STUDIES IN PORPHYRIA .5. DRUG OXIDATION RATES IN HEREDITARY HEPATIC PORPHYRIA

被引:0
|
作者
ANDERSON, KE [1 ]
ALVARES, AP [1 ]
SASSA, S [1 ]
KAPPAS, A [1 ]
机构
[1] ROCKEFELLER UNIV,NEW YORK,NY 10021
关键词
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
引用
收藏
页码:47 / 54
页数:8
相关论文
共 50 条
  • [31] Hepatocellular Carcinoma in Acute Hepatic Porphyria: A Meta-Analysis of Observational Studies
    Singal, Ashwani K.
    Reddy, Rewanth K.
    Gudiwada, Mohan C.
    Jasti, Jaswant J.
    Anderson, Karl E.
    DIGESTIVE DISEASES AND SCIENCES, 2024, 69 (11) : 4268 - 4274
  • [32] ENHANCED BRAIN 5-HYDROXYTRYPTAMINE (5-HT) TURNOVER IN RATS WITH HEPATIC PORPHYRIA
    LITMAN, DA
    CORREIA, MA
    FEDERATION PROCEEDINGS, 1983, 42 (03) : 370 - 370
  • [33] STUDIES IN PORPHYRIA .2. EVIDENCE FOR A DEFICIENCY OF STEROID DELTA-4-5-ALPHA-REDUCTASE ACTIVITY IN ACUTE INTERMITTENT PORPHYRIA
    BRADLOW, HL
    GILLETTE, PN
    GALLAGHER, TF
    KAPPAS, A
    JOURNAL OF EXPERIMENTAL MEDICINE, 1973, 138 (04): : 754 - 763
  • [34] UROPORPHYRINOGEN DECARBOXYLASE IN ERYTHROCYTES - STUDIES ON PRIMARY GENETIC ENZYME DEFECT IN CHRONIC HEPATIC PORPHYRIA
    TIEPERMANN, RV
    DOSS, M
    JOURNAL OF CLINICAL CHEMISTRY AND CLINICAL BIOCHEMISTRY, 1978, 16 (09): : 513 - 517
  • [35] ACTIVITY OF HEPATIC 5-AMINOLEVULINATE SYNTHASE DURING EXPERIMENTAL PORPHYRIA AND MITOCHONDRIAL BIOGENESIS
    BEATTIE, DS
    PATTON, GM
    HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1973, 354 (08): : 855 - 855
  • [36] HEREDITARY HEPATIC PORPHYRIA WITH DELTA-AMINOLEVULINATE DEHYDRASE DEFICIENCY - IMMUNOLOGICAL CHARACTERIZATION OF THE NON-CATALYTIC ENZYME
    DEVERNEUIL, H
    DOSS, M
    BRUSCO, N
    BEAUMONT, C
    NORDMANN, Y
    HUMAN GENETICS, 1985, 69 (02) : 174 - 177
  • [37] 5-Aminolevulinate Dehydratase Porphyria (ADP): Evidence for Hepatic ALAS1 Induction
    Gou, Eric
    Chan, Amy
    Simon, Amy
    Querbes, William
    Anderson, Karl E.
    HEPATOLOGY, 2017, 66 : 441A - 442A
  • [38] Secondary coproporphyrinuria in a patient with the full clinical picture of a hereditary acute hepatic porphyria. A misleading clinical and biochemical course
    Oberndorfer, S
    Hitzenberger, P
    Gruber, W
    Seidel, J
    Urbanits, S
    Doss, M
    Grisold, W
    JOURNAL OF NEUROLOGY, 2002, 249 (09) : 1325 - 1326
  • [39] STUDIES IN PORPHYRIA .8. RELATIONSHIP OF THE 5-ALPHA-REDUCTIVE METABOLISM OF STEROID-HORMONES TO CLINICAL EXPRESSION OF THE GENETIC DEFECT IN ACUTE INTERMITTENT PORPHYRIA
    ANDERSON, KE
    BRADLOW, HL
    SASSA, S
    KAPPAS, A
    AMERICAN JOURNAL OF MEDICINE, 1979, 66 (04): : 644 - 650
  • [40] HEPATIC HEME METABOLISM IN PORPHYRIA-CUTANEA-TARDA (PCT) - ENZYMATIC STUDIES AND THEIR RELATION TO LIVER ULTRASTRUCTURE
    BLEKKENHORST, GH
    PIMSTONE, NR
    WEBBER, BL
    EALES, L
    ANNALS OF CLINICAL RESEARCH, 1976, 8 : 108 - 121