Hereditary coproporphyria in Germany: Clinical-biochemical studies in 53 patients

Clinical Biochemistry

Volumn 33, Issue 6, 2000, Pages 465-473

  Kühnel, Alexandra ^a   Gross, Ulrich ^a   Doss, Manfred O ^a,b  

^a UNIVERSITY HOSPITAL MARBURG   (Germany)

^b PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

Acute hepatic porphyria; Coproporphyrinogen oxidase; Fecal isomer ratio; Heme arginate; Hereditary coproporphyria; Neurologic manifestation

Indexed keywords

COPROPORPHYRIN;

ABDOMINAL PAIN; ADOLESCENT; ADULT; AGED; ARTICLE; CARDIOVASCULAR DISEASE; CLINICAL ARTICLE; FEMALE; GERMANY; HEPATIC PORPHYRIA; HUMAN; MALE; MENTAL DISEASE; NEUROLOGIC DISEASE; PORPHYRIA; PRIORITY JOURNAL; SCHOOL CHILD; SKIN DISEASE; URINE LEVEL;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; AMINOLEVULINIC ACID; ARGININE; CHILD; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; COPROPORPHYRINOGEN OXIDASE; COPROPORPHYRINS; FECES; FEMALE; GERMANY; HEME; HETEROZYGOTE; HUMANS; ISOMERISM; MALE; MIDDLE AGED; PORPHOBILINOGEN; PORPHYRIAS, HEPATIC; UROPORPHYRINS;

EID: 0033741406     PISSN: 00099120     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0009-9120(00)00159-4     Document Type: Article

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