Výsledky vyhledávání - Neumann, Hartmut P
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Maternal and Fetal Outcomes in Pheochromocytoma and Pregnancy: a multi-center retrospective cohort study and systematic review of literature Autor Bancos, Irina, Atkinson, Elizabeth, Eng, Charis, Young, William F., Neumann, Hartmut P. H.
Vydáno 2020Text -
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Germline and somatic DNA methylation and epigenetic regulation of KILLIN in renal cell carcinoma Autor Bennett, Kristi L., Campbell, Rebecca, Ganapathi, Shireen, Zhou, Ming, Rini, Brian, Ganapathi, Ram, Neumann, Hartmut P.H., Eng, Charis
Vydáno 2011Text -
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Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome Autor Manuelian, Tamara, Hellwage, Jens, Meri, Seppo, Caprioli, Jessica, Noris, Marina, Heinen, Stefan, Jozsi, Mihaly, Neumann, Hartmut P.H., Remuzzi, Giuseppe, Zipfel, Peter F.
Vydáno 2003Text -
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Growth characteristics and therapeutic decision markers in von Hippel-Lindau disease patients with renal cell carcinoma Autor Schuhmacher, Patrick, Kim, Emily, Hahn, Felix, Sekula, Peggy, Jilg, Cordula Annette, Leiber, Christian, Neumann, Hartmut P., Schultze-Seemann, Wolfgang, Walz, Gerd, Zschiedrich, Stefan
Vydáno 2019Text -
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Evaluation of a functional epigenetic approach to identify promoter region methylation in phaeochromocytoma and neuroblastoma Autor Margetts, Caroline D E, Morris, Mark, Astuti, Dewi, Gentle, Dean C, Cascon, Alberto, McRonald, Fiona E, Catchpoole, Daniel, Robledo, Mercedes, Neumann, Hartmut P H, Latif, Farida, Maher, Eamonn R
Vydáno 2008Text -
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Hemangioblastoma and von Hippel-Lindau disease: genetic background, spectrum of disease, and neurosurgical treatment Autor Klingler, Jan-Helge, Gläsker, Sven, Bausch, Birke, Urbach, Horst, Krauss, Tobias, Jilg, Cordula A., Steiert, Christine, Puzik, Alexander, Neumann-Haefelin, Elke, Kotsis, Fruzsina, Agostini, Hansjürgen, Neumann, Hartmut P.H., Beck, Jürgen
Vydáno 2020Text -
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Profiling of Somatic Mutations in Phaeochromocytoma and Paraganglioma by Targeted Next Generation Sequencing Analysis Autor Luchetti, Andrea, Walsh, Diana, Rodger, Fay, Clark, Graeme, Martin, Tom, Irving, Richard, Sanna, Mario, Yao, Masahiro, Robledo, Mercedes, Neumann, Hartmut P. H., Woodward, Emma R., Latif, Farida, Abbs, Stephen, Martin, Howard, Maher, Eamonn R.
Vydáno 2015Text -
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Germ-Line Mutations in the von Hippel–Lindau Tumor-Suppressor Gene Are Similar to Somatic von Hippel–Lindau Aberrations in Sporadic Renal Cell Carcinoma Autor Whaley, Jean M., Naglich, Joseph, Gelbert, Lawrence, Hsia, Y. Edward, Lamiell, James M., Green, Jane S., Collins, Debra, Neumann, Hartmut P. H., Laidlaw, Jana, Li, Fred P., Klein-Szanto, Andres J. P., Seizinger, Bernd R., Kley, Nikolai
Vydáno 1994Text -
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Pathogenicity of DNA Variants and Double Mutations in Multiple Endocrine Neoplasia Type 2 and Von Hippel-Lindau Syndrome Autor Erlic, Zoran, Hoffmann, Michael M., Sullivan, Maren, Franke, Gerlind, Peczkowska, Mariola, Harsch, Igor, Schott, Matthias, Gabbert, Helmut E., Valimäki, Matti, Preuss, Simon F., Hasse-Lazar, Kornelia, Waligorski, Dariusz, Robledo, Mercedes, Januszewicz, Andrzej, Eng, Charis, Neumann, Hartmut P. H.
Vydáno 2010Text -
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Impact of Screening Kindreds for SDHD p.Cys11X as a Common Mutation Associated with Paraganglioma Syndrome Type 1 Autor Pęczkowska, Mariola, Erlic, Zoran, Hoffmann, Michael M., Furmanek, Mariusz, Ćwikła, Jarosław, Kubaszek, Agata, Prejbisz, Aleksander, Szutkowski, Zbigniew, Kawecki, Andrzej, Chojnowski, Krzysztof, Lewczuk, Anna, Litwin, Mieczysław, Szyfter, Witold, Walter, Martin A., Sullivan, Maren, Eng, Charis, Januszewicz, Andrzej, Neumann, Hartmut P. H.
Vydáno 2008Text -
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Characteristics of Intracranial Aneurysms in the Else Kröner-Fresenius Registry of Autosomal Dominant Polycystic Kidney Disease Autor Neumann, Hartmut P.H., Malinoc, Angelica, Bacher, Janina, Nabulsi, Zinaida, Ivanovas, Vera, Bruechle, Nadine Ortiz, Mader, Irina, Hoffmann, Michael M., Riegler, Peter, Kraemer-Guth, Annette, Burchardi, Christian, Schaeffner, Elke, Martin, Rodolfo S., Azurmendi, Pablo J., Zerres, Klaus, Jilg, Cordula, Eng, Charis, Gläsker, Sven
Vydáno 2012Text -
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Early-Onset Renal Cell Carcinoma as a Novel Extraparaganglial Component of SDHB-Associated Heritable Paraganglioma Autor Vanharanta, Sakari, Buchta, Mary, McWhinney, Sarah R., Virta, Sanna K., Peçzkowska, Mariola, Morrison, Carl D., Lehtonen, Rainer, Januszewicz, Andrzej, Järvinen, Heikki, Juhola, Matti, Mecklin, Jukka-Pekka, Pukkala, Eero, Herva, Riitta, Kiuru, Maija, Nupponen, Nina N., Aaltonen, Lauri A., Neumann, Hartmut P. H., Eng, Charis
Vydáno 2004Text -
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Integrative genetic, epigenetic and pathological analysis of paraganglioma reveals complex dysregulation of NOTCH signaling Autor Cama, Alessandro, Verginelli, Fabio, Lotti, Lavinia Vittoria, Napolitano, Francesco, Morgano, Annalisa, D’Orazio, Andria, Vacca, Michele, Perconti, Silvia, Pepe, Felice, Romani, Federico, Vitullo, Francesca, di Lella, Filippo, Visone, Rosa, Mannelli, Massimo, Neumann, Hartmut P. H., Raiconi, Giancarlo, Paties, Carlo, Moschetta, Antonio, Tagliaferri, Roberto, Veronese, Angelo, Sanna, Mario, Mariani-Costantini, Renato
Vydáno 2013Text