congenital anomalies are more common in people with cerebral palsy (CP) compared to the non‐CP population. In our population‐based study, 23.4% of persons with CP had a congenital anomaly (CA) but 7% of the cohort had anomalies that were unlikely to be pathogenic.
Susan M. Reid +4 more
wiley +1 more source
Predictive risk factors for moderate to severe hyperbilirubinemia [PDF]
Einstein (São Paulo), 2007 Objective: to describe predictive factors for severity of neonataljaundice in newborn infants treated at the University Neonatal Clinic,highlighting maternal, obstetric and neonatal factors.
Gláucia Macedo de Lima +3 more
doaj
Rh Negative Status and Isoimmunization Update: A Case-Based Approach to Care [PDF]
, 2003 Prior to the 1970s and the advent of Rho (D) immune globulin (RIG) for Rh negative women, hemolytic disease of the newborn led to morbidity, long-term disabilities, and mortality.
Hanson, Lisa +3 more
core +1 more source
Pediatric Discovery, Volume 2, Issue 4, December 2024.This study allowed the characterization of pediatric patients with swallowing disorders seen in a multidisciplinary clinic. This overview provides healthcare personnel with an understanding of the complexity of swallowing disorders and their relationships to various medical conditions in children.
Silvia J. Galvis‐Blanco +9 more
wiley +1 more source
Deficiência de glicose-6-fosfato desidrogenase eritrocitária em recém-nascidos do sexo masculino e sua relação com a icterícia neonatal [PDF]
, 2010 Glucose-6-phosphate dehydrogenase (G6PD) deficiency, the commonest red cell enzymopathy in humans, has an X-linked inheritance. The major clinical manifestations are drug induced hemolytic anemia, neonatal jaundice and chronic nonspherocytic hemolytic ...
AMORIM, Maria do Socorro T. +6 more
core +1 more source
Small Science, Volume 4, Issue 12, December 2024.This study explores how nanoplastics (NPs) influence the binding behavior of serum albumin (SA) in varying pH environments, noting that low pH reduces perfluorooctane sulfonate but not perfluorooctanoic acid interactions, independent of NP adsorption. Perfluoroalkyl and polyfluoroalkyl substances significantly inhibit SA–NP aggregation. Furthermore, PN
Zongshan Zhao +10 more
wiley +1 more source
British Journal of Haematology, Volume 205, Issue 5, Page 1985-1994, November 2024.In the upper left corner is an image of the structure of the G6PD tetramer. In the lower left corner is a blow‐up of the region in one monomer surrounding the Arg454 amino acid; this residue is close to the binding site for the substrate G6P (pink) and the substrate NADP (light brown).
Simonetta Costa +17 more
wiley +1 more source
Risk Factors for Kernicterus in Neonatal Jaundice
Gomal Journal of Medical Sciences, 2010 Background: Kernicterus is a neurologic syndrome resulting from deposition of unconjugated bilirubin in the basal ganglia and brain stem nuclei. The aim of this study was to identify the risk factors for kernicterus in neonatal jaundice.
Hussain Bux Korejo +5 more
doaj
Neonatal hyperbilirubinemia [PDF]
, 2008 This issue of eMedRef provides information to clinicians on the pathophysiology, diagnosis, and therapeutics of neonatal ...
Brandes, Lisa
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