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Results of search for 'au:"Hadchouel, M"', page 6 of 7
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Authors
Alagille, D
Alvarez, F
Bernard, O
Brechot, C
Brunelle, F
Cresteil, D
Deleuze, J F
Dhorne-Pollet, S
Dumont, M
Gautier, M
Hadchouel, M
Jacquemin, E
Maggiore, G
Meunier-Rotival, M
Odievre, M
Odièvre, M
Pollet, N
Pourcel, C
Scotto, J
Tiollais, P
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Topics
Adolescent
Alagille Syndrome
Animals
Child
Child, Preschool
Cholestasis
Female
Hepatitis B Surface Antigens
Humans
Infant
Infant, Newborn
Liver
Male
analysis
blood
complications
etiology
genetics
metabolism
pathology
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Your search returned 134 results.
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101.
Genetic cholestatic liver diseases: the example of progressive familial intrahepatic cholestasis and related disorders.
[electronic resource]
by
Baussan, C
Cresteil, D
Gonzales, E
Raynaud, N
Dumont, M
Bernard, O
Hadchouel, M
Jacquemin, E
Producer:
20040928
In:
Acta gastro-enterologica Belgica
vol. 67
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102.
Glomerular mesangiolipidosis in Alagille syndrome (arteriohepatic dysplasia).
[electronic resource]
by
Habib, R
Dommergues, J P
Gubler, M C
Hadchouel, M
Gautier, M
Odievre, M
Alagille, D
Producer:
19901227
In:
Pediatric nephrology (Berlin, Germany)
vol. 1
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103.
Hepatitis B surface antigen gene expression is regulated by sex steroids and glucocorticoids in transgenic mice.
[electronic resource]
by
Farza, H
Salmon, A M
Hadchouel, M
Moreau, J L
Babinet, C
Tiollais, P
Pourcel, C
Producer:
19870406
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 84
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104.
Abnormal lipoprotein pattern in patients with Alagille syndrome depends on Icterus severity.
[electronic resource]
by
Davit-Spraul, A
Pourci, M L
Atger, V
Cambillau, M
Hadchouel, M
Moatti, N
Legrand, A
Producer:
19961106
In:
Gastroenterology
vol. 111
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105.
Jagged1 mutations in alagille syndrome.
[electronic resource]
by
Spinner, N B
Colliton, R P
Crosnier, C
Krantz, I D
Hadchouel, M
Meunier-Rotival, M
Producer:
20010222
In:
Human mutation
vol. 17
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106.
Pattern of expression of gamma-glutamyl transpeptidase in rat liver and kidney during development: study by immunochemistry and in situ hybridization.
[electronic resource]
by
Jacquemin, E
Bulle, F
Bernaudin, J F
Wellman, M
Hugon, R N
Guellaen, G
Hadchouel, M
Producer:
19900921
In:
Journal of pediatric gastroenterology and nutrition
vol. 11
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107.
Biliary tract involvement in children with histiocytosis X.
[electronic resource]
by
Pariente, D
Bacadi, D
Schmit, P
Brunelle, F
Chaumont, P
Hadchouel, M
Amédée-Manesme, O
Bernard, O
Producer:
19870512
In:
Annales de radiologie
vol. 29
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108.
Defect of multidrug-resistance 3 gene expression in a subtype of progressive familial intrahepatic cholestasis.
[electronic resource]
by
Deleuze, J F
Jacquemin, E
Dubuisson, C
Cresteil, D
Dumont, M
Erlinger, S
Bernard, O
Hadchouel, M
Producer:
19960802
In:
Hepatology (Baltimore, Md.)
vol. 23
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109.
Autoimmune hepatitis associated with anti-actin antibodies in children and adolescents.
[electronic resource]
by
Maggiore, G
Veber, F
Bernard, O
Hadchouel, M
Homberg, J C
Alvarez, F
Hadchouel, P
Alagille, D
Producer:
19940504
In:
Journal of pediatric gastroenterology and nutrition
vol. 17
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110.
Liver disease associated with anti-liver-kidney microsome antibody in children.
[electronic resource]
by
Maggiore, G
Bernard, O
Homberg, J C
Hadchouel, M
Alvarez, F
Hadchouel, P
Odièvre, M
Alagille, D
Producer:
19860402
In:
The Journal of pediatrics
vol. 108
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111.
Hepatocyte nuclear factor 1 inactivation results in hepatic dysfunction, phenylketonuria, and renal Fanconi syndrome.
[electronic resource]
by
Pontoglio, M
Barra, J
Hadchouel, M
Doyen, A
Kress, C
Bach, J P
Babinet, C
Yaniv, M
Producer:
19960423
In:
Cell
vol. 84
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112.
Ursodeoxycholic acid therapy in pediatric patients with progressive familial intrahepatic cholestasis.
[electronic resource]
by
Jacquemin, E
Hermans, D
Myara, A
Habes, D
Debray, D
Hadchouel, M
Sokal, E M
Bernard, O
Producer:
19970320
In:
Hepatology (Baltimore, Md.)
vol. 25
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113.
A retrospective study of the role of delta agent infection in children with HBsAg-positive chronic hepatitis.
[electronic resource]
by
Maggiore, G
Hadchouel, M
Sessa, F
Vinci, M
Craxì, A
Marzani, M D
De Giacomo, C
Alagille, D
Producer:
19850318
In:
Hepatology (Baltimore, Md.)
vol. 5
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114.
Mutations in JAGGED1 gene are predominantly sporadic in Alagille syndrome.
[electronic resource]
by
Crosnier, C
Driancourt, C
Raynaud, N
Dhorne-Pollet, S
Pollet, N
Bernard, O
Hadchouel, M
Meunier-Rotival, M
Producer:
19990607
In:
Gastroenterology
vol. 116
Online resources:
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115.
Seroimmunologic classification of chronic hepatitis in 57 children.
[electronic resource]
by
Odièvre, M
Maggiore, G
Homberg, J C
Saadoun, F
Couroucé, A M
Yvart, J
Hadchouel, M
Alagille, D
Producer:
19830623
In:
Hepatology (Baltimore, Md.)
vol. 3
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116.
A new cause of progressive intrahepatic cholestasis: 3 beta-hydroxy-C27-steroid dehydrogenase/isomerase deficiency.
[electronic resource]
by
Jacquemin, E
Setchell, K D
O'Connell, N C
Estrada, A
Maggiore, G
Schmitz, J
Hadchouel, M
Bernard, O
Producer:
19940929
In:
The Journal of pediatrics
vol. 125
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117.
Sclerosing cholangitis with neonatal onset.
[electronic resource]
by
Amedee-Manesme, O
Bernard, O
Brunelle, F
Hadchouel, M
Polonovski, C
Baudon, J J
Beguet, P
Alagille, D
Producer:
19870910
In:
The Journal of pediatrics
vol. 111
Online resources:
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118.
Construction of an integrated physical and gene map of human chromosome 20p12 providing candidate genes for Alagille syndrome.
[electronic resource]
by
Pollet, N
Boccaccio, C
Dhorne-Pollet, S
Driancourt, C
Raynaud, N
Auffray, C
Hadchouel, M
Meunier-Rotival, M
Producer:
19970902
In:
Genomics
vol. 42
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119.
Budd-Chiari syndrome in children: report of 22 cases.
[electronic resource]
by
Gentil-Kocher, S
Bernard, O
Brunelle, F
Hadchouel, M
Maillard, J N
Valayer, J
Hay, J M
Alagille, D
Producer:
19880811
In:
The Journal of pediatrics
vol. 113
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120.
Interstitial deletion of the short arm of chromosome 20 in arteriohepatic dysplasia (Alagille syndrome).
[electronic resource]
by
Zhang, F
Deleuze, J F
Aurias, A
Dutrillaux, A M
Hugon, R N
Alagille, D
Thomas, G
Hadchouel, M
Producer:
19900214
In:
The Journal of pediatrics
vol. 116
Online resources:
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