Zobrazeno 1 - 10
of 256
pro vyhledávání: '"S Cabrol"'
Autor:
Elodie Fiot, Delphine Zénaty, Priscilla Boizeau, Jérémie Haignere, Sophie Dos Santos, Juliane Léger, J C Carel, S Cabrol, P Chanson, S Christin-Maitre, C Courtillot, B Donadille, J Dulon, M Houang, M Nedelcu, I Netchine, M Polak, S Salenave, D Samara-Boustani, D Simon, P Touraine, M Viaud, H Bony, K Braun, R Desailloud, A M Bertrand, B Mignot, F Schillo, P Barat, V Kerlan, C Metz, E Sonnet, Y Reznik, V Ribault, H Carla, I Tauveron, C Bensignor, F Huet, B Verges, O Chabre, C Dupuis, A Spiteri, M Cartigny, C Stuckens, J Weill, A Lienhardt, C Naud-Saudreau, F Borson-Chazot, A Brac de la Perriere, M Pugeat, T Brue, R Reynaud, G Simonin, F Paris, C Sultan, B Leheup, G Weryha, S Baron, B Charbonnel, S Dubourdieu, E Baechler, P Fenichel, K Wagner, F Compain, H Crosnier, C Personnier, B Delemer, A C Hecart, P F Souchon, M De Kerdanet, F Galland, S Nivot-Adamiak, M Castanet, C Lecointre, O Richard, N Jeandidier, S Soskin, P Lecomte, M Pepin-Donat, P Pierre
Publikováno v:
European Journal of Endocrinology
European Journal of Endocrinology, 2019, 180 (6), pp.397-406. ⟨10.1530/EJE-18-0878⟩
European Journal of Endocrinology, BioScientifica, 2019, 180 (6), pp.397-406. ⟨10.1530/EJE-18-0878⟩
European Journal of Endocrinology, 2019, 180 (6), pp.397-406. ⟨10.1530/EJE-18-0878⟩
European Journal of Endocrinology, BioScientifica, 2019, 180 (6), pp.397-406. ⟨10.1530/EJE-18-0878⟩
ObjectiveTurner Syndrome is associated with several phenotypic conditions associated with a higher risk of subsequent comorbidity. We aimed to evaluate the prevalence of congenital malformations and the occurrence of age-related comorbid conditions a
Publikováno v:
La Presse Médicale. 43:981-993
Pulmonary arterial hypertension (PAH) is characterized by vasoconstriction, in situ thrombosis, and vascular remodeling of small pulmonary arteries. It induces a fixed pulmonary arterial obstruction, persistent elevation of pulmonary arterial resista
Autor:
A Linglart, S Cabrol, P Berlier, C Stuckens, K Wagner, M de Kerdanet, C Limoni, J-C Carel, J-L Chaussain
Publikováno v:
European Journal of Endocrinology. 164:891-897
ObjectiveAdult height deficit seen in Turner syndrome (TS) originates, in part, from growth retardation in utero and throughout the first 3 years of life. Earlier diagnosis enables earlier therapeutic intervention, such as with recombinant human GH (
Autor:
Helmuth G. Dörr, Carol Worrell, S. Cabrol, Sojung Lee, Javier de las Heras, Lisa Öhl, Philip Murray, Satz Mengensatzproduktion, Fida Bacha, L. Perin, Brigid Gregg, Christof Schöfl, Thomas M.K. Völkl, M. Jésuran-Perelroizen, Denise L. Jacobson, Christine Yu, Rohan Hazra, Manfred Rauh, Silva A. Arslanian, Olaf Hiort, Tracie L. Miller, Jun Mishina, M. Colle, Y. Le Bouc, Druck Reinhardt Druck Basel, Robert Gut, Robert L. Rosenfield, Peter E. Clayton, Toshiaki Tanaka, Hala Tfayli, William Borkowsky, Linda A. DiMeglio, Larry K. Kociolek, Dan Hanson, Judith L. Ross, Peter A. Lee, Russell B. Van Dyke, R. Coutant, Giampiero I. Baroncelli, Hajime Togari, Eleonora Dati, Kunjal Patel, Susumu Yokoya, John Germak, Silvano Bertelloni, Mitchell E. Geffner, Kenji Fujieda, Yoshiki Seino, Kenan Qin, P. Czernichow, Graeme C.M. Black, Margarita Silio, Anne-Marie Kappelgaard
Publikováno v:
Hormone Research in Paediatrics. 76:I-VI
Autor:
V. Bélien-Pallet, Arnaud Petit, Anne Auvrignon, S. Cabrol, Judith Landman-Parker, Sylvie Fasola, Guy Leverger
Publikováno v:
Archives de Pédiatrie. 17:1637-1644
Resume La survenue d’un deficit corticotrope cortico-induit symptomatique chez 8 enfants hospitalises pour leucemie aigue lymphoblastique (LAL) nous a menes a la realisation d’un travail prospectif, entre mai 2006 et mai 2007, afin de mieux carac
Autor:
Salah Azzi, Yves Le Bouc, Muriel Houang, Laurence Perin, Anne-Marie Bertrand, Marie-Line Jacquemont, Virginie Steunou, Graziella Pinto, Claudine Heinrichs, Sylvie Rossignol, Guy-André Loeuille, Marie-Noëlle Dufourg, Marie-Charles Raux M.-C.R. Demay, Elżbieta Petriczko, Fabienne Danton, Nathalie Thibaud, Blandine Esteva, Jean-Claude Carel, S Cabrol, Irène Netchine, Alexandra Rousseau, C Gicquel
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 92:3148-3154
Context: Russell-Silver syndrome (RSS), characterized by intrauterine and postnatal growth retardation, dysmorphic features, and frequent body asymmetry, spares cranial growth. Maternal uniparental disomy for chromosome 7 (mUPD7) is found in 5–10%
Autor:
Benjamin Sztrymf, S. Cabrol, Xavier Jaïs, E. Fadel, Florence Parent, Sophie Maitre, Colas Tcherakian, O. Sitbon, Sacha Mussot, J. Le Pavec, G. Simonneau, Marc Humbert, P. Dartevelle, Dominique Musset
Publikováno v:
Revue des Maladies Respiratoires. 24:497-508
Resume Introduction L’hypertension pulmonaire postembolique (HTP PE) est une affection rare, caracterisee par la persistance et l’organisation fibreuse de caillots au sein des arteres pulmonaires. La consequence de cette obstruction est une augme
Autor:
Philippe Dartevelle, Elie Fadel, Gérald Simonneau, Xavier Jaïs, Ratiba Haddad Si Ali, Rogério Souza, S. Cabrol, Olivier Sitbon, Marc Humbert
Publikováno v:
The Journal of Heart and Lung Transplantation. 26:357-362
Pulmonary thromboendarterectomy may be a cure for patients with chronic thromboembolic pulmonary hypertension (CTEPH) with proximal obstruction. Conversely, short-term prognosis is poor for inoperable CTEPH patients with distal obstruction. Vascular
Autor:
S. Cabrol
Publikováno v:
Annales d'Endocrinologie. 68:2-9
Turner syndrome occurs in 1:5000 live births (1:2,500 females) and is caused not only by X-chromosome monosomy, but also in a large degree, by the presence of a mosaicism (45,X) and/or an abnormal X or Y chromosome (deletion, isochromosome X, dicentr
Publikováno v:
European Heart Journal. 27:589-595
Aims Data on long-term efficacy of bosentan in unselected idiopathic pulmonary arterial hypertension (IPAH) patients are lacking. We aimed to describe the long-term outcome of consecutive IPAH patients treated first-line with bosentan. Methods and re