SAT-321 Bilateral Cortical Sparing Adrenalectomy For Treatment Of Pheochromocytoma In A MEN2-a Mutation Carrier: 19 Year Follow-up

por de Almeida, Tobias, Leitão, Cristiane, Maia, Ana, Koff, Walter, Czepielewski, Mauro
Publicado 2019

SUN-319 Failure Of Pasireotide To Control Hypoglycemia In A Men-1 Patient With Metastatic Insulinoma

por de Almeida, Tobias, Bertoluci, Marcello, Barkan, Sabrina, Marobin, Roberta, Czepielewski, Mauro
Publicado 2019

Fungus ball of the paranasal sinuses: Report of two cases and literature review

por Bosi, Guilherme Rasia, de Braga, Gustavo Lisbôa, de Almeida, Tobias Skrebsky, de Carli, Adriana
Publicado 2012

SAT-253 Long-Term Management and Successful Pregnancy of a Patient with a TSH Secreting Macroadenoma Treated with Octreotide

por de Almeida, Tobias Skrebsky, Salla, Rafaela Fenalti, Casagrande, Alessandra, Costenaro, Fabíola, Czepielewski, Mauro Antonio
Publicado 2020

SUN-932 Successful Response of Temozolomide (TMZ) in two Patients with Metastatic Pheochromocytoma/Paragangliomas (PPGLs)

por de Almeida, Tobias Skrebsky, Borges, Roberta P, Laís, Janeczko, Becker, Giovana Caroline Marx, Rodrigues, Ticiana Costa, Czepielewski, Mauro Antonio
Publicado 2020

Enhancing Cushing’s disease diagnosis: exploring the impact of desmopressin on ACTH gradient during BIPSS

por de Almeida, Tobias Skrebsky, Rodrigues, Ticiana da Costa, Costenaro, Fabíola, Scaffaro, Leandro Armani, Farenzena, Maurício, Gastaldo, Fernando, Czepielewski, Mauro Antônio
Publicado 2023

Complex consequences of Cantu syndrome SUR2 variant R1154Q in genetically modified mice

por Zhang, Haixia, Hanson, Alex, de Almeida, Tobias Scherf, Emfinger, Christopher, McClenaghan, Conor, Harter, Theresa, Yan, Zihan, Cooper, Paige E., Brown, G. Schuyler, Arakel, Eric C., Mecham, Robert P., Kovacs, Atilla, Halabi, Carmen M., Schwappach, Blanche, Remedi, Maria S., Nichols, Colin G.
Publicado 2021

Management of hypopituitarism: a perspective from the Brazilian Society of Endocrinology and Metabolism

por Garmes, Heraldo Mendes, Boguszewski, César Luiz, Miranda, Paulo Augusto Carvalho, Martins, Manoel Ricardo Alves, da Silva, Silvia Regina Correa, Abucham, Julio Zaki, Musolino, Nina Rosa de Castro, Vilar, Lucio, Portari, Luiz Henrique Corrêa, Gadelha, Mônica Roberto, Kasuki, Leandro, Naves, Luciana Ansaneli, Czepielewski, Mauro Antônio, de Almeida, Tobias Skrebsky, Duarte, Felipe Henning Gaia, Glezer, Andrea, Bronstein, Marcello Delano
Publicado 2021

Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies

por Iqbal, Maria, Maroofian, Reza, Çavdarlı, Büşranur, Riccardi, Florence, Field, Michael, Banka, Siddharth, Bubshait, Dalal K., Li, Yun, Hertecant, Jozef, Baig, Shahid Mahmood, Dyment, David, Efthymiou, Stephanie, Abdullah, Uzma, Makhdoom, Ehtisham Ul Haq, Ali, Zafar, Scherf de Almeida, Tobias, Molinari, Florence, Mignon-Ravix, Cécile, Chabrol, Brigitte, Antony, Jayne, Ades, Lesley, Pagnamenta, Alistair T., Jackson, Adam, Douzgou, Sofia, Beetz, Christian, Karageorgou, Vasiliki, Vona, Barbara, Rad, Aboulfazl, Baig, Jamshaid Mahmood, Sultan, Tipu, Alvi, Javeria Raza, Maqbool, Shazia, Rahman, Fatima, Toosi, Mehran Beiraghi, Ashrafzadeh, Farah, Imannezhad, Shima, Karimiani, Ehsan Ghayoor, Sarwar, Yasra, Khan, Sheraz, Jameel, Muhammad, Noegel, Angelika A., Budde, Birgit, Altmüller, Janine, Motameny, Susanne, Höhne, Wolfgang, Houlden, Henry, Nürnberg, Peter, Wollnik, Bernd, Villard, Laurent, Alkuraya, Fowzan Sami, Osmond, Matthew, Hussain, Muhammad Sajid, Yigit, Gökhan
Publicado 2021