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Results:
1-14
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Results: 14
Authors:
Spinner, NB
Colliton, RP
Crosnier, C
Krantz, ID
Hadchouel, M
Meunier-Rotival, M
Citation: Nb. Spinner et al., Jagged1 mutations in Alagille syndrome, HUM MUTAT, 17(1), 2001, pp. 18-33
Authors:
Davit-Spraul, A
Cosson, C
Couturier, M
Hadchouel, M
Legrand, A
Lemonnier, F
Therond, P
Citation: A. Davit-spraul et al., Standard treatment of alpha-tocopherol in alagille patients with severe cholestasis is insufficient, PEDIAT RES, 49(2), 2001, pp. 232-236
Authors:
Lykavieris, P
Hadchouel, M
Chardot, C
Bernard, O
Citation: P. Lykavieris et al., Outcome of liver disease in children with Alagille syndrome: a study of 163 patients, GUT, 49(3), 2001, pp. 431-435
Authors:
Jacquemin, E
de Vree, JML
Cresteil, D
Sokal, EM
Sturm, E
Dumont, M
Scheffer, GL
Paul, M
Burdelski, M
Bosma, PJ
Bernard, O
Hadchouel, M
Elferink, RPJO
Citation: E. Jacquemin et al., The wide spectrum of multidrug resistance 3 deficiency: From neonatal cholestasis to cirrhosis of adulthood, GASTROENTY, 120(6), 2001, pp. 1448-1458
Authors:
Pourcel, C
Jaubert, J
Hadchouel, M
Wu, X
Schweizer, J
Citation: C. Pourcel et al., A new family of genes and pseudogenes potentially expressing testis- and brain-specific leucine zipper proteins in man and mouse, GENE, 249(1-2), 2000, pp. 105-113
Authors:
Crosnier, C
Attie-Bitach, T
Encha-Razavi, F
Audollent, S
Soudy, F
Hadchouel, M
Meunier-Rotival, M
Vekemans, M
Citation: C. Crosnier et al., JAGGED1 gene expression during human embryogenesis elucidates the wide phenotypic spectrum of Alagille syndrome, HEPATOLOGY, 32(3), 2000, pp. 574-581
Authors:
Hadchouel, M
Citation: M. Hadchouel, Notch signalling pathway and human diseases, J HEPATOL, 32, 2000, pp. 1-2
Authors:
Hadchouel, M
Citation: M. Hadchouel, Should we treat children with chronic hepatitis C with interferon?, ARCH PED, 6, 1999, pp. 178S-179S
Authors:
Jacquemin, E
Hadchouel, M
Citation: E. Jacquemin et M. Hadchouel, Genetic basis of progressive familial intrahepatic cholestasis, J HEPATOL, 31(2), 1999, pp. 377-381
Authors:
Faivre, L
Houssin, D
Valayer, J
Brouard, J
Hadchouel, M
Bernard, O
Citation: L. Faivre et al., Long-term outcome of liver transplantation in patients with glycogen storage disease type Ia, J INH MET D, 22(6), 1999, pp. 723-732
Authors:
Jacquemin, E
Cresteil, D
Manouvrier, S
Boute, O
Hadchouel, M
Citation: E. Jacquemin et al., Heterozygous non-sense mutation of the MDR3 gene in familial intrahepatic cholestasis of pregnancy, LANCET, 353(9148), 1999, pp. 210-211
Authors:
Davit-Spraul, A
Atger, V
Pourci, ML
Hadchouel, M
Legrand, A
Moatti, N
Citation: A. Davit-spraul et al., Cholesterol efflux from Fu5AH cells to the serum of patients with Alagillesyndrome: importance of the HDL-phospholipids free cholesterol ratio and of the HDL size distribution, J LIPID RES, 40(2), 1999, pp. 328-335
Authors:
Jansen, PLM
Strautnieks, SS
Jacquemin, E
Hadchouel, M
Sokal, EM
Hooiveld, GJEJ
Koning, JH
De Jager-Krikken, A
Kuipers, F
Stellaard, F
Bijleveld, CMA
Gouw, A
Van Goor, H
Thompson, RJ
Muller, M
Citation: Plm. Jansen et al., Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis, GASTROENTY, 117(6), 1999, pp. 1370-1379
Authors:
Crosnier, C
Driancourt, C
Raynaud, N
Dhorne-Pollet, S
Pollet, N
Bernard, O
Hadchouel, M
Meunier-Rotival, M
Citation: C. Crosnier et al., Mutations in JAGGED1 gene are predominantly sporadic in alagille syndrome, GASTROENTY, 116(5), 1999, pp. 1141-1148
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