Zobrazeno 1 - 10
of 737
pro vyhledávání: '"Delmar, M."'
Autor:
Paula B. Araujo, Mirna S. Carvallo, Ana P. Vidal, João B. Nascimento, Julia M. Wo, Erika O. Naliato, Silvio H. Cunha Neto, Flavia L. Conceição, Rosita Fontes, Vinicius V. de Lima, Denise P. Carvalho, Paula Soares, Jorge Lima, Delmar M. Lourenço, Alice Helena D. Violante
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Composite pheochromocytoma (CP) is a very rare tumor originating from neural crest cells, predominantly composed of pheochromocytoma (PCC), a chromaffin cell tumor arising in adrenal medulla, and ganglioneuroma, a tumor derived from autonomic ganglio
Externí odkaz:
https://doaj.org/article/d4f54fad152e4ea69f9f9102ddb27fb2
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:
Frontiers in Endocrinology, Vol 11 (2020)
Externí odkaz:
https://doaj.org/article/a7e2dee8bce44c8296153d287d017888
Autor:
Naiara C. B. Dantas, Carlos E. L. Soares, Manoel R. A. Martins, Delmar M. Lourenço, Ana R. P. Quidute
Publikováno v:
Frontiers in Endocrinology, Vol 10 (2019)
Context: Overall, giant prolactinomas are rare tumors (4%), especially those larger than 60 mm (1%). Despite the predominance of macroadenoma documented in multiple endocrine neoplasia type 1 (MEN1)-related prolactinoma, only three giant prolactinoma
Externí odkaz:
https://doaj.org/article/4a44dd5883d941d1bf2769cef83373c2
Autor:
Stephen J. Marx, Delmar M. Lourenço
Publikováno v:
Frontiers in Endocrinology, Vol 9 (2018)
Externí odkaz:
https://doaj.org/article/12ae1b93e1b84cb399da3461759de1b7
Akademický článek
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Akademický článek
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Publikováno v:
In Clinics July 2013 68(7):1039-1056
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:
Coutinho, Flavia L. *, Lourenco, Delmar M., Jr., Toledo, Rodrigo A., Montenegro, Fabio L.M., Toledo, Sergio P.A.
Publikováno v:
In Clinics April 2012 67 Supplement 1:169-172