CARDIOMYOPATHIE HYPERTROPHIQUE PDF

La cardiomyopathie hypertrophique (CMH) est une maladie génétique de transmission autosomique dominante couramment traitée par inotropes négatifs. Report of the World Health Organisation/International Society and Federation of Cardiology Task force on the definition and classification of. High level of physical training can lead cardiovascular quantitative and qualitative adaptations. These clinical, electrical and echocardiographic adaptations are.

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Cardiomyopathie hypertrophique – EM|consulte

Synonyme s cardiomyopathie obstructive familiale ;familial hypertrophic myocardiopathy ;familial obstructive cardiomyopathy ;familial obstructive myocardiopathy ;myocardiopathie hypertrophique familiale ;myocardiopathie obstructive familiale ;familial HCM familial hypertrophic cardiomyopathy.

The version of the gene table of monogenic neuromuscular disorders nuclear genome Bonne G, Rivier F, Hamroun D Neuromuscular hjpertrophique NMD, 27, 12, p.

The version of the gene table of monogenic neuromuscular disorders nuclear genome Type de document: NMD, 26, 12, p. The version of the gene table of monogenic neuromuscular disorders nuclear genome Kaplan JC, Hamroun D Neuromuscular disorders: NMD, 25, p.

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The authors and the editorial office regret the oversight of the journal reference under the title at the start of the Gene Table on page which should read: The version of the gene table of monogenic neuromuscular disorders nuclear genome Kaplan JC Neuromuscular disorders: NMD, 24, 12, p.

Hypertrophic Cardiomyopathy Overview Type de document: NMD, 23, 12, p. GeneReviews, sp. NMD, 22, 12, p.

Laing early onset distal myopathy: Journal of hypsrtrophique, neurosurgery and psychiatry, 77, 2, p. Truncated cardiac myosin-binding protein C are substrates and inhibitors of the ubiquitin-proteasome system abstract: A new mouse model of familial hypertrophic cardiomyopathy exhibits instability of the EK mutant cardiac myosin-binding protein C abstract: Gene profiling during progressive muscle dysfunction induced by human cardiac myosin binding protein C expression in Drosophila abstract: Mutations in the gamma-2 subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: Human molecular genetics, 10, 11, p.

End-stage hypertrophic cardiomyopathy in a cat.

Genetic and molecular basis of cardiac arrhythmias: European heart journal, 20, p. La cardiomyopathie hypertrophique familiale: American journal of human genetics The, 55, p.

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Infantile familial cardiomyopathy due to mitochondrial complex I and IV associated deficiency. NMD, 3, 1, p Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy Watkins H, Rosenzweig A, Hwang DS, et al. New England Journal of Medicine The,The version of the gene table of monogenic neuromuscular disorders nuclear genome.

Kaplan JCAuteur.