UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Sudden cardiac death in childhood hypertrophic cardiomyopathy is best predicted by a combination of electrocardiogram risk‐score and HCMRisk‐Kids score

Acta Paediatrica, 2021-11, Vol.110 (11), p.3105-3115

2021

Volltextzugriff (PDF)

Cardiomyopathy and Exercise Intolerance in Muscle Glycogen Storage Disease 0

The New England journal of medicine, 2007-10, Vol.357 (15), p.1507-1514

2007

Volltextzugriff (PDF)

Biomarkers and Proteomics in Sarcomeric Hypertrophic Cardiomyopathy in the Young-FGF-21 Highly Associated with Overt Disease

Journal of cardiovascular development and disease, 2024-04, Vol.11 (4), p.105

2024

Volltextzugriff (PDF)

Electrocardiographic amplitudes: a new risk factor for sudden death in hypertrophic cardiomyopathy

European heart journal, 2010-02, Vol.31 (4), p.439-449

2010

Volltextzugriff (PDF)

Screening for Critical Congenital Heart Defects in Sweden

Obstetrical & gynecological survey, 2024-04, Vol.79 (4), p.185-187

2024

Volltextzugriff (PDF)

Indications and management of implantable cardioverter-defibrillator therapy in childhood hypertrophic cardiomyopathy: A position statement from the AEPC Working Group on Basic Science, Genetics and Myocardial Disease and the AEPC Working Group on Cardiac Dysrhythmias and Electrophysiology

Cardiology in the young, 2023-05, Vol.33 (5), p.681-698

2023

Volltextzugriff (PDF)

Screening for Critical Congenital Heart Defects in Sweden

Pediatrics (Evanston), 2023, Vol.152 (4)

2023

Volltextzugriff (PDF)

Indications and management of implantable cardioverter-defibrillator therapy in childhood hypertrophic cardiomyopathy: A position statement from the AEPC Working Group on Basic Science, Genetics and Myocardial Disease and the AEPC Working Group on Cardiac Dysrhythmias and Electrophysiology - ERRATUM

Cardiology in the young, 2024-02, Vol.34 (2), p.469-1

2024

Volltextzugriff (PDF)

Management of cardiac aspects in children with Noonan syndrome – results from a European clinical practice survey among paediatric cardiologists

European journal of medical genetics, 2022-01, Vol.65 (1), p.104372-104372, Article 104372

2022

Volltextzugriff (PDF)

What Aspects of Phenotype Determine Risk for Sudden Cardiac Death in Pediatric Hypertrophic Cardiomyopathy?

Journal of cardiovascular development and disease, 2022-04, Vol.9 (5), p.124

Östman-Smith, Ingegerd

2022

Volltextzugriff (PDF)

Hypertrophic cardiomyopathy due to sarcomeric gene mutations is characterized by impaired energy metabolism irrespective of the degree of hypertrophy

Journal of the American College of Cardiology, 2003-05, Vol.41 (10), p.1776-1782

2003

Volltextzugriff (PDF)

High ECG Risk-Scores Predict Late Gadolinium Enhancement on Magnetic Resonance Imaging in HCM in the Young

Pediatric cardiology, 2021-03, Vol.42 (3), p.492-500

2021

Volltextzugriff (PDF)

Hypertrophic cardiomyopathy in childhood and adolescence - strategies to prevent sudden death

Fundamental & clinical pharmacology, 2010-10, Vol.24 (5), p.637-652

Östman-Smith, Ingegerd

2010

Volltextzugriff (PDF)

Beta-Blockers in Pediatric Hypertrophic Cardiomyopathies

Reviews on recent clinical trials, 2014-01, Vol.9 (2), p.82-85

Östman-Smith, Ingegerd

2014

Volltextzugriff (PDF)

Conflicting results on the role of electrocardiogram in risk stratification for sudden cardiac death in childhood hypertrophic cardiomyopathy

European journal of preventive cardiology, 2023-04, Vol.30 (6), p.e31-e33

2023

Volltextzugriff (PDF)

Impact of pulse oximetry screening on the detection of duct dependent congenital heart disease: a Swedish prospective screening study in 39,821 newborns

BMJ, 2009-01, Vol.338 (7687), p.145-149

International edition, 2009

Volltextzugriff (PDF)

Lessons From a Genotype-Phenotype Study About the Clinical Spectrum of Hypertrophic Cardiomyopathy Associated With Noonan Syndrome With Multiple Lentigines and PTPN11-Mutations

Circulation. Genomic and precision medicine, 2023-08, Vol.16 (4), p.e004206-362

Östman-Smith, Ingegerd

2023

Volltextzugriff (PDF)

Factors associated with excess female mortality in obstructive hypertrophic cardiomyopathy

European journal of preventive cardiology, 2022-08, Vol.29 (11), p.1545-1556

2022

Volltextzugriff (PDF)

Predictors of risk for sudden death in childhood hypertrophic cardiomyopathy: the importance of the ECG risk score

Open heart, 2017, Vol.4 (2), p.e000658-e000658

2017

Volltextzugriff (PDF)

Differential diagnosis between left ventricular hypertrophy and cardiomyopathy in childhood

Journal of electrocardiology, 2014-09, Vol.47 (5), p.661-668

Östman-Smith, Ingegerd, MD, PhD

2014

Volltextzugriff (PDF)

Short atrioventricular delay pacing therapy in young and old patients with hypertrophic obstructive cardiomyopathy: good long-term results and a low need for reinterventions

Europace (London, England), 2018-10, Vol.20 (10), p.1683-1691

2018

Volltextzugriff (PDF)

Differentiation of athlete's heart from pathological forms of cardiac hypertrophy by means of geometric indices derived from cardiovascular magnetic resonance

Journal of cardiovascular magnetic resonance, 2005-01, Vol.7 (3), p.551-558

2005

Volltextzugriff (PDF)

Mutations of the Light Meromyosin Domain of the β-Myosin Heavy Chain Rod in Hypertrophic Cardiomyopathy

Circulation research, 2002-02, Vol.90 (3), p.263-269

2002

Volltextzugriff (PDF)

Quality of life in asymptomatic children and adolescents before and after diagnosis of hypertrophic cardiomyopathy through family screening

Journal of clinical nursing, 2013-01, Vol.22 (1-2), p.211-221

2013

Volltextzugriff (PDF)

Morbidity and resource usage after myectomy- or pacing-treatment in hypertrophic obstructive cardiomyopathy: A case-control study

International journal of cardiology, 2021-01, Vol.322, p.197-203

2021

Volltextzugriff (PDF)

1 – 25 von 65

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(65)
Mit Volltextzugriff
(56)

Publikationsform

Artikel
(64)
Tagungsberichte
(1)

Sprache

Englisch
(64)
Schwedisch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Sudden cardiac death in childhood hypertrophic cardiomyopathy is best predicted by a combination of electrocardiogram risk‐score and HCMRisk‐Kids score

Cardiomyopathy and Exercise Intolerance in Muscle Glycogen Storage Disease 0

Biomarkers and Proteomics in Sarcomeric Hypertrophic Cardiomyopathy in the Young-FGF-21 Highly Associated with Overt Disease

Electrocardiographic amplitudes: a new risk factor for sudden death in hypertrophic cardiomyopathy

Screening for Critical Congenital Heart Defects in Sweden

Indications and management of implantable cardioverter-defibrillator therapy in childhood hypertrophic cardiomyopathy: A position statement from the AEPC Working Group on Basic Science, Genetics and Myocardial Disease and the AEPC Working Group on Cardiac Dysrhythmias and Electrophysiology

Screening for Critical Congenital Heart Defects in Sweden

Indications and management of implantable cardioverter-defibrillator therapy in childhood hypertrophic cardiomyopathy: A position statement from the AEPC Working Group on Basic Science, Genetics and Myocardial Disease and the AEPC Working Group on Cardiac Dysrhythmias and Electrophysiology - ERRATUM

Management of cardiac aspects in children with Noonan syndrome – results from a European clinical practice survey among paediatric cardiologists

What Aspects of Phenotype Determine Risk for Sudden Cardiac Death in Pediatric Hypertrophic Cardiomyopathy?

Hypertrophic cardiomyopathy due to sarcomeric gene mutations is characterized by impaired energy metabolism irrespective of the degree of hypertrophy

High ECG Risk-Scores Predict Late Gadolinium Enhancement on Magnetic Resonance Imaging in HCM in the Young

Hypertrophic cardiomyopathy in childhood and adolescence - strategies to prevent sudden death

Beta-Blockers in Pediatric Hypertrophic Cardiomyopathies

Conflicting results on the role of electrocardiogram in risk stratification for sudden cardiac death in childhood hypertrophic cardiomyopathy

Impact of pulse oximetry screening on the detection of duct dependent congenital heart disease: a Swedish prospective screening study in 39,821 newborns

Lessons From a Genotype-Phenotype Study About the Clinical Spectrum of Hypertrophic Cardiomyopathy Associated With Noonan Syndrome With Multiple Lentigines and PTPN11-Mutations

Factors associated with excess female mortality in obstructive hypertrophic cardiomyopathy

Predictors of risk for sudden death in childhood hypertrophic cardiomyopathy: the importance of the ECG risk score

Differential diagnosis between left ventricular hypertrophy and cardiomyopathy in childhood

Short atrioventricular delay pacing therapy in young and old patients with hypertrophic obstructive cardiomyopathy: good long-term results and a low need for reinterventions

Differentiation of athlete's heart from pathological forms of cardiac hypertrophy by means of geometric indices derived from cardiovascular magnetic resonance

Mutations of the Light Meromyosin Domain of the β-Myosin Heavy Chain Rod in Hypertrophic Cardiomyopathy

Quality of life in asymptomatic children and adolescents before and after diagnosis of hypertrophic cardiomyopathy through family screening

Morbidity and resource usage after myectomy- or pacing-treatment in hypertrophic obstructive cardiomyopathy: A case-control study

Suchergebnisse filtern