About: Philippe Charron

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	researcher (en) 연구원 (ko) ricercatore (it) 研究者 (ja) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq)
rdfs:label	Philippe Charron (en) Philippe Charron (es) Philippe Charron (nl) Philippe Charron (sl) Philippe Charron (ast)
skos:prefLabel	Philippe Charron (en) Philippe Charron (es) Philippe Charron (nl) Philippe Charron (sl) Philippe Charron (ast)
name	Philippe Charron (en) Philippe Charron (es) Philippe Charron (nl) Philippe Charron (sl) Philippe Charron (ast)
given name	wds:Q51581875-A626F1D3-7843-47D2-82C3-0834F116928E
given name	Philippe
instance of	wds:Q51581875-DF961FE7-B0E5-40BB-A15A-BC51D805FC65
instance of	Homo sapiens
occupation	wds:Q51581875-694F893C-45D9-49BB-BF92-4F1B963EF60D
sex or gender	wds:Q51581875-22d795ed-46e6-4af0-27a5-69a772ecec9c
VIAF ID	wds:Q51581875-4882FEE3-1773-481D-9941-8871C586C34F
IdRef ID	wds:Q51581875-C4D2B4EE-463D-4C97-82D8-06F449B04BB0
date of birth	wds:Q51581875-1571E20D-B9BE-41C2-A40E-242E05E892FE
educated at	wds:Q51581875-3FA84145-890D-4E3D-8CFF-D50EAB8E12AC
PLWABN ID	wds:Q51581875-90E47EAC-3EEE-4490-A94A-0C40FCF943FA
family name	wds:Q51581875-1D9C327C-B8AA-4E70-9557-79C60CC5231B
WorldCat Identities ID (superseded)	wds:Q51581875-9DCB6C8D-D912-417D-86F9-4BB37C64C5F8
VIAF ID	http://viaf.org/viaf/88149841839302840166
IdRef ID	http://www.idref.fr/123379458/id
occupation	researcher
sex or gender	male
VIAF ID	88149841839302840166
IdRef ID	123379458
date of birth	1949-01-01 00:00:00Z (xsd:dateTime)
educated at	Assistance Publique – Hôpitaux de Paris
PLWABN ID	9810603027905606
family name	Charron
WorldCat Identities ID (superseded)	viaf-88149841839302840166
ORCID iD	wds:Q51581875-4DDBA77C-0570-41EB-9CA1-DFF142775561
ORCID iD	https://orcid.org/0000-0002-1782-1118
ORCID iD	0000-0002-1782-1118
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q51581875
is author of	Relation between QT duration and maximal wall thickness in familial hypertrophic cardiomyopathy A potential link between peroxisome proliferator-activated receptor signalling and the pathogenesis of arrhythmogenic right ventricular cardiomyopathy. Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial Diseases. Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene Familial dilated cardiomyopathy: clinical features in French families. Epidemiology of desmin and cardiac actin gene mutations in a european population of dilated cardiomyopathy. 2013 ESC Guidelines on cardiac pacing and cardiac resynchronization therapy: the Task Force on cardiac pacing and resynchronization therapy of the European Society of Cardiology (ESC). Developed in collaboration with the European Heart Rhythm Associ Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped children Natural history of Barth syndrome: a national cohort study of 22 patients FHL2 expression and variants in hypertrophic cardiomyopathy Genetic advances in sarcomeric cardiomyopathies: state of the art. Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy Characterization of a Unique Genetic Variant in the β1-adrenoceptor Gene and Evaluation of its Role in Idiopathic Dilated Cardiomyopathy Mutations in the ANKRD1 gene encoding CARP are responsible for human dilated cardiomyopathy Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy Clinical genetics in cardiology Current state of knowledge on aetiology, diagnosis, management, and therapy of myocarditis: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases. Mutational analysis of the beta- and delta-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathy Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC). Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy Triage strategy for urgent management of cardiac tamponade: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases Isolated left ventricular non-compaction in adults: clinical and echocardiographic features in 105 patients. Results from a French registry Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations. Homozygotes for a R869G Mutation in the β -myosin Heavy Chain Gene have a Severe Form of Familial Hypertrophic Cardiomyopathy Genotype–phenotype correlations in familial hypertrophic cardiomyopathy A comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genes Multifocal ectopic Purkinje-related premature contractions: a new SCN5A-related cardiac channelopathy Brugada syndrome in pure black Africans Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers Atlas of the clinical genetics of human dilated cardiomyopathy Accuracy of European diagnostic criteria for familial hypertrophic cardiomyopathy in a genotyped population Functional characterization of the cAMP-binding proteins Epac in cardiac myocytes Epidemiology of walker-related injuries and deaths in the United States Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy Early identification of mutation carriers in familial hypertrophic cardiomyopathy by combined echocardiography and tissue Doppler imaging Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers. Desmosomal cadherins are decreased in explanted arrhythmogenic right ventricular dysplasia/cardiomyopathy patient hearts Screening of genes encoding junctional candidates in arrhythmogenic right ventricular cardiomyopathy/dysplasia.

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