Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Arthur Sorlin"'
Autor:
Nicolas Richard, Martin Kaufmann, Arnaud Wiedemann, Marie-Laure Kottler, Arthur Sorlin, Nick Demers, François Feillet, Georges Weryha, Hervé Mittre, Nadia Coudray, Jérémy Do Cao, Genevieve Abeguile, Brigitte Dousset, Arnaud Molin, Laurent Mainard, Glenville Jones, Pierre Journeau
Publikováno v:
Journal of Bone and Mineral Research. 32:1893-1899
Vitamin D requires a two-step activation by hydroxylation: The first step is catalyzed by hepatic 25-hydroxylase (CYP2R1, 11p15.2) and the second one is catalyzed by renal 1α-hydroxylase (CYP27B1, 12q13.1), which produces the active hormonal form of
Autor:
Arthur Sorlin, Thomas Cuny, P. Journeau, Georges Weryha, M. Agopiantz, Beatrice Lebon-Labich, Bruno Leheup
Publikováno v:
Annales d'Endocrinologie
Annales d'Endocrinologie, Elsevier Masson, 2016, 77 (1), pp.7-13. ⟨10.1016/j.ando.2016.01.002⟩
Annales d'Endocrinologie, Elsevier Masson, 2016, 77 (1), pp.7-13. ⟨10.1016/j.ando.2016.01.002⟩
International audience; Background: McCune-Albright syndrome is a rare disorder characterized by endocrine disorders, café-au-lait spots and fibrous dysplasia of bone that occurs early in life.Methods: A series of 14 pediatric cases were followed be
Autor:
Arnaud Wiedemann, David Cheillan, Bettina Montaut-Verient, Arthur Sorlin, Gilbert Briand, François Feillet, Emmanuelle Schmitt
Publikováno v:
Neuropediatrics
Neuropediatrics, Thieme Publishing, 2016, 47 (03), pp.179-181. ⟨10.1055/s-0036-1578798⟩
Neuropediatrics, Thieme Publishing, 2016, 47 (03), pp.179-181. ⟨10.1055/s-0036-1578798⟩
International audience; Peroxisome biogenesis disorders (PBD) are a heterogeneous group of disorders due to PEX genesmutations, with a broad clinical spectrum comprising severe neonatal disease to mild presentation. Recently, Berendse et al reported
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5331760588b9959f8cf2aedeee9bc731
https://hal.univ-lorraine.fr/hal-01661724
https://hal.univ-lorraine.fr/hal-01661724