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Plos One|August 23, 2014
Generation and characterisation of novel pancreatic adenocarcinoma xenograft models and corresponding primary cell linesAnna B Wennerström, Inger Marie Bowitz Lothe, Vandana Sandhu, et al.
Scandinavian Journal of Gastroenterology|December 24, 2005
Estimated prevalence of hereditary cancers and the need for surveillance in a Norwegian county, TelemarkAstrid T Stormorken, Geir Hoff, Jarle Norstein, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|December 16, 2020
Aplastic anaemiaSofie Hagestande, Ann Kristin Kvam, Inger Marie Bowitz Lothe, et al.
Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]|April 9, 2013
Improved survival and quality of life in patients undergoing R1 pancreatic resection compared to patients with locally advanced unresectable pancreatic adenocarcinomaTom Nordby, Tone Ikdahl, Inger Marie Bowitz Lothe, et al.
Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]|February 5, 2019
Clinical relevance of pancreatobiliary and intestinal subtypes of ampullary and duodenal adenocarcinoma: Pattern of recurrence, chemotherapy, and survival after pancreatoduodenectomyInger Marie Bowitz Lothe, Dyre Kleive, Ewa Pomianowska, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|July 22, 2005
Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancerAstrid T Stormorken, Inger Marie Bowitz-Lothe, Tove Norèn, et al.
Scandinavian Journal of Gastroenterology|April 20, 2013
Opportunities of improvement in the management of pancreatic and periampullary tumorsTom Nordby, Tone Ikdahl, Inger Marie Bowitz Lothe, et al.
Leukemia & Lymphoma|April 18, 2009
Alterations in regulators of the extracellular matrix in non-Hodgkin lymphomasHelene F S Negaard, Katja Svennevig, Svein Olav Kolset, et al.
Familial Cancer|October 24, 2003
The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumoursAstrid T Stormorken, Wolfram Müller, Annika Lindblom, et al.
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