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Volumn 21, Issue 3, 1998, Pages 186-190

Alterations of hepatic peroxisomes in tyrosinaemia type I: Return to fetal type?

Author keywords

[No Author keywords available]

Indexed keywords

TYROSINE;

EID: 0031879412     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005351129336     Document Type: Conference Paper
Times cited : (5)

References (9)
  • 1
    • 0029584743 scopus 로고
    • Secondary alterations of human hepatocellular peroxisomes
    • Roels F, De Bie S, Schutgens RBH, Besley GTN, eds. Diagnosis of Human Peroxisomal Diseases. A Handbook
    • De Craemer D (1995) Secondary alterations of human hepatocellular peroxisomes. In Roels F, De Bie S, Schutgens RBH, Besley GTN, eds. Diagnosis of Human Peroxisomal Diseases. A Handbook. J Inker Metab Dis 18 (supplement 1): 181-213.
    • (1995) J Inker Metab Dis , vol.18 , Issue.1 SUPPL. , pp. 181-213
    • De Craemer, D.1
  • 5
    • 0029613813 scopus 로고
    • Practical guide for morphometry of human peroxisomes on electron micrographs
    • Roels F, De Bie S, Schutgens RBH, Besley GTN, eds. Diagnosis of Human Peroxisomal Diseases. A Handbook
    • Kerckaert I, De Craemer D, Van Limbergen G (1995) Practical guide for morphometry of human peroxisomes on electron micrographs. In Roels F, De Bie S, Schutgens RBH, Besley GTN, eds. Diagnosis of Human Peroxisomal Diseases. A Handbook. J Inher Metab Dis 18 (supplement 1): 172-180.
    • (1995) J Inher Metab Dis , vol.18 , Issue.1 SUPPL. , pp. 172-180
    • Kerckaert, I.1    De Craemer, D.2    Van Limbergen, G.3
  • 7
    • 0029618344 scopus 로고
    • Liver and chorion cytochemistry
    • Roels F, De Bie S, Schutgens RBH, Besley GTN, eds. Diagnosis of Human Peroxisomal Diseases. A Handbook
    • Roels F, De Prest B, De Pestel G (1995) Liver and chorion cytochemistry. In Roels F, De Bie S, Schutgens RBH, Besley GTN, eds. Diagnosis of Human Peroxisomal Diseases. A Handbook. J Inher Metab Dis 18 (supplement 1): 155-171.
    • (1995) J Inher Metab Dis , vol.18 , Issue.1 SUPPL. , pp. 155-171
    • Roels, F.1    De Prest, B.2    De Pestel, G.3
  • 9
    • 84920314492 scopus 로고    scopus 로고
    • Hereditary tyrosinaemia type I: An ultrastructural study of 7 patients treated with NTBC
    • Remotti H, Samuelsson BM, Hjalmarsson O, Holme E, Conradi N (1997) Hereditary tyrosinaemia type I: an ultrastructural study of 7 patients treated with NTBC. J Inher Metab Dis 20 (supplement 1): 14.
    • (1997) J Inher Metab Dis , vol.20 , Issue.1 SUPPL. , pp. 14
    • Remotti, H.1    Samuelsson, B.M.2    Hjalmarsson, O.3    Holme, E.4    Conradi, N.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.