Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Muriel Meier"'
Autor:
Chong Ae Kim, Mona Nemani, Robert K. Semple, Stephen O'Rahilly, Jocelyne Magré, Etienne Bridel, Jacqueline Capeau, Marc Delepine, Soazig Le Lay, Haquima El Mourabit, Isabelle Dugail, Claudia da Costa Leite, Mark Lathrop, Muriel Meier, Emilie Boutet, Débora Romeo Bertola
Publikováno v:
Journal of Clinical Endocrinology and Metabolism
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2008, 93, pp.1129-34. ⟨10.1210/jc.2007-1328⟩
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2008, 93, pp.1129-34. ⟨10.1210/jc.2007-1328⟩
International audience; CONTEXT: Berardinelli-Seip congenital lipodystrophy (BSCL) is a rare recessive disease characterized by near absence of adipose tissue, resulting in severe dyslipidemia and insulin resistance. In most reported cases, BSCL is d
Autor:
Jocelyne Magré, Muriel Meier, Jean Y. Park, Arnaud Basdevant, Karine Clément, Jean-Marc Guettier, Elaine Cochran, Phillip Gorden, Christine Poitou
Partial lipodystrophy (PL) is most commonly characterized by loss of subcutaneous fat in the extremities with preservation of truncal fat and is associated with insulin resistance, diabetes and hyperlipidaemia. Recombinant human leptin (r-metHuLeptin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56bc478b56a46d86faed25a791724649
https://europepmc.org/articles/PMC2578870/
https://europepmc.org/articles/PMC2578870/
Autor:
C. Ronald Kahn, E. Seemanova, Jean-Jacques Robert, Jacqueline Capeau, Chong Ae Kim, Lionel Van Maldergem, Corinne Vigouroux, Mark Lathrop, Didier Lacombe, Olivier Lascols, Muriel Meier, Vanessa R. Panz, Nadia Tubiana-Rufi, Paul Czernichow, Marc Delepine, J. Antonie Maassen, Charles R. Buchanan, Jocelyne Magré
Publikováno v:
Diabetes. 52(6)
Berardinelli-Seip congenital lipodystrophy (BSCL) is a heterogeneous genetic disease characterized by near absence of adipose tissue and severe insulin resistance. We have previously identified mutations in the seipin gene in a subset of our patients
Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13
Autor:
N. Baudic, M. Lanza, Stephen O'Rahilly, H. Loret, P. Bogalho, Frédéric Huet, Philippe Labrune, Bourut C, O. Trygstad, J. A. Maassen, C R Kahn, Didier Lacombe, J.-J. Robert, Eric M. Sobel, Corinne Vigouroux, M. De Kerdanet, A. Bachy, Jacqueline Capeau, P. Tric, Frederick J. Raal, Barry I Joffe, T. Stephenson, André Mégarbané, Lionel Van Maldergem, F. H. D'abronzo, J. L. Medina, Jocelyne Magré, Roger Assan, A. Nivelon-Chevalier, Alain Verloes, Muriel Meier, Paul Czernichow, Fumihiko Matsuda, S. Savasta, E. Seemanova, Vanessa R. Panz, N. Tubiana-Rufi, G. Loyson, Jean Weissenbach, Eliane Khallouf, Florin Grigorescu, P. Freitas, Tobias Gedde-Dahl, Marc Delepine, Jeanette C. Papp, J. Navarro, Mark Lathrop, Meraida Polak, F. Bonnicci
Publikováno v:
Nature genetics. 28(4)
Congenital generalized lipodystrophy, or Berardinelli-Seip syndrome (BSCL), is a rare autosomal recessive disease characterized by a near-absence of adipose tissue from birth or early infancy and severe insulin resistance. Other clinical and biologic
Autor:
Muriel Meier, Corinne Vigouroux, Jacqueline Capeau, Constantinos Sinaniotis, Christina Karayanni, Martine Caron, Charalambos G Hadjiathanasiou, C. Stavrinadis, Jocelyne Magré, Christèle Desbois-Mouthon
Publikováno v:
ResearcherID
Autor:
Martine Moreau, C. Mazière, Jacques Polonovski, E. Alsat, Véronique Barbu, J.C. Mazière, Sopia Goldstein, Muriel Meier
Publikováno v:
Biochimie. 71(3)
Polyclonal antibodies were prepared by immunization of rabbits with partially purified LDL receptor obtained from human placental microvilli. The antiserum reacted with membranes from human placental microvilli and human fibroblasts, as assessed by i
Autor:
Johan Auwerx, Jean Weissenbach, Lluis Fajas, G Gyapay, Jocelyne Magré, Corinne Vigouroux, Olivier Lascols, Muriel Meier, Jacqueline Capeau, Eliane Khallouf
Reference NCEM-ARTICLE-1998-001doi:10.2337/diabetes.47.3.490View record in PubMed Record created on 2009-04-02, modified on 2017-05-12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f289d8347d1c07020d4300ccbdfc5d2d
https://infoscience.epfl.ch/record/135448
https://infoscience.epfl.ch/record/135448
Autor:
Nina Badertscher, Ralph P. Braun, Michel Wensing, Ryan Tandjung, Muriel Meier, Antonio Cozzio, Brigitte Tag, Thomas Rosemann
Publikováno v:
BMC Health Services Research, 14, 581
BMC Health Services Research, 14, 1, pp. 581
BMC Health Services Research
BMC Health Services Research, 14, 1, pp. 581
BMC Health Services Research
Background The rising incidence of melanoma – Switzerland has the highest incidence in Europe - is a major public health challenge. Swiss dermatologist introduced the “Swiss Skin Cancer Day” (SSCD) in 2006, which provides skin cancer screening