Zobrazeno 1 - 10
of 210
pro vyhledávání: '"Isabelle, Rousseau"'
Autor:
Totelin, Laurence
Publikováno v:
Bulletin of the History of Medicine, 2016 Apr 01. 90(1), 141-142.
Externí odkaz:
https://www.jstor.org/stable/26310795
Autor:
Vanden Broeck-Parant, Jean
Publikováno v:
Antiquité Classique, 2016 Jan 01. 85, 396-397.
Externí odkaz:
https://www.jstor.org/stable/90005548
Autor:
Colorado, Jaime Hernández
Publikováno v:
Foro Internacional, 2012 Jan 01. 521 (207), 248-254.
Externí odkaz:
https://www.jstor.org/stable/41636519
Autor:
Jaime Hernández Colorado
Publikováno v:
Foro Internacional, Vol 52, Iss 1 (2012)
Externí odkaz:
https://doaj.org/article/ca86b97c38674834ad5c0c6a662506f4
Autor:
Alba, Carlos
Publikováno v:
Foro Internacional, 2002 Jan 01. 421 (167), 231-235.
Externí odkaz:
https://www.jstor.org/stable/27739116
Autor:
Philippe Mudry
Publikováno v:
Gesnerus. 72:353
Autor:
Isabelle Rousseau
Publikováno v:
Foro Internacional, Vol 60, Iss 2 (2020)
En el marco de la reforma energética, en 2014, las leyes de Hidrocarburos y de la Industria Eléctrica incluyeron herramientas para prevenir, mitigar o reparar los posibles daños que la presencia de la infraestructura de los megaproyectos del secto
Externí odkaz:
https://doaj.org/article/9fd425a6d4c74bf7bcb6107a9aa00bca
Publikováno v:
Journal of Pediatric Endocrinology and Diabetes. 2:81-85
McCune–Albright syndrome (MAS) is a rare genetic disorder which presents across a broad clinical spectrum. The characteristic features are café-au-lait macules, fibrous dysplasia of the bone (FD), and hyperfunctioning endocrinopathies. A 10-year-o
Autor:
Isabelle Rousseau
Publikováno v:
Soins Cadres. 31:29-32
Autor:
Celia Rodd, Arati Mokashi, Glenville Jones, Maury Pinsk, R. Todd Alexander, Caroline Zuijdwijk, Indra R. Gupta, Karlpiet Schlingmann, Munier Nour, Isabelle Rousseau-Nepton, Karine Khatchadourian, Martin Kaufmann, Danièle Pacaud
Publikováno v:
Hormone Research in Paediatrics. 94:124-132
Objectives: Biallelic pathogenic variants in CYPA24A1 and SLC34A1 are causes of idiopathic infantile hypercalcemia. Pathogenic variants in both may also give rise to hypercalciuria with nephrocalcinosis or nephrolithiasis without previous hypercalcem