IMMUNOREACTIVE UROPORPHYRINOGEN DECARBOXYLASE IN THE LIVER IN PORPHYRIA CUTANEA TARDA

The Lancet

Volumn 326, Issue 8449, 1985, Pages 229-233

  Elder, GeorgeH ^a,b   De Salamanca, RafaelE ^a,b   Urquhart, AndrewJ ^a,b   Munoz, JuanJ ^a,b   Bonkovsky, HerbertL ^a,b  

^a CARDIFF UNIVERSITY   (United Kingdom)

^b VA MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

UROPORPHYRINOGEN DECARBOXYLASE;

CASE REPORT; FAMILIAL DISEASE; HUMAN; LIVER; PORPHYRIA CUTANEA TARDA; PRIORITY JOURNAL;

EID: 84920238259     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(85)90287-9     Document Type: Article

References (25)

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3. Decreased activity of hepatic uroporphyrinogen decarboxylase in sporadic porphyria cutanea tarda
4. Hereditary and non-hereditary form of chronic hepatic porphyria: Different behaviour of uroporphyrinogen decarboxylase in liver and erythrocytes
5. Decreased hepatic uroporphyrinogen decarboxylase activity in porphyria cutanea tarda
6. Familial and sporadic porphyria cutanea tarda: Two different diseases
7. Identification of two types of porphyria cutanea tarda by measurement of erythrocyte uroporphyrinogen decarboxylase
8. Porphyria cutanea tarda in South Africa. Metabolic basis of disordered haem biosynthesis
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19. Human uroporphyrinogen decarboxylase. Do tissue-specific isoenzymes exist ?
20. Quantative and Qualitative porphyrin excretion in normal subjects
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25. Assignment of the gene for uroporphyrinogen decarboxylase to human chromosome 1 by somatic cell hybridization and specific enzyme immunoassay.