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10篇 您的检索式：作者名="Manghisi"

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		题名	作者	年代	出处	被引量
	1	The treatment of chronic hepatitis C not responding to interferon显示文摘	CozzolongoR Cuppone R Manghisi OG	2002	Curr Pharm Des2002，8，11：	1
	2	The treatment of chronic hepatitis C not responding to interferon显示文摘	Cozzolongo R Cuppone R Manghisi O G	2002	Curr Pharm Des2002，8，11：	1
	3	A new prognostic system for hepatocellular carcinoma: a retrospective study of 435 patients:the Cancer of the Liver Italian Program (CLIP) investigators 显示文摘	Manghisi G	1998	Hepatology1998，28，3：	1
	4	Onset of type 1 diabetes mellitus during peginterferon α-2b plus ribavirin treatment for chronic hepatitis C显示文摘	Raffaele Cozzolongo Corrado Betterle Paolo Fabris Maria Paola Albergoni Elsa Lanzilotta Onofrio G. Manghisi	2006	European Journal of Gastroenterology & Hepatology2006，，6：	1
	5	Onset of type 1 diabetes mellitus during peginterferon α-2b plus ribavirin treatment for chronic hepatitis C显示文摘	Raffaele Cozzolongo Corrado Betterle Paolo Fabris Maria Paola Albergoni Elsa Lanzilotta Onofrio G. Manghisi	2006	European Journal of Gastroenterology & Hepatology2006，，6：	1
	6	The treatment of chronic hepatitis C not responding to interfer- on 显示文摘	Cozzolongo R Cuppone R Manghisi OG	2002	Curr Pharm Des2002，8，11：	1
	7	The treatment of chronic hepatitis C not responding to interferon 显示文摘	Cozzolongo R Cuppone R Manghisi OG	2002	Curr Pharm Des2002，8，11：	1
	8	The treatment of chronic hepatitis C not responding to interferon 显示文摘	Cozzolongo R Cuppone R Manghisi OG	2002	Curr Pharm Des2002，8，11：	1
	9	Coinheritance of germline mutations in APC and MUTYH genes defines the clinical outcome of adenomatous polyposis syndromes显示文摘Familial adenomatous polyposis(FAP)and MUTYH-associ-ated polyposis(MAP)are colon cancer predisposition syn-dromes.FAP is an autosomal dominant inherited condition caused by germline mutations in the adenomatous polyposis coli(APC)gene and characterized by hundreds to thousands of colorectal adenomas.	Giovanna Forte Filomena Cariola Antonia Lucia Buonadonna Anna Filomena Guglielmi Andrea Manghisi Katia De Marco Valentina Grossi Candida Fasano Martina Lepore Signorile Paola Sanese Rosanna Bagnulo Nicoletta Resta b Vittoria Disciglio Cristiano Simone	2023	Genes & Diseases2023，10，4：	0
	10	A novel STK11 gene mutation (c.388dupG,p.Glu130Glyfs∗33) in a Peutz-Jeghers family and evidence of higher gastric cancer susceptibility associated with alterations in STK11 region aa 107-170显示文摘Peutz-Jeghers syndrome(PJS)is a rare autosomal dominant disorder characterized by mucocutaneous pigmentation and gastrointestinal(GI)hamartomatous polyposis and is associated with an increased risk of gastrointestinal,breast,gynecologic and other extra-GI malignancies.The serine/threonine kinase 11(STK11)gene has been identi-fied as a pathogenic factor in PJS.STK11 is a tumor sup-pressor gene located on chromosome 19p13.3 and includes 9 coding exons.1 The STK11 protein is composed of 433 amino acids(aa)and comprises a kinase catalytic region(aa 49e309)as well as N-and C-terminal regulatory domains.	Giovanna Forte Filomena Cariola Katia De Marco Andrea Manghisi Filomena Anna Guglielmi Raffaele Armentano Giuseppe Lippolis Pietro Giorgio Cristiano Simone Vittoria Disciglio	2022	Genes & Diseases2022，9，2：	0

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