About: Dominique Germain

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An Entity of Type : foaf:Person, within Data Space : data.idref.fr associated with source document(s)

Attributes	Values
type	Person
sameAs	Germain, Dominique Germain, Dominique
alternative label	Germain, Dominique P.
preferred label	Germain, Dominique
name	Dominique Germain
dbpedia-owl:citizenship	http://sws.geonames.org/3017382/
Language	http://lexvo.org/id/iso639-3/fra
Given name	Dominique
familyName	Germain
has biographical i...tion (Deprecated)	Directeur d'une thèse en médecine générale à l'Université Versailles-Saint Quentin en Yvelines en 2009 Professeur de génétique médicale à l'Université de Versailles, membre de l'UMR 1179 - Handicap neuromusculaire : physiopathologie, biothérapie et pharmacologie appliquées (END-ICAP) en 2019
gender	male
ORCID iD	0000-0002-8355-007X
Scopus ID	7006706457
is sameAs of	Germain, Dominique Germain, Dominique Germain, Dominique Germain, Dominique Germain, Dominique
is Thesis advisor of	http://www.sudoc.fr/139606629/id http://www.sudoc.fr/049513494/id
is Author of	http://www.sudoc.fr/041694821/id http://www.sudoc.fr/043308899/id Non-invasive evaluation of arterial involvement in patients affected with Fabry disease Screening patients with hypertrophic cardiomyopathy for Fabry disease using a filter-paper test: the FOCUS study Humoral immune response to SARS-CoV-2 vaccination after a booster vaccine dose in two kidney transplant recipients with fabry disease and variable secondary immunosuppressive regimens MALADIE DE FABRY ET MALADIE DE GAUCHER, CARACTERISATION MOLECULAIRE, CORRELATIONS GENOTYPE/PHENOTYPE ET PERSPECTIVES THERAPEUTIQUES https://serval.unil.ch/notice/serval:BIB_8A051DBE6C82#id Screening for Fabry disease in male patients with end-stage renal disease in western France The role of CNVs in the etiology of rare autosomal recessive disorders: the example of TRAPPC9-associated intellectual disability http://www.sudoc.fr/059948523/id Fluorescence-assisted mismatch analysis (FAMA) for exhaustive screening of the α-galactosidase A gene and detection of carriers in Fabry disease Maladie de Fabry en cardiologie revue de la littérature et point de vue d'experts [Fabry disease in cardiology practice Literature review and expert point of view] Mutation spectrum in the ABCC6 gene and genotype–phenotype correlations in a French cohort with pseudoxanthoma elasticum http://www.sudoc.fr/246545410/id Correlations between cytogenetics and morphology in myelodysplastic syndromes https://archive-ouverte.unige.ch/unige:148842#id Fabry disease: a review of current management strategies Clinical and molecular delineation of Tetrasomy 9p syndrome: Report of 12 new cases and literature review Pseudoxanthoma elasticum: evidence for the existence of a pseudogene highly homologous to the ABCC6gene End-stage renal disease in patients with Fabry disease: natural history data from the Fabry Registry Familial occurrence and heritable connective tissue disorders in cervical artery dissection. http://hub.abes.fr/edp/periodical/medsci/2013/volume_29/issue_67/medsci2013296-7p579/w https://serval.unil.ch/notice/serval:BIB_C8A8921BAB45#id https://serval.unil.ch/notice/serval:BIB_8DEE63EC54AF#id
is primary topic of	http://www.idref.fr/139615547
is Opponent of	http://www.sudoc.fr/235017981/id
is Thesis referee of	http://www.sudoc.fr/235905496/id

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