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A Cantafora

Showing results (101-110 of 105) with videos related to

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Human Mutation|May 25, 1999
Rapid screening of the LDL receptor point mutation FH-Genoa/Palermo. Mutation in brief no. 238. OnlineG Marino, S Travali, T Reyes, et al.
Journal of Internal Medicine|November 21, 2008
Severe HDL deficiency due to novel defects in the ABCA1 transporterL Pisciotta, L Bocchi, C Candini, et al.
Gastroenterology|April 28, 2000
Impaired human gallbladder lipid absorption in cholesterol gallstone disease and its effect on cholesterol solubility in bileS G Corradini, W Elisei, L Giovannelli, et al.
Hepatology (Baltimore, Md.)|August 8, 1998
The human gallbladder increases cholesterol solubility in bile by differential lipid absorption: a study using a new in vitro model of isolated intra-arterially perfused gallbladderS Ginanni Corradini, C Ripani, P Della Guardia, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 9, 2000
Clinical expression of familial hypercholesterolemia in clusters of mutations of the LDL receptor gene that cause a receptor-defective or receptor-negative phenotypeS Bertolini, A Cantafora, M Averna, et al.
Pageof 11

Showing results (101-110 of 105) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 105 results.
Human Mutation|May 25, 1999
Rapid screening of the LDL receptor point mutation FH-Genoa/Palermo. Mutation in brief no. 238. OnlineG Marino, S Travali, T Reyes, et al.
Journal of Internal Medicine|November 21, 2008
Severe HDL deficiency due to novel defects in the ABCA1 transporterL Pisciotta, L Bocchi, C Candini, et al.
Gastroenterology|April 28, 2000
Impaired human gallbladder lipid absorption in cholesterol gallstone disease and its effect on cholesterol solubility in bileS G Corradini, W Elisei, L Giovannelli, et al.
Hepatology (Baltimore, Md.)|August 8, 1998
The human gallbladder increases cholesterol solubility in bile by differential lipid absorption: a study using a new in vitro model of isolated intra-arterially perfused gallbladderS Ginanni Corradini, C Ripani, P Della Guardia, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 9, 2000
Clinical expression of familial hypercholesterolemia in clusters of mutations of the LDL receptor gene that cause a receptor-defective or receptor-negative phenotypeS Bertolini, A Cantafora, M Averna, et al.
Pageof 11