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 ... Related articles - All 2 versions
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 ... Related articles - All 4 versions
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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