Le Kremlin-Bicêtre

Dec 5, 2024 | jhltonline.org | Le Kremlin-Bicêtre |Vascular diseases

Abbreviation 6MWD (6-minute walk distance) ActRIIA-Fc (human activin receptor IIA with the fragment crystallizable) AEOIs (adverse events of interest) ANCOVA (analysis of covariance) CI (cardiac Index) CO (cardiac output) eGFR (estimated glomerular filtration rate) eRAP (estimated right atrial pressure) ESC/ERS (European Society of Cardiology/European Respiratory Society) GDFs (growth differentiation factors) HL (Hodges-Lehmann) HR (hazard ratio) LS (least squares) mPAP (mean pulmonary artery...

Nov 27, 2024 | publications.ersnet.org | Gábor Kovács |Marc Humbert |Hôpital Bicêtre |Le Kremlin-Bicêtre

Original Research Article Prognostic relevance of Exercise Pulmonary Hypertension: Results of the multi-center PEX-NET Clinical Research Collaboration ArticleInfo & Metrics This is a PDF-only article. Please click on the PDF link above to read it.

Nov 14, 2024 | publications.ersnet.org | Marc Humbert |Faculté de Médecine |Le Kremlin-Bicêtre |Paul M Hassoun

IntroductionPulmonary arterial hypertension (PAH) is a debilitating, progressive disease marked by the remodelling and narrowing of the pulmonary vasculature [1–4].

Nov 6, 2024 | bmcpublichealth.biomedcentral.com | Aix Marseille Univ |Institut Paoli-Calmettes |Université de Nantes |Le Kremlin-Bicêtre

Our pooled sample comprised 4 025 respondents. Half were women and half had tertiary education. The mean age was 49 years (SD = 17.3) and the mean financial deprivation score was 38.9 (SD = 22.9). A statistically significant difference in socio-demographic characteristics was observed between the two studies we analyzed (i.e., HLS19 and SLAVACO) (Table 1). Furthermore, the average HLS19-Q12 score was higher than the average HLS19-NAV score (63.4 vs. 51.4).

Oct 20, 2024 | rbmojournal.com | Le Kremlin-Bicêtre

KeywordsPersistent Müllerian duct syndromeAnti-Müllerian hormoneInfertilityCryptorchidismAzoospermiaExploratory laparoscopyINTRODUCTIONPersistent Müllerian Duct Syndrome (PMDS) is a rare autosomal recessive syndrome caused by mutations in the anti-Müllerian hormone (AMH) or AMH receptor II (AMH-RII) genes, transmitted either in a homozygous or a compound heterozygous manner.