S. Hughes

发表

Novel Mutation in Desmoplakin Causes Arrhythmogenic Left Ventricular Cardiomyopathy

M. Simpson, J. Mogensen, P. Syrris, 2005, Circulation.

P Arrhythmogenic Cardiomyopathy Left-Dominant Arrhythmogenic Cardiomyopathy An UnderRecognized Clinical Entity

D. Pennell, R. Merrifield, P. Syrris, 2008 .

Left-dominant arrhythmogenic cardiomyopathy: an under-recognized clinical entity.

Dudley J Pennell, Sanjay K Prasad, Robert Merrifield, 2008, Journal of the American College of Cardiology.

New insights into the pathology of inherited cardiomyopathy

W. McKenna, S. Hughes, William J McKenna, 2005, Heart.

Long-term adaptive versus maladaptive remodelling of the pulmonary autograft after the Ross operation.

M. Yacoub, V. Tsang, P. Sarathchandra, 2020, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

Desmoglein-2 mutations in arrhythmogenic right ventricular cardiomyopathy: a genotype-phenotype characterization of familial disease.

P. Syrris, S. Sen-Chowdhry, W. McKenna, 2006, European heart journal.

Interruption of the aorta with multilobulated arch aneurysms: a new clinicopathologic entity.

M. Yacoub, P. Kilner, T. Hsia, 2007, The Journal of thoracic and cardiovascular surgery.

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

J. Mogensen, T. Kubo, W. McKenna, 2004, The Lancet.

A case of fatal ephedra intake associated with lipofuscin accumulation, caspase activation and cleavage of myofibrillary proteins

J. Gardin, D. Latchman, L. Saravolatz, 2005, European journal of heart failure.

Heart failure in a woman with SLE, anti-phospholipid syndrome and Fabry’s disease

D. Isenberg, S. Hughes, T. Butters, 2013, Lupus.

Heart muscle disease

S. Hughes, 2002 .

Cardiomyopathy Novel Mutation in Desmoplakin Causes Arrhythmogenic Left Ventricular

M. Simpson, J. Mogensen, P. Syrris, 2010 .

cardiomyopathyinsights into the pathology of inherited

W. McKenna, S. Hughes, 2007 .

Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families.

E. Behr, M. Christiansen, P. Syrris, 2008, European heart journal.

Differential Expression of the Fibroblast Growth Factor Receptor (FGFR) Multigene Family in Normal Human Adult Tissues

S. Hughes, S E Hughes, 1997, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Valvular Heart Disease

S. Hughes, 2013 .

GAA repeat expansion mutation mouse models of Friedreich ataxia exhibit oxidative stress leading to progressive neuronal and cardiac pathology.

M. Pook, Z. Webster, S. Hughes, 2006, Genomics.

Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome: natural history.

P. Elliott, J. Mogensen, J. Holton, 2005, Journal of the American College of Cardiology.

Detection of apoptosis using in situ markers for DNA strand breaks in the failing human heart. Fact or epiphenomenon?

S. Hughes, 2003, The Journal of pathology.

The pathology of hypertrophic cardiomyopathy

S. Hughes, 2004, Histopathology.

Early functional and transcriptomic changes in the myocardium predict outcome in a long-term rat model of sepsis.

M. Singer, M. Bauer, J. Carré, 2013, Clinical science.

Aortic Root Characteristics of Human Pulmonary Autografts

Magdi H. Yacoub, M. Yacoub, S. Edwards, 2000, Circulation.

The fibroblast growth factor and receptor multigene families

P. Hall, S. Hughes, Sian E. Hughes, 1993, The Journal of pathology.

Letter regarding article by Norman et al, "Novel mutation in desmoplakin causes arrhythmogenic left ventricular cardiomyopathy" - Response

M. Simpson, J. Mogensen, P. Syrris, 2006 .

Cardiac involvement in acute thrombotic thrombocytopenic purpura: association with troponin T and IgG antibodies to ADAMTS 13

J. McEwan, H. Cohen, M. Scully, 2009, Journal of thrombosis and haemostasis : JTH.

Expression of basic and acidic fibroblast growth factors and their receptor in normal and atherosclerotic human arteries.

D. Crossman, P. Hall, S. Hughes, 1993, Cardiovascular Research.

GAA repeat expansion mutation mouse models of Friedreich ataxia exhibit oxidative stress leading to progressive neuronal and cardiac pathology.

M. Pook, S. Hughes, L. Lawrence, 2006, Genomics.

Cardiac involvement in acute thrombotic thrombocytopenic purpura: association with troponin T and IgG antibodies to ADAMTS 13

J. McEwan, H. Cohen, M. Scully, 2009, Journal of thrombosis and haemostasis : JTH.

Early functional and transcriptomic changes in the myocardium predict outcome in a long-term rat model of sepsis.

M. Singer, M. Bauer, A. Rudiger, 2013, Clinical science.