✦ LIBER ✦

Significance of the DNA synthesis in hypertrophic cardiomyopathies

✍ Scribed by L. Matturri; B. Biondo; B. Colombo; A. M. Lavezzi; L. Rossi

Publisher: Springer
Year: 1997
Tongue: English
Weight: 698 KB
Volume: 92
Category: Article
ISSN: 0300-8428
DOI: 10.1007/bf00805568

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Prognostic significance of morphologic a

Prognostic significance of morphologic abnormalities in hypertrophic cardiomyopathy

📂 Article 📅 1990 🏛 Springer 🌐 English ⚖ 95 KB

Significant regional heterogeneity of co

Significant regional heterogeneity of coronary flow reserve in paediatric hypertrophic cardiomyopathy

✍ Eiji Tadamura; Muneo Yoshibayashi; Toshiya Yonemura; Takashi Kudoh; Shigeto Kubo 📂 Article 📅 2000 🏛 Springer 🌐 English ⚖ 136 KB

Clinical significance of N-terminal-prob

Clinical significance of N-terminal-probrain natriuretic peptide in hypertrophic cardiomyopathy

✍ Georgios K. Efthimiadis; Areti Hitoglou-Makedou; Georgios Giannakoulas; Anastasi 📂 Article 📅 2007 🏛 Springer 🌐 English ⚖ 229 KB

Prognostic significance of myocardial fi

Prognostic significance of myocardial fibrosis in hypertrophic cardiomyopathy using cardiovascular magnetic resonance

✍ Rory O'Hanlon; Agata Grasso; Michael Roughton; James C Moon; Susan Clarke; Ricar 📂 Article 📅 2010 🏛 BioMed Central 🌐 English ⚖ 66 KB

Management of arrhythmias in hypertrophi

Management of arrhythmias in hypertrophic cardiomyopathy

✍ J. T. Stewart; W. J. McKenna 📂 Article 📅 1994 🏛 Springer US 🌐 English ⚖ 661 KB

A DNA resequencing array for pathogenic

A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy

✍ Siv Fokstuen; Robert Lyle; Analia Munoz; Corinne Gehrig; René Lerch; Andreas Per 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 227 KB

## Communicated by Michel Goossens Hypertrophic cardiomyopathy (HCM) is a heterogeneous autosomal dominant cardiac disorder with a prevalence of 1 in 500. Over 450 different pathogenic mutations in at least 16 genes have been identified so far. The large allelic and genetic heterogeneity of HCM r