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Jump to: 2022 | 2019 | 2016
Number of items: 4.

2022

Loos, Martin, Al-Saeedi, Mohammed, Hinz, Ulf, Mehrabi, Arianeb, Schneider, Martin, Berchtold, Christoph, Mueller-Stich, Beat P., Schmidt, Thomas, Kulu, Yakup, Hoffmann, Katrin, Strobel, Oliver, Hackert, Thilo and Buechler, Markus W. (2022). Categorization of Differing Types of Total Pancreatectomy. JAMA Surg., 157 (2). S. 120 - 129. CHICAGO: AMER MEDICAL ASSOC. ISSN 2168-6262

2019

Hueneburg, Robert, Aretz, Stefan ORCID: 0000-0002-5228-1890, Buettner, Reinhard, Daum, Severin, Engel, Christoph ORCID: 0000-0002-7247-282X, Fechner, Guido, Habermann, Jens K., Heling, Dominik, Hoffmann, Katrin, Holinski-Feder, Elke, Kloor, Matthias, von Knebel-Doeberitz, Magnus, Loeffler, Markus, Moeslein, Gabriela, Perne, Claudia, Redler, Silke, Riess, Olaf, Schmiegel, Wolff, Seufferlein, Thomas, Siebers-Renelt, Ulrike, Steinke-Lange, Verena, Tecklenburg, Johanna, Vangala, Deepak, Vilz, Tim, Weitz, Juergen, Wiedenmann, Bertram, Strassburg, Christian P. and Nattermann, Jacob (2019). Current recommendations for surveillance, risk reduction and therapy in Lynch syndrome patients. Z. Gastroent., 57 (11). S. 1309 - 1321. STUTTGART: GEORG THIEME VERLAG KG. ISSN 1439-7803

2016

Seemanova, Eva, Varon, Raymonda, Vejvalka, Jan, Jarolim, Petr ORCID: 0000-0002-9612-8652, Seeman, Pavel, Chrzanowska, Krystyna H., Digweed, Martin, Resnick, Igor, Kremensky, Ivo, Saar, Kathrin ORCID: 0000-0002-4483-1557, Hoffmann, Katrin, Dutrannoy, Veronique, Karbasiyan, Mohsen, Ghani, Mehdi, Baric, Ivo, Tekin, Mustafa ORCID: 0000-0002-3525-7960, Kovacs, Peter, Krawczak, Michael ORCID: 0000-0003-2603-1502, Reis, Andre ORCID: 0000-0002-6301-6363, Sperling, Karl and Nothnagel, Michael ORCID: 0000-0001-8305-7114 (2016). The Slavic NBN Founder Mutation: A Role for Reproductive Fitness? PLoS One, 11 (12). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1932-6203

Willkomm, Lena, Heredia, Raul, Hoffmann, Katrin, Wang, Haicui, Voit, Thomas, Hoffman, Eric P. and Cirak, Sebahattin (2016). Homozygous mutation in Atlastin GTPase 1 causes recessive hereditary spastic paraplegia. J. Hum. Genet., 61 (6). S. 571 - 574. NEW YORK: NATURE PUBLISHING GROUP. ISSN 1435-232X

This list was generated on Tue Jun 4 02:43:03 2024 CEST.