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Noninvasive peripheral perfusion index as a possible tool for screening for critical left heart obstruction

Acta Paediatrica, 2007-10, Vol.96 (10), p.1455-1459

2007

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A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by DSP mutations

Clinical and experimental dermatology, 2014-01, Vol.39 (1), p.30-34

2014

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New skeletal myopathy and cardiomyopathy associated with a missense mutation in MYH7

Neurology, 2007-06, Vol.68 (23), p.2041-2042

2007

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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

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ECG risk score: A powerful predictor of sudden death in hypertrophic cardiomyopathy - genotype correlates

Heart, lung & circulation, 2014, Vol.23, p.e14-e15

Ostman-Smith, I

2014

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Age- and gender-specific mortality rates in childhood hypertrophic cardiomyopathy

European heart journal, 2008-05, Vol.29 (9), p.1160-1167

2008

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Mutations in cis can confound genotype-phenotype correlations in hypertrophic cardiomyopathy

Journal of medical genetics, 2001-06, Vol.38 (6), p.385-387

2001

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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

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Reduction by oral propranolol treatment of left ventricular hypertrophy secondary to pressure‐overload in the rat

British journal of pharmacology, 1995-11, Vol.116 (6), p.2703-2709

Östman‐Smith, I.

1995

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Screening for Critical Congenital Heart Defects in Sweden

Pediatrics (Evanston), 2023-10, Vol.152 (4)

2023

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Prenatal diagnosis and successful preterm delivery of a fetus with long QT syndrome

BJOG : an international journal of obstetrics and gynaecology, 2000-08, Vol.107 (8), p.1049-1051

2000

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Screening for Critical Congenital Heart Defects in Sweden

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

2024

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Reduction by β‐adrenoceptor blockade of hypoxia‐induced right heart hypertrophy in the rat

British journal of pharmacology, 1995-11, Vol.116 (6), p.2698-2702

Östman‐Smith, I.

1995

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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

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Diagnosis of hypertrophic cardiomyopathy and screening for the phenotype suggestive of gene carriage in familial disease: a simple echocardiographic procedure

Journal of medical screening, 2000-01, Vol.7 (2), p.82-90

2000

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Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

Human molecular genetics, 2001-05, Vol.10 (11), p.1215-1220

2001

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Infant Ross procedure for recurrent aortic stenosis

Heart (British Cardiac Society), 1996-11, Vol.76 (5), p.449-450, Article 449

1996

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P1245In a prospective randomized study in familial hypertrophic cardiomyopathy, metoprolol maintains exercise-performance, with lower myocardial oxygen-cost, and prevents deterioration in exercise-ability

European heart journal, 2019-10, Vol.40 (Supplement_1)

2019

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A cohort study of childhood hypertrophic cardiomyopathy improved survival following high-dose beta-adrenoceptor antagonist treatment

Journal of the American College of Cardiology, 1999-11, Vol.34 (6), p.1813-1822

1999

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A cohort study of neurodevelopmental outcome in children with DiGeorge syndrome following cardiac surgery

Archives of disease in childhood, 2003-01, Vol.88 (1), p.61-64

2003

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A.P.15

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.835-835

2014

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A comparison of MRI and echocardiography in hypertrophic cardiomyopathy

British journal of radiology, 1999-03, Vol.72 (855), p.258-264

1999

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Cardiac sympathetic nerves as the final common pathway in the induction of adaptive cardiac hypertrophy

Clinical science (1979), 1981-09, Vol.61 (3), p.265-272

Ostman-Smith, I

1981

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Echocardiographic and electrocardiographic identification of those children with hypertrophic cardiomyopathy who should be considered at high-risk of dying suddenly

Cardiology in the young, 2005-12, Vol.15 (6), p.632-642

2005

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Middle aortic syndrome in a boy with arteriohepatic dysplasia (Alagille syndrome)

Pediatric cardiology, 1997-05, Vol.18 (3), p.232-234

1997

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Noninvasive peripheral perfusion index as a possible tool for screening for critical left heart obstruction

A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by DSP mutations

New skeletal myopathy and cardiomyopathy associated with a missense mutation in MYH7

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

ECG risk score: A powerful predictor of sudden death in hypertrophic cardiomyopathy - genotype correlates

Age- and gender-specific mortality rates in childhood hypertrophic cardiomyopathy

Mutations in cis can confound genotype-phenotype correlations in hypertrophic cardiomyopathy

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

Reduction by oral propranolol treatment of left ventricular hypertrophy secondary to pressure‐overload in the rat

Screening for Critical Congenital Heart Defects in Sweden

Prenatal diagnosis and successful preterm delivery of a fetus with long QT syndrome

Screening for Critical Congenital Heart Defects in Sweden

Reduction by β‐adrenoceptor blockade of hypoxia‐induced right heart hypertrophy in the rat

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

Diagnosis of hypertrophic cardiomyopathy and screening for the phenotype suggestive of gene carriage in familial disease: a simple echocardiographic procedure

Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

Infant Ross procedure for recurrent aortic stenosis

P1245In a prospective randomized study in familial hypertrophic cardiomyopathy, metoprolol maintains exercise-performance, with lower myocardial oxygen-cost, and prevents deterioration in exercise-ability

A cohort study of childhood hypertrophic cardiomyopathy improved survival following high-dose beta-adrenoceptor antagonist treatment

A cohort study of neurodevelopmental outcome in children with DiGeorge syndrome following cardiac surgery

A.P.15

A comparison of MRI and echocardiography in hypertrophic cardiomyopathy

Cardiac sympathetic nerves as the final common pathway in the induction of adaptive cardiac hypertrophy

Echocardiographic and electrocardiographic identification of those children with hypertrophic cardiomyopathy who should be considered at high-risk of dying suddenly

Middle aortic syndrome in a boy with arteriohepatic dysplasia (Alagille syndrome)

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