Paula Louise Hedley
Citeret af
Citeret af
The genetic basis of long QT and short QT syndromes: a mutation update
PL Hedley, P Jørgensen, S Schlamowitz, R Wangari, J Moolman‐Smook, ...
Human mutation 30 (11), 1486-1511, 2009
Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death
M Nyegaard, MT Overgaard, MT Søndergaard, M Vranas, ER Behr, ...
The American Journal of Human Genetics 91 (4), 703-712, 2012
Danish premature birth rates during the COVID-19 lockdown
G Hedermann, PL Hedley, M Bækvad-Hansen, H Hjalgrim, K Rostgaard, ...
Archives of Disease in Childhood-Fetal and Neonatal Edition 106 (1), 93-95, 2021
Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population
PA Brink, L Crotti, V Corfield, A Goosen, G Durrheim, P Hedley, ...
Circulation 112 (17), 2602-2610, 2005
The genetic basis of Brugada syndrome: a mutation update.
PL Hedley, P Jørgensen, S Schlamowitz, J Moolman-Smook, JK Kanters, ...
Hum Mutat 30 (9), 1256-1266, 2009
Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives
PS Andersen, O Havndrup, L Hougs, KM Sørensen, M Jensen, LA Larsen, ...
Human mutation 30 (3), 363-370, 2009
High Prevalence of Long QT Syndrome–Associated SCN5A Variants in Patients With Early-Onset Lone Atrial Fibrillation
MS Olesen, L Yuan, B Liang, AG Holst, N Nielsen, JB Nielsen, PL Hedley, ...
Circulation: Cardiovascular Genetics 5 (4), 450-459, 2012
Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation
MS Olesen, T Jespersen, JB Nielsen, B Liang, DV Møller, P Hedley, ...
Cardiovascular research 89 (4), 786-793, 2011
Increased risk of preterm delivery and pre‐eclampsia in women with polycystic ovary syndrome and hyperandrogenaemia
KV Naver, J Grinsted, SO Larsen, PL Hedley, FS Jørgensen, ...
BJOG: An International Journal of Obstetrics & Gynaecology 121 (5), 575-581, 2014
Neural control of heart rate is an arrhythmia risk modifier in long QT syndrome
PJ Schwartz, E Vanoli, L Crotti, C Spazzolini, C Ferrandi, A Goosen, ...
Journal of the American College of Cardiology 51 (9), 920-929, 2008
The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy
DV Møller, PS Andersen, P Hedley, MK Ersbøll, H Bundgaard, ...
European Journal of Human Genetics 17 (10), 1241-1249, 2009
Adipose expression of adipocytokines in women with polycystic ovary syndrome
PF Svendsen, M Christiansen, PL Hedley, L Nilas, SB Pedersen, ...
Fertility and sterility 98 (1), 235-241, 2012
Therapeutic hypothermia and ventricular fibrillation storm in early repolarization syndrome
R Bastiaenen, PL Hedley, M Christiansen, ER Behr
Heart rhythm 7 (6), 832-834, 2010
Relative atrial natriuretic peptide deficiency and inadequate renin and angiotensin II suppression in obese hypertensive men
CL Asferg, SJ Nielsen, UB Andersen, A Linneberg, DV Møller, PL Hedley, ...
Hypertension 62 (1), 147-153, 2013
Fc gamma receptor IIIB (FcγRIIIB) polymorphisms are associated with clinical malaria in Ghanaian children
B Adu, D Dodoo, S Adukpo, PL Hedley, FKN Arthur, TA Gerds, SO Larsen, ...
Public Library of Science 7 (9), e46197, 2012
Leptin, adiponectin, and their ratio as markers of insulin resistance and cardiometabolic risk in childhood obesity
C Frithioff‐Bøjsøe, MAV Lund, U Lausten‐Thomsen, PL Hedley, ...
Pediatric diabetes 21 (2), 194-202, 2020
Mitochondrial haplogroups modify the risk of developing hypertrophic cardiomyopathy in a Danish population
CM Hagen, FH Aidt, PL Hedley, MK Jensen, O Havndrup, JK Kanters, ...
PloS one 8 (8), e71904, 2013
High‐efficiency multiplex capillary electrophoresis single strand conformation polymorphism (multi‐CE‐SSCP) mutation screening of SCN5A: a rapid genetic …
J Hofman‐Bang, ER Behr, P Hedley, J Tfelt‐Hansen, JK Kanters, ...
Clinical genetics 69 (6), 504-511, 2006
The role of Lamin A/C mutations in Danish patients with idiopathic dilated cardiomyopathy
DV Møller, TT Pham, F Gustafsson, P Hedley, MK Ersbøll, H Bundgaard, ...
European journal of heart failure 11 (11), 1031-1035, 2009
A novel Myosin essential light chain mutation causes hypertrophic cardiomyopathy with late onset and low expressivity
PS Andersen, PL Hedley, SP Page, P Syrris, JC Moolman-Smook, ...
Biochemistry research international 2012, 2012
Systemet kan ikke foretage handlingen nu. Prøv igen senere.
Artikler 1–20