-
1
-
-
0023148932
-
Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): Review of 80 cases
-
Alagille D, Estrada A, Hadchouel M, Gautier M, Odievre M, Dommergues JP. Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases. J Pediatr 1987;110:195-200
-
(1987)
J Pediatr
, vol.110
, pp. 195-200
-
-
Alagille, D.1
Estrada, A.2
Hadchouel, M.3
Gautier, M.4
Odievre, M.5
Dommergues, J.P.6
-
2
-
-
0024339022
-
Human ontogeny of the bile duct to portal space ratio
-
Kahn E, Markowitz J, Aiges H, Daum F. Human ontogeny of the bile duct to portal space ratio. Hepatology 1989;10:21-23
-
(1989)
Hepatology
, vol.10
, pp. 21-23
-
-
Kahn, E.1
Markowitz, J.2
Aiges, H.3
Daum, F.4
-
3
-
-
0016439420
-
Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur
-
Alagille D, Odievre M, Gautier M, Dommergues JP. Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur. J Pediatr 1975;86:63-71
-
(1975)
J Pediatr
, vol.86
, pp. 63-71
-
-
Alagille, D.1
Odievre, M.2
Gautier, M.3
Dommergues, J.P.4
-
4
-
-
0017578990
-
Hereditary cholestasis combined with peripheral pulmonary stenosis and other anomalies
-
Henriksen NT, Langmark F, Sorland SJ, Fausa O, Landaas S, Aagenaes O. Hereditary cholestasis combined with peripheral pulmonary stenosis and other anomalies. Acta Paediatr Scand 1977;66:7-15
-
(1977)
Acta Paediatr Scand
, vol.66
, pp. 7-15
-
-
Henriksen, N.T.1
Langmark, F.2
Sorland, S.J.3
Fausa, O.4
Landaas, S.5
Aagenaes, O.6
-
5
-
-
0026655225
-
Cytokeratin immunohistochemical examination of liver biopsies in infants with Alagille syndrome and biliary atresia
-
Treem WR, Krzymowski GA, Cartun RW, Pedersen CA, Hyams JS, Berman M. Cytokeratin immunohistochemical examination of liver biopsies in infants with Alagille syndrome and biliary atresia. J Pediatr Gastroenterol Nutr 1992;15:73-80
-
(1992)
J Pediatr Gastroenterol Nutr
, vol.15
, pp. 73-80
-
-
Treem, W.R.1
Krzymowski, G.A.2
Cartun, R.W.3
Pedersen, C.A.4
Hyams, J.S.5
Berman, M.6
-
6
-
-
0026037503
-
Paucity of interlobular bile ducts: Arteriohepatic dysplasia and nonsyndromic duct paucity
-
Kahn E. Paucity of interlobular bile ducts: arteriohepatic dysplasia and nonsyndromic duct paucity. Perspect Pediatr Pathol 1991;14:168-215
-
(1991)
Perspect Pediatr Pathol
, vol.14
, pp. 168-215
-
-
Kahn, E.1
-
7
-
-
0023551346
-
Syndromic paucity of the intrahepatic bile ducts: Diagnostic difficulty; severe morbidity throughout early childhood
-
Deprettere A, Portmann B, Mowat AP. Syndromic paucity of the intrahepatic bile ducts: diagnostic difficulty; severe morbidity throughout early childhood. J Pediatr Gastroenterol Nutr 1987;6:865-871
-
(1987)
J Pediatr Gastroenterol Nutr
, vol.6
, pp. 865-871
-
-
Deprettere, A.1
Portmann, B.2
Mowat, A.P.3
-
8
-
-
0033017848
-
Features of Alagille syndrome in 92 patients: Frequency and relation to prognosis
-
Emerick KM, Rand EB, Goldmuntz E, Krantz ID, Spinner NB, Piccoli DA. Features of Alagille syndrome in 92 patients: frequency and relation to prognosis. Hepatology 1999;29:822-829
-
(1999)
Hepatology
, vol.29
, pp. 822-829
-
-
Emerick, K.M.1
Rand, E.B.2
Goldmuntz, E.3
Krantz, I.D.4
Spinner, N.B.5
Piccoli, D.A.6
-
10
-
-
16444386224
-
Autosomal dominant inheritance of Williams-Beuren syndrome in a father and son with haploinsufficiency for FKBP6
-
Metcalfe K, Simeonov E, Beckett W, Donnai D, Tassabehji M. Autosomal dominant inheritance of Williams-Beuren syndrome in a father and son with haploinsufficiency for FKBP6. Clin Dysmorphol 2005;14:61-65
-
(2005)
Clin Dysmorphol
, vol.14
, pp. 61-65
-
-
Metcalfe, K.1
Simeonov, E.2
Beckett, W.3
Donnai, D.4
Tassabehji, M.5
-
14
-
-
0029015848
-
Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: Evaluation of 235 patients
-
Lowery MC, Morris CA, Ewart A, et al. Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: evaluation of 235 patients. Am J Hum Genet 1995;57:49-53
-
(1995)
Am J Hum Genet
, vol.57
, pp. 49-53
-
-
Lowery, M.C.1
Morris, C.A.2
Ewart, A.3
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