Early‐onset, progressive, frequent, extensive, and severe bone mineral and renal complications in multiple endocrine neoplasia type 1–associated primary hyperparathyroidism von Lourenço, Delmar M, Coutinho, Flavia L, Toledo, Rodrigo A, Montenegro, Fabio LM, Correia‐Deur, Joya EM, Toledo, Sergio PA

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Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS von Agrawal, Nishant, Jiao, Yuchen, Sausen, Mark, Leary, Rebecca, Bettegowda, Chetan, Roberts, Nicholas J, Bhan, Sheetal, Ho, Allen S, Khan, Zubair, Bishop, Justin, Westra, William H, Wood, Laura D, Hruban, Ralph H, Tufano, Ralph P, Robinson, Bruce, Dralle, Henning, Toledo, Sergio P. A, Toledo, Rodrigo A, Morris, Luc G. T, Ghossein, Ronald A, Fagin, James A, Chan, Timothy A, Velculescu, Victor E, Vogelstein, Bert, Kinzler, Kenneth W, Papadopoulos, Nickolas, Nelkin, Barry D, Ball, Douglas W

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Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study von Daly, Adrian F, Tichomirowa, Maria A, Petrossians, Patrick, Heliövaara, Elina, Jaffrain-Rea, Marie-Lise, Barlier, Anne, Naves, Luciana A, Ebeling, Tapani, Karhu, Auli, Raappana, Antti, Cazabat, Laure, De Menis, Ernesto, Montañana, Carmen Fajardo, Raverot, Gerald, Weil, Robert J, Sane, Timo, Maiter, Dominique, Neggers, Sebastian, Yaneva, Maria, Tabarin, Antoine, Verrua, Elisa, Eloranta, Eija, Murat, Arnaud, Vierimaa, Outi, Salmela, Pasi I, Emy, Philippe, Toledo, Rodrigo A, Sabaté, Maria Isabel, Villa, Chiara, Popelier, Marc, Salvatori, Roberto, Jennings, Juliet, Longás, Ángel Ferrandez, Labarta Aizpún, José Ignacio, Georgitsi, Marianthi, Paschke, Ralf, Ronchi, Cristina, Valimaki, Matti, Saloranta, Carola, De Herder, Wouter, Cozzi, Renato, Guitelman, Mirtha, Magri, Flavia, Lagonigro, Maria Stefania, Halaby, Georges, Corman, Vinciane, Hagelstein, Marie-Thérèse, Vanbellinghen, Jean-François, Barra, Gustavo Barcelos, Gimenez-Roqueplo, Anne-Paule, Cameron, Fergus J, Borson-Chazot, Françoise, Holdaway, Ian, Toledo, Sergio P. A, Stalla, Günter K, Spada, Anna, Zacharieva, Sabina, Bertherat, Jerome, Brue, Thierry, Bours, Vincent, Chanson, Philippe, Aaltonen, Lauri A, Beckers, Albert

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In vivo and in vitro oncogenic effects of HIF2A mutations in pheochromocytomas and paragangliomas von Toledo, Rodrigo A, Qin, Yuejuan, Srikantan, Subramanya, Morales, Nicole Paes, Li, Qun, Deng, Yilun, Kim, Sang-Woo, Pereira, Maria Adelaide A, Toledo, Sergio P A, Su, Xiaoping, Aguiar, Ricardo C T, Dahia, Patricia L M

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Spectrum and Prevalence of FP/TMEM127 Gene Mutations in Pheochromocytomas and Paragangliomas von Yao, Li, Schiavi, Francesca, Cascon, Alberto, Qin, Yuejuan, Inglada-Pérez, Lucia, King, Elizabeth E, Toledo, Rodrigo A, Ercolino, Tonino, Rapizzi, Elena, Ricketts, Christopher J, Mori, Luigi, Giacchè, Mara, Mendola, Antonella, Taschin, Elisa, Boaretto, Francesca, Loli, Paola, Iacobone, Maurizio, Rossi, Gian-Paolo, Biondi, Bernadette, Lima-Junior, José Viana, Kater, Claudio E, Bex, Marie, Vikkula, Miikka, Grossman, Ashley B, Gruber, Stephen B, Barontini, Marta, Persu, Alexandre, Castellano, Maurizio, Toledo, Sergio P. A, Maher, Eamonn R, Mannelli, Massimo, Opocher, Giuseppe, Robledo, Mercedes, Dahia, Patricia L. M

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Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10 von Frank-Raue, Karin, Rybicki, Lisa A., Erlic, Zoran, Schweizer, Heiko, Winter, Aurelia, Milos, Ioana, Toledo, Sergio P.A., Toledo, Rodrigo A., Tavares, Marcos R., Alevizaki, Maria, Mian, Caterina, Siggelkow, Heide, Hüfner, Michael, Wohllk, Nelson, Opocher, Giuseppe, Dvořáková, Šárka, Bendlova, Bela, Czetwertynska, Małgorzata, Skasko, Elżbieta, Barontini, Marta, Sanso, Gabriela, Vorländer, Christian, Maia, Ana Luiza, Patocs, Attila, Links, Thera P., de Groot, Jan Willem, Kerstens, Michiel N., Valk, Gerlof D., Miehle, Konstanze, Musholt, Thomas J., Biarnes, Josefina, Damjanovic, Svetozar, Muresan, Mihaela, Wüster, Christian, Fassnacht, Martin, Peczkowska, Mariola, Fauth, Christine, Golcher, Henriette, Walter, Martin A., Pichl, Josef, Raue, Friedhelm, Eng, Charis, Neumann, Hartmut P.H.

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A HIF1α Regulatory Loop Links Hypoxia and Mitochondrial Signals in Pheochromocytomas von Dahia, Patricia L. M, Ross, Ken N, Wright, Matthew E, Hayashida, César Y, Santagata, Sandro, Barontini, Marta, Kung, Andrew L, Sanso, Gabriela, Powers, James F, Tischler, Arthur S, Hodin, Richard, Heitritter, Shannon, Moore, Francis, Dluhy, Robert, Sosa, Julie Ann, Ocal, I. Tolgay, Benn, Diana E, Marsh, Deborah J, Robinson, Bruce G, Schneider, Katherine, Garber, Judy, Arum, Seth M, Korbonits, Márta, Grossman, Ashley, Pigny, Pascal, Toledo, Sérgio P. A, Nosé, Vania, Li, Cheng, Stiles, Charles D

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Germline Mutation in the Aryl Hydrocarbon Receptor Interacting Protein Gene in Familial Somatotropinoma von Toledo, Rodrigo A., Lourenço, Delmar M., Liberman, Bernardo, Cunha-Neto, Malebranche B. C., Cavalcanti, Maria G., Moyses, Cinthia B., Toledo, Sergio P. A., Dahia, Patricia L. M.

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Bone mineral density analysis in patients with primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 after total parathyroidectomy von Coutinho, Flavia L., Lourenço Jr, Delmar M., Toledo, Rodrigo A., Montenegro, Fabio L. M., Correia-Deur, Joya E. M., Toledo, Sergio P. A.

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Somatotroph pituitary adenoma with acromegaly and autosomal dominant polycystic kidney disease: SSTR5 polymorphism and PKD1 mutation von Syro, Luis V., Sundsbak, Jamie L., Scheithauer, Bernd W., Toledo, Rodrigo A., Camargo, Mauricio, Heyer, Christina M., Sekiya, Tomoko, Uribe, Humberto, Escobar, Jorge I., Vasquez, Martin, Rotondo, Fabio, Toledo, Sergio P. A., Kovacs, Kalman, Horvath, Eva, Babovic-Vuksanovic, Dusica, Harris, Peter C.

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A HIF1[alpha] Regulatory Loop Links Hypoxia and Mitochondrial Signals in Pheochromocytomas: e8 von Dahia, Patricia LM, Ross, Ken N, Wright, Matthew E, Hayashida, César Y, Santagata, Sandro, Barontini, Marta, Kung, Andrew L, Sanso, Gabriela, Powers, James F, Tischler, Arthur S, Hodin, Richard, Heitritter, Shannon, Jr, Francis Moore, Dluhy, Robert, Sosa, Julie Ann, Ocal, I Tolgay, Benn, Diana E, Marsh, Deborah J, Robinson, Bruce G, Schneider, Katherine, Garber, Judy, Arum, Seth M, Korbonits, Márta, Grossman, Ashley, Pigny, Pascal, Toledo, Sérgio PA, Nosé, Vania, Li, Cheng, Stiles, Charles D

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Partial monosomy 13 and 21 due to a familial 13/21 translocation von Otto, P G, Toledo, S, Richieri-Costa, A, Otto, P A, Vianna-Morgante, A M, Kasahara, S

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