메뉴 건너뛰기




Volumn 16, Issue 9, 2010, Pages 1049-1053

Recurrent liver failure in a 25-year-old female

Author keywords

[No Author keywords available]

Indexed keywords

ARGININOSUCCINATE SYNTHASE; COTRIMOXAZOLE; QUETIAPINE; UREA;

EID: 77956922117     PISSN: 15276465     EISSN: 15276473     Source Type: Journal    
DOI: 10.1002/lt.22118     Document Type: Article
Times cited : (22)

References (26)
  • 1
    • 0022504127 scopus 로고
    • Fulminant and sub-fulminant liver failure: Definitions and causes
    • Bernuau J, Rueff B, Benhamou JP. Fulminant and sub-fulminant liver failure: definitions and causes. Semin Liver Dis 1986;6:97-106.
    • (1986) Semin Liver Dis , vol.6 , pp. 97-106
    • Bernuau, J.1    Rueff, B.2    Benhamou, J.P.3
  • 2
    • 0034024049 scopus 로고    scopus 로고
    • Acute liver failure: Clinical features, outcome analysis, and applicability of prognostic criteria
    • Shakil AO, Kramer D, Mazariegos GV, Fung JJ, Rakela J. Acute liver failure: clinical features, outcome analysis, and applicability of prognostic criteria. Liver Transpl 2000;6:163-169.
    • (2000) Liver Transpl , vol.6 , pp. 163-169
    • Shakil, A.O.1    Kramer, D.2    Mazariegos, G.V.3    Fung, J.J.4    Rakela, J.5
  • 3
    • 0037126649 scopus 로고    scopus 로고
    • Results of a prospective study of acute liver failure at 17 tertiary care centers in the United States
    • Ostapowicz G, Fontana RJ, Schiødt FV, Larson A, Davern TJ, Han SH, et al. Results of a prospective study of acute liver failure at 17 tertiary care centers in the United States. Ann Intern Med 2002;137:947-954.
    • (2002) Ann Intern Med , vol.137 , pp. 947-954
    • Ostapowicz, G.1    Fontana, R.J.2    Schiødt, F.V.3    Larson, A.4    Davern, T.J.5    Han, S.H.6
  • 6
    • 0025335712 scopus 로고
    • Heterogeneity of mutations in argininosuccinate synthetase causing human citrullinemia
    • Kobayashi K, Jackson MJ, Tick DB, O'Brien WE, Beaudet AL. Heterogeneity of mutations in argininosuccinate synthetase causing human citrullinemia. J Biol Chem 1990;265:11361-11367.
    • (1990) J Biol Chem , vol.265 , pp. 11361-11367
    • Kobayashi, K.1    Jackson, M.J.2    Tick, D.B.3    O'Brien, W.E.4    Beaudet, A.L.5
  • 7
    • 0028019772 scopus 로고
    • Mutations in argininosuccinate synthetase mRNA of Japanese patients, causing classical citrullinemia
    • Kobayashi K, Shaheen N, Terazono H, Saheki T. Mutations in argininosuccinate synthetase mRNA of Japanese patients, causing classical citrullinemia. Am J Hum Genet 1994;55:1103-1112.
    • (1994) Am J Hum Genet , vol.55 , pp. 1103-1112
    • Kobayashi, K.1    Shaheen, N.2    Terazono, H.3    Saheki, T.4
  • 8
    • 0033037729 scopus 로고    scopus 로고
    • The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein
    • Kobayashi K, Sinasac DS, Iijima M, Boright AP, Begum L, Lee JR, et al. The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein. Nat Genet 1999;22:159-163.
    • (1999) Nat Genet , vol.22 , pp. 159-163
    • Kobayashi, K.1    Sinasac, D.S.2    Iijima, M.3    Boright, A.P.4    Begum, L.5    Lee, J.R.6
  • 10
    • 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;47:333-341.
    • (2002) J Hum Genet , vol.47 , pp. 333-341
    • Saheki, T.1    Kobayashi, K.2
  • 12
    • 75149172953 scopus 로고    scopus 로고
    • Ornithine transcarbamoylase deficiency presenting with acute liver failure
    • Mustafa A, Clarke JT. Ornithine transcarbamoylase deficiency presenting with acute liver failure. J Inherit Metab Dis 2006;29:586.
    • (2006) J Inherit Metab Dis , vol.29 , pp. 586
    • Mustafa, A.1    Clarke, J.T.2
  • 16
    • 0031646276 scopus 로고    scopus 로고
    • The phenotype of ostensibly healthy women who are carriers for ornithine transcarbamylase deficiency
    • (Baltimore)
    • Maestri NE, Lord C, Glynn M, Bale A, Brusilow SW. The phenotype of ostensibly healthy women who are carriers for ornithine transcarbamylase deficiency. Medicine (Baltimore) 1998;77:389-397.
    • (1998) Medicine , vol.77 , pp. 389-397
    • Maestri, N.E.1    Lord, C.2    Glynn, M.3    Bale, A.4    Brusilow, S.W.5
  • 17
    • 0025296601 scopus 로고
    • Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus. A cause of postpartum coma
    • Arn PH, Hauser ER, Thomas GH, Herman G, Hess D, Brusilow SW. Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus. A cause of postpartum coma. N Engl J Med 1990;322:1652-1655.
    • (1990) N Engl J Med , vol.322 , pp. 1652-1655
    • Arn, P.H.1    Hauser, E.R.2    Thomas, G.H.3    Herman, G.4    Hess, D.5    Brusilow, S.W.6
  • 18
    • 56049119171 scopus 로고    scopus 로고
    • The role of molecular testing and enzyme analysis in the management of hypomorphic citrullinemia
    • Dimmock DP, Trapane P, Feigenbaum A, Keegan CE, Cederbaum S, Gibson J, et al. The role of molecular testing and enzyme analysis in the management of hypomorphic citrullinemia. Am J Med Genet A 2008;146A:2885-2890.
    • (2008) Am J Med Genet A , vol.146 A , pp. 2885-2890
    • Dimmock, D.P.1    Trapane, P.2    Feigenbaum, A.3    Keegan, C.E.4    Cederbaum, S.5    Gibson, J.6
  • 19
    • 0026085434 scopus 로고
    • Recurrent acute fatty liver of pregnancy associated with a fatty-acid oxidation defect in the offspring
    • Schoeman MN, Batey RG, Wilcken B. Recurrent acute fatty liver of pregnancy associated with a fatty-acid oxidation defect in the offspring. Gastroenterology 1991;100:544-548.
    • (1991) Gastroenterology , vol.100 , pp. 544-548
    • Schoeman, M.N.1    Batey, R.G.2    Wilcken, B.3
  • 21
    • 0022568610 scopus 로고
    • Dangers of non-compliance in Wilson's disease
    • Walshe JM, Dixon AK. Dangers of non-compliance in Wilson's disease. Lancet 1986;1:845-847.
    • (1986) Lancet , vol.1 , pp. 845-847
    • Walshe, J.M.1    Dixon, A.K.2
  • 23
    • 66149190943 scopus 로고    scopus 로고
    • Reactivation of hepatitis B
    • Hoofnagle JH. Reactivation of hepatitis B. Hepatology 2009;49(suppl):S156-S165.
    • (2009) Hepatology , vol.49 , Issue.SUPPL.
    • Hoofnagle, J.H.1
  • 25
    • 77956895077 scopus 로고    scopus 로고
    • Recurrent acute hepatic dysfunction in severe anorexia nervosa
    • doi:10.1002/eat.20775
    • Dowman J, Arulraj R, Chesner I. Recurrent acute hepatic dysfunction in severe anorexia nervosa. Int J Eat Disord; doi:10.1002/eat.20775.
    • Int J Eat Disord
    • Dowman, J.1    Arulraj, R.2    Chesner, I.3
  • 26
    • 69149097823 scopus 로고    scopus 로고
    • Fulminant liver failure after vancomycin in a sulfasalazine-induced DRESS syndrome: Fatal recurrence after liver transplantation
    • Mennicke M, Zawodniak A, Keller M, Wilkens L, Yawalkar N, Stickel F, et al. Fulminant liver failure after vancomycin in a sulfasalazine-induced DRESS syndrome: fatal recurrence after liver transplantation. Am J Transplant 2009;9:2197-2202.
    • (2009) Am J Transplant , vol.9 , pp. 2197-2202
    • Mennicke, M.1    Zawodniak, A.2    Keller, M.3    Wilkens, L.4    Yawalkar, N.5    Stickel, F.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.