Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Delmar M. Lourenço Jr."'
Autor:
Delmar M. Lourenço Jr., Flavia L. Coutinho, Rodrigo A. Toledo, Tatiana Denck Gonçalves, Fabio L. M. Montenegro, Sergio P. A. Toledo
Publikováno v:
Clinics, Vol 67, Pp 99-108 (2012)
Primary hyperparathyroidism associated with multiple endocrine neoplasia type I (hyperparathyroidism/multiple endocrine neoplasia type 1) differs in many aspects from sporadic hyperparathyroidism, which is the most frequently occurring form of hyperp
Externí odkaz:
https://doaj.org/article/5566a23bd35f4a9a9959d6d4d935ce29
Autor:
Rodrigo A. Toledo, Tomoko Sekiya, Viviane C. Longuini, Flavia L. Coutinho, Delmar M. Lourenço Jr., Sergio P. A. Toledo
Publikováno v:
Clinics, Vol 67, Pp 3-6 (2012)
The finished version of the human genome sequence was completed in 2003, and this event initiated a revolution in medical practice, which is usually referred to as the age of genomic or personalized medicine. Genomic medicine aims to be predictive, p
Externí odkaz:
https://doaj.org/article/71b8c145ce00462682ccfcdca324e784
Autor:
Joya Emilie M. Correia-Deur, Rodrigo A. Toledo, Alice T. Imazawa, Delmar M. Lourenço Jr., Marilza C. L. Ezabella, Marcos R. Tavares, Sergio P. A. Toledo
Publikováno v:
Clinics, Vol 64, Iss 5, Pp 379-386 (2009)
INTRODUCTION: Medullary thyroid carcinoma may occur in a sporadic (s-medullary thyroid carcinoma, 75%) or in a multiple endocrine neoplasia type 2 form (MEN2, 25%). These clinical forms differ in many ways, as s-medullary thyroid carcinoma cases are
Externí odkaz:
https://doaj.org/article/7ea05c9457c648d6b74e178bf56c6a6e
Autor:
Flavia L. Coutinho, Delmar M. Lourenco Jr., Rodrigo A. Toledo, Fabio L. M. Montenegro, Sergio P. A. Toledo
Publikováno v:
Clinics, Vol 67, Pp 169-172 (2012)
The bone mineral density increments in patients with sporadic primary hyperparathyroidism after parathyroidectomy have been studied by several investigators, but few have investigated this topic in primary hyperparathyroidism associated with multiple
Externí odkaz:
https://doaj.org/article/4272f6c2cbd94d109839cdcc690bfd13
Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study
Autor:
Rui M B Maciel, Cleber P Camacho, Lígia V M Assumpção, Natassia E Bufalo, André L Carvalho, Gisah A de Carvalho, Luciana A Castroneves, Francisco M de Castro Jr, Lucieli Ceolin, Janete M Cerutti, Rossana Corbo, Tânia M B L Ferraz, Carla V Ferreira, M Inez C França, Henrique C R Galvão, Fausto Germano-Neto, Hans Graf, Alexander A L Jorge, Ilda S Kunii, Márcio W Lauria, Vera L G Leal, Susan C Lindsey, Delmar M Lourenço Jr, Léa M Z Maciel, Patrícia K R Magalhães, João R M Martins, M Cecília Martins-Costa, Gláucia M F S Mazeto, Anelise I Impellizzeri, Célia R Nogueira, Edenir I Palmero, Cencita H C N Pessoa, Bibiana Prada, Débora R Siqueira, Maria Sharmila A Sousa, Rodrigo A Toledo, Flávia O F Valente, Fernanda Vaisman, Laura S Ward, Shana S Weber, Rita V Weiss, Ji H Yang, Magnus R Dias-da-Silva, Ana O Hoff, Sergio P A Toledo, Ana L Maia
Publikováno v:
Endocrine Connections, Vol 8, Iss 3, Pp 289-298 (2019)
Multiple endocrine neoplasia type 2 (MEN2) is an autosomal dominant genetic disease caused by RET gene germline mutations that is characterized by medullary thyroid carcinoma (MTC) associated with other endocrine tumors. Several reports have demonstr
Externí odkaz:
https://doaj.org/article/37d0d78e06b24b48bb6c7725c95f14cc
Publikováno v:
Clinics, Vol 68, Iss 7, Pp 1039-1056 (2013)
Inherited endocrine tumors have been increasingly recognized in clinical practice, although some difficulties still exist in differentiating these conditions from their sporadic endocrine tumor counterparts. Here, we list the 12 main topics that coul
Externí odkaz:
https://doaj.org/article/4f99b932e0fe4feeb1a7576cb8d12027
Autor:
Rodrigo A. Toledo, Berenice B. Mendonca, Maria Candida B. V. Fragoso, Iberê C. Soares, Madson Q. Almeida, Michelle B. Moraes, Delmar M. Lourenço-Jr, Venâncio A. F. Alves, Marcello D. Bronstein, Sergio P. A. Toledo
Publikováno v:
Clinics, Vol 65, Iss 4, Pp 407-415 (2010)
OBJECTIVE: Non-pituitary tumors have been reported in a subset of patients harboring germline mutations in the aryl hydrocarbon receptor-interacting protein (AIP) gene. However, no detailed investigations of non-pituitary tumors of AIP-mutated patien
Externí odkaz:
https://doaj.org/article/bd3acfd134e94c3fb447bd7d6ce60425
Autor:
Sergio PA Toledo, Delmar M Lourenço Jr, Marcelo Augusto Santos, Marcos R Tavares, Rodrigo A Toledo, Joya Emilie de Menezes Correia-Deur
Publikováno v:
Clinics, Vol 64, Iss 7, Pp 699-706 (2009)
Hypercalcitoninemia has frequently been reported as a marker for medullary thyroid carcinoma. Currently, calcitonin measurements are mostly useful in the evaluation of tumor size and progression, and as an index of biochemical improvement of medullar
Externí odkaz:
https://doaj.org/article/ccccee9b581a4300ac534f51105fff18