Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Fabio Y Tanno"'
Autor:
Gustavo F C Fagundes, Felipe Freitas-Castro, Lucas S Santana, Ana Caroline F Afonso, Janaina Petenuci, Mariana F A Funari, Augusto G Guimaraes, Felipe L Ledesma, Maria Adelaide A Pereira, Carolina R Victor, Marcela S M Ferrari, Fernando M A Coelho, Victor Srougi, Fabio Y Tanno, Jose L Chambo, Ana Claudia Latronico, Berenice B Mendonca, Maria Candida B V Fragoso, Ana O Hoff, Madson Q Almeida
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism.
ContextLimited information is available concerning the genetic spectrum of pheochromocytoma and paraganglioma (PPGL) patients in South America. Germline SDHB large deletions are very rare worldwide, but most of the individuals harboring the SDHB exon
Autor:
Maria Candida Barisson Villares Fragoso, Fernando Ide Yamauchi, Madson Q. Almeida, Berenice B. Mendonca, Ana Claudia Latronico, Sheila Aparecida Coelho Siqueira, Jose Luis Chambo, Ana O. Hoff, Silvia C Soares, Francisco Tibor Dénes, Augusto G Guimaraes, Janaina Petenuci, Roberto Iglesias Lopes, Anna Flavia Figueredo Benedetti, Maria Adelaide Albergaria Pereira, Gustavo F C Fagundes, Fabio Y Tanno, Victor Srougi, Maria Claudia Nogueira Zerbini, Ana Caroline F Afonso
Publikováno v:
Clinical Endocrinology. 95:117-124
Objective Few and conflicting reports have characterized the genetics of paediatric pheochromocytomas and paragangliomas (PPGLs). This study aimed to investigate the clinical and genetic features of Brazilian children with PPGL. Patients and methods
Autor:
Bruna Pilan, Ana Claudia Latronico, Antonio Lerario, Anna Flavia Figueredo Benedetti, Victor Srougi, Luciano F. Drager, Leticia A P Vilela, Tatiana S Goldbaum, Luiz Aparecido Bortolotto, Berenice B. Mendonca, Marcela Rassi-Cruz, Maria Adelaide Albergaria Pereira, Fabio R. Faucz, Lucas Santos de Santana, Aline C B S Cavalcante, Fabio Y Tanno, Jose Luis Chambo, Andrea Gutierrez Maria, Maria Candida Barisson Villares Fragoso, Francisco Cesar Carnevale, Maria Claudia Nogueira Zerbini, Edra London, Madson Q. Almeida, Constantine A. Stratakis
Publikováno v:
Endocr Relat Cancer
Familial primary aldosteronism (PA) is rare and mostly diagnosed in early-onset hypertension (HT). However, ‘sporadic’ bilateral adrenal hyperplasia (BAH) is the most frequent cause of PA and remains without genetic etiology in most cases. Our ai
Autor:
Ana Alice W Maciel, Thais C Freitas, Gustavo F C Fagundes, Janaina Petenuci, Leticia A P Vilela, Luciana P Brito, Tatiana S Goldbaum, Maria Claudia N Zerbini, Felipe L Ledesma, Fabio Y Tanno, Victor Srougi, Jose L Chambo, Maria Adelaide A Pereira, Fernando M A Coelho, Aline C B S Cavalcante, Francisco C Carnevale, Bruna Pilan, Andrea Pio-Abreu, João V Silveira, Fernanda M Consolim-Colombo, Luiz A Bortolotto, Ana Claudia Latronico, Maria Candida B V Fragoso, Luciano F Drager, Berenice B Mendonca, Madson Q Almeida
Publikováno v:
The Journal of clinical endocrinology and metabolism.
Context Primary aldosteronism (PA) screening relies on an elevated aldosterone to renin ratio with a minimum aldosterone level, which varies from 10 to 15 ng/dL (277-415.5 pmol/L) using immunoassay. Objective To evaluate intra-individual coefficient
Autor:
Maria Cbv Fragoso, Vidhush K. Yarlagadda, Miguel Srougi, Jose Luis Chambo, John Phillips, Fabio Y Tanno, Jennifer Gordetsky, Jonathan Bloom, Victor Srougi, Soroush Rais-Bahrami, Madson Q. Almeida, Luciana Schultz
Publikováno v:
International Journal of Urology. 27:463-468
Objectives To develop a preoperative nomogram that would predict the risk of a postoperative complication for pheochromocytoma patients undergoing adrenalectomy using an international database. Methods We retrospectively analyzed preoperative variabl
Autor:
Jennifer B. Gordetsky, John Phillips, Andrew M. Fang, Jennifer Rosen, Ava Saidian, Jose Luis Chambo, Soroush Rais-Bahrami, Victor Srougi, Jonathan Bloom, Sejong Bae, Fabio Y Tanno
Publikováno v:
J Robot Surg
While multiple studies have demonstrated that minimally invasive surgical (MIS) techniques are a safe and efficacious approach to adrenalectomy for pheochromocytomas (PC), these studies have only been small comparative studies. The aim of this multi-
Autor:
Marcos F. Dall'Oglio, Juliana M. Sousa-Canavez, Fabio Y. Tanno, Bruno C. Tiseo, Alexandre Crippa, Sabrina T. dos Reis, Katia R. M. Leite, Miguel Srougi
Publikováno v:
International Brazilian Journal of Urology, Vol 37, Iss 2, Pp 180-186 (2011)
PURPOSE: Metastatic renal cell carcinoma (RCC) is one of the most treatment-resistant malignancies and nephrectomy, isolated or combined with systemic chemotherapy typically has limited or no effectiveness. We report our initial results in patients t
Externí odkaz:
https://doaj.org/article/704a0ae72d0c440c8d83203c6561c8b0
Autor:
Gustavo F Fagundes, Madson Q Almeida, Lucas Santana, Felipe Castro, Ana Caroline Afonso, Janaina Petenuci, Mariana Funari, Augusto G Guimarães, Elaine V Sales, Ana Vieites, Gabriela Sanso, Felipe L Ledesma, Sheila Siqueira, Maria Adelaide A Pereira, Fabio Y Tanno, Vitor Srougi, Jose L Chambo, Carolina R Victor, Marcela S Ferrari, Fernando M Coelho, Silvia C Soares, Ana Claudia Latronico, Berenice B Mendonca, Maria Candida BV Fragoso, Ana O Hoff
Publikováno v:
Journal of the Endocrine Society. 6:A134-A134
Background Pheochromocytomas and paragangliomas (PPGLs) have the highest degree of heritability among endocrine tumors. Currently, ∼40% of PPGL individuals have a genetic germline pathogenic variant and exist at least 12 different genetic syndromes
Autor:
Gustavo F C Fagundes, Ana Claudia Latronico, Ana O. Hoff, Maria Claudia Nogueira Zerbini, Delmar M. Lourenço, Antonio M. Lerario, Victor Srougi, Berenice B. Mendonca, Fabio Y Tanno, Janaina Petenuci, Sheila Aparecida Coelho Siqueira, Ericka B. Trarbach, Joya Emilie Correa D’Eur, Jose Luis Chambo, Maria Adelaide Albergaria Pereira, Maria Candida Barisson Villares Fragoso, Fernando Ide Yamauchi, Madson Q. Almeida
Publikováno v:
Journal of the Endocrine Society
Context Von Hippel-Lindau (VHL) disease is an autosomal dominant syndrome caused by germline mutations in the VHL gene. Guidelines recommend pheochromocytoma (PHEO) biochemical screening should start at age 5 years. Objective Genotype–phenotype cor
Autor:
Berenice B. Mendonca, Fabio Y Tanno, Augusto G Guimaraes, Janaina Petenuci, Gustavo F C Fagundes, Ana Claudia Latronico, Fábio Luiz de Menezes Montenegro, Ana O. Hoff, Aurea Luiza F. Magalhães, João Evangelista Bezerra Neto, Maria Claudia Nogueira Zerbini, Ana Caroline F Afonso, Jose Luis Chambo, Maria Candida Barisson Villares Fragoso, Anna Flavia Figueredo Benedetti, George Barberio Coura-Filho, Maria Adelaide Albergaria Pereira, Madson Q. Almeida, Flavia T. Mota, Victor Srougi, Marcela S. S. Ferrari, Sheila Aparecida Coelho Siqueira
Publikováno v:
Endocrine. 72(2)