📇 Rhumatologue · LA CHAUSSEE ST VICTOR · (41) · Libéral
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1 raison identifiée
Délais de RDV courts dans la région
86 rhumatos / 100 000 hab. — département bien doté
✨ Génération du profil synthétique IA en cours…
Indicateurs publics agrégés sur 250 M+ d'œuvres scientifiques (OpenAlex, PubMed). Traduits ici en langage patient.
Influence scientifique
Données ANS publiques (Licence Ouverte 2.0) · Enrichissements MonRhumato 100 % opt-in · Toute personne référencée peut demander la suppression ou la rectification.
6
6 articles ont été cités au moins 6fois par d'autres chercheurs — preuve que ses travaux sont repris par la communauté médicale.
h-index
Total citations reçues
169
Nombre de fois où d'autres équipes ont mentionné ses publications dans leurs propres travaux.
Publications totales
9
Articles, revues et chapitres référencés dans les bases académiques internationales.
Articles influents
3
Publications ayant marqué leur domaine — chacune citée au moins 10 fois par d'autres chercheurs.
i10-index
Thématiques principales
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.
Head-to-head comparison of eight late gadolinium-enhanced cardiac MR (LGE CMR) sequences at 1.5 tesla: From bench to bedside
2011ArticleJournal of Magnetic Resonance Imaging
Concordance rate differences of 3 noninvasive imaging techniques to measure carotid stenosis in clinical routine practice: results of the CARMEDAS multicenter study.
2004ArticleStroke
Source : HAL — archive ouverte CCSD/CNRS (couvre articles, chapitres EMC, communications congrès, thèses).
CABINET DU DR CARMEN ROTARU
TOUR DE CONSULTATION 3 RUE ROBERT DEBRE, 41260 LA CHAUSSEE ST VICTOR
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).
Journal of magnetic resonance imaging : JMRI · 2011
AbstractPurpose:To compare—theoretically and experimentally—clinically available two‐dimensional/three‐dimensional (2D/3D), breathhold and non‐breathhold, inversion‐recovery (IR) gradient‐echo (GRE) sequences used to differentiate between nonviable injured and normal myocardium with late gadolinium‐enhanced techniques (IR‐GRE2D sequence is used as a reference), and to evaluate their respective clinical benefit.Materials and Methods:Six breathhold (2D‐IR‐GRE, 3D‐IR‐GRE, balanced steady‐state free precession 2D‐IR‐bSSFP and 3D‐IR‐bSSFP, phase‐sensitive 2D‐PSIR‐GRE, and 2D‐PSIR‐bSSFP) and two non‐breathhold late gadolinium‐enhanced techniques (single‐shot 2D‐ssbSSFP and 2D‐PSIR‐ssbSSFP) were consecutively performed in 32 coronary artery disease patients with chronic myocardial infarction. Qualitative assessment and manual planimetry were performed by two independent observers. Quantitative assessment was based on percentage signal intensity elevation between injured and normal myocardium and contrast‐to‐noise ratio. Theoretical simulations were compared with experimental measurements performed on phantoms with various concentrations of gadolinium.Results:The 3D‐IR‐GRE image quality appeared better than the other 2D and 3D sequences, showing better delineation of complex nontransmural lesions, with significantly higher percentage signal intensity and contrast‐to‐noise ratio. PSIR techniques appeared more limited in differentiating sub‐endocardial lesions and intracavity blood pool, but in all other cases were comparable to the other techniques. Single‐shot PSIR‐ssbSSFP appeared to be a valuable alternative technique when breathhold cannot be achieved.Conclusion:We recommend 3D‐IR‐GRE as the method of choice for late gadolinium‐enhanced cardiac magnetic resonance imaging in clinical practice. J. Magn. Reson. Imaging 2011;. © 2011 Wiley Periodicals, Inc.
American journal of medical genetics. Part A · 2015
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder characterized by congenital malformations of the great toes and progressive heterotopic ossification of connective tissue that begins during the first decade of life. Our patient presented with intrauterine growth retardation, respiratory distress, neonatal onset soft tissue masses, bilateral hallux valgus, and congenital anomalies of the thyroid and uterus. She was initially diagnosed with atypical infantile myofibromatosis based on clinical and pathological findings. She underwent whole‐exome sequencing (WES) as part of the FORGE study to identify the gene for infantile myofibromatosis; however a de novo dominant mutation in ACVR1 (NM_001105.4:c.617G>A) revised the diagnosis to FOP. This patient highlights the utility of WES as an early diagnostic tool in the investigation of patients with unusual presentations of rare diseases, thereby providing clinicians with accurate molecular diagnoses and the opportunity to tailor clinical management to improve patient care. © 2015 Wiley Periodicals, Inc.
International journal of pediatric otorhinolaryngology · 2013
Source PubMed · Recherche par auteur (homonymes possibles, vérifier l'affiliation).
Journal of magnetic resonance imaging : JMRI · 2011 · Comparative Study
Viallon M, Jacquier A, Rotaru C, Delattre BM, et al.
Investigative radiology · 2007 · Comparative Study
Croisille P, Rotaru C, Janier M, Hiba B
International journal of pediatric otorhinolaryngology · 2013 · Case Reports
Sklar M, Rotaru C, Grynspan D, Bromwich M
American journal of medical genetics. Part A · 2015 · Case Reports
Liu H, Sawyer SL, Gos M, Grynspan D, et al.