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5 raisons identifiées
Auteur de référence en rhumatologie
28 articles scientifiques publiés — un praticien à la pointe de la recherche
Encadrant universitaire
Forme la prochaine génération de rhumatologues (1 thèse dirigée)
Expérience confirmée
18 ans d'exercice en rhumatologie — recul clinique solide
Disponibilité géographique
2 lieux d'exercice — choisissez celui qui vous arrange
Délais de RDV courts dans la région
146.3 rhumatos / 100 000 hab. — département bien doté
18ans d'exercice (thèse 2008)
✨ Génération du profil synthétique IA en cours…
Données ANS publiques (Licence Ouverte 2.0) · Enrichissements MonRhumato 100 % opt-in · Toute personne référencée peut demander la suppression ou la rectification.
Source : catalogue national des thèses theses.fr (ABES). Ne couvre que les doctorats / HDR — les thèses d'exercice (DES) sont archivées dans les SCD universitaires.
Source theses.fr — signal de direction d'équipe / statut PU-PH (à confirmer via le site universitaire).
Indicateurs publics agrégés sur 250 M+ d'œuvres scientifiques (OpenAlex, PubMed). Traduits ici en langage patient.
Influence scientifique
53
53 articles ont été cités au moins 53fois par d'autres chercheurs — preuve que ses travaux sont repris par la communauté médicale.
h-index
Total citations reçues
15 679
Nombre de fois où d'autres équipes ont mentionné ses publications dans leurs propres travaux.
Publications totales
334
Articles, revues et chapitres référencés dans les bases académiques internationales.
Articles influents
96
Publications ayant marqué leur domaine — chacune citée au moins 10 fois par d'autres chercheurs.
i10-index
Thématiques principales
Affiliations FR : Université de Lorraine
Source : OpenAlex (CC0, OurResearch). Indicateurs académiques agrégés sur 250 M+ d'œuvres.
Articles déposés en accès libre sur l'archive ouverte des universités françaises (HAL) — gage d'activité de recherche en France.
Cardiac MRI differentiates classical idiopathic pulmonary arterial hypertension from lung phenotype and group 3 pulmonary hypertension
2026ArticleRespiratory Medicine and Research
Prognostic factors in interstitial lung disease-associated pulmonary hypertension: data from the HYPID cohort and the French Pulmonary Hypertension Registry
2026ArticleEuropean Respiratory Journal
Evolving paradigms in pulmonary hypertension: Highlights of the 6th French Pulmonary Hypertension Network Meeting
2025ArticleRespiratory Medicine and Research
Initial therapy in patients with pulmonary arterial hypertension and cardiovascular comorbidities
2025ArticleEuropean Respiratory Journal
Change in sleep quality Induced by adaptive servo-ventilation for central sleep apnea: 6-month follow-up of the multicenter nationwide French FACIL-VAA cohort
2024ArticleChest
Long‐term follow‐up of neutrophil activation after severe‐to‐critical SARS‐CoV ‐2 infection: A longitudinal study
2024ArticleAllergy
Pulmonary vascular phenotype identified in patients with GDF2 ( BMP9 ) or BMP10 variants: an international multicentre study
2024ArticleEuropean Respiratory Journal
Outcomes and risk assessment in pulmonary veno-occlusive disease
2024ArticleERJ Open Research
Source : HAL — archive ouverte CCSD/CNRS (couvre articles, chapitres EMC, communications congrès, thèses).
SERVICE DE SOINS SNCF
5 B R SAINT-LEON, 54000 NANCY
CHRU NANCY - HOPITAUX DE BRABOIS
R DU MORVAN, 54511 VANDOEUVRE LES NANCY CEDEX
Secteur de conventionnement non disponible (médecin hospitalier ou non présent dans l'Annuaire santé CNAM des libéraux conventionnés).
Lien Doctolib = recherche Google site:doctolib.fr (le 1er résultat est presque toujours le profil correct s'il existe).
The Lancet. Respiratory medicine · 2022
American journal of respiratory and critical care medicine · 2021
Abstract Rationale The relationship between the initial treatment strategy and survival in pulmonary arterial hypertension (PAH) remains uncertain. Objectives To evaluate the long-term survival of patients with PAH categorized according to the initial treatment strategy. Methods A retrospective analysis of incident patients with idiopathic, heritable, or anorexigen-induced PAH enrolled in the French Pulmonary Hypertension Registry (January 2006 to December 2018) was conducted. Survival was assessed according to the initial strategy: monotherapy, dual therapy, or triple-combination therapy (two oral medications and a parenteral prostacyclin). Measurements and Main Results Among 1,611 enrolled patients, 984 were initiated on monotherapy, 551 were initiated on dual therapy, and 76 were initiated on triple therapy. The triple-combination group was younger and had fewer comorbidities but had a higher mortality risk. The survival rate was higher with the use of triple therapy (91% at 5 yr) as compared with dual therapy or monotherapy (both 61% at 5 yr) (P < 0.001). Propensity score matching of age, sex, and pulmonary vascular resistance also showed significant differences between triple therapy and dual therapy (10-yr survival, 85% vs. 65%). In high-risk patients (n = 243), the survival rate was higher with triple therapy than with monotherapy or dual therapy, whereas there was no difference between monotherapy and double therapy. In intermediate-risk patients (n = 1,134), survival improved with an increasing number of therapies. In multivariable Cox regression, triple therapy was independently associated with a lower risk of death (hazard ratio, 0.29; 95% confidence interval, 0.11–0.80; P = 0.017). Among the 148 patients initiated on a parenteral prostacyclin, those on triple therapy had a higher survival rate than those on monotherapy or dual therapy. Conclusions Initial triple-combination therapy that includes parenteral prostacyclin seems to be associated with a higher survival rate in PAH, particularly in the youngest high-risk patients.
The European respiratory journal · 2022
IntroductionContemporary risk assessment tools categorise patients with pulmonary arterial hypertension (PAH) as low, intermediate or high risk. A minority of patients achieve low risk status with most remaining intermediate risk. Our aim was to validate a four-stratum risk assessment approach categorising patients as low, intermediate-low, intermediate-high or high risk, as proposed by the Comparative, Prospective Registry of Newly Initiated Therapies for Pulmonary Hypertension (COMPERA) investigators.MethodsWe evaluated incident patients from the French PAH Registry and applied a four-stratum risk method at baseline and at first reassessment. We applied refined cut-points for three variables: World Health Organization functional class, 6-min walk distance and N-terminal pro-brain natriuretic peptide. We used Kaplan–Meier survival analyses and Cox proportional hazards regression to assess survival according to three-stratum and four-stratum risk approaches.ResultsAt baseline (n=2879), the four-stratum approach identified four distinct risk groups and performed slightly better than a three-stratum method for predicting mortality. Four-stratum model discrimination was significantly higher than the three-stratum method when applied during follow-up and refined risk categories among subgroups with idiopathic PAH, connective tissue disease-associated PAH, congenital heart disease and portopulmonary hypertension. Using the four-stratum approach, 53% of patients changed risk category from baseline compared to 39% of patients when applying the three-stratum approach. Those who achieved or maintained a low risk status had the best survival, whereas there were more nuanced differences in survival for patients who were intermediate-low and intermediate-high risk.ConclusionsThe four-stratum risk assessment method refined risk prediction, especially within the intermediate risk category of patients, performed better at predicting survival and was more sensitive to change than the three-stratum approach.
Source PubMed · Recherche par auteur (homonymes possibles, vérifier l'affiliation).
Respiratory medicine and research · 2026 · Journal Article
Valentin S, Odille F, Fraix A, Pace N, et al.
Respiratory medicine · 2025 · Journal Article
Watrin C, Baptista BR, Chabot F, Chaouat A, et al.
Respiratory medicine and research · 2025 · Journal Article
Boucly A, Beauvais A, Lacoste-Palasset T, Jevnikar M, et al.
Respiratory medicine and research · 2025 · Journal Article
Farkouh C, Chaouat A, Guillaumot A, Baptista BR, et al.
ERJ open research · 2024 · Journal Article
Boucly A, Solinas S, Beurnier A, Jaïs X, et al.
Respiratory medicine · 2023 · Journal Article
Perez T, Roche N, Nunes H, Burgel PR, et al.
Respiratory medicine and research · 2022 · Journal Article
Basin S, Valentin S, Maurac A, Poussel M, et al.
American journal of respiratory and critical care medicine · 2021 · Evaluation Study
Boucly A, Savale L, Jaïs X, Bauer F, et al.
The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2021 · Journal Article
Dauriat G, Reynaud-Gaubert M, Cottin V, Lamia B, et al.
American journal of respiratory and critical care medicine · 2020 · Journal Article
Jutant EM, Jaïs X, Girerd B, Savale L, et al.
The European respiratory journal · 2019 · Journal Article
Savale L, Habibi A, Lionnet F, Maitre B, et al.
The European respiratory journal · 2019 · Case Reports
Maurac A, Lardenois É, Eyries M, Ghigna MR, et al.
The European respiratory journal · 2026 · Journal Article
Diesler R, Turquier S, Reynaud-Gaubert M, Lestelle F, et al.
Respiratory medicine and research · 2023 · Journal Article
Thoré P, Staentzel J, Valentin S, Guillaumot A, et al.
Inflammatory bowel diseases · 2023 · Journal Article
Valentin S, Renel B, Manneville F, Caron B, et al.
The European respiratory journal · 2026 · Editorial
Piper AJ, Adir Y, Hill NS, Chaouat A
Obesity surgery · 2025 · Journal Article
Groshaeny L, Gomez E, Valentin S, Thore P, et al.
Acta oto-laryngologica · 2023 · Editorial
Benamron H, Chaouat A, Carpentier N, Jankowski R, et al.
The European respiratory journal · 2021 · Journal Article
Adir Y, Humbert M, Chaouat A
The European respiratory journal · 2025 · Letter
Jevnikar M, Brenot P, Kularatne M, Rodière A, et al.
Frontiers in medicine · 2024 · Case Reports
Pequignot B, Chaouat A, Chabot F, Levy B, et al.
The European respiratory journal · 2026 · Editorial
Piper AJ, Adir Y, Hill NS, Chaouat A
The Lancet. Respiratory medicine · 2022 · Meta-Analysis
Lacasse Y, Casaburi R, Sliwinski P, Chaouat A, et al.
The Lancet. Respiratory medicine · 2022 · Meta-Analysis
Lacasse Y, Casaburi R, Sliwinski P, Chaouat A, et al.
Respiration; international review of thoracic diseases · 2020 · Journal Article
Faure M, Valentin S, Zysman M, Sitbon O, et al.
The Lancet. Respiratory medicine · 2022 · Clinical Trial, Phase III
Jaïs X, Brenot P, Bouvaist H, Jevnikar M, et al.
Swiss medical weekly · 2022 · Journal Article
Lechartier B, Chaouat A, Aubert JD, Schwitter J, et al.
Supplementary Materials for “Novel Role of Von Willebrand Factor-αvβ3 Integrin in Human Pulmonary Artery Smooth Muscle Cell”.
This dataset contains the supplementary materials for “Novel Role of Von Willebrand Factor-αvβ3 Integrin in Human Pulmonary Artery Smooth Muscle Cell”, including spplementary figures, detailed experimental methods, table
Supplementary Materials for “Novel Role of Von Willebrand Factor-αvβ3 Integrin in Human Pulmonary Artery Smooth Muscle Cell”.
This dataset contains the supplementary materials for “Novel Role of Von Willebrand Factor-αvβ3 Integrin in Human Pulmonary Artery Smooth Muscle Cell”, including spplementary figures, detailed experimental methods, table
Source : DataCite — DOIs pour datasets, logiciels, protocoles, registres patient. Hors articles (déjà couverts).
The European respiratory journal · 2022 · Journal Article
Boucly A, Weatherald J, Savale L, de Groote P, et al.
BMC pulmonary medicine · 2019 · Journal Article
Carette H, Zysman M, Morelot-Panzini C, Perrin J, et al.
Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine · 2019 · Journal Article
Magne F, Gomez E, Marchal O, Malvestio P, et al.