about
Mutations in calmodulin cause ventricular tachycardia and sudden cardiac deathMutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillationThe genetic basis of Brugada syndrome: a mutation updateThe genetic basis of long QT and short QT syndromes: a mutation updateThe role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygoteDiagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relativesFc γ receptor IIIB (FcγRIIIB) polymorphisms are associated with clinical malaria in Ghanaian children.Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.High-efficiency multiplex capillary electrophoresis single strand conformation polymorphism (multi-CE-SSCP) mutation screening of SCN5A: a rapid genetic approach to cardiac arrhythmia.[Short QT syndrome as an inherited condition].Long QT syndrome in South Africa: the results of comprehensive genetic screening.Combined gating and trafficking defect in Kv11.1 manifests as a malignant long QT syndrome phenotype in a large Danish p.F29L founder family.Hereditary hemochromatosis (HFE) genotypes in heart failure: relation to etiology and prognosisPolymorphisms in the RNASE3 gene are associated with susceptibility to cerebral malaria in Ghanaian childrenThe role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.MicroRNAs in cardiac arrhythmia: DNA sequence variation of MiR-1 and MiR-133A in long QT syndromeMitochondrial haplogroups modify the risk of developing hypertrophic cardiomyopathy in a Danish population.The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.MT-CYB mutations in hypertrophic cardiomyopathy.HIV-1 Vertical Transmission in Zimbabwe in 622 Mother and Infant Pairs: Rethinking the Contribution of Mannose Binding Lectin Deficiency in Africa.Adipokines in umbilical cord blood from children born large for gestational age.A novel Myosin essential light chain mutation causes hypertrophic cardiomyopathy with late onset and low expressivityHigh prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation.Relative atrial natriuretic peptide deficiency and inadequate renin and angiotensin II suppression in obese hypertensive men.Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population.Obese hypertensive men have plasma concentrations of C-reactive protein similar to that of obese normotensive men.Pregnancy-associated plasma protein-A (PAPP-A) and the proform of the eosinophil major basic protein (ProMBP) are associated with increased risk of death in heart failure patients.MT-CYB mutations in hypertrophic cardiomyopathy.Maternal Serum Resistin Is Reduced in First Trimester Preeclampsia Pregnancies and Is a Marker of Clinical Severity.Metabolic rather than body composition measurements are associated with lower serum natriuretic peptide concentrations in normal weight and obese men.Longitudinal changes in C-reactive protein, proform of eosinophil major basic protein, and pregnancy-associated plasma protein-A during weight changes in obese children.Adipose expression of adipocytokines in women with polycystic ovary syndrome.A necrogenomic registry's potential.Including ethical considerations in models for first-trimester screening for pre-eclampsia.Cytochrome P450 polymorphism and postoperative cognitive dysfunction.Ethical issues related to screening for preeclampsia.The role of Lamin A/C mutations in Danish patients with idiopathic dilated cardiomyopathy.Reference values for fasting serum resistin in healthy children and adolescents.Reference values for serum leptin in healthy non-obese children and adolescents.
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Paula Louise Hedley
@ast
Paula Louise Hedley
@en
Paula Louise Hedley
@es
Paula Louise Hedley
@nl
Paula Louise Hedley
@sl
type
label
Paula Louise Hedley
@ast
Paula Louise Hedley
@en
Paula Louise Hedley
@es
Paula Louise Hedley
@nl
Paula Louise Hedley
@sl
altLabel
Paula Louise Hedley
@en
prefLabel
Paula Louise Hedley
@ast
Paula Louise Hedley
@en
Paula Louise Hedley
@es
Paula Louise Hedley
@nl
Paula Louise Hedley
@sl
P1053
E-6156-2011
P106
P1153
8861656700
P21
P31
P3829
P496
0000-0001-5801-960X