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Mycobacterium abscessus-Induced Granuloma Formation Is Strictly Dependent on TNF Signaling and Neutrophil Trafficking

PLoS pathogens, 2016-11, Vol.12 (11), p.e1005986-e1005986

2016

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Brugada syndrome and atrial fibrillation: pathophysiology and genetics

Europace (London, England), 2011-07, Vol.13 (7), p.913-915

2011

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Sexual risk behaviour and donor deferral in Europe

Vox sanguinis, 2014-11, Vol.107 (4), p.420-427

2014

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Sudden cardiac arrest in sports – need for uniform registration: A Position Paper from the Sport Cardiology Section of the European Association for Cardiovascular Prevention and Rehabilitation

European journal of preventive cardiology, 2016-04, Vol.23 (6), p.657-667

2016

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The Phenotype Standardization Project: Improving Pharmacogenetic Studies of Serious Adverse Drug Reactions

Clinical pharmacology and therapeutics, 2011-06, Vol.89 (6), p.784-785

2011

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Sudden arrhythmic death syndrome: a national survey of sudden unexplained cardiac death

Heart (British Cardiac Society), 2007-05, Vol.93 (5), p.601-605

2007

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Characterisation of hypertensive heart disease: pathological insights from a sudden cardiac death cohort to inform clinical practice

Journal of human hypertension, 2022-03, Vol.36 (3), p.246-253

2022

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Cardiological assessment of first-degree relatives in sudden arrhythmic death syndrome

The Lancet (British edition), 2003-11, Vol.362 (9394), p.1457-1459

2003

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Andersen-Tawil syndrome: multi-system deep phenotyping of a large UK cohort

Journal of neurology, neurosurgery and psychiatry, 2022-06, Vol.93 (6), p.A95-A95

2022

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Kreuth IV: European consensus proposals for treatment of haemophilia with coagulation factor concentrates

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-05, Vol.23 (3), p.370-375

2017

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Mitral annular disjunction in idiopathic ventricular fibrillation patients: just a bystander or a potential cause?

European heart journal cardiovascular imaging, 2024-05, Vol.25 (6), p.764-770

2024

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Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage disease

International journal of cardiology, 2016-05, Vol.210, p.41-44

2016

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Research in haemophilia B - approaching the request for high evidence levels in a rare disease

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-01, Vol.21 (1), p.4-20

2015

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The magnitude of sudden cardiac death in the young: a death certificate-based review in England and Wales

Europace (London, England), 2009-10, Vol.11 (10), p.1353-1358

2009

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Sudden unexplained death in infants and children: the role of undiagnosed inherited cardiac conditions

Europace (London, England), 2014-12, Vol.16 (12), p.1706-1713

2014

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Utility of high and standard right precordial leads during ajmaline testing for the diagnosis of Brugada syndrome

Heart (British Cardiac Society), 2010-12, Vol.96 (23), p.1904-1908

2010

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Getting to the heart of the matter: investigating the idiopathic sudden cardiac death of a previous well soldier

Journal of the Royal Army Medical Corps, 2019-10, Vol.165 (5), p.377-379

2019

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Homozygous Mutation of Desmocollin-2 in Arrhythmogenic Right Ventricular Cardiomyopathy with Mild Palmoplantar Keratoderma and Woolly Hair

Cardiology, 2009-01, Vol.113 (1), p.28-34

2009

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Pode-se aprender Openmusic em três dias?

Orfeu, 2017-12, Vol.2 (1)

Malt, Mikhail

2017

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Takotsubo cardiomyopathy and the long-QT syndrome: an insult to repolarization reserve

Europace (London, England), 2009-06, Vol.11 (6), p.697-700

2009

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PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome

Neurology, 2003-06, Vol.60 (11), p.1811

2003

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High-efficiency multiplex capillary electrophoresis single strand conformation polymorphism (multi-CE-SSCP) mutation screening of SCN5A: a rapid genetic approach to cardiac arrhythmia

Clinical genetics, 2006-06, Vol.69 (6), p.504-511

2006

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Drug-induced arrhythmia: pharmacogenomic prescribing?

European heart journal, 2013-01, Vol.34 (2), p.89-95

2013

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Kreuth III: European consensus proposals for treatment of haemophilia with coagulation factor concentrates

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-05, Vol.20 (3), p.322-325

2014

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Clinical trial report: the electrocardiographic response to ajmaline provocation in healthy subjects

Europace (London, England), 2023-05, Vol.25 (Supplement_1)

2023

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Mycobacterium abscessus-Induced Granuloma Formation Is Strictly Dependent on TNF Signaling and Neutrophil Trafficking

Brugada syndrome and atrial fibrillation: pathophysiology and genetics

Sexual risk behaviour and donor deferral in Europe

Sudden cardiac arrest in sports – need for uniform registration: A Position Paper from the Sport Cardiology Section of the European Association for Cardiovascular Prevention and Rehabilitation

The Phenotype Standardization Project: Improving Pharmacogenetic Studies of Serious Adverse Drug Reactions

Sudden arrhythmic death syndrome: a national survey of sudden unexplained cardiac death

Characterisation of hypertensive heart disease: pathological insights from a sudden cardiac death cohort to inform clinical practice

Cardiological assessment of first-degree relatives in sudden arrhythmic death syndrome

Andersen-Tawil syndrome: multi-system deep phenotyping of a large UK cohort

Kreuth IV: European consensus proposals for treatment of haemophilia with coagulation factor concentrates

Mitral annular disjunction in idiopathic ventricular fibrillation patients: just a bystander or a potential cause?

Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage disease

Research in haemophilia B - approaching the request for high evidence levels in a rare disease

The magnitude of sudden cardiac death in the young: a death certificate-based review in England and Wales

Sudden unexplained death in infants and children: the role of undiagnosed inherited cardiac conditions

Utility of high and standard right precordial leads during ajmaline testing for the diagnosis of Brugada syndrome

Getting to the heart of the matter: investigating the idiopathic sudden cardiac death of a previous well soldier

Homozygous Mutation of Desmocollin-2 in Arrhythmogenic Right Ventricular Cardiomyopathy with Mild Palmoplantar Keratoderma and Woolly Hair

Pode-se aprender Openmusic em três dias?

Takotsubo cardiomyopathy and the long-QT syndrome: an insult to repolarization reserve

PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome

High-efficiency multiplex capillary electrophoresis single strand conformation polymorphism (multi-CE-SSCP) mutation screening of SCN5A: a rapid genetic approach to cardiac arrhythmia

Drug-induced arrhythmia: pharmacogenomic prescribing?

Kreuth III: European consensus proposals for treatment of haemophilia with coagulation factor concentrates

Clinical trial report: the electrocardiographic response to ajmaline provocation in healthy subjects

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