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Hepatic porphyrias current concepts
Postgraduate Medicine, 1977Acute intermittent porphyria, variegate porphyria, and hereditary coproporphyria are hepatic porphyrias due to enzyme defects that are inherited as autosomal dominants. Porphyria cutanea tarda is considered an acquired disorder. Similar drugs or circumstances are precipitants of acute attacks in all three inherited hepatic porphyrias.
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Drugs and the Hepatic Porphyrias
Clinics in Haematology, 1980A G, Smith, F, De Matteis
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Fortschritte der Medizin, 1978
Among the different types of hepatic porphyrias, acute intermittent porphyria (AIP) and the group of chronic hepatic porphyrias (CHP) are most frequently seen in Europe. Both diseases are supposed to be inherited, but clinical manifestation mostly occurs following endogenous and especially exogenous stimulation. While recurrent attacks of abdominal and
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Among the different types of hepatic porphyrias, acute intermittent porphyria (AIP) and the group of chronic hepatic porphyrias (CHP) are most frequently seen in Europe. Both diseases are supposed to be inherited, but clinical manifestation mostly occurs following endogenous and especially exogenous stimulation. While recurrent attacks of abdominal and
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A Membrane-Bound Diacylglycerol Species Induces PKCϵ-Mediated Hepatic Insulin Resistance
Cell Metabolism, 2020Kun Lyu, Dongyan Zhang, Mario Kahn
exaly
Defects in a liver-bone axis contribute to hepatic osteodystrophy disease progression
Cell Metabolism, 2022Jing Wu, Xiang Lu, Yi Cao
exaly
Targeted delivery of hyaluronic acid nanomicelles to hepatic stellate cells in hepatic fibrosis rats
Acta Pharmaceutica Sinica B, 2020Yao Fu, Tijia Chen, Zhirong Zhang
exaly
Surgical therapy of hepatic colorectal metastasis
Ca-A Cancer Journal for Clinicians, 1999Yuman Fong
exaly