-
1
-
-
0000135411
-
Embryogenèse des voies biliaires
-
Desmet VJ. Embryogenèse des voies biliaires. Médecine Thérapeutique 1995;1:227-35.
-
(1995)
Médecine Thérapeutique
, vol.1
, pp. 227-235
-
-
Desmet, V.J.1
-
2
-
-
0026061287
-
Normal and abnormal development of human intrahepatic bile ducts. An immunohistochemical perspective
-
Abramowsky CR, Bernstein J, Rosenberg HS, eds. Basel: Karger
-
Blankenberg TA, Lund JK, Reubner BH. Normal and abnormal development of human intrahepatic bile ducts. An immunohistochemical perspective. In: Abramowsky CR, Bernstein J, Rosenberg HS, eds. Perspectives in Pediatric Pathology. Transplantation Pathology-Hepatic Morphogenesis. Vol. 14. Basel: Karger, 1991:143-67.
-
(1991)
Perspectives in Pediatric Pathology. Transplantation Pathology-Hepatic Morphogenesis
, vol.14
, pp. 143-167
-
-
Blankenberg, T.A.1
Lund, J.K.2
Reubner, B.H.3
-
3
-
-
0027991665
-
The developing human biliary system at the porta hepatis level between 29 days and 8 weeks of gestation: A way to understanding biliary atresia. Part 1
-
Tan CEL, Moscoso GJ. The developing human biliary system at the porta hepatis level between 29 days and 8 weeks of gestation: a way to understanding biliary atresia. Part 1. Pathol Int 1994;44:587-99.
-
(1994)
Pathol Int
, vol.44
, pp. 587-599
-
-
Tan, C.E.L.1
Moscoso, G.J.2
-
4
-
-
0015184790
-
Morphogenesis of intrahepatic bile ducts of the human fetus. Light and electron microscopic study
-
Koga A. Morphogenesis of intrahepatic bile ducts of the human fetus. Light and electron microscopic study. Z Anat Entwicklungsgesch 1971;135:156-84.
-
(1971)
Z Anat Entwicklungsgesch
, vol.135
, pp. 156-184
-
-
Koga, A.1
-
5
-
-
0001775398
-
Über die erste Entstehung der nicht kapillaren intrahepatischen Gallengänge beim Menschen
-
Hammar JA. Über die erste Entstehung der nicht kapillaren intrahepatischen Gallengänge beim Menschen. Z Mikrosk Anat Forsch 1926; 5:59-89.
-
(1926)
Z Mikrosk Anat Forsch
, vol.5
, pp. 59-89
-
-
Hammar, J.A.1
-
6
-
-
0033791668
-
Study of the malformation of ductal plate of the liver in Meckel syndrome and review of other syndromes presenting this anomaly
-
Sergi C, Adam S, Kahl P, Otto HF. Study of the malformation of ductal plate of the liver in Meckel syndrome and review of other syndromes presenting this anomaly. Pediatr Dev Pathol 2000;3:568-83.
-
(2000)
Pediatr Dev Pathol
, vol.3
, pp. 568-583
-
-
Sergi, C.1
Adam, S.2
Kahl, P.3
Otto, H.F.4
-
7
-
-
0002398167
-
Embryology of the liver and intrahepatic biliary tract, and an overview of malformations of the bile duct
-
Bircher J, Benhamou J-P, McIntyre N, Rizzetto M, Rodés J, eds. Oxford: Oxford University Press
-
Desmet VJ, Van Eyken P, Roskams T. Embryology of the liver and intrahepatic biliary tract, and an overview of malformations of the bile duct. In: Bircher J, Benhamou J-P, McIntyre N, Rizzetto M, Rodés J, eds. Oxford Textbook of Clinical Hepatology. 2nd ed. Vol. 1. Oxford: Oxford University Press, 1999:51-61.
-
(1999)
Oxford Textbook of Clinical Hepatology. 2nd Ed.
, vol.1
, pp. 51-61
-
-
Desmet, V.J.1
Van Eyken, P.2
Roskams, T.3
-
8
-
-
0035990952
-
The correlation between portal myofibroblasts and the development of intrahepatic bile ducts and arterial branches in human liver
-
Libbrecht L, Cassiman D, Desmet V, Roskams T. The correlation between portal myofibroblasts and the development of intrahepatic bile ducts and arterial branches in human liver. Liver 2002;22:1-7.
-
(2002)
Liver
, vol.22
, pp. 1-7
-
-
Libbrecht, L.1
Cassiman, D.2
Desmet, V.3
Roskams, T.4
-
9
-
-
0036893031
-
Relationship between vascular development and vascular differentiation during liver organogenesis in humans
-
Gouysse G, Couvelard A, Frachon S, Bouvier R, Nejjari M, Dauge MC, et al. Relationship between vascular development and vascular differentiation during liver organogenesis in humans. J Hepatol 2002;37:730-40.
-
(2002)
J Hepatol
, vol.37
, pp. 730-740
-
-
Gouysse, G.1
Couvelard, A.2
Frachon, S.3
Bouvier, R.4
Nejjari, M.5
Dauge, M.C.6
-
10
-
-
0024213059
-
The development of the intrahepatic bile ducts in man: A keratin-immunohistochemical study
-
Van Eyken P, Sciot R, Callea F, Van der Steen K, Moerman P, Desmet VJ. The development of the intrahepatic bile ducts in man: a keratin- immunohistochemical study. Hepatology 1988;8:1586-95.
-
(1988)
Hepatology
, vol.8
, pp. 1586-1595
-
-
Van Eyken, P.1
Sciot, R.2
Callea, F.3
Van Der Steen, K.4
Moerman, P.5
Desmet, V.J.6
-
11
-
-
0027220730
-
Development of human peribiliary capillary plexus: A lectin-histochemical and immunohistochemical study
-
Terada T, Nakanuma Y. Development of human peribiliary capillary plexus: a lectin-histochemical and immunohistochemical study. Hepatology 1993;18:529-36.
-
(1993)
Hepatology
, vol.18
, pp. 529-536
-
-
Terada, T.1
Nakanuma, Y.2
-
12
-
-
0036336713
-
The onecut transcription factor HNF6 is required for normal development of the biliary tract
-
Clotman F, Lannoy VJ, Reber M, Cereghini S, Cassiman D, Jacquemin P, et al. The onecut transcription factor HNF6 is required for normal development of the biliary tract. Development 2002;129:1819-28.
-
(2002)
Development
, vol.129
, pp. 1819-1828
-
-
Clotman, F.1
Lannoy, V.J.2
Reber, M.3
Cereghini, S.4
Cassiman, D.5
Jacquemin, P.6
-
13
-
-
0036336513
-
Bile system morphogenesis defects and liver dysfunction upon targeted deletion of HNF1β
-
Coffinier C, Gresh L, Fiette L, Tronche F, Schütz G, Babinet C, et al. Bile system morphogenesis defects and liver dysfunction upon targeted deletion of HNF1β. Development 2002;129:1829-38.
-
(2002)
Development
, vol.129
, pp. 1829-1838
-
-
Coffinier, C.1
Gresh, L.2
Fiette, L.3
Tronche, F.4
Schütz, G.5
Babinet, C.6
-
14
-
-
0032897080
-
Embryonic lethality and vascular defects in mice lacking the Notch ligand Jagged 1
-
Xue Y, Gao X, Lindsell CE, Norton CR, Chang B, Hicks C, et al. Embryonic lethality and vascular defects in mice lacking the Notch ligand Jagged 1. Hum Mol Genet 1999;8:723-30.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 723-730
-
-
Xue, Y.1
Gao, X.2
Lindsell, C.E.3
Norton, C.R.4
Chang, B.5
Hicks, C.6
-
15
-
-
0033839965
-
JAGGED 1 gene expression during human embryogenesis elucidates the wide phenotypic spectrum of Alagille syndrome
-
Crosnier C, Attie-Bitach T, Encha-Razavi F, Audollent S, Soudy F, Hadchouel M, et al. JAGGED 1 gene expression during human embryogenesis elucidates the wide phenotypic spectrum of Alagille syndrome. Hepatology 2000;32:574-81.
-
(2000)
Hepatology
, vol.32
, pp. 574-581
-
-
Crosnier, C.1
Attie-Bitach, T.2
Encha-Razavi, F.3
Audollent, S.4
Soudy, F.5
Hadchouel, M.6
-
16
-
-
0032737819
-
Hepatic Jagged-1 expression studies
-
Louis AA, Van Eyken P, Haber PA, Hicks C, Weinmaster G, Taub R, et al. Hepatic Jagged-1 expression studies. Hepatology 1999;30:1269-75.
-
(1999)
Hepatology
, vol.30
, pp. 1269-1275
-
-
Louis, A.A.1
Van Eyken, P.2
Haber, P.A.3
Hicks, C.4
Weinmaster, G.5
Taub, R.6
-
17
-
-
0020338292
-
The unit-concept of hepatic parenchyma - A re-examination based on angioarchitectural studies
-
Matsumoto R, Kawakami M. The unit-concept of hepatic parenchyma - a re-examination based on angioarchitectural studies. Acta Pathol Jpn 1982;32:285-314.
-
(1982)
Acta Pathol Jpn
, vol.32
, pp. 285-314
-
-
Matsumoto, R.1
Kawakami, M.2
-
18
-
-
0017355516
-
The ductal plate malformation. A study of the intrahepatic ile-duct lesion in infantile polycystic disease and congenital hepatic fibrosis
-
Jorgensen MJ. The ductal plate malformation. A study of the intrahepatic ile-duct lesion in infantile polycystic disease and congenital hepatic fibrosis. Acta Pathol Microbiol Scand A 1976;257 (Suppl):33-44.
-
(1976)
Acta Pathol Microbiol Scand A
, vol.257
, Issue.SUPPL.
, pp. 33-44
-
-
Jorgensen, M.J.1
-
19
-
-
26244437334
-
Etiologie, anatomopathologie, évolution des lésons d'origine génétique de l'arbre biliaire
-
7-002-A-10
-
Desmet VJ. Etiologie, anatomopathologie, évolution des lésons d'origine génétique de l'arbre biliaire. Encycl Med Chir, Hépatologie 2000;7-002-A-10.
-
(2000)
Encycl Med Chir, Hépatologie
-
-
Desmet, V.J.1
-
20
-
-
0026737604
-
Congenital diseases of intrahepatic bile ducts: Variations on the theme "ductal plate malformation"
-
Desmet VJ. Congenital diseases of intrahepatic bile ducts: variations on the theme "ductal plate malformation". Hepatology 1992;16:1069-83.
-
(1992)
Hepatology
, vol.16
, pp. 1069-1083
-
-
Desmet, V.J.1
-
21
-
-
0031609085
-
Pathogenesis of ductal plate abnormalities
-
Desmet VJ. Pathogenesis of ductal plate abnormalities. Mayo Clin Proc 1998;73:80-9.
-
(1998)
Mayo Clin Proc
, vol.73
, pp. 80-89
-
-
Desmet, V.J.1
-
23
-
-
0037900924
-
Molecular pathology and genetics of congenital hepatorenal fibrocystic syndromes
-
Johnson CA, Gissen P, Sergi C. Molecular pathology and genetics of congenital hepatorenal fibrocystic syndromes. J Med Genet 2003;40:311-9.
-
(2003)
J Med Genet
, vol.40
, pp. 311-319
-
-
Johnson, C.A.1
Gissen, P.2
Sergi, C.3
-
24
-
-
0026636283
-
What is congenital hepatic fibrosis?
-
Desmet VJ. What is congenital hepatic fibrosis? Histopathology 1992;20:465-77.
-
(1992)
Histopathology
, vol.20
, pp. 465-477
-
-
Desmet, V.J.1
-
25
-
-
0000536989
-
Cholestatic syndromes of infancy and childhood
-
Zakim D, Boyer TD, eds. Philadelphia: WB Saunders
-
Desmet VJ, Callea F. Cholestatic syndromes of infancy and childhood. In: Zakim D, Boyer TD, eds. Hepatology. A Textbook of Liver Disease. 2nd ed. Vol. 2. Philadelphia: WB Saunders, 1990:1355-95.
-
(1990)
Hepatology. A Textbook of Liver Disease. 2nd Ed.
, vol.2
, pp. 1355-1395
-
-
Desmet, V.J.1
Callea, F.2
-
26
-
-
0037371324
-
Mutations in PRKCSH cause isolated autosomal dominant polycystic liver disease
-
Li A, Davila S, Furu L, Qian Q, Tian X, Kamath PS, et al. Mutations in PRKCSH cause isolated autosomal dominant polycystic liver disease. Am J Hum Genet 2003;72:691-703.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 691-703
-
-
Li, A.1
Davila, S.2
Furu, L.3
Qian, Q.4
Tian, X.5
Kamath, P.S.6
-
27
-
-
1842427829
-
Abnormal hepatocystin caused by truncating PRKCSH mutations leads to autosomal dominant polycystic liver disease
-
Drenth JPH, Tahvanainen E, te Morsche RHM, Tahvanainen P, Kääriäinen H, Höckerstedt K, et al. Abnormal hepatocystin caused by truncating PRKCSH mutations leads to autosomal dominant polycystic liver disease. Hepatology 2004;39:924-31.
-
(2004)
Hepatology
, vol.39
, pp. 924-931
-
-
Drenth, J.P.H.1
Tahvanainen, E.2
Te Morsche, R.H.M.3
Tahvanainen, P.4
Kääriäinen, H.5
Höckerstedt, K.6
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