Author/Creator: Elliott, P M - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Elliott, P M

1. 073 Evaluation of clinical markers of early disease expression and the ability to predict genotype in families with HCM and mutations in cardiac myosin binding protein C. (16th May 2012)

Authors:: Page, S P; Kounas, S; Syrris, P; Christiansen, M I; Rune-Hansen, F; Andersen, P S; Elliott, P M; McKenna, W J
Journal:: Heart
Issue:: Volume 98(2012)Supplement 1
Page Start:: A41
Record Type:: Journal Article
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2. A case of transient hypertrophic cardiomyopathy. Issue 1015 (3rd April 2010)

Authors:: Cahill, T J; Coats, C J; Elliott, P M
Journal:: Postgraduate medical journal
Issue:: Volume 86:Issue 1015(2010)
Page Start:: 310
Record Type:: Journal Article
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3. A new mutation of the cardiac troponin T gene causing familial hypertrophic cardiomyopathy without left ventricular hypertrophy. Issue 5 (1st November 1999)

Authors:: Varnava, A; Baboonian, C; Davison, F; de Cruz, L; Elliott, P M; Davies, M J; McKenna, W J
Journal:: Heart
Issue:: Volume 82:Issue 5(1999)
Page Start:: 621
Record Type:: Journal Article
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4. Abnormal cardiopulmonary exercise variables in asymptomatic relatives of patients with dilated cardiomyopathy who have left ventricular enlargement. Issue 5 (1st May 2000)

Authors:: Mahon, N G; Sharma, S; Elliott, P M; Baig, M K; Norman, M W; Barbeyto, S; McKenna, W J
Journal:: Heart
Issue:: Volume 83:Issue 5(2000)
Page Start:: 511
Record Type:: Journal Article
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5. B-type natriuretic peptide predicts disease severity in children with hypertrophic cardiomyopathy. Issue 10 (10th December 2007)

Authors:: Kaski, J P; Tomé-Esteban, M T; Mead-Regan, S; Pantazis, A; Marek, J; Deanfield, J E; McKenna, W J; Elliott, P M
Journal:: Heart
Issue:: Volume 94:Issue 10(2008)
Page Start:: 1307
Record Type:: Journal Article
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6. Cardiac abnormalities in patients with Leber's hereditary optic neuropathy. Issue 7 (1st July 2003)

Authors:: Sorajja, P; Sweeney, M G; Chalmers, R; Sachdev, B; Syrris, P; Hanna, M; Wood, N D; McKenna, W J; Elliott, P M
Journal:: Heart
Issue:: Volume 89:Issue 7(2003)
Page Start:: 791
Record Type:: Journal Article
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7. Cardiopulmonary responses to exercise in patients with hypertrophic cardiomyopathy. Issue 1 (1st July 1998)

Authors:: Jones, S; Elliott, P M; Sharma, S; McKenna, W J; Whipp, B J
Journal:: Heart
Issue:: Volume 80:Issue 1(1998)
Page Start:: 60
Record Type:: Journal Article
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8. Coronary microvascular dysfunction in male patients with Anderson-Fabry disease and the effect of treatment with α galactosidase A. Issue 3 (5th August 2005)

Authors:: Elliott, P M; Kindler, H; Shah, J S; Sachdev, B; Rimoldi, O E; Thaman, R; Tome, M T; McKenna, W J; Lee, P; Camici, P G
Journal:: Heart
Issue:: Volume 92:Issue 3(2006)
Page Start:: 357
Record Type:: Journal Article
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9. Diagnostic utility of metabolic exercise testing in a patient with cardiovascular disease. Issue 4 (1st April 1999)

Authors:: Elliott, P M; Hanna, M G; Ward, S A; Chinnery, P F; Turnbull, D M; Wood, N W; McKenna, W J
Journal:: Heart
Issue:: Volume 81:Issue 4(1999)
Page Start:: 441
Record Type:: Journal Article
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10. Effects of enzyme replacement therapy on the cardiomyopathy of Anderson–Fabry disease: a randomised, double-blind, placebo-controlled clinical trial of agalsidase alfa. Issue 2 (4th May 2007)

Authors:: Hughes, D A; Elliott, P M; Shah, J; Zuckerman, J; Coghlan, G; Brookes, J; Mehta, A B
Journal:: Heart
Issue:: Volume 94:Issue 2(2008)
Page Start:: 153
Record Type:: Journal Article
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