Search Results - Neumann, Hartmut P

The Approach to the Patient with Paraganglioma by Neumann, Hartmut P. H., Eng, Charis

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Genetic stratification of inherited and sporadic phaeochromocytoma and paraganglioma: implications for precision medicine by Casey, Ruth, Neumann, Hartmut P H, Maher, Eamonn R

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Diagnosis of extra-adrenal phaeochromocytoma after nephrectomy by Barski, Dimitri, Ezziddin, Samer, Heikaus, Sebastian, Neumann, Hartmut P.H.

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Maternal and Fetal Outcomes in Pheochromocytoma and Pregnancy: a multi-center retrospective cohort study and systematic review of literature by Bancos, Irina, Atkinson, Elizabeth, Eng, Charis, Young, William F., Neumann, Hartmut P. H.

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Max Schottelius: Pioneer in Pheochromocytoma by Bausch, Birke, Tischler, Arthur S., Schmid, Kurt W., Leijon, Helena, Eng, Charis, Neumann, Hartmut P. H.

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Clinical Features of Paraganglioma Syndromes by Boedeker, Carsten Christof, Neumann, Hartmut P.H., Offergeld, Christian, Maier, Wolfgang, Falcioni, Maurizio, Berlis, Ansgar, Schipper, Joerg

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Juxtacondylar Approach in Temporal Paraganglioma Surgery: When and Why? by Schipper, Joerg, Spetzger, Uwe, Tatagiba, Marcos, Rosahl, Steffen, Neumann, Hartmut P.H., Boedeker, Carsten Christof, Maier, Wolfgang

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Germline and somatic DNA methylation and epigenetic regulation of KILLIN in renal cell carcinoma by Bennett, Kristi L., Campbell, Rebecca, Ganapathi, Shireen, Zhou, Ming, Rini, Brian, Ganapathi, Ram, Neumann, Hartmut P.H., Eng, Charis

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Clinical decision making in small non-functioning VHL-related incidentalomas by Därr, Roland, Kater, Jonas, Sekula, Peggy, Bausch, Birke, Krauss, Tobias, Bode, Christoph, Walz, Gerd, Neumann, Hartmut P, Zschiedrich, Stefan

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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 by Manuelian, Tamara, Hellwage, Jens, Meri, Seppo, Caprioli, Jessica, Noris, Marina, Heinen, Stefan, Jozsi, Mihaly, Neumann, Hartmut P.H., Remuzzi, Giuseppe, Zipfel, Peter F.

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Growth characteristics and therapeutic decision markers in von Hippel-Lindau disease patients with renal cell carcinoma by Schuhmacher, Patrick, Kim, Emily, Hahn, Felix, Sekula, Peggy, Jilg, Cordula Annette, Leiber, Christian, Neumann, Hartmut P., Schultze-Seemann, Wolfgang, Walz, Gerd, Zschiedrich, Stefan

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Evaluation of a functional epigenetic approach to identify promoter region methylation in phaeochromocytoma and neuroblastoma by 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

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Hemangioblastoma and von Hippel-Lindau disease: genetic background, spectrum of disease, and neurosurgical treatment by 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

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Profiling of Somatic Mutations in Phaeochromocytoma and Paraganglioma by Targeted Next Generation Sequencing Analysis by 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.

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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 by 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

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Pathogenicity of DNA Variants and Double Mutations in Multiple Endocrine Neoplasia Type 2 and Von Hippel-Lindau Syndrome by 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.

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Impact of Screening Kindreds for SDHD p.Cys11X as a Common Mutation Associated with Paraganglioma Syndrome Type 1 by 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.

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Characteristics of Intracranial Aneurysms in the Else Kröner-Fresenius Registry of Autosomal Dominant Polycystic Kidney Disease by 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

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Early-Onset Renal Cell Carcinoma as a Novel Extraparaganglial Component of SDHB-Associated Heritable Paraganglioma by 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

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Integrative genetic, epigenetic and pathological analysis of paraganglioma reveals complex dysregulation of NOTCH signaling by 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

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