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Respiratory motion reduction with a dual gating approach in myocardial perfusion SPECT: Effect on left ventricular functional parameters

Journal of nuclear cardiology, 2018-10, Vol.25 (5), p.1633-1641

2018

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Genetics of dilated cardiomyopathy

Annals of medicine (Helsinki), 2007, Vol.39 (2), p.91-107

2007

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Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy

Journal of cardiovascular magnetic resonance, 2011-06, Vol.13 (1), p.30-30, Article 30

2011

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High-Throughput Phosphotyrosine Profiling Using SH2 Domains

Molecular cell, 2007-06, Vol.26 (6), p.899-915

2007

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Platelet function testing: Current practice among clinical centres in Northern Europe

Haemophilia : the official journal of the World Federation of Hemophilia, 2022-07, Vol.28 (4), p.642-648

2022

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Serum lipidomics meets cardiac magnetic resonance imaging: profiling of subjects at risk of dilated cardiomyopathy

PloS one, 2011-01, Vol.6 (1), p.e15744-e15744

2011

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POSH2 is a RING finger E3 ligase with Rac1 binding activity through a partial CRIB domain

FEBS letters, 2010-09, Vol.584 (18), p.3867-3872

2010

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Early familial dilated cardiomyopathy: identification with determination of disease state parameter from cine MR image data

Radiology, 2008-10, Vol.249 (1), p.88

2008

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Idiopathic dilated cardiomyopathy and chronic atrial fibrillation

Clinical physiology and functional imaging, 2014-03, Vol.34 (2), p.133-137

2014

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Identification of preferred protein interactions by phage-display of the human Src homology-3 proteome

EMBO reports, 2006-02, Vol.7 (2), p.186-191

2006

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Left atrial appendage volume increased in more than half of patients with cryptogenic stroke

PloS one, 2013-11, Vol.8 (11), p.e79519-e79519

2013

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Plasma N-terminal pro-B-type natriuretic peptide in the detection of aortic valve stenosis

Scandinavian journal of clinical and laboratory investigation, 2023-11, Vol.83 (7), p.489-494

2023

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A novel mutation, Ser143Pro, in the lamin A/C gene is common in finnish patients with familial dilated cardiomyopathy

European heart journal, 2004-05, Vol.25 (10), p.885-893

2004

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Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland

Journal of molecular medicine (Berlin, Germany), 2002-07, Vol.80 (7), p.412-422

2002

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Lamin A/C Mutation Affecting Primarily the Right Side of the Heart

Cardiogenetics, 2013-04, Vol.3 (1), p.e1-e1

2013

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Description of A/C gene mutation related dilated cardiomyopathy with gadolinium- enhanced magnetic resonance imaging

Journal of cardiovascular magnetic resonance, 2011-02, Vol.13 (S1), p.M5-M5, Article M5

2011

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Clinical disease presentation and ECG characteristics of LMNA mutation carriers

Open heart, 2017-01, Vol.4 (1), p.e000474-e000474

2017

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Increased ventilatory response to exercise in symptomatic and asymptomatic LMNA mutation carriers: a follow‐up study

Clinical physiology and functional imaging, 2017-01, Vol.37 (1), p.8-16

2017

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A new common mutation in the cardiac beta-myosin heavy chain gene in Finnish patients with hypertrophic cardiomyopathy

Annals of medicine (Helsinki), 2014-09, Vol.46 (6), p.424-429

2014

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Pregnancy and childbirth in carriers of the lamin A/C-gene mutation

European journal of heart failure, 2010-06, Vol.12 (6), p.630-633

2010

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Characterization of familial and sporadic arrhythmogenic right ventricular cardiomyopathy in Finland

Annals of medicine (Helsinki), 2007, Vol.39 (4), p.312-318

2007

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Arachidonic acid increases matrix metalloproteinase 9 secretion and expression in human monocytic MonoMac 6 cells

Lipids in health and disease, 2009-03, Vol.8 (1), p.11-11, Article 11

2009

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Cardiac Autonomic Control in Relation to Other Prognostic Markers in Idiopathic Dilated Cardiomyopathy

World Journal of Cardiovascular Diseases, 2015, Vol.5 (5), p.107-119

2015

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No variants in the cardiac actin gene in Finnish patients with dilated or hypertrophic cardiomyopathy

The American heart journal, 2002-06, Vol.143 (6), p.E6-E6

2002

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A novel mutation, Arg71Thr, in the δ-sarcoglycan gene is associated with dilated cardiomyopathy

Journal of molecular medicine (Berlin, Germany), 2003-12, Vol.81 (12), p.795-800

2003

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Respiratory motion reduction with a dual gating approach in myocardial perfusion SPECT: Effect on left ventricular functional parameters

Genetics of dilated cardiomyopathy

Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy

High-Throughput Phosphotyrosine Profiling Using SH2 Domains

Platelet function testing: Current practice among clinical centres in Northern Europe

Serum lipidomics meets cardiac magnetic resonance imaging: profiling of subjects at risk of dilated cardiomyopathy

POSH2 is a RING finger E3 ligase with Rac1 binding activity through a partial CRIB domain

Early familial dilated cardiomyopathy: identification with determination of disease state parameter from cine MR image data

Idiopathic dilated cardiomyopathy and chronic atrial fibrillation

Identification of preferred protein interactions by phage-display of the human Src homology-3 proteome

Left atrial appendage volume increased in more than half of patients with cryptogenic stroke

Plasma N-terminal pro-B-type natriuretic peptide in the detection of aortic valve stenosis

A novel mutation, Ser143Pro, in the lamin A/C gene is common in finnish patients with familial dilated cardiomyopathy

Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland

Lamin A/C Mutation Affecting Primarily the Right Side of the Heart

Description of A/C gene mutation related dilated cardiomyopathy with gadolinium- enhanced magnetic resonance imaging

Clinical disease presentation and ECG characteristics of LMNA mutation carriers

Increased ventilatory response to exercise in symptomatic and asymptomatic LMNA mutation carriers: a follow‐up study

A new common mutation in the cardiac beta-myosin heavy chain gene in Finnish patients with hypertrophic cardiomyopathy

Pregnancy and childbirth in carriers of the lamin A/C-gene mutation

Characterization of familial and sporadic arrhythmogenic right ventricular cardiomyopathy in Finland

Arachidonic acid increases matrix metalloproteinase 9 secretion and expression in human monocytic MonoMac 6 cells

Cardiac Autonomic Control in Relation to Other Prognostic Markers in Idiopathic Dilated Cardiomyopathy

No variants in the cardiac actin gene in Finnish patients with dilated or hypertrophic cardiomyopathy

A novel mutation, Arg71Thr, in the δ-sarcoglycan gene is associated with dilated cardiomyopathy

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