Rezultaty - Neumann, Hartmut P
- Rezultaty 1 - 20 Rezultaty od 26
- Idź do następnej strony
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Maternal and Fetal Outcomes in Pheochromocytoma and Pregnancy: a multi-center retrospective cohort study and systematic review of literature od Bancos, Irina, Atkinson, Elizabeth, Eng, Charis, Young, William F., Neumann, Hartmut P. H.
Wydane 2020Text -
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Germline and somatic DNA methylation and epigenetic regulation of KILLIN in renal cell carcinoma od Bennett, Kristi L., Campbell, Rebecca, Ganapathi, Shireen, Zhou, Ming, Rini, Brian, Ganapathi, Ram, Neumann, Hartmut P.H., Eng, Charis
Wydane 2011Text -
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Clinical decision making in small non-functioning VHL-related incidentalomas od Därr, Roland, Kater, Jonas, Sekula, Peggy, Bausch, Birke, Krauss, Tobias, Bode, Christoph, Walz, Gerd, Neumann, Hartmut P, Zschiedrich, Stefan
Wydane 2020Text -
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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 od Manuelian, Tamara, Hellwage, Jens, Meri, Seppo, Caprioli, Jessica, Noris, Marina, Heinen, Stefan, Jozsi, Mihaly, Neumann, Hartmut P.H., Remuzzi, Giuseppe, Zipfel, Peter F.
Wydane 2003Text -
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Growth characteristics and therapeutic decision markers in von Hippel-Lindau disease patients with renal cell carcinoma od Schuhmacher, Patrick, Kim, Emily, Hahn, Felix, Sekula, Peggy, Jilg, Cordula Annette, Leiber, Christian, Neumann, Hartmut P., Schultze-Seemann, Wolfgang, Walz, Gerd, Zschiedrich, Stefan
Wydane 2019Text -
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Evaluation of a functional epigenetic approach to identify promoter region methylation in phaeochromocytoma and neuroblastoma od 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
Wydane 2008Text -
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Hemangioblastoma and von Hippel-Lindau disease: genetic background, spectrum of disease, and neurosurgical treatment od 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
Wydane 2020Text -
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Profiling of Somatic Mutations in Phaeochromocytoma and Paraganglioma by Targeted Next Generation Sequencing Analysis od 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.
Wydane 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 od 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
Wydane 1994Text -
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Pathogenicity of DNA Variants and Double Mutations in Multiple Endocrine Neoplasia Type 2 and Von Hippel-Lindau Syndrome od 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.
Wydane 2010Text -
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Impact of Screening Kindreds for SDHD p.Cys11X as a Common Mutation Associated with Paraganglioma Syndrome Type 1 od 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.
Wydane 2008Text -
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Characteristics of Intracranial Aneurysms in the Else Kröner-Fresenius Registry of Autosomal Dominant Polycystic Kidney Disease od 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
Wydane 2012Text -
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Early-Onset Renal Cell Carcinoma as a Novel Extraparaganglial Component of SDHB-Associated Heritable Paraganglioma od 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
Wydane 2004Text -
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Integrative genetic, epigenetic and pathological analysis of paraganglioma reveals complex dysregulation of NOTCH signaling od 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
Wydane 2013Text