Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Laurence Chardon"'
Autor:
Cécile Nozières, Karim Chikh, Françoise Borson-Chazot, Bernard Goichot, Laurence Chardon, Valérie Hervieu, Thomas Walter, Catherine Lombard-Bohas
Publikováno v:
European Journal of Endocrinology
European Journal of Endocrinology, BioScientifica, 2016, 174 (3), pp.335-41. ⟨10.1530/EJE-15-0917⟩
European Journal of Endocrinology, BioScientifica, 2016, 174 (3), pp.335-41. ⟨10.1530/EJE-15-0917⟩
ObjectivesInappropriate calcitonin (CT) release, a major feature of medullary thyroid cancer (MTC), may occur in neuroendocrine tumors (NETs). The aims of this retrospective study were to assess i) the characteristics and prognosis of CT-producing NE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f564d700d8f08915a69aa17893f54fa3
https://hal.archives-ouvertes.fr/hal-01850353
https://hal.archives-ouvertes.fr/hal-01850353
Autor:
Xavier Chopin-Laly, Laurence Chardon, Thomas Walter, Jean-Yves Scoazec, Anne-Gaelle Caffin, Catherine Lombard-Bohas, Véronique Raverot, Jean-Alain Chayvialle
Publikováno v:
European Journal of Cancer. 48:1766-1773
Chromogranin A (CgA) is the principal tumour marker for gastroenteropancreatic neuroendocrine tumours (GEPNET). Combining serum CgA and pancreatic polypeptide (PP) levels may increase the sensitivity of tumour markers in the diagnosis of GEPNET.(1) T
Autor:
Michel Bovier-Lapierre, Laurence Chardon, Alain Lachaux, Laurence Michel-Calemard, Bernard Dingeon, Philippe Moulin, Agnès Sassolas
Publikováno v:
European journal of pediatrics. 168(8)
Abetalipoproteinemia (ABL; OMIM 200100) is an inherited disorder resulting from mutations in the microsomal triglyceride transfer protein gene and characterized by a major lipid malabsorption leading to extremely low plasma cholesterol and triglyceri