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DF Bishop, S Clavero, N Mohandas… - Molecular medicine ( …, 2011 - ncbi.nlm.nih.gov
Congenital erythropoietic porphyria (CEP) is an autosomal recessive disorder due to the deficient
activity of uroporphyrinogen III synthase (UROS). Knock-in mouse models were generated for
the common, hematologically severe human genotype, C73R/C73R, and milder ...
JK Dowman, BK Gunson, DF Mirza… - Liver …, 2011 - Wiley Online Library
Page 1. 1 LT-11-056 Liver transplantation for acute intermittent porphyria is complicated by a
high rate of hepatic artery thrombosis ... Abbreviations AIP acute intermittent porphyria ALA
5-aminolaevulinic acid HAT hepatic artery thrombosis LT liver transplantation ...
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JA Emamaullee, A Thiesen… - Journal of …, 2011 - Wiley Online Library
A 61-year-old woman was investigated because of an episode of pain in the right upper quadrant
of her abdomen that radiated into the mid-back. Her past history included a cholecystectomy
and hysterectomy and, 11 years previously, she had an episode of blistering on her ...
All 3 versions
[HTML] from nih.govJK Wickliffe, SZ Abdel-Rahman, C Lee… - Molecular …, 2011 - ncbi.nlm.nih.gov
Porphyria cutanea tarda (PCT) is a cutaneous porphyria with sporadic (type 1) and familial (type
2) subtypes, both resulting from decreased hepatic uroporphyrinogen decarboxylase
(UROD) activity. Environmental and genetic factors are involved in the development of ...
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JK Dowman, BK Gunson, S Bramhall… - Annals of internal …, 2011 - Am Coll Physicians
TO THE EDITOR: In their recent article on the cost-effectiveness of dabigatran versus
warfarin, Freeman and colleagues (1) did not ac- count for some of the highest costs associated
with warfarin admin- istration. Each time that prothrombin time is measured, the logistics ...
Related articles - All 3 versions

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