Hypertrophe Kardiomyopathie als Sarkomererkrankung-Reference-Cited by-同舟云学术

Hypertrophe Kardiomyopathie als Sarkomererkrankung

Published:2004-06 Issue:6 Volume:152 Page:649-658
ISSN:0026-9298
Container-title:Monatsschrift Kinderheilkunde
language:de
Short-container-title:Monatsschr Kinderheilkd

Author:

Kilter H.,Böhm M.

Publisher

Springer Science and Business Media LLC

Subject

Surgery,Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00112-004-0957-5.pdf

Reference45 articles.

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2. Anan R, Shono H, Kisanuki A et al. (1998) Patients with familial hypertrophic cardiomyopathy caused by a Phe110Ile missense mutation in the cardiac troponin T gene have variable cardiac morphologies and a favourable prognosis. Circulation 98:391–397

3. Blair E, Redwood C, Ashrafian H et al. (2001) Mutations in the γ2 subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis. Hum Mol Genet 10:1215–1220

4. Bonne G, Carrier L, Richard P et al. (1998) Familial hypertrophic cardiomyopathy: from mutations to functional defects. Circ Res 83:580–593

5. Brugada R, Kelsey W, Lechin M et al. (1997) Role of candidate modifier genes on the phenotypic expression of hypertrophy in patients with hypertrophic cardiomyopathy. J Invest Med 45:542–551

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1. Andere Herzkrankheiten;Pädiatrie;2007