N. O'connell

发表

Additive hypocholesterolemic effect of psyllium and cholestyramine in the hamster: influence on fecal sterol and bile acid profiles.

K. Setchell, B. Daggy, N. O'connell, 1997, Journal of lipid research.

Serum Unconjugated Bile Acids as a Test for Intestinal Bacterial Overgrowth in Dogs

K. Setchell, T. Melgarejo, D. Williams, 2000, Digestive Diseases and Sciences.

Differences in the metabolism and disposition of ursodeoxycholic acid and of its taurine‐conjugated species in patients with primary biliary cirrhosis

A. Larghi, P. Invernizzi, P. Battezzati, 1999, Hepatology.

Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC‐1] and Byler syndrome): Evidence for heterogeneity

N. Freimer, V. Carlton, K. Setchell, 1997, Hepatology.

Effect of psyllium in hypercholesterolemia at two monounsaturated fatty acid intakes.

P. Corey, T. Wolever, V. Fulgoni, 1997, The American journal of clinical nutrition.

delta 22-Ursodeoxycholic acid, a unique metabolite of administered ursodeoxycholic acid in rats, indicating partial beta-oxidation as a major pathway for bile acid metabolism.

K. Setchell, B. Kren, C. Rodrigues, 1995, Biochemistry.

A new cause of progressive intrahepatic cholestasis: 3 beta-hydroxy-C27-steroid dehydrogenase/isomerase deficiency.

K. Setchell, G. Maggiore, M. Hadchouel, 1994, The Journal of pediatrics.

Liver disease caused by failure to racemize trihydroxycholestanoic acid: gene mutation and effect of bile acid therapy.

A. Moser, K. Setchell, Robert H. Squires, 2003, Gastroenterology.

Endogenous ursodeoxycholic acid and cholic acid in liver disease due to cystic fibrosis

K. Setchell, P. Lewindon, Jeffery L. Smith, 2004, Hepatology.

Identification of a new inborn error in bile acid synthesis: mutation of the oxysterol 7alpha-hydroxylase gene causes severe neonatal liver disease.

R. Lathe, D. Russell, K. Setchell, 1998, The Journal of clinical investigation.

Genetic defects in bile acid conjugation cause fat-soluble vitamin deficiency.

P. Rosenthal, D. Russell, Sohela Shah, 2013, Gastroenterology.

Ileal resection/dysfunction in childhood predisposes to lithogenic bile only after puberty.

K. Setchell, J. Heubi, N. O'connell, 1992, Gastroenterology.

Bile acid conjugation in early stage cholestatic liver disease before and during treatment with ursodeoxycholic acid.

G. Galatola, K. Setchell, A. Hofmann, 1996, Clinica chimica acta; international journal of clinical chemistry.

A new amino acid derivative of ursodeoxycholate, (N-L-Glutamyl)-UDCA (UDCA-Glu), to selectively release UDCA in the colon.

K. Setchell, C. Clerici, R. Pellicciari, 2009, Anticancer research.

3α-6α-Dihydroxy-7α-fluoro-5β-cholanoate (UPF-680), physicochemical and physiological properties of a new fluorinated bile acid that prevents 17α-ethynyl-estradiol-induced cholestasis in rats

K. Setchell, C. Clerici, A. Morelli, 2006 .

Tryptophan intake influences infants' sleep latency.

L. Birch, L. Steinberg, M. Picciano, 1992, The Journal of nutrition.

Effect of ursodeoxycholic acid on hypertransaminasaemia and bile acid composition in patients undergoing bone marrow transplantation--a double-blind randomized control study.

M. Martelli, F. Aversa, K. Setchell, 1996, The Italian journal of gastroenterology.

Influence of Breast Feeding, and Adapted and Hydrolyzed Formulas on Biliary Bile Acids in Newborn Guinea Pigs

K. Setchell, C. Colombo, A. Marini, 2003, Neonatology.

Edinburgh Research Explorer Identification of a new inborn error in bile acid synthesis: Mutation of the oxysterol 7 alpha-hydroxylase gene causes severe neonatal liver disease

M. Schwarz, D. L. Davis, K. Setchell, 2018 .