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X Chromosome Contribution to the Genetic Architecture of Primary Biliary Cholangitis.
Asselta R, Paraboschi EM, Gerussi A, Cordell HJ, Mells GF, Sandford RN, Jones DE, Nakamura M, Ueno K, Hitomi Y, Kawashima M, Nishida N, Tokunaga K, Nagasaki M, Tanaka A, Tang R, Li Z, Shi Y, Liu X, Xiong M, Hirschfield G, Siminovitch KA; Canadian-US PBC Consortium; Italian PBC Genetics Study Group; UK-PBC Consortium; Japan PBC-GWAS Consortium; Carbone M, Cardamone G, Duga S, Gershwin ME, Seldin MF, Invernizzi P. Asselta R, et al. Among authors: invernizzi p. Gastroenterology. 2021 Jun;160(7):2483-2495.e26. doi: 10.1053/j.gastro.2021.02.061. Epub 2021 Mar 4. Gastroenterology. 2021. PMID: 33675743 Free PMC article.
Ursodeoxycholic acid therapy in primary biliary cirrhosis.
Podda M, Crosignani A, Battezzati PM, Quagliuolo M, Valsania C, Invernizzi P, Zuin M. Podda M, et al. Among authors: invernizzi p. Ital J Gastroenterol. 1996 Feb-Mar;28(2):114-7. Ital J Gastroenterol. 1996. PMID: 8782007 Review.
Blood fetal microchimerism in primary biliary cirrhosis.
Invernizzi P, De Andreis C, Sirchia SM, Battezzati PM, Zuin M, Rossella F, Perego F, Bignotto M, Simoni G, Podda M. Invernizzi P, et al. Clin Exp Immunol. 2000 Dec;122(3):418-22. doi: 10.1046/j.1365-2249.2000.01381.x. Clin Exp Immunol. 2000. PMID: 11122249 Free PMC article.
Ten-year combination treatment with colchicine and ursodeoxycholic acid for primary biliary cirrhosis: a double-blind, placebo-controlled trial on symptomatic patients.
Battezzati PM, Zuin M, Crosignani A, Allocca M, Invernizzi P, Selmi C, Villa E, Podda M. Battezzati PM, et al. Among authors: invernizzi p. Aliment Pharmacol Ther. 2001 Sep;15(9):1427-34. doi: 10.1046/j.1365-2036.2001.01018.x. Aliment Pharmacol Ther. 2001. PMID: 11552915 Free article. Clinical Trial.
497 results