Ostman-Smith I - Search Results

1

Hypertrophic cardiomyopathy due to sarcomeric gene mutations is characterized by impaired energy metabolism irrespective of the degree of hypertrophy.

Crilley JG, Boehm EA, Blair E, Rajagopalan B, Blamire AM, Styles P, McKenna WJ, Ostman-Smith I, Clarke K, Watkins H. Crilley JG, et al. J Am Coll Cardiol. 2003 May 21;41(10):1776-82. doi: 10.1016/s0735-1097(02)03009-7. J Am Coll Cardiol. 2003. PMID: 12767664 Free article.

2

A comparison of MRI and echocardiography in hypertrophic cardiomyopathy.

Devlin AM, Moore NR, Ostman-Smith I. Devlin AM, et al. Br J Radiol. 1999 Mar;72(855):258-64. doi: 10.1259/bjr.72.855.10396215. Br J Radiol. 1999. PMID: 10396215 Clinical Trial.

3

A cohort study of childhood hypertrophic cardiomyopathy: improved survival following high-dose beta-adrenoceptor antagonist treatment.

Ostman-Smith I, Wettrell G, Riesenfeld T. Ostman-Smith I, et al. J Am Coll Cardiol. 1999 Nov 15;34(6):1813-22. doi: 10.1016/s0735-1097(99)00421-0. J Am Coll Cardiol. 1999. PMID: 10577575 Free article. Clinical Trial.

4

Diagnosis of hypertrophic cardiomyopathy and screening for the phenotype suggestive of gene carriage in familial disease: a simple echocardiographic procedure.

Devlin AM, Ostman-Smith I. Devlin AM, et al. J Med Screen. 2000;7(2):82-90. doi: 10.1136/jms.7.2.82. J Med Screen. 2000. PMID: 11002448

5

Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis.

Blair E, Redwood C, Ashrafian H, Oliveira M, Broxholme J, Kerr B, Salmon A, Ostman-Smith I, Watkins H. Blair E, et al. Hum Mol Genet. 2001 May 15;10(11):1215-20. doi: 10.1093/hmg/10.11.1215. Hum Mol Genet. 2001. PMID: 11371514

6

Mutations in cis can confound genotype-phenotype correlations in hypertrophic cardiomyopathy.

Blair E, Price SJ, Baty CJ, Ostman-Smith I, Watkins H. Blair E, et al. J Med Genet. 2001 Jun;38(6):385-8. doi: 10.1136/jmg.38.6.385. J Med Genet. 2001. PMID: 11424919 Free PMC article. No abstract available.

7

Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy.

Blair E, Redwood C, de Jesus Oliveira M, Moolman-Smook JC, Brink P, Corfield VA, Ostman-Smith I, Watkins H. Blair E, et al. Circ Res. 2002 Feb 22;90(3):263-9. doi: 10.1161/hh0302.104532. Circ Res. 2002. PMID: 11861413

8

A simple method for assessing the regression or progression of ventricular hypertrophy in the growing child and adult: the value of left ventricular wall-to-cavity ratios.

Ostman-Smith I, Devlin AM. Ostman-Smith I, et al. Eur J Echocardiogr. 2001 Mar;2(1):22-30. doi: 10.1053/euje.2000.0053. Eur J Echocardiogr. 2001. PMID: 11882422

9

Mutation analysis of AMP-activated protein kinase subunits in inherited cardiomyopathies: implications for kinase function and disease pathogenesis.

Oliveira SM, Ehtisham J, Redwood CS, Ostman-Smith I, Blair EM, Watkins H. Oliveira SM, et al. J Mol Cell Cardiol. 2003 Oct;35(10):1251-5. doi: 10.1016/s0022-2828(03)00237-2. J Mol Cell Cardiol. 2003. PMID: 14519435

10

Differentiation of athlete's heart from pathological forms of cardiac hypertrophy by means of geometric indices derived from cardiovascular magnetic resonance.

Petersen SE, Selvanayagam JB, Francis JM, Myerson SG, Wiesmann F, Robson MD, Ostman-Smith I, Casadei B, Watkins H, Neubauer S. Petersen SE, et al. J Cardiovasc Magn Reson. 2005;7(3):551-8. doi: 10.1081/jcmr-200060631. J Cardiovasc Magn Reson. 2005. PMID: 15959967

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