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Volumn 8, Issue 5, 2003, Pages 357-374

Neonatal hepatitis syndrome

Author keywords

Conjugated hyperbilirubinaemia; Giant cell hepatitis; Infant; Metabolic liver disease; Neonatal hepatitis syndrome; Neonatal liver failure

Indexed keywords

25 HYDROXYVITAMIN D; ALPHA TOCOPHEROL; BILIRUBIN GLUCURONIDE; COLESTYRAMINE; PHENOBARBITAL; RETINOL; RIFAMPICIN; VITAMIN; VITAMIN D; VITAMIN K GROUP;

EID: 0141894364     PISSN: 10842756     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1084-2756(03)00093-9     Document Type: Review
Times cited : (49)

References (92)
  • 1
    • 0037313267 scopus 로고    scopus 로고
    • Differential developmental regulation of rat liver canalicular membrane transporters bsep and mrp2
    • Tomer G, Ananthanarayanan M, Weymann A et al. Differential developmental regulation of rat liver canalicular membrane transporters bsep and mrp2. Pediatr Res 2003;53:288-94.
    • (2003) Pediatr Res , vol.53 , pp. 288-294
    • Tomer, G.1    Ananthanarayanan, M.2    Weymann, A.3
  • 2
    • 0029908965 scopus 로고    scopus 로고
    • Neonatal liver failure
    • Shneider BL. Neonatal liver failure. Curr Opin Pediatr 1996;8:495-501.
    • (1996) Curr Opin Pediatr , vol.8 , pp. 495-501
    • Shneider, B.L.1
  • 3
    • 0034924076 scopus 로고    scopus 로고
    • Identification of neonatal liver failure and perinatal hemochromatosis in Canada
    • Jackson R, Roberts EA. Identification of neonatal liver failure and perinatal hemochromatosis in Canada. Paediatr Child Health 2001;6:248-50.
    • (2001) Paediatr Child Health , vol.6 , pp. 248-250
    • Jackson, R.1    Roberts, E.A.2
  • 4
    • 0023637483 scopus 로고
    • Morbidity after percutaneous liver biopsy
    • Lichtman S, Guzman C, Moore DL et al. Morbidity after percutaneous liver biopsy. Arch Dis Child 1987;62:901-4.
    • (1987) Arch Dis Child , vol.62 , pp. 901-904
    • Lichtman, S.1    Guzman, C.2    Moore, D.L.3
  • 5
    • 0026714658 scopus 로고
    • Polymerase chain reaction to detect human cytomegalovirus in livers of infants with neonatal hepatitis
    • Chang MH, Huang HH, Huang ES et al. Polymerase chain reaction to detect human cytomegalovirus in livers of infants with neonatal hepatitis. Gastroenterology 1992;103:1022-5.
    • (1992) Gastroenterology , vol.103 , pp. 1022-1025
    • Chang, M.H.1    Huang, H.H.2    Huang, E.S.3
  • 6
    • 0030848707 scopus 로고    scopus 로고
    • Extreme hyperbilirubinaemia in Zimbabwean neonates: Neurodevelopmental outcome at 4 months
    • Wolf MJ, Beunen G, Casaer P et al. Extreme hyperbilirubinaemia in Zimbabwean neonates: neurodevelopmental outcome at 4 months. Eur J Pediatr 1997;156:803-7.
    • (1997) Eur J Pediatr , vol.156 , pp. 803-807
    • Wolf, M.J.1    Beunen, G.2    Casaer, P.3
  • 7
    • 0036828817 scopus 로고    scopus 로고
    • Maternal-infant transmission of hepatitis C virus infection
    • Roberts EA, Yeung L. Maternal-infant transmission of hepatitis C virus infection. Hepatology 2002;36:S106-13.
    • (2002) Hepatology , vol.36
    • Roberts, E.A.1    Yeung, L.2
  • 8
    • 0027221496 scopus 로고
    • Cholestatic hepatitis in children infected with the human immunodeficiency virus
    • Persaud D, Bangaru B, Greco MA et al. Cholestatic hepatitis in children infected with the human immunodeficiency virus. Pediatr Infect Dis J 1993;12:492-8.
    • (1993) Pediatr Infect Dis J , vol.12 , pp. 492-498
    • Persaud, D.1    Bangaru, B.2    Greco, M.A.3
  • 9
    • 0029994964 scopus 로고    scopus 로고
    • Anemia, blueberry-muffin rash, and hepatomegaly in a newborn infant
    • Silver MM, Hellmann J, Zielenska M et al. Anemia, blueberry-muffin rash, and hepatomegaly in a newborn infant. J Pediatr 1996;128:579-86.
    • (1996) J Pediatr , vol.128 , pp. 579-586
    • Silver, M.M.1    Hellmann, J.2    Zielenska, M.3
  • 10
    • 0022881135 scopus 로고
    • Fulminant hepatic failure with intractable ascites due to an echovirus 11 infection successfully managed with a peritoneo-venous (LeVeen) shunt
    • Gillam GL, Stokes KB, McLellan J et al. Fulminant hepatic failure with intractable ascites due to an echovirus 11 infection successfully managed with a peritoneo-venous (LeVeen) shunt. J Pediatr Gastroenterol Nutr 1986;5:476-80.
    • (1986) J Pediatr Gastroenterol Nutr , vol.5 , pp. 476-480
    • Gillam, G.L.1    Stokes, K.B.2    McLellan, J.3
  • 11
    • 0036246828 scopus 로고    scopus 로고
    • Jaundice as an early diagnostic sign of urinary tract infection in infancy
    • Garcia FJ, Nager AL. Jaundice as an early diagnostic sign of urinary tract infection in infancy. Pediatrics 2002;109:846-51.
    • (2002) Pediatrics , vol.109 , pp. 846-851
    • Garcia, F.J.1    Nager, A.L.2
  • 13
    • 0032822507 scopus 로고    scopus 로고
    • Prognosis of biliary atresia in the era of liver transplantation: French national study from 1986 to 1996
    • Chardot C, Carton M, Spire-Bendelac N et al. Prognosis of biliary atresia in the era of liver transplantation: French national study from 1986 to 1996. Hepatology 1999;30:606-11.
    • (1999) Hepatology , vol.30 , pp. 606-611
    • Chardot, C.1    Carton, M.2    Spire-Bendelac, N.3
  • 14
    • 0025811352 scopus 로고
    • Biliary atresia and the polysplenia syndrome
    • Karrer FM, Hall RJ, Lilly JR. Biliary atresia and the polysplenia syndrome. J Pediatr Surg 1991;26:524-7.
    • (1991) J Pediatr Surg , vol.26 , pp. 524-527
    • Karrer, F.M.1    Hall, R.J.2    Lilly, J.R.3
  • 15
    • 0028915437 scopus 로고
    • Biliary atresia and the polysplenia syndrome: Its impact on final outcome
    • Vasquez J, Lopez Gutierrez JC, Gamez M et al. Biliary atresia and the polysplenia syndrome: its impact on final outcome. J Pediatr Surg 1995;30:485-7.
    • (1995) J Pediatr Surg , vol.30 , pp. 485-487
    • Vasquez, J.1    Lopez Gutierrez, J.C.2    Gamez, M.3
  • 16
    • 0028938593 scopus 로고
    • Reovirus 3 not detected by reverse transcriptase-mediated polymerase chain reaction analysis of preserved tissue from infants with cholestatic liver disease
    • Steele MI, Marshall CM, Lloyd RE et al. Reovirus 3 not detected by reverse transcriptase-mediated polymerase chain reaction analysis of preserved tissue from infants with cholestatic liver disease. Hepatology 1995;21:697-702.
    • (1995) Hepatology , vol.21 , pp. 697-702
    • Steele, M.I.1    Marshall, C.M.2    Lloyd, R.E.3
  • 17
    • 0031023069 scopus 로고    scopus 로고
    • Lack of evidence for rotavirus by polymerase chain reaction/enzyme immunoassay of hepatobiliary samples from children with biliary atresia
    • Bobo L, Ojeh C, Chiu D et al. Lack of evidence for rotavirus by polymerase chain reaction/enzyme immunoassay of hepatobiliary samples from children with biliary atresia. Pediatr Res 1997;41:229-34.
    • (1997) Pediatr Res , vol.41 , pp. 229-234
    • Bobo, L.1    Ojeh, C.2    Chiu, D.3
  • 18
    • 0026088992 scopus 로고
    • Neonatal hepatitis and extrahepatic biliary atresia associated with cytomegalovirus infection in twins
    • Hart MH, Kaufman SS, Vanderhoof JA et al. Neonatal hepatitis and extrahepatic biliary atresia associated with cytomegalovirus infection in twins. Am J Dis Child 1991;145:302-5.
    • (1991) Am J Dis Child , vol.145 , pp. 302-305
    • Hart, M.H.1    Kaufman, S.S.2    Vanderhoof, J.A.3
  • 19
    • 0030008314 scopus 로고    scopus 로고
    • Biliary atresia, cytomegalovirus, and age at referral
    • Tarr PI, Haas JE, Christie DL. Biliary atresia, cytomegalovirus, and age at referral. Pediatrics 1996;97:828-31.
    • (1996) Pediatrics , vol.97 , pp. 828-831
    • Tarr, P.I.1    Haas, J.E.2    Christie, D.L.3
  • 20
    • 0026564554 scopus 로고
    • Rejection of murine congenic bile ducts: A model for immune mediated bile duct disease
    • Schreiber RA, Kleinman RE, Barksdale EM et al. Rejection of murine congenic bile ducts: a model for immune mediated bile duct disease. Gastroenterology 1992;102:924-30.
    • (1992) Gastroenterology , vol.102 , pp. 924-930
    • Schreiber, R.A.1    Kleinman, R.E.2    Barksdale, E.M.3
  • 21
    • 0028864785 scopus 로고
    • Choledochal cysts: Lessons from a 20 year experience
    • Stringer MD, Dhawan A, Davenport M et al. Choledochal cysts: lessons from a 20 year experience. Arch Dis Child 1995;73:528-31.
    • (1995) Arch Dis Child , vol.73 , pp. 528-531
    • Stringer, M.D.1    Dhawan, A.2    Davenport, M.3
  • 22
    • 0023195906 scopus 로고
    • Sclerosing cholangitis with neonatal onset
    • Amedee-Manesme O, Bernard O, Brunelle F et al. Sclerosing cholangitis with neonatal onset. J Pediatr 1987;111:225-9.
    • (1987) J Pediatr , vol.111 , pp. 225-229
    • Amedee-Manesme, O.1    Bernard, O.2    Brunelle, F.3
  • 23
    • 4244079126 scopus 로고
    • Expanding the spectrum of neonatal cholestatic liver disease
    • Mulberg AE, Arora S, Grand RJ et al. Expanding the spectrum of neonatal cholestatic liver disease. Hepatology 1992;16:192A.
    • (1992) Hepatology , vol.16
    • Mulberg, A.E.1    Arora, S.2    Grand, R.J.3
  • 24
    • 0027366236 scopus 로고
    • Neonatal sclerosing cholangitis in two siblings: A category of progressive intrahepatic cholestasis
    • Baker AJ, Portmann B, Westaby D et al. Neonatal sclerosing cholangitis in two siblings: a category of progressive intrahepatic cholestasis. J Pediatr Gastroenterol Nutr 1993;17:317-22.
    • (1993) J Pediatr Gastroenterol Nutr , vol.17 , pp. 317-322
    • Baker, A.J.1    Portmann, B.2    Westaby, D.3
  • 25
  • 26
    • 0036556044 scopus 로고    scopus 로고
    • Alagille syndrome associated with angiographic moyamoya
    • Connor SE, Hewes D, Ball C et al. Alagille syndrome associated with angiographic moyamoya. Childs Nerv Syst 2002;18:186-90.
    • (2002) Childs Nerv Syst , vol.18 , pp. 186-190
    • Connor, S.E.1    Hewes, D.2    Ball, C.3
  • 29
    • 0030817924 scopus 로고    scopus 로고
    • Outcome of hepatobiliary scanning in neonatal hepatitis syndrome
    • Gilmour SM, Hershkop M, Reifen R et al. Outcome of hepatobiliary scanning in neonatal hepatitis syndrome. J Nucl Med 1997;38:1279-82.
    • (1997) J Nucl Med , vol.38 , pp. 1279-1282
    • Gilmour, S.M.1    Hershkop, M.2    Reifen, R.3
  • 30
    • 0028269284 scopus 로고
    • Arteriohepatic dysplasia and cardiovascular malformations
    • Silberbach M, Lashley D, Reller MD et al. Arteriohepatic dysplasia and cardiovascular malformations. Am Heart J 1991;127:695-9.
    • (1991) Am Heart J , vol.127 , pp. 695-699
    • Silberbach, M.1    Lashley, D.2    Reller, M.D.3
  • 31
    • 0027146371 scopus 로고
    • Ocular anomalies in the Alagille syndrome (arteriohepatic dysplasia)
    • Brodsky MC, Cunniff C. Ocular anomalies in the Alagille syndrome (arteriohepatic dysplasia). Ophthalmology 1993;100:1767-74.
    • (1993) Ophthalmology , vol.100 , pp. 1767-1774
    • Brodsky, M.C.1    Cunniff, C.2
  • 32
    • 0030935555 scopus 로고    scopus 로고
    • Orthotopic liver transplantation reverse the adverse nutritional changes of end-stage liver disease in children
    • Holt RIG, Broide E, Buchman CR et al. Orthotopic liver transplantation reverse the adverse nutritional changes of end-stage liver disease in children. Am J Clin Nutr 1997;65:534-42.
    • (1997) Am J Clin Nutr , vol.65 , pp. 534-542
    • Holt, R.I.G.1    Broide, E.2    Buchman, C.R.3
  • 33
    • 0033822023 scopus 로고    scopus 로고
    • Does liver transplantation affect growth pattern in Alagille syndrome?
    • Quiros-Tejeira RE, Ament ME, Heyman MB et al. Does liver transplantation affect growth pattern in Alagille syndrome? Liver Transpl 2000;6:582-7.
    • (2000) Liver Transpl , vol.6 , pp. 582-587
    • Quiros-Tejeira, R.E.1    Ament, M.E.2    Heyman, M.B.3
  • 35
    • 0032930909 scopus 로고    scopus 로고
    • Mutations in JAGGED1 gene are predominantly sporadic in Alagille syndrome
    • Crosnier C, Driancourt C, Raynaud N et al. Mutations in JAGGED1 gene are predominantly sporadic in Alagille syndrome. Gastroenterology 1999;116:1141-8.
    • (1999) Gastroenterology , vol.116 , pp. 1141-1148
    • Crosnier, C.1    Driancourt, C.2    Raynaud, N.3
  • 36
    • 0035261057 scopus 로고    scopus 로고
    • Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patients
    • Colliton RP, Bason L, Lu FM et al. Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patients. Hum Mutat 2001;17:151-2.
    • (2001) Hum Mutat , vol.17 , pp. 151-152
    • Colliton, R.P.1    Bason, L.2    Lu, F.M.3
  • 37
    • 0035003805 scopus 로고    scopus 로고
    • The DSL domain in mutant JAG1 ligand is essential for the severity of the liver defect in Alagille syndrome
    • Yuan ZR, Okaniwa M, Nagata I et al. The DSL domain in mutant JAG1 ligand is essential for the severity of the liver defect in Alagille syndrome. Clin Genet 2001;59:330-7.
    • (2001) Clin Genet , vol.59 , pp. 330-337
    • Yuan, Z.R.1    Okaniwa, M.2    Nagata, I.3
  • 39
    • 0034041588 scopus 로고    scopus 로고
    • Prognosis of alpha-1-antitrypsin deficiency-related liver disease in the era of paediatric liver transplantation
    • Francavilla R, Castellaneta SP, Hadzic N et al. Prognosis of alpha-1-antitrypsin deficiency-related liver disease in the era of paediatric liver transplantation. J Hepatol 2000;32:986-92.
    • (2000) J Hepatol , vol.32 , pp. 986-992
    • Francavilla, R.1    Castellaneta, S.P.2    Hadzic, N.3
  • 40
    • 0033813172 scopus 로고    scopus 로고
    • Liver transplantation for alpha-1-antitrypsin deficiency in children
    • Prachalias AA, Kalife M, Francavilla R et al. Liver transplantation for alpha-1-antitrypsin deficiency in children. Transpl Int 2000;13:207-10.
    • (2000) Transpl Int , vol.13 , pp. 207-210
    • Prachalias, A.A.1    Kalife, M.2    Francavilla, R.3
  • 41
    • 0029934054 scopus 로고    scopus 로고
    • Neonatal cholestasis as the presenting feature in cystic fibrosis
    • Lykavieris P, Bernard O, Hadchouel M. Neonatal cholestasis as the presenting feature in cystic fibrosis. Arch Dis Child 1996;75:67-70.
    • (1996) Arch Dis Child , vol.75 , pp. 67-70
    • Lykavieris, P.1    Bernard, O.2    Hadchouel, M.3
  • 42
    • 0030966950 scopus 로고    scopus 로고
    • Mutations in the fumarylaceto-acetate hydrotase gene causing hereditary tyrosinemia type I: Overview
    • St-Louis M, Tanguay RM. Mutations in the fumarylaceto-acetate hydrotase gene causing hereditary tyrosinemia type I: overview. Hum Mutat 1997;9:291-9.
    • (1997) Hum Mutat , vol.9 , pp. 291-299
    • St-Louis, M.1    Tanguay, R.M.2
  • 43
    • 0031871486 scopus 로고    scopus 로고
    • Tyrosinaemia type I and NTBC (2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione)
    • Holme E, Lindstedt S. Tyrosinaemia type I and NTBC (2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione). J Inherit Metab Dis 1998;21:507-17.
    • (1998) J Inherit Metab Dis , vol.21 , pp. 507-517
    • Holme, E.1    Lindstedt, S.2
  • 44
    • 0029097210 scopus 로고
    • Molecular basis of hereditary fructose intolerance: Mutations and polymorphisms in the human aldolase B gene
    • Tolan DR. Molecular basis of hereditary fructose intolerance: mutations and polymorphisms in the human aldolase B gene. Hum Mutat 1995;6:210-8.
    • (1995) Hum Mutat , vol.6 , pp. 210-218
    • Tolan, D.R.1
  • 45
    • 0037032455 scopus 로고    scopus 로고
    • Structural and functional analysis of aldolase B mutants related to hereditary fructose intolerance
    • Esposito G, Vitagliano L, Santamaria R et al. Structural and functional analysis of aldolase B mutants related to hereditary fructose intolerance. FEBS Lett 2002;531:152-6.
    • (2002) FEBS Lett , vol.531 , pp. 152-156
    • Esposito, G.1    Vitagliano, L.2    Santamaria, R.3
  • 46
    • 0033515560 scopus 로고    scopus 로고
    • The Niemann-Pick C1 protein resides in a vesicular compartment linked to retrograde transport of multiple tysosomal cargo
    • Neufeld EB, Wastney M, Patel S et al. The Niemann-Pick C1 protein resides in a vesicular compartment linked to retrograde transport of multiple tysosomal cargo. J Biol Chem 1999;274:9627-35.
    • (1999) J Biol Chem , vol.274 , pp. 9627-9635
    • Neufeld, E.B.1    Wastney, M.2    Patel, S.3
  • 47
    • 0031970926 scopus 로고    scopus 로고
    • Niemann-Pick disease type C and defective peroxisomal beta-oxidation of branched-chain substrates
    • Sequeira JS, Vellodi A, Vanier MT et al. Niemann-Pick disease type C and defective peroxisomal beta-oxidation of branched-chain substrates. J Inherit Metab Dis 1998;21:149-54.
    • (1998) J Inherit Metab Dis , vol.21 , pp. 149-154
    • Sequeira, J.S.1    Vellodi, A.2    Vanier, M.T.3
  • 48
    • 0027305869 scopus 로고
    • Niemann-Pick disease type C: Diagnosis and outcome in children, with particular reference to liver disease
    • Kelly DA, Portmann B, Mowat AP et al. Niemann-Pick disease type C: diagnosis and outcome in children, with particular reference to liver disease. J Pediatr 1993;123:242-7.
    • (1993) J Pediatr , vol.123 , pp. 242-247
    • Kelly, D.A.1    Portmann, B.2    Mowat, A.P.3
  • 49
    • 0028303784 scopus 로고
    • Evidence for defective primary bile acid secretion in children with progressive familial intrahepatic cholestasis (Byler disease)
    • Jacquemin E, Dumont M, Bernard O et al. Evidence for defective primary bile acid secretion in children with progressive familial intrahepatic cholestasis (Byler disease). Eur J Pediatr 1994;153:424-8.
    • (1994) Eur J Pediatr , vol.153 , pp. 424-428
    • Jacquemin, E.1    Dumont, M.2    Bernard, O.3
  • 50
    • 0031907132 scopus 로고    scopus 로고
    • A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis
    • Bull LN, van Eijk MJ, Pawlikowska L et al. A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis. Nat Genet 1998;18:219-24.
    • (1998) Nat Genet , vol.18 , pp. 219-224
    • Bull, L.N.1    Van Eijk, M.J.2    Pawlikowska, L.3
  • 51
    • 0033652101 scopus 로고    scopus 로고
    • A missense mutation in FIC1 is associated with Greenland familial cholestasis
    • Klomp LW, Bull LN, Knisely AS et al. A missense mutation in FIC1 is associated with Greenland familial cholestasis. Hepatology 2000;32:1337-41.
    • (2000) Hepatology , vol.32 , pp. 1337-1341
    • Klomp, L.W.1    Bull, L.N.2    Knisely, A.S.3
  • 52
    • 12644268207 scopus 로고    scopus 로고
    • Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC-1] and Byler syndrome): Evidence for heterogeneity
    • Bull LNCV, Stricker NL, Baharloo S et al. Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC-1] and Byler syndrome): evidence for heterogeneity. Hepatology 1997;26:155-64.
    • (1997) Hepatology , vol.26 , pp. 155-164
    • Bull, L.N.C.V.1    Stricker, N.L.2    Baharloo, S.3
  • 53
    • 0036186424 scopus 로고    scopus 로고
    • Benign recurrent intrahepatic cholestasis progressing to progressive familial intrahepatic cholestasis: Low GGT chotestasis is a clinical continuum
    • van Ooteghem NA, Klomp LW, van Berge-Henegouwen GP et al. Benign recurrent intrahepatic cholestasis progressing to progressive familial intrahepatic cholestasis: low GGT chotestasis is a clinical continuum. J Hepatol 2002;36:439-43.
    • (2002) J Hepatol , vol.36 , pp. 439-443
    • Van Ooteghem, N.A.1    Klomp, L.W.2    Van Berge-Henegouwen, G.P.3
  • 54
    • 0032711405 scopus 로고    scopus 로고
    • Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis
    • Jansen PL, Strautnieks SS, Jacquemin E et al. Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis. Gastroenterology 1999;117:1370-9.
    • (1999) Gastroenterology , vol.117 , pp. 1370-1379
    • Jansen, P.L.1    Strautnieks, S.S.2    Jacquemin, E.3
  • 55
    • 0036790453 scopus 로고    scopus 로고
    • The role of bile salt export pump mutations in progressive familiar intrahepatic chotestasis type II
    • Wang L, Soroka CJ, Boyer JL. The role of bile salt export pump mutations in progressive familiar intrahepatic chotestasis type II. J Clin Invest 2002;110:965-72.
    • (2002) J Clin Invest , vol.110 , pp. 965-972
    • Wang, L.1    Soroka, C.J.2    Boyer, J.L.3
  • 56
    • 0010572547 scopus 로고    scopus 로고
    • Mutations in the MDR3 gene are responsible for a subtype of progressive familial intrahepatic cholestasis (PFIC)
    • Jacquemin E, de Vree JML, Sturm E et al. Mutations in the MDR3 gene are responsible for a subtype of progressive familial intrahepatic cholestasis (PFIC) [abstr]. Hepatology 1997;26:248A.
    • (1997) Hepatology , vol.26
    • Jacquemin, E.1    De Vree, J.M.L.2    Sturm, E.3
  • 57
    • 0035045719 scopus 로고    scopus 로고
    • The wide spectrum of multidrug resistance 3 deficiency: From neonatal cholestasis to cirrhosis of adulthood
    • Jacquemin E, De Vree JM, Cresteil D et al. The wide spectrum of multidrug resistance 3 deficiency: from neonatal cholestasis to cirrhosis of adulthood. Gastroenterology 2001;120:1448-58.
    • (2001) Gastroenterology , vol.120 , pp. 1448-1458
    • Jacquemin, E.1    De Vree, J.M.2    Cresteil, D.3
  • 58
    • 0019521476 scopus 로고
    • Severe familial cholestasis in North American Indian children: A clinical model of microfilament dysfunction?
    • Weber AM, Tuchweber B, Yousef I et al. Severe familial cholestasis in North American Indian children: a clinical model of microfilament dysfunction? Gastroenterology 1981;81:653-62.
    • (1981) Gastroenterology , vol.81 , pp. 653-662
    • Weber, A.M.1    Tuchweber, B.2    Yousef, I.3
  • 59
    • 0033809652 scopus 로고    scopus 로고
    • North American Indian cirrhosis in children: A review of 30 cases
    • Drouin E, Russo P, Tuchweber B et al. North American Indian cirrhosis in children: a review of 30 cases. J Pediatr Gastroenterol Nutr 2000;31:395-404.
    • (2000) J Pediatr Gastroenterol Nutr , vol.31 , pp. 395-404
    • Drouin, E.1    Russo, P.2    Tuchweber, B.3
  • 60
    • 0036918537 scopus 로고    scopus 로고
    • A missense mutation (R565W) in cirhin (FLJ14728) in North American Indian childhood cirrhosis
    • Chagnon P, Michaud J, Mitchell G et al. A missense mutation (R565W) in cirhin (FLJ14728) in North American Indian childhood cirrhosis. Am J Hum Genet 2002;71:1443-9.
    • (2002) Am J Hum Genet , vol.71 , pp. 1443-1449
    • Chagnon, P.1    Michaud, J.2    Mitchell, G.3
  • 61
    • 0033795071 scopus 로고    scopus 로고
    • Mapping of the locus for cholestasis-lymphedema syndrome (Aagenaes syndrome) to a 6.6-cM interval on chromosome 15q
    • Bull LN, Roche E, Song EJ et al. Mapping of the locus for cholestasis-lymphedema syndrome (Aagenaes syndrome) to a 6.6-cM interval on chromosome 15q. Am J Hum Genet 2000;67:994-9.
    • (2000) Am J Hum Genet , vol.67 , pp. 994-999
    • Bull, L.N.1    Roche, E.2    Song, E.J.3
  • 62
    • 0033768556 scopus 로고    scopus 로고
    • Liver disease caused by disorders of bile acid synthesis
    • Bove KE. Liver disease caused by disorders of bile acid synthesis. Clin Liver Dis 2000;4:831-48.
    • (2000) Clin Liver Dis , vol.4 , pp. 831-848
    • Bove, K.E.1
  • 63
    • 0028942689 scopus 로고
    • Familial giant cell hepatitis with low bile acid concentration and increased urinary excretion of specific bile alcohols: A new inborn error of bile acid synthesis?
    • Clayton PT, Casteels M, Mieli-Vergani G et al. Familial giant cell hepatitis with low bile acid concentration and increased urinary excretion of specific bile alcohols: a new inborn error of bile acid synthesis? Pediatr Res 1995;37:424-31.
    • (1995) Pediatr Res , vol.37 , pp. 424-431
    • Clayton, P.T.1    Casteels, M.2    Mieli-Vergani, G.3
  • 64
    • 0032211865 scopus 로고    scopus 로고
    • Identification of a new inborn error in bile acid synthesis: Mutation of the oxysterol 7alpha-hydroxylase gene causes severe neonatal liver disease
    • Setchell KD, Schwarz M, O'Connell NC et al. Identification of a new inborn error in bile acid synthesis: mutation of the oxysterol 7alpha-hydroxylase gene causes severe neonatal liver disease. J Clin Invest 1998;102:1690-703.
    • (1998) J Clin Invest , vol.102 , pp. 1690-1703
    • Setchell, K.D.1    Schwarz, M.2    O'Connell, N.C.3
  • 65
    • 0037219301 scopus 로고    scopus 로고
    • Liver disease caused by failure to racemize trihydroxycholestanoic acid: Gene mutation and effect of bile acid therapy
    • Setchell KD, Heubi JE, Bove KE et al. Liver disease caused by failure to racemize trihydroxycholestanoic acid: gene mutation and effect of bile acid therapy. Gastroenterology 2003;124:217-32.
    • (2003) Gastroenterology , vol.124 , pp. 217-232
    • Setchell, K.D.1    Heubi, J.E.2    Bove, K.E.3
  • 66
    • 0032729864 scopus 로고    scopus 로고
    • Genotype-phenotype correlations in disorders of peroxisome biogenesis
    • Moser HW. Genotype-phenotype correlations in disorders of peroxisome biogenesis. Mol Genet Metab 1999;68:316-27.
    • (1999) Mol Genet Metab , vol.68 , pp. 316-327
    • Moser, H.W.1
  • 67
    • 0034255179 scopus 로고    scopus 로고
    • Peroxisome biogenesis disorders: Genetics and cell biology
    • Gould SJ, Valle D. Peroxisome biogenesis disorders: genetics and cell biology. Trends Genet 2000;16:340-5.
    • (2000) Trends Genet , vol.16 , pp. 340-345
    • Gould, S.J.1    Valle, D.2
  • 68
    • 0036103162 scopus 로고    scopus 로고
    • PEX1 mutations in complementation group 1 of Zellweger spectrum patients correlate with severity of disease
    • Preuss N, Brosius U, Biermanns M et al. PEX1 mutations in complementation group 1 of Zellweger spectrum patients correlate with severity of disease. Pediatr Res 2002;51:706-14.
    • (2002) Pediatr Res , vol.51 , pp. 706-714
    • Preuss, N.1    Brosius, U.2    Biermanns, M.3
  • 70
    • 0033912761 scopus 로고    scopus 로고
    • Neonatal hemochromatosis: The importance of early recognition of liver failure
    • Vohra P, Haller C, Emre S et al. Neonatal hemochromatosis: the importance of early recognition of liver failure. J Pediatr 2000;136:537-41.
    • (2000) J Pediatr , vol.136 , pp. 537-541
    • Vohra, P.1    Haller, C.2    Emre, S.3
  • 71
    • 0034845503 scopus 로고    scopus 로고
    • Classification and genetic features of neonatal haemochromatosis: A study of 27 affected pedigrees and molecular analysis of genes implicated in iron metabolism
    • Kelly AL, Lunt PW, Rodrigues F et al. Classification and genetic features of neonatal haemochromatosis: a study of 27 affected pedigrees and molecular analysis of genes implicated in iron metabolism. J Med Genet 2001;38:599-610.
    • (2001) J Med Genet , vol.38 , pp. 599-610
    • Kelly, A.L.1    Lunt, P.W.2    Rodrigues, F.3
  • 72
    • 0027723516 scopus 로고
    • Tissue iron and copper quantitation in perinatal hemochromatosis and other perinatal liver diseases. Comparison with a large perinatal control population, including cases with chronic liver disease
    • Silver MM, Valberg LS, Lines LD et al. Tissue iron and copper quantitation in perinatal hemochromatosis and other perinatal liver diseases. Comparison with a large perinatal control population, including cases with chronic liver disease. Am J Pathol 1993;143:1312-25.
    • (1993) Am J Pathol , vol.143 , pp. 1312-1325
    • Silver, M.M.1    Valberg, L.S.2    Lines, L.D.3
  • 73
    • 0037373702 scopus 로고    scopus 로고
    • Progress in treatment and outcome for children with neonatal haemochromatosis
    • Flynn DM, Mohan N, McKiernan P et al. Progress in treatment and outcome for children with neonatal haemochromatosis. Arch Dis Child Fetal Neonatal Ed 2003;88:F124-7.
    • (2003) Arch Dis Child Fetal Neonatal Ed , vol.88
    • Flynn, D.M.1    Mohan, N.2    McKiernan, P.3
  • 74
    • 0028351940 scopus 로고
    • Renal proximal tubular dysgenesis associated with severe neonatal hemosiderotic liver disease
    • Bale PM, Kan AE, Dorney SF. Renal proximal tubular dysgenesis associated with severe neonatal hemosiderotic liver disease. Pediatr Pathol 1994;14:479-89.
    • (1994) Pediatr Pathol , vol.14 , pp. 479-489
    • Bale, P.M.1    Kan, A.E.2    Dorney, S.F.3
  • 75
    • 0036431028 scopus 로고    scopus 로고
    • Infantile citrullinemia caused by citrin deficiency with increased dibasic amino acids
    • Ben-Shalom E, Kobayashi K, Shaag A et al. Infantile citrullinemia caused by citrin deficiency with increased dibasic amino acids. Mol Genet Metab 2002;77:202-8.
    • (2002) Mol Genet Metab , vol.77 , pp. 202-208
    • Ben-Shalom, E.1    Kobayashi, K.2    Shaag, A.3
  • 76
    • 0036299910 scopus 로고    scopus 로고
    • Mitochondrial aspartate glutamate carrier (citrin) deficiency as the cause of adult-onset type II citrullinemia (CTLN2) and idiopathic neonatal hepatitis (NICCD)
    • Saheki T, Kobayashi K. Mitochondrial aspartate glutamate carrier (citrin) deficiency as the cause of adult-onset type II citrullinemia (CTLN2) and idiopathic neonatal hepatitis (NICCD). J Hum Genet 2002;47:333-41.
    • (2002) J Hum Genet , vol.47 , pp. 333-341
    • Saheki, T.1    Kobayashi, K.2
  • 77
    • 0036460375 scopus 로고    scopus 로고
    • Neonatal intrahepatic cholestasis caused by citrin deficiency: Severe hepatic dysfunction in an infant requiring liver transplantation
    • Tamamori A, Okano Y, Ozaki H et al. Neonatal intrahepatic cholestasis caused by citrin deficiency: severe hepatic dysfunction in an infant requiring liver transplantation. Eur J Pediatr 2002;161:609-13.
    • (2002) Eur J Pediatr , vol.161 , pp. 609-613
    • Tamamori, A.1    Okano, Y.2    Ozaki, H.3
  • 78
    • 0029986408 scopus 로고    scopus 로고
    • Absence of the canalicular isoform of the MRP gene-encoded conjugate export pump from the hepatocytes in Dubin-Johnson syndrome
    • Kartenbeck J, Leuschner U, Mayer R et al. Absence of the canalicular isoform of the MRP gene-encoded conjugate export pump from the hepatocytes in Dubin-Johnson syndrome. Hepatology 1996;23:1061-6.
    • (1996) Hepatology , vol.23 , pp. 1061-1066
    • Kartenbeck, J.1    Leuschner, U.2    Mayer, R.3
  • 79
    • 0030994468 scopus 로고    scopus 로고
    • A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome
    • Paulusma CC, Kool M, Bosma PJ et al. A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome. Hepatology 1997;25:1539-42.
    • (1997) Hepatology , vol.25 , pp. 1539-1542
    • Paulusma, C.C.1    Kool, M.2    Bosma, P.J.3
  • 80
    • 0036830243 scopus 로고    scopus 로고
    • Trafficking and functional defects by mutations of the ATP-binding domains in MRP2 in patients with Dubin-Johnson syndrome
    • Hashimoto K, Uchiumi T, Konno T et al. Trafficking and functional defects by mutations of the ATP-binding domains in MRP2 in patients with Dubin-Johnson syndrome. Hepatology 2002;36:1236-45.
    • (2002) Hepatology , vol.36 , pp. 1236-1245
    • Hashimoto, K.1    Uchiumi, T.2    Konno, T.3
  • 81
    • 0037229540 scopus 로고    scopus 로고
    • A common Dubin-Johnson syndrome mutation impairs protein maturation and transport activity of MRP2 (ABCC2)
    • Keitel V, Nies AT, Brom M et al. A common Dubin-Johnson syndrome mutation impairs protein maturation and transport activity of MRP2 (ABCC2). Am J Physiol Gastrointest Liver Physiol 2003;284:G165-74.
    • (2003) Am J Physiol Gastrointest Liver Physiol , vol.284
    • Keitel, V.1    Nies, A.T.2    Brom, M.3
  • 82
    • 0036117708 scopus 로고    scopus 로고
    • Treatment of severe cholestasis in neonatal Dubin-Johnson syndrome with ursodeoxycholic acid
    • Regev RH, Stolar O, Raz A et al. Treatment of severe cholestasis in neonatal Dubin-Johnson syndrome with ursodeoxycholic acid. J Perinat Med 2002;30:185-7.
    • (2002) J Perinat Med , vol.30 , pp. 185-187
    • Regev, R.H.1    Stolar, O.2    Raz, A.3
  • 83
    • 0026315199 scopus 로고
    • Congenital structural abnormalities in biliary atresia: Evidence for etiopathogenic heterogeneity and therapeutic implications
    • Silveira TR, Salzano FM, Howard ER et al. Congenital structural abnormalities in biliary atresia: evidence for etiopathogenic heterogeneity and therapeutic implications. Acta Paediatr Scand 1991;80:1192-9.
    • (1991) Acta Paediatr Scand , vol.80 , pp. 1192-1199
    • Silveira, T.R.1    Salzano, F.M.2    Howard, E.R.3
  • 84
    • 0031812150 scopus 로고    scopus 로고
    • Down syndrome, transient myeloproliferative disorder, and infantile liver fibrosis
    • Schwab M, Niemeyer C, Schwarzer U. Down syndrome, transient myeloproliferative disorder, and infantile liver fibrosis. Med Pediatr Oncol 1998;31:159-65.
    • (1998) Med Pediatr Oncol , vol.31 , pp. 159-165
    • Schwab, M.1    Niemeyer, C.2    Schwarzer, U.3
  • 85
    • 0036153957 scopus 로고    scopus 로고
    • Incidence and treatment of potentially lethal diseases in transient leukemia of Down syndrome: Pediatric Oncology Group Study
    • Al-Kasim F, Doyle JJ, Massey GV et al. Incidence and treatment of potentially lethal diseases in transient leukemia of Down syndrome: Pediatric Oncology Group Study. J Pediatr Hematol Oncol 2002;24:9-13.
    • (2002) J Pediatr Hematol Oncol , vol.24 , pp. 9-13
    • Al-Kasim, F.1    Doyle, J.J.2    Massey, G.V.3
  • 87
    • 0036363045 scopus 로고    scopus 로고
    • Hepatobiliary disease in neonatal lupus: Prevalence and clinical characteristics in cases enrolled in a national registry
    • Lee LA, Sokol RJ, Buyon JP. Hepatobiliary disease in neonatal lupus: prevalence and clinical characteristics in cases enrolled in a national registry. Pediatrics 2002;109:E11.
    • (2002) Pediatrics , vol.109
    • Lee, L.A.1    Sokol, R.J.2    Buyon, J.P.3
  • 88
    • 0031932806 scopus 로고    scopus 로고
    • A case of severe neonatal lupus erythematosus without cardiac or cutaneous involvement
    • Selander B, Cedergren S, Domanski H. A case of severe neonatal lupus erythematosus without cardiac or cutaneous involvement. Acta Paediatr 1998;87:105-7.
    • (1998) Acta Paediatr , vol.87 , pp. 105-107
    • Selander, B.1    Cedergren, S.2    Domanski, H.3
  • 89
    • 0026632774 scopus 로고
    • Fate of infants with neonatal hepatitis: Pediatric surgeons dilemma
    • Suita S, Arima T, Ishii K et al. Fate of infants with neonatal hepatitis: pediatric surgeons dilemma. J Pediatr Surg 1992;27:696-9.
    • (1992) J Pediatr Surg , vol.27 , pp. 696-699
    • Suita, S.1    Arima, T.2    Ishii, K.3
  • 90
    • 0024327345 scopus 로고
    • Resting energy expenditure in infants and children with extrahepatic biliary atresia
    • Pierro A, Koletzko B, Carnielli V et al. Resting energy expenditure in infants and children with extrahepatic biliary atresia. J Pediatr Surg 1989;24:534-8.
    • (1989) J Pediatr Surg , vol.24 , pp. 534-538
    • Pierro, A.1    Koletzko, B.2    Carnielli, V.3
  • 91
    • 0027202803 scopus 로고
    • Effect of rifampin in the treatment of pruritus in hepatic cholestasis
    • Gregorio GV, Batt CS, Mowat AP et al. Effect of rifampin in the treatment of pruritus in hepatic cholestasis. Arch Dis Child 1993;69:141-3.
    • (1993) Arch Dis Child , vol.69 , pp. 141-143
    • Gregorio, G.V.1    Batt, C.S.2    Mowat, A.P.3
  • 92
    • 0036614010 scopus 로고    scopus 로고
    • Partial external biliary diversion for intractable pruritus and xanthomas in Alagille syndrome
    • Emerick KM, Whitington PF. Partial external biliary diversion for intractable pruritus and xanthomas in Alagille syndrome. Hepatology 2002;35:1501-6.
    • (2002) Hepatology , vol.35 , pp. 1501-1506
    • Emerick, K.M.1    Whitington, P.F.2


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