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Hereditary Coproporphyria

Known as: CPO DEFICIENCY, hereditary coproporphyria porphyria, Coproporphyrinogen Oxidase Deficiency 
An autosomal dominant porphyria that is due to a deficiency of COPROPORPHYRINOGEN OXIDASE in the LIVER, the sixth enzyme in the 8-enzyme biosynthetic… 
National Institutes of Health

Papers overview

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Review
2014
Review
2014
OBJECTIVE We report a successful treatment with lamotrigine of a patient with hereditary coproporphyria presenting with affective… 
2010
2010
Objective:  Pain physicians should also be aware of rare complications that can occur after intrathecal pump (ITP) placement. One… 
2002
2002
BACKGROUND Dual porphyrias are characterized by two independent disturbances of porphyrin metabolism. PATIENT AND METHODS At… 
2002
2002
The response of magnetization to magnetic field was studied in permalloy film on Mo(0 0 1) stepped surface grown by molecular… 
1990
1990
We report self-consistent surface electronic-structure calculations for metals across the lanthanide series. We have used the… 
1987
1987
An appendectomy operation was undertaken in a 29-year-old patient with signs of an acute crisis of hereditary coproporphyria… 
1981
1981
Chlorinated bisphenol antibacterial and antifungal agents are potent inhibitors of torula yeast glucose-6-phosphate dehydrogenase… 
1978
1978
The genetically transmitted hepatic porphyrias are inborn errors of porphyrin and heme biosynthesis. The group includes… 
1970
1970
SYMPTOMS of acute intermittent porphyria may be associated with three forms of hepatic porphyria: acute intermittent, variegate…