About: Corinne Vigouroux

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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	Vigouroux, Corinne (19..-....) Vigouroux, Corinne (19..-....) Vigouroux, Corinne (19..-....)
Life Event	http://www.idref.fr/084062835/birth
preferred label	Vigouroux, Corinne (19..-....)
name	Corinne Vigouroux
Language	http://lexvo.org/id/iso639-3/fra
isni:identifierValid	0000000431908927
Given name	Corinne
familyName	Vigouroux
has biographical i...tion (Deprecated)	Directrice de thèse à l'Université Pierre et Marie Curie - Paris 6 en 2010 Maître de conférences des universités-Praticien hospitalier
gender	female
ORCID iD	0000-0002-8181-4721
ISI Researcher ID	DZB-5061-2022
Scopus ID	7003800580
is sameAs of	Vigouroux, Corinne (19..-....) Vigouroux, Corinne (19..-....) Vigouroux, Corinne (19..-....) Vigouroux, Corinne (19..-....) Vigouroux, Corinne (19..-....)
is Thesis advisor of	http://www.sudoc.fr/219470766/id Fonctions adipocytaires de la seipine, mécanismes physiopathologiques de la Lipodystrophie Congénitale de Berardinelli-Seip (BSCL) http://www.sudoc.fr/19070683X/id http://www.sudoc.fr/08406305X/id http://www.sudoc.fr/19129442X/id http://www.sudoc.fr/150513046/id http://www.sudoc.fr/095385991/id http://www.sudoc.fr/247957496/id Liposdystrophies partielles liées à des mutations de la périlipine et des lamines A/C http://www.sudoc.fr/249063549/id
is Praeses of	http://www.sudoc.fr/197849504/id http://www.sudoc.fr/203944275/id http://www.sudoc.fr/225375613/id http://www.sudoc.fr/268710007/id http://www.sudoc.fr/27223706X/id http://www.sudoc.fr/267989776/id
is Author of	http://www.sudoc.fr/059958995/id Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies Peroxisome proliferator‐activated receptor gamma‐ligand‐binding domain mutations associated with familial partial lipodystrophy type 3 disrupt human trophoblast fusion and fibroblast migration Two Decades after Mandibuloacral Dysplasia Discovery: Additional Cases and Comprehensive View of Disease Characteristics Rôles biologiques à multiples facettes de l’adiponectine Biallelic CAV1 null variants induce Congenital Generalized Lipodystrophy with achalasia Short title: CAV1, generalized lipodystrophy and achalasia Lipodystrophic syndromes due to LMNA mutations: recent developments on biomolecular aspects, pathophysiological hypotheses and therapeutic perspectives What have we learned form monogenic forms of severe insulin resistance associated with PCOS/HAIRAN? Cardiovascular complications of lipodystrophic syndromes – focus on laminopathies http://id.erudit.org/iderudit/013187ar#id Leptin, adiponectin, lipodystrophic and severe insulin resistance syndromes Seipin localizes at endoplasmic-reticulum-mitochondria contact sites to control mitochondrial calcium import and metabolism in adipocytes Ciliopathy due to POC1A deficiency: clinical and metabolic features, and cellular modeling Lipodystrophic syndromes: From diagnosis to treatment Metabolic complications affecting adipose tissue, lipid and glucose metabolism associated with HIV antiretroviral treatment Molecular and Cellular Bases of Lipodystrophy Syndromes Efficient adenoviral transduction of 3T3-F442A preadipocytes without affecting adipocyte differentiation Inappropriately low glycated hemoglobin values and hemolysis in HIV-infected patients. Impact of protease inhibitors on circulating PCSK9 levels in HIV-infected antiretroviral-naive patients from an ongoing prospective cohort LIPE-related lipodystrophic syndrome: clinical features and disease modeling using adipose stem cells http://hub.abes.fr/edp/periodical/mnut/2011/volume_47/issue_2/mnut1120005/w Functional Human Beige Adipocytes From Induced Pluripotent Stem Cells Therapeutic use of recombinant methionyl human leptin. Human lipodystrophies: genetic and acquired diseases of adipose tissue. Therapeutic indications and metabolic effects of metreleptin in patients with lipodystrophy syndromes: Real-life experience from a national reference network Looking at New Unexpected Disease Targets in LMNA-Linked Lipodystrophies in the Light of Complex Cardiovascular Phenotypes: Implications for Clinical Practice http://www.sudoc.fr/246553251/id SYNDROMES DE RESISTANCE A L'INSULINE AVEC LIPODYSTROPHIE, ETUDE CLINIQUE, BIOLOGIQUE ET MOLECULAIRE Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: towards recommendation for molecular testing and management MFN2-associated lipomatosis: Clinical spectrum and impact on adipose tissue Partial lipodystrophy with severe insulin resistance and adult progeria Werner syndrome. One-year metreleptin therapy decreases PCSK9 serum levels in diabetic patients with monogenic lipodystrophy syndromes Monogenic forms of lipodystrophic syndromes - diagnosis, detection, and practical management considerations from clinical cases Diagnostic Challenge in PLIN1-Associated Familial Partial Lipodystrophy Functional Human Beige Adipocytes From Induced Pluripotent Stem Cells Maladaptative autophagy impairs adipose function in Congenital Generalized Lipodystrophy due to cavin-1 deficiency Adherence with metreleptin therapy and health self-perception in patients with lipodystrophic syndromes Acquired Generalized Lipodystrophy: A New Cause of Anti-PD-1 Immune-Related Diabetes Seipin regulates ER-lipid droplet contacts and cargo delivery A Novel Lamin A Mutant Responsible for Congenital Muscular Dystrophy Causes Distinct Abnormalities of the Cell Nucleus [Mutltifaceted biological roles of leptin] Immune deficiency could be an early risk factor for altered insulin sensitivity in antiretroviral-naive HIV-1-infected patients: the ANRS COPANA cohort. https://serval.unil.ch/notice/serval:BIB_2ED3068C9528#id Laminopathies’ Treatments Systematic Review: A Contribution Towards a ‘Treatabolome’ EPHX1 mutations cause a lipoatrophic diabetes syndrome due to impaired epoxide hydrolysis and increased cellular senescence Cardiometabolic assessment of lamin A/C gene mutation carriers: A phenotype-genotype correlation. Lipodystrophy-Linked LMNA p.R482W Mutation Induces Clinical Early Atherosclerosis and In Vitro Endothelial Dysfunction https://serval.unil.ch/notice/serval:BIB_2A58E13A9E9B#id Metabolic risk factors in young adults infected with HIV since childhood compared with the general population PIK3R1 Mutations Cause Syndromic Insulin Resistance with Lipoatrophy New Anti-Müllerian Hormone Target Genes Involved in Granulosa Cell Survival in Women With Polycystic Ovary Syndrome Progerin Expression Induces Inflammation, Oxidative Stress and Senescence in Human Coronary Endothelial Cells Irisin levels in LMNA-associated partial lipodystrophies ADH1B, the adipocyte-enriched alcohol dehydrogenase, plays an essential, cell-autonomous role in human adipogenesis Loss of thymidine phosphorylase activity disrupts adipocyte differentiation and induces insulin-resistant lipoatrophic diabetes Diagnosis, risk factors and management of diabetes mellitus in HIV-infected persons in France: A real-life setting study <scp>RIPK3</scp> dampens mitochondrial bioenergetics and lipid droplet dynamics in metabolic liver disease LMNA mutations resulting in lipodystrophy and HIV protease inhibitors trigger vascular smooth muscle cell senescence and calcification: Role of ZMPSTE24 downregulation Hypoglycaemia revealing heterozygous insulin receptor mutations. Hyperinsulinemia and insulin signalling in the pathogenesis and the clinical course of hepatocellular carcinoma Chrom3D: three-dimensional genome modeling from Hi-C and nuclear lamin-genome contacts https://orbi.uliege.be/handle/2268/194348#id

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