Diagnosis of extra-adrenal phaeochromocytoma after nephrectomy

por Barski, Dimitri, Ezziddin, Samer, Heikaus, Sebastian, Neumann, Hartmut P.H.
Publicado 2014

Max Schottelius: Pioneer in Pheochromocytoma

por Bausch, Birke, Tischler, Arthur S., Schmid, Kurt W., Leijon, Helena, Eng, Charis, Neumann, Hartmut P. H.
Publicado 2017

Clinical decision making in small non-functioning VHL-related incidentalomas

por Därr, Roland, Kater, Jonas, Sekula, Peggy, Bausch, Birke, Krauss, Tobias, Bode, Christoph, Walz, Gerd, Neumann, Hartmut P, Zschiedrich, Stefan
Publicado 2020

Growth characteristics and therapeutic decision markers in von Hippel-Lindau disease patients with renal cell carcinoma

por Schuhmacher, Patrick, Kim, Emily, Hahn, Felix, Sekula, Peggy, Jilg, Cordula Annette, Leiber, Christian, Neumann, Hartmut P., Schultze-Seemann, Wolfgang, Walz, Gerd, Zschiedrich, Stefan
Publicado 2019

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

por 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
Publicado 2008

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

por 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
Publicado 2020

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

por 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.
Publicado 2015

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

por 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
Publicado 2012

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

por 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
Publicado 2013

Primary hyperparathyroidism as first manifestation in multiple endocrine neoplasia type 2A: an international multicenter study

por Larsen, Louise Vølund, Mirebeau-Prunier, Delphine, Imai, Tsuneo, Alvarez-Escola, Cristina, Hasse-Lazar, Kornelia, Censi, Simona, Castroneves, Luciana A, Sakurai, Akihiro, Kihara, Minoru, Horiuchi, Kiyomi, Barbu, Véronique Dorine, Borson-Chazot, Francoise, Gimenez-Roqueplo, Anne-Paule, Pigny, Pascal, Pinson, Stephane, Wohllk, Nelson, Eng, Charis, Aydogan, Berna Imge, Saranath, Dhananjaya, Dvorakova, Sarka, Castinetti, Frederic, Patocs, Attila, Bergant, Damijan, Links, Thera P, Peczkowska, Mariola, Hoff, Ana O, Mian, Caterina, Dwight, Trisha, Jarzab, Barbara, Neumann, Hartmut P H, Robledo, Mercedes, Uchino, Shinya, Barlier, Anne, Godballe, Christian, Mathiesen, Jes Sloth
Publicado 2020

Comparison of Pheochromocytoma-Specific Morbidity and Mortality Among Adults With Bilateral Pheochromocytomas Undergoing Total Adrenalectomy vs Cortical-Sparing Adrenalectomy

por Neumann, Hartmut P. H., Tsoy, Uliana, Bancos, Irina, Amodru, Vincent, Walz, Martin K., Tirosh, Amit, Kaur, Ravinder Jeet, McKenzie, Travis, Qi, Xiaoping, Bandgar, Tushar, Petrov, Roman, Yukina, Marina Y., Roslyakova, Anna, van der Horst-Schrivers, Anouk N. A., Berends, Annika M. A., Hoff, Ana O., Castroneves, Luciana Audi, Ferrara, Alfonso Massimiliano, Rizzati, Silvia, Mian, Caterina, Dvorakova, Sarka, Hasse-Lazar, Kornelia, Kvachenyuk, Andrey, Peczkowska, Mariola, Loli, Paola, Erenler, Feyza, Krauss, Tobias, Almeida, Madson Q., Liu, Longfei, Zhu, Feizhou, Recasens, Mònica, Wohllk, Nelson, Corssmit, Eleonora P. M., Shafigullina, Zulfiya, Calissendorff, Jan, Grozinsky-Glasberg, Simona, Kunavisarut, Tada, Schalin-Jäntti, Camilla, Castinetti, Frederic, Vlček, Petr, Beltsevich, Dmitry, Egorov, Viacheslav I., Schiavi, Francesca, Links, Thera P., Lechan, Ronald M., Bausch, Birke, Young, William F., Eng, Charis
Publicado 2019

Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy

por Otto, Edgar A., Hurd, Toby W., Airik, Rannar, Chaki, Moumita, Zhou, Weibin, Stoetzel, Corinne, Patil, Suresh B., Levy, Shawn, Ghosh, Amiya K., Murga-Zamalloa, Carlos A., van Reeuwijk, Jeroen, Letteboer, Stef J.F., Sang, Liyun, Giles, Rachel H., Liu, Qin, Coene, Karlien L. M., Estrada-Cuzcano, Alejandro, Collin, Rob W. J., McLaughlin, Heather M., Held, Susanne, Kasanuki, Jennifer M., Ramaswami, Gokul, Conte, Jinny, Lopez, Irma, Washburn, Joseph, MacDonald, James, Hu, Jinghua, Yamashita, Yukiko, Maher, Eamonn R., Guay-Woodford, Lisa, Neumann, Hartmut P.H., Obermüller, Nicholas, Koenekoop, Robert K., Bergmann, Carsten, Bei, Xiaoshu, Lewis, Richard A., Katsanis, Nicholas, Lopes, Vanda, Williams, David S., Lyons, Robert H., Dang, Chi V., Brito, Daniela A., Dias, Mónica Bettencourt, Zhang, Xinmin, Nürnberg, Gudrun, Nürnberg, Peter, Pierce, Eric, Jackson, Peter, Antignac, Corinne, Saunier, Sophie, Roepman, Ronald, Dollfus, Helene, Khanna, Hemant, Hildebrandt, Friedhelm
Publicado 2010