Zobrazeno 1 - 10
of 556
pro vyhledávání: '"Hadchouel M"'
Publikováno v:
Science, 1985 Dec 01. 230(4730), 1160-1163.
Externí odkaz:
https://www.jstor.org/stable/1695510
Autor:
Davit-Spraul, A. 1, *, †, Atger, V. §, Pourci, M.L. *, †, Hadchouel, M. **, Legrand, A. †, ††, Moatti, N. *, §
Publikováno v:
In Journal of Lipid Research February 1999 40(2):328-335
Autor:
Bungener, Martine, Hadchouel, M
Publikováno v:
La Presse Médicale
La Presse Médicale, Elsevier Masson, 2012, 41 (9 Part1), pp.841-846. ⟨10.1016/j.lpm.2012.02.050⟩
La Presse Médicale, Elsevier Masson, 2012, 41 (9 Part1), pp.841-846. ⟨10.1016/j.lpm.2012.02.050⟩
International audience; Key points Fraud is only a part of misconduct in research. Very few French research Institutions have a scientific integrity office, and their prevention. The Institut national de la santé et de la recherche médicale (Inserm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::ad2cbd3f297f5501829bd06b480c8743
https://hal-cnrs.archives-ouvertes.fr/hal-03478604
https://hal-cnrs.archives-ouvertes.fr/hal-03478604
Autor:
Jacquemin, E, de Vree, JML, Cresteil, D, Sokal, EM, Sturm, E, Dumont, M, Scheffer, GL, Paul, M, Burdelski, M, Bernard, O, Hadchouel, M, Elferink, RPJO
Publikováno v:
Gastroenterology, 120(6), 1448-1458. W B SAUNDERS CO-ELSEVIER INC
Background & Aims: We have specified the features of progressive familial intrahepatic cholestasis type 3 and investigated in 31 patients whether a defect of the multidrug resistance 3 gene (MDR3) underlies this phenotype. Methods: MDR3 sequencing li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::d5808b7b5919a55c747836ae56454574
https://research.rug.nl/en/publications/7d555be3-8fe1-4d12-81d6-f415089dd702
https://research.rug.nl/en/publications/7d555be3-8fe1-4d12-81d6-f415089dd702
Autor:
Deleuze, F., Hadchouel, M.
Alagille syndrome (AGS) is a clinically defined disorder characterized by cholestatic liver disease with bile duct paucity, peculiar facies, structural heart defects, vertebral anomalies, and ocular abnormalities. Multiple patients with various cytog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6dfb947e4b043da9a78985ffe1da5540
https://europepmc.org/articles/PMC1914723/
https://europepmc.org/articles/PMC1914723/
Publikováno v:
Gastroentérologie Clinique et Biologique / Research and Clinics in Hepatology and Gastroenterology
Gastroentérologie Clinique et Biologique / Research and Clinics in Hepatology and Gastroenterology, Elsevier Masson, 1995, 19 (6-7), pp.587-596
Gastroentérologie Clinique et Biologique / Research and Clinics in Hepatology and Gastroenterology, Elsevier Masson, 1995, 19 (6-7), pp.587-596
National audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e6deebc38251d4b92347ad20c71e3dfb
https://hal.inrae.fr/hal-02711912
https://hal.inrae.fr/hal-02711912
Publikováno v:
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::6cd36ed251ca6d6dbb1c38fb800e1bef
https://pubmed.ncbi.nlm.nih.gov/7842097
https://pubmed.ncbi.nlm.nih.gov/7842097