Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Joelle Deibener"'
Autor:
François Chabot, Maurice Tanguy, Eliane Albuisson, Marine Fauny, Joelle Deibener, Damien Mandry, Damien Loeuille, Olivier Huttin, Isabelle Chary-Valckenaere, Elodie Bauer
Publikováno v:
Medicine
The objectives of this study were to describe the prevalence and characteristics of radiographic lesions of the hands, and calcifications of the spine on computer tomography scans (CT-scans), and to investigate the relationships between radiographic
Autor:
Aurélien Guffroy, Marc Michel, Jean-Christophe Weber, Jean Sibilia, Simon Gravier, Jacques-Eric Gottenberg, Laurent Arnaud, Anne-Sophie Korganow, C. Martinez, Eric Hachulla, Benjamin Dervieux, Joelle Deibener-Kaminsky
Publikováno v:
Seminars in Arthritis and Rheumatism. 46:509-512
Objectives Systemic capillary leak syndrome (Clarkson's disease) is a rare entity characterized by recurrent and unpredictable attacks of capillary leakage of plasma fluid and proteins throughout the endothelium. Some cases are secondary. We describe
Autor:
Constantinos Papadopoulos, David Orlikowski, Hélène Prigent, Arnaud Lacour, Céline Tard, Alain Furby, Julien Praline, Guilhem Solé, Jean-Yves Hogrel, Marie De Antonio, Claudio Semplicini, Joelle Deibener-Kaminsky, Pierre Kaminsky, Bruno Eymard, Nadjib Taouagh, Barbara Perniconi, Dalil Hamroun, Pascal Laforêt, G. Bassez, A.-L. Bedat-Millet, A. Behin, B. Eymard, S. Leonard-Louis, T. Stojkovic, A. Canal, V. Decostre, F. Bouhour, F. Boyer, C. Caillaud, Y. Castaing, F. Chapon, P. Cintas, I. Durieu, A. Echaniz-Laguna, L. Feasson, X. Ferrer, R. Froissart, M. Piraud, D. Germain, K. Benistan, N. Guffon-Fouilhoux, H. Journel, P. Labauge, A. Levy, A. Magot, Y. Péréon, M.-C. Minot-Myhié, A. Nadaj-Pakleza, C. Nathier, N. Pellegrini, P. Petiot, F. Lofaso, A. Dutry, D. Renard, S. Sacconi, C. Desnuelle, E. Salort-Campana, J. Pouget, V. Tiffreau, D. Vincent, F. Zagnoli
Publikováno v:
Molecular Genetics and Metabolism
Molecular Genetics and Metabolism, 2017, Molecular genetics and metabolism, 122 (1-2), pp.80-85. ⟨10.1016/j.ymgme.2017.06.007⟩
Molecular Genetics and Metabolism, Elsevier, 2017, Molecular genetics and metabolism, 122 (1-2), pp.80-85. ⟨10.1016/j.ymgme.2017.06.007⟩
Molecular Genetics and Metabolism, 2017, Molecular genetics and metabolism, 122 (1-2), pp.80-85. ⟨10.1016/j.ymgme.2017.06.007⟩
Molecular Genetics and Metabolism, Elsevier, 2017, Molecular genetics and metabolism, 122 (1-2), pp.80-85. ⟨10.1016/j.ymgme.2017.06.007⟩
Background The efficacy of enzyme replacement therapy (ERT) in patients at an advanced stage of Pompe disease has only been addressed in a few studies. Our objective was to assess the long term effects of ERT in a cohort of patients with severe Pompe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2eca040ef3e520953509b66aeb672813
https://hal.univ-lille.fr/hal-02369159
https://hal.univ-lille.fr/hal-02369159
Autor:
Béatrice Brembilla-Perrot, Mathias Poussel, Lelia Pruna, Bruno Chenuel, Joelle Deibener, Pierre Kaminsky
Publikováno v:
Medicine. 90:262-268
Myotonic dystrophy type 1 (DM1) is a multisystemic disorder characterized by muscle weakness and multiple organ impairment, especially the eyes, lung, and heart. We conducted the current study to analyze the prevalence and intercorrelation among thes
Publikováno v:
Laboratory Hematology. 17:1-5
BACKGROUND Abdominal pain is a common symptom underlying a variety of disorders with different prognoses. Neutrophilia or lymphopenia have been used as prognostic markers in several stress- or infection-mediated disorders. We studied the clinical rel
Publikováno v:
Intensive care medicine. 40(6)
Autor:
Laetitia Peultier-Celli, Roland Jaussaud, Pierre Kaminsky, Joëlle Deibener-Kaminsky, François Feillet, Philippe Perrin
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
BackgroundFabry disease (FD) is a rare inherited lysosomal storage disorder caused by the deficiency of the enzyme alpha-galactosidase A. This deficiency leads to an accumulation of glycosphingolipids leading to progressive and multisystemic disease,
Externí odkaz:
https://doaj.org/article/486d5a9d8f28423e87c028f37922cae5
Autor:
E. Jeannesson, Pierre Kaminsky, F Barbé, Joelle Deibener, Marc Klein, Jean Marie Escanyé, Paul Walker, Brigitte Dousset
Publikováno v:
Growth Hormone & IGF Research
Growth Hormone & IGF Research, 2012, 22 (6), pp.240-244. 〈10.1016/j.ghir.2012.08.001〉
Growth Horm IGF Res
Growth Horm IGF Res, 2012, 22 (6), pp.240-4. ⟨10.1016/j.ghir.2012.08.001⟩
Growth Hormone & IGF Research, 2012, 22 (6), pp.240-244. ⟨10.1016/j.ghir.2012.08.001⟩
Growth Horm IGF Res, 2012, 22 (6), pp.240-4. 〈10.1016/j.ghir.2012.08.001〉
Growth Hormone & IGF Research, 2012, 22 (6), pp.240-244. 〈10.1016/j.ghir.2012.08.001〉
Growth Horm IGF Res
Growth Horm IGF Res, 2012, 22 (6), pp.240-4. ⟨10.1016/j.ghir.2012.08.001⟩
Growth Hormone & IGF Research, 2012, 22 (6), pp.240-244. ⟨10.1016/j.ghir.2012.08.001⟩
Growth Horm IGF Res, 2012, 22 (6), pp.240-4. 〈10.1016/j.ghir.2012.08.001〉
International audience; OBJECTIVE: The aim of the study was to determine the respective impact of thyroxine and growth hormone on in vivo skeletal mitochondrial function assessed via post exercise phosphocreatine recovery. DESIGN: The hind leg muscle
Publikováno v:
Chest. 106(4)
A diagnosis of sarcoidosis was evoked in a 61-year-old man on clinical and histologic bases. Nevertheless, a bile duct carcinoma was disclosed in association with the discovery of generalized sarcoid-like granulomas. This is only the third time that