Zobrazeno 1 - 10
of 381
pro vyhledávání: '"M, Hadchouel"'
Publikováno v:
Journal of Lipid Research, Vol 40, Iss 2, Pp 328-335 (1999)
We have previously described the lipoprotein abnormalities in cholestatic children with paucity of interlobular bile ducts (PILBD), and we have shown that two different profiles emerged among these patients, depending on the level of lecithin:cholest
Externí odkaz:
https://doaj.org/article/f206e3e7434b4adabab14371d521b7f6
Publikováno v:
Archives of Disease in Childhood. 75:67-70
Between 1960 and 1994 cystic fibrosis was found in nine out of 1474 infants investigated for neonatal cholestasis. Four had delay in passing meconium. In all patients cholestatic jaundice was present during the first 48 hours and in three patients ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8c2071c456ab061b18da03bbff00227
https://doi.org/10.1136/adc.75.1.67
https://doi.org/10.1136/adc.75.1.67
Autor:
Fathi Moussa, André Rassat, René Céolin, François Trivin, Claude Fabre, H. Szwarc, M. Hadchouel, Pierre-Yves Sizaret, Virginie Greugny
Publikováno v:
Fullerene Science and Technology. 4:21-29
High amounts of micronized C60 have been injected intraperitoneally into Swiss mice. Until the fourteenth day, they were still alive without any behaviour trouble. C60 was well absorbed, and found localized in spleen and liver. Inside the liver, C60
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32a01f047e88c2e6d3d3cc7350ad5948
https://doi.org/10.1080/10641229608001534
https://doi.org/10.1080/10641229608001534
Publikováno v:
Biochemical and Biophysical Research Communications. 208:957-963
Type I hereditary tyrosinemia results from an inherited deficiency in fumarylacetoacetate hydrolase, the enzyme involved in the last step in tyrosine catabolic pathway. The cloning of the cDNA encoding FAH in human has opened the way to genetic treat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c8a65b5ef84b8e91045a263b63a542a
https://doi.org/10.1006/bbrc.1995.1427
https://doi.org/10.1006/bbrc.1995.1427
Autor:
C, Baussan, D, Cresteil, E, Gonzales, N, Raynaud, M, Dumont, O, Bernard, M, Hadchouel, E, Jacquemin
Publikováno v:
Acta gastro-enterologica Belgica. 67(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c7f3966e6ecdcda1f731e4da66980513
https://pubmed.ncbi.nlm.nih.gov/15285575
https://pubmed.ncbi.nlm.nih.gov/15285575
Autor:
F, Gauthier, M, Hadchouel
Publikováno v:
La Revue du praticien. 50(19)
Congenital disorders of the bile ducts manifesting as neonatal cholestasis, are: biliary atresia, Alagille syndrome and neonatal sclerosing cholangitis. Biliary atresia must be considered as a neonatal surgical emergency: diagnosis and therapeutic in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2aad4c9f3a25f7c4122bacd432e7b400
https://pubmed.ncbi.nlm.nih.gov/11213458
https://pubmed.ncbi.nlm.nih.gov/11213458
Publikováno v:
Human mutation. 17(1)
Mutations in the human JAGGED1 gene cause Alagille syndrome, an autosomal dominant developmental disorder. The gene encodes a transmembrane protein which is a ligand of Notch receptors. We report 23 mutations in previously undescribed probands, inclu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e421c1b06d0bc963192d2b71f026848b
https://pubmed.ncbi.nlm.nih.gov/11139247
https://pubmed.ncbi.nlm.nih.gov/11139247
Autor:
Alain Aurias, Chantal Desmaze, A M Dutrillaux, M Hadchouel, Jean-François Deleuze, Gareth J. Thomas
Publikováno v:
Journal of Medical Genetics. 29:233-235
We report a cytogenetic and molecular study of a series of patients with Alagille syndrome. All 14 patients were studied with high resolution banding techniques and eight of them were also analysed with non-radioactive in situ hybridisation of the co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87a3fbcb4dcd1628aa076ce20cac2172
https://doi.org/10.1136/jmg.29.4.233
https://doi.org/10.1136/jmg.29.4.233
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 161(10)
The immunotherapeutic effect of DNA-mediated immunization against chronic hepatitis B virus (HBV) infection has been evaluated in transgenic mice expressing the sequences that code for the envelope proteins of HBV in the liver. In this model of HBV c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2c264ee06f2cf2b4d413b9baf018bef7
https://pubmed.ncbi.nlm.nih.gov/9820533
https://pubmed.ncbi.nlm.nih.gov/9820533
Autor:
M, Hadchouel, M, Fabre
Publikováno v:
Annales de pathologie. 15(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e00d43a947df237f9e083e57c2fa0b1b
https://pubmed.ncbi.nlm.nih.gov/8540921
https://pubmed.ncbi.nlm.nih.gov/8540921