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6篇 您的检索式：作者名="Markus Raderer"

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		题名	作者	年代	出处	被引量
	1	Lanreotide in Metastatic Enteropancreatic Neuroendocrine Tumors显示文摘	Martyn E. Caplin Marianne Pavel Jaros?aw B. ?wik?a Alexandria T. Phan Markus Raderer Eva Sedlá?ková Guillaume Cadiot Edward M. Wolin Jaume Capdevila Lucy Wall Guido Rindi Alison Langley Séverine Martinez Jo?lle Blumberg Philippe Ruszniewski	2014	The New England Journal of Medicine2014，，：	3
	2	Esophageal cancer: a critical evaluation of systemic second - line therapy 显示文摘	Christiane Maria Rosina Markus Raderer	2011	J Clin Oncol2011，29，35：	1
	3	18F-fluorodeoxyglucose positron emission tomography (18F-FDG-PET) does not visualize follicular lymphoma of the duodenum显示文摘	Martha Hoffmann Andreas Chott Andreas Püsp?k Ulrich J?ger Kurt Kletter Markus Raderer	2004	Annals of Hematology2004，，5：	1
	4	18F-fluorodeoxyglucose positron emission tomography (18F-FDG-PET) does not visualize follicular lymphoma of the duodenum显示文摘	Martha Hoffmann Andreas Chott Andreas Püsp?k Ulrich J?ger Kurt Kletter Markus Raderer	2004	Annals of Hematology2004，，5：	1
	5	Cardiovascular biomarkers in patients with cancer and their association with all-cause mortality显示文摘	Pavo Noemi Raderer Markus Hulsmann Martin Neuhold Stephanie Adlbrecht Christopher Strunk Guido Goliasch Georg Gisslinger Heinz Steger Gunther G Hejna Michael Kostler Wolfgang Zochbauer-Muller Sabine Marosi Christine Kornek Gabriela Auerbach Leo Schneider	2015	Heart2015，，：	1
	6	Running in the family:MALT lymphoma and autoimmune disease in mother and daughter显示文摘Gastric B-cell lymphoma of the mucosa associated lym-phoid tissue(MALT) lymphoma is one of the most com-mon forms of extranodal lymphoma.In addition to in-fection with Helicobacter pylori(H.pylori),the presence of an underlying autoimmune disease has also been associated with MALT lymphoma development.To date,no familial predisposition for MALT lymphomas has been reported as opposed to other types of lymphoma.A 65-year-old woman was admitted at our institution in 1998 with a diagnosis of H.pylori positive gastric MALT lymphoma and the presence of chronic autoim-mune thyroiditis was established on further work-up.H.pylori eradication did not result in regression of the lymphoma and RT-PCR showed the presence of the t(11;18)(q21;q21) translocation.About 1.5 years after H.pylori eradication,chemotherapy with cladribine resulted in complete remission.Due to lymphoma re-currence 13 mo later,radiotherapy to the stomach(46 Gy) resulted in minimal residual disease without further progression.The patient developed a second malig-nancy(Epstein-Bar virus-associated anaplastic large cell lymphoma in the mediastinum) in 2004 which initially responded to two courses of chemotherapy,but she re-fused further therapy and died of progressive lympho-ma in 2006.In 2008,her 55 years old daughter with a long standing Sj gren's syndrome was diagnosed with MALT lymphoma of the right parotid,but no evidence of gastric involvement or H.pylori infection was found.Currently,she is alive without therapy and undergoing regular check-ups.To our knowledge,this is the first report of MALT lymphoma in a f irst-degree relative of a patient with gastric MALT lymphoma in the context of two autoimmune diseases without a clearly established familial background.	Barbara Kiesewetter Marlene Troch Leonhard Müllauer Markus Raderer	2012	World Journal of Gastrointestinal Oncology2012，4，2：	0

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