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66 Should we offer multi-gene testing to all patients with breast cancer: a cost-effectiveness analysis

International journal of gynecological cancer, 2019-09, Vol.29 (Suppl 3), p.A36-A37

2019

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Factors associated with non-compliance with hormone therapy cessation before screening mammography

Climacteric : the journal of the International Menopause Society, 2011-04, Vol.14 (2), p.268-274

2011

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Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome

Circulation (New York, N.Y.), 2001-03, Vol.103 (9), p.1256-1263

2001

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Detection of viruses in myocardial tissues by polymerase chain reaction. evidence of adenovirus as a common cause of myocarditis in children and adults

Journal of the American College of Cardiology, 2003-08, Vol.42 (3), p.466-472

2003

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Mutations in Cypher/ZASP in patients with Dilated cardiomyopathy and left ventricular non-compaction

Journal of the American College of Cardiology, 2003-12, Vol.42 (11), p.2014-2027

2003

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The failing heart

Nature (London), 2002-01, Vol.415 (6868), p.227-233

2002

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Mutations in the muscle LIM protein and α-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis

Molecular genetics and metabolism, 2003-09, Vol.80 (1), p.207-215

2003

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Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in children

Circulation (New York, N.Y.), 2005-09, Vol.112 (11), p.1612-1617

2005

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Clinical characterization of left ventricular noncompaction in children: A relatively common form of cardiomyopathy

Circulation (New York, N.Y.), 2003-11, Vol.108 (21), p.2672-2678

2003

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Genetic analysis in patients with left ventricular noncompaction and evidence for genetic heterogeneity

Molecular genetics and metabolism, 2006-05, Vol.88 (1), p.71-77

2006

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Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

The Journal of clinical investigation, 2000-09, Vol.106 (5), p.655-662

2000

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Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, α- dystrobrevin and FK Binding Protein-12

Molecular genetics and metabolism, 2004-06, Vol.82 (2), p.162-166

2004

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The "final common pathway" hypothesis and inherited cardiovascular disease. The role of cytoskeletal proteins in dilated cardiomyopathy

Herz, 2000-05, Vol.25 (3), p.168-175

2000

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A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathy

Human molecular genetics, 2005-12, Vol.14 (23), p.3587-3593

2005

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Etiologies of cardiomyopathy and heart failure

Nature medicine, 1999-03, Vol.5 (3), p.266-267

1999

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Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome

Human molecular genetics, 2002-02, Vol.11 (3), p.337-345

2002

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Detection of adenoviral genome in the myocardium of adult patients with idiopathic left ventricular dysfunction

Circulation (New York, N.Y.), 1999-03, Vol.99 (10), p.1348-1354

1999

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The detection of cardiotropic viruses in the myocardium of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy

Journal of the American College of Cardiology, 2002-03, Vol.39 (5), p.892-895

2002

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Association of Viral Genome with Graft Loss in Children after Cardiac Transplantation

The New England journal of medicine, 2001-05, Vol.344 (20), p.1498-1503

2001

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Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompaction

Molecular genetics and metabolism, 2002-12, Vol.77 (4), p.319-325

2002

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Adenovirus infection in the lung results in graft failure after lung transplantation

The Journal of thoracic and cardiovascular surgery, 1998-10, Vol.116 (4), p.617-623

1998

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Molecular remodelling of dystrophin in patients with end-stage cardiomyopathies and reversal in patients on assistance-device therapy

The Lancet (British edition), 2002-03, Vol.359 (9310), p.936-941

2002

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Molecular normalization of dystrophin in the failing left and right ventricle of patients treated with either pulsatile or continuous flow-type ventricular assist devices

Journal of the American College of Cardiology, 2004-03, Vol.43 (5), p.811-817

2004

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Association of Parvovirus B19 genome in children with myocarditis and cardiac allograft rejection : Diagnosis using the polymerase chain reaction

Circulation (New York, N.Y.), 1997-11, Vol.96 (10), p.3549-3554

1997

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66 Should we offer multi-gene testing to all patients with breast cancer: a cost-effectiveness analysis

Factors associated with non-compliance with hormone therapy cessation before screening mammography

Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome

Detection of viruses in myocardial tissues by polymerase chain reaction. evidence of adenovirus as a common cause of myocarditis in children and adults

Mutations in Cypher/ZASP in patients with Dilated cardiomyopathy and left ventricular non-compaction

Quantifying cancer risk from exposures to medical imaging in the Risk of Pediatric and Adolescent Cancer Associated with Medical Imaging (RIC) Study: research methods and cohort profile

The failing heart

Mutations in the muscle LIM protein and α-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis

Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in children

Clinical characterization of left ventricular noncompaction in children: A relatively common form of cardiomyopathy

Genetic analysis in patients with left ventricular noncompaction and evidence for genetic heterogeneity

Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, α- dystrobrevin and FK Binding Protein-12

The "final common pathway" hypothesis and inherited cardiovascular disease. The role of cytoskeletal proteins in dilated cardiomyopathy

A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathy

Etiologies of cardiomyopathy and heart failure

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome

Detection of adenoviral genome in the myocardium of adult patients with idiopathic left ventricular dysfunction

The detection of cardiotropic viruses in the myocardium of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy

Association of Viral Genome with Graft Loss in Children after Cardiac Transplantation

Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompaction

Adenovirus infection in the lung results in graft failure after lung transplantation

Molecular remodelling of dystrophin in patients with end-stage cardiomyopathies and reversal in patients on assistance-device therapy

Molecular normalization of dystrophin in the failing left and right ventricle of patients treated with either pulsatile or continuous flow-type ventricular assist devices

Association of Parvovirus B19 genome in children with myocarditis and cardiac allograft rejection : Diagnosis using the polymerase chain reaction

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