Characterization of endolymphatic sac tumors and von Hippel-Lindau disease in the International Endolymphatic Sac Tumor Registry von Bausch, Birke, Wellner, Ulrich, Peyre, Mathieu, Boedeker, Carsten C., Hes, Frederik J., Anglani, Mariagiulia, de Campos, Jose M., Kanno, Hiroshi, Maher, Eamonn R., Krauss, Tobias, Sansó, Gabriela, Barontini, Marta, Letizia, Claudio, Hader, Claudia, Schiavi, Francesca, Zanoletti, Elisabetta, Suárez, Carlos, Offergeld, Christian, Malinoc, Angelica, Zschiedrich, Stefan, Glasker, Sven, Bobin, Serge, Sterkers, Olivier, Ba Huy, Patrice Tran, Giraud, Sophie, Links, Thera, Eng, Charis, Opocher, Giuseppe, Richard, Stephane, Neumann, Hartmut P. H.

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A decision aid to rule out pneumonia and reduce unnecessary prescriptions of antibiotics in primary care patients with cough and fever von Steurer, Johann, Held, Ulrike, Spaar, Anne, Bausch, Birke, Zoller, Marco, Hunziker, Roger, Bachmann, Lucas M

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Evidence of MEN-2 in the Original Description of Classic Pheochromocytoma von Neumann, Hartmut P.H, Vortmeyer, Alexander, Schmidt, Dieter, Werner, Martin, Erlic, Zoran, Cascon, Alberto, Bausch, Birke, Januszewicz, Andrzej, Eng, Charis

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

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Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions von Vuorela, Pia, Ala-Mello, Sirpa, Saloranta, Carola, Penttinen, Maila, Pöyhönen, Minna, Huoponen, Kirsi, Borozdin, Wiktor, Bausch, Birke, Botzenhart, Elke M, Wilhelm, Christian, Kääriäinen, Helena, Kohlhase, Jürgen

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Long-term prognosis of patients with pediatric pheochromocytoma von Bausch, Birke, Wellner, Ulrich, Bausch, Dirk, Schiavi, Francesca, Barontini, Marta, Sanso, Gabriela, Walz, Martin K, Peczkowska, Mariola, Weryha, Georges, Dall'Igna, Patrizia, Cecchetto, Giovanni, Bisogno, Gianni, Moeller, Lars C, Bockenhauer, Detlef, Patocs, Attila, Rácz, Karoly, Zabolotnyi, Dmitry, Yaremchuk, Svetlana, Dzivite-Krisane, Iveta, Castinetti, Frederic, Taieb, David, Malinoc, Angelica, von Dobschuetz, Ernst, Roessler, Jochen, Schmid, Kurt W, Opocher, Giuseppe, Eng, Charis, Neumann, Hartmut P H

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Somatic deletion of the NF1 gene in a neurofibromatosis type 1-associated malignant melanoma demonstrated by digital PCR von Rübben, Albert, Bausch, Birke, Nikkels, Arjen

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Minimally Invasive Surgery (MIS) in Children and Adolescents with Pheochromocytomas and Retroperitoneal Paragangliomas: Experiences in 42 Patients von Walz, Martin K., Iova, Laura D., Deimel, Judith, Neumann, Hartmut P. H., Bausch, Birke, Zschiedrich, Stefan, Groeben, Harald, Alesina, Pier F.

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Hemangioblastoma and von Hippel-Lindau disease: genetic background, spectrum of disease, and neurosurgical treatment von 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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Evaluation of Laboratory and Sonographic Parameters for Detection of Portal Hypertension in Patients with Common Variable Immunodeficiency von Globig, Anna-Maria, Strohmeier, Valentina, Surabattula, Rambabu, Leeming, Diana J., Karsdal, Morten A., Heeg, Maximilian, Kindle, Gerhard, Goldacker, Sigune, von Spee-Mayer, Caroline, Proietti, Michele, Bausch, Birke, Bettinger, Dominik, Schultheiß, Michael, Thimme, Robert, Schuppan, Detlef, Warnatz, Klaus

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Distinct Clinical Features of Paraganglioma Syndromes Associated With SDHB and SDHD Gene Mutations von Neumann, Hartmut P. H, Pawlu, Christian, Pęczkowska, Mariola, Bausch, Birke, McWhinney, Sarah R, Muresan, Mihaela, Buchta, Mary, Franke, Gerlind, Klisch, Joachim, Bley, Thorsten A, Hoegerle, Stefan, Boedeker, Carsten C, Opocher, Giuseppe, Schipper, Jörg, Januszewicz, Andrzej, Eng, Charis, for the European-American Paraganglioma Study Group

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Preventive medicine of von Hippel–Lindau disease-associated pancreatic neuroendocrine tumors von Krauss, Tobias, Ferrara, Alfonso Massimiliano, Links, Thera P, Wellner, Ulrich, Bancos, Irina, Kvachenyuk, Andrey, Villar Gómez de las Heras, Karina, Yukina, Marina Y, Petrov, Roman, Bullivant, Garrett, von Duecker, Laura, Jadhav, Swati, Ploeckinger, Ursula, Welin, Staffan, Schalin-Jäntti, Camilla, Gimm, Oliver, Pfeifer, Marija, Ngeow, Joanne, Hasse-Lazar, Kornelia, Sansó, Gabriela, Qi, Xiaoping, Ugurlu, M Umit, Diaz, Rene E, Wohllk, Nelson, Peczkowska, Mariola, Aberle, Jens, Lourenço, Delmar M, Pereira, Maria A A, Fragoso, Maria C B V, Hoff, Ana O, Almeida, Madson Q, Violante, Alice H D, Quidute, Ana R P, Zhang, Zhewei, Recasens, Mònica, Díaz, Luis Robles, Kunavisarut, Tada, Wannachalee, Taweesak, Sirinvaravong, Sirinart, Jonasch, Eric, Grozinsky-Glasberg, Simona, Fraenkel, Merav, Beltsevich, Dmitry, Egorov, Viacheslav I, Bausch, Dirk, Schott, Matthias, Tiling, Nikolaus, Pennelli, Gianmaria, Zschiedrich, Stefan, Därr, Roland, Ruf, Juri, Denecke, Timm, Link, Karl-Heinrich, Zovato, Stefania, von Dobschuetz, Ernst, Yaremchuk, Svetlana, Amthauer, Holger, Makay, Özer, Patocs, Attila, Walz, Martin K, Huber, Tobias B, Seufert, Jochen, Hellman, Per, Kim, Raymond H, Kuchinskaya, Ekaterina, Schiavi, Francesca, Malinoc, Angelica, Reisch, Nicole, Jarzab, Barbara, Barontini, Marta, Januszewicz, Andrzej, Shah, Nalini, Young, William F, Opocher, Giuseppe, Eng, Charis, Neumann, Hartmut P H, Bausch, Birke

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65 YEARS OF THE DOUBLE HELIX: Genetics informs precision practice in the diagnosis and management of pheochromocytoma von Neumann, Hartmut P, Young, William F, Krauss, Tobias, Bayley, Jean-Pierre, Schiavi, Francesca, Opocher, Giuseppe, Boedeker, Carsten C, Tirosh, Amit, Castinetti, Frederic, Ruf, Juri, Beltsevich, Dmitry, Walz, Martin, Groeben, Harald-Thomas, von Dobschuetz, Ernst, Gimm, Oliver, Wohllk, Nelson, Pfeifer, Marija, Lourenço, Delmar M, Peczkowska, Mariola, Patocs, Attila, Ngeow, Joanne, Makay, Özer, Shah, Nalini S, Tischler, Arthur, Leijon, Helena, Pennelli, Gianmaria, Villar Gómez de las Heras, Karina, Links, Thera P, Bausch, Birke, Eng, Charis

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Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and SDHAF2 for Gene-Informed Prevention von Bausch, B, Schiavi, F, Ni, Y, Welander, J, Patocs, A, Ngeow, J, Wellner, U, Malinoc, A, Taschin, E, Barbon, G, Lanza, V, Soderkvist, P, Stenman, A, Fraenkel, M, Walter, MA, Peczkowska, M, Prejbisz, A, Jarzab, B, Hasse-Lazar, K, Petersenn, S, Moeller, LC, Meyer, A, Reisch, N, Trupka, A, Brase, C, Galiano, M, Preuss, SF, Kwok, P, Lendvai, N, Berisha, G, Makay, O, Boedeker, CC, Weryha, G, Racz, K, Januszewicz, A, Walz, MK, Gimm, O, Opocher, G, Eng, C, Neumann, HPH

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Maternal and fetal outcomes in phaeochromocytoma and pregnancy: a multicentre retrospective cohort study and systematic review of literature von Bancos, Irina, Atkinson, Elizabeth, Eng, Charis, Young, William F, Neumann, Hartmut P H, Yukina, Marina, Cohen, Debbie L, Waguespack, Steven G, Pereira, Maria Adelaide Albergaria, He, Xin, Bandgar, Tushar, Donatini, Gianluca, Qi, Xiao-Ping, Cohn, Aviva, Letizia, Claudio, Fishbein, Lauren, Kaur, Ravinder Jeet, Murad, Mohammad H, Gruber, Lucinda, Jimenez, Camilo, Petramala, Luigi, Beltsevich, Dmitry, Walz, Martin K, Corssmit, Eleonora P.M., Wohllk, Nelson, Links, Thera P, Ferrara, Alfonso Massimiliano, Tsoy, Uliana, Donegan, Diane, Peczkowska, Mariola, Timmers, Henri J, Ebbehoj, Andreas, Kirschner, Lawrence S, Kunavisarut, Tada, Larsson, Catharina, Kudlai, Inna, Hasse-Lazar, Kornelia, Barczyński, Marcin, Deutschbein, Timo, Rasmussen, Åse Krogh, Dvorakova, Sarka, Miller, Julie A, Liu, Longfei, Bennett, Bonita, Huang, Ya-Sheng, Yu, Zhi-xian, Kumar Jaiswal, Sanjeet, Shah, Nalini, Dullaart, Robin P.F, Akker, Scott A, Drake, William M, Boaretto, Francesca, Barbon, Giovanni, Taschin, Elisa, Schiavi, Francesca, Grineva, Elena, Skierczynski, Paul, Fassnacht, Martin, Calissendorff, Jan, Juhlin, C Christofer, Vlĕek, Petr, Li, Minghao, Jonasch, Eric, Prokop, Larry, Jovanovic, Milan, Lechan, Ronald M, Erenler, Feyza, Garla, Vishnu, Bobryk, Maryna, Kovalenko, Andrey Y, Hodson, Emma, Jenner, Bernadette, Simpson, Helen L, Shafigullina, Zulfiya, Martins Bugalho, Maria João, Rizzati, Silvia, Fraenkel, Merav, Sherlock, Mark, Sarma, Dipti, Kaimal Saikia, Uma, Quinkler, Marcus, Zschiedrich, Stefan, Bausch, Birke, Zavrashvili, Nino, Søndergaard, Esben, Mathiesen, Jes Sloth, Robaczyk, Maciej G, Poulsen, Per Løgstrup, Vasilkova, Volha, Costa-Barbosa, Flavia A, Kater, Claudio E, Yildirim Simsir, Ilgin, Ugurlu, M. Umit, Soyaltin, Utku E, Makay, Özer, Ivanov, Nikita V, Opocher, Giuseppe, Egorov, Viacheslav I, Petrov, Roman, Khudiakova, Natalia V

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Therapy Algorithm for Portal Vein Thrombosis in Liver Cirrhosis: The Internist's Point of View von Rössle, Martin, Bausch, Birke, Klinger, Christoph

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Comparison of Pheochromocytoma-Specific Morbidity and Mortality Among Adults With Bilateral Pheochromocytomas Undergoing Total Adrenalectomy vs Cortical-Sparing Adrenalectomy von 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, Vlcek, Petr, Beltsevich, Dmitry, Egorov, Viacheslav I, Schiavi, Francesca, Links, Thera P, Lechan, Ronald M, Bausch, Birke, Young, Jr, William F, Eng, Charis

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Alu-Alu recombination underlies the vast majority of large VHL germline deletions: Molecular characterization and genotype-phenotype correlations in VHL patients von Franke, Gerlind, Bausch, Birke, Hoffmann, Michael M, Cybulla, Markus, Wilhelm, Christian, Kohlhase, Jürgen, Scherer, Gerd, Neumann, Hartmut P.H

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Clinical and Genetic Characteristics of Patients with Neurofibromatosis Type 1 and Pheochromocytoma von Bausch, Birke, Borozdin, Wiktor, Neumann, Hartmut P.H

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Predictors and Prevalence of Paraganglioma Syndrome Associated With Mutations of the SDHC Gene von Schiavi, Francesca, Boedeker, Carsten C, Bausch, Birke, Peçzkowska, Mariola, Gomez, Clara Fuentes, Strassburg, Thomas, Pawlu, Christian, Buchta, Mary, Salzmann, Maren, Hoffmann, Michael M, Berlis, Ansgar, Brink, Ingo, Cybulla, Markus, Muresan, Mihaela, Walter, Martin A, Forrer, Flavio, Välimäki, Matti, Kawecki, Andrzej, Szutkowski, Zbigniew, Schipper, Jörg, Walz, Martin K, Pigny, Pascal, Bauters, Catherine, Willet-Brozick, Joan E, Baysal, Bora E, Januszewicz, Andrzej, Eng, Charis, Opocher, Giuseppe, Neumann, Hartmut P. H, European-American Paraganglioma Study Group, for the

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