Výsledky vyhledávání - "Priscila S. Signorini"

A ten-year clinical update of a largeRETp.Gly533Cys kindred with medullary thyroid carcinoma emphasizes the need for an individualized assessment of affected relatives

Autor: Magnus R. Dias-da-Silva, Susan C. Lindsey, Teresa S. Kasamatsu, Alberto L. Machado, Janete M. Cerutti, Camila P. Salim, Rui M. B. Maciel, Flávia O. F. Valente, Cleber P. Camacho, Ana O. Hoff, Priscila S. Signorini, Rosana Delcelo, Maria Inez C. Franca

Publikováno v: Clinical Endocrinology. 80:235-245

SummaryObjective Reviewing the clinical outcomes of a large kindred with a RET p.Gly533Cys mutation, 10 years after the first description of this kindred, has provided an important set of clinical data for healthcare decision-making. Design and Patie

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dabaafc8507bb3f761feef87eca3ce85
https://doi.org/10.1111/cen.12264

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Extended RET gene analysis in patients with apparently sporadic medullary thyroid cancer: clinical benefits and cost

Autor: Misaki Y. Sittoni, Priscila S. Signorini, Cleber P. Camacho, Flávia O. F. Valente, Ji H. Yang, Magnus R. Dias-da-Silva, Susan C. Lindsey, Janete M. Cerutti, Ilda S. Kunii, Fausto Germano-Neto, Rui M. B. Maciel, Rosana Delcelo

Publikováno v: Hormonescancer. 3(4)

RET sequencing has become an important tool in medullary thyroid cancer (MTC) evaluation and should be performed even in the absence of family history of MTC. The most commonly studied exons in index cases are 8, 10, 11, and 13–16. To address the A

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4d5a0e77c578074a7a1b86baa75d8f0
https://pubmed.ncbi.nlm.nih.gov/22648435

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Early diagnosis of multiple endocrine neoplasia type 2B: a challenge for physicians

Autor: Flávia O. F. Valente, Mariana N. L. Oliveira, Ilda S. Kunii, Priscila S. Signorini, Rosa Paula M. Biscolla, Susan C. Lindsey, Ana O. Hoff, Janete M. Cerutti, Rui M. B. Maciel, Cleber P. Camacho

Publikováno v: Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 52, Issue: 8, Pages: 1393-1398, Published: NOV 2008
Arquivos Brasileiros de Endocrinologia & Metabologia v.52 n.8 2008
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM

BACKGROUND: The hereditary form of medullary thyroid carcinoma may occur isolated as a familial medullary thyroid carcinoma (FMTC) or as part of Multiple Endocrine Neoplasia 2A (MEN2A) and 2B (MEN2B). MEN2B is a rare syndrome, its phenotype may usual

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbf6fa1571ddd2bb5cc0f346d403f673
https://pubmed.ncbi.nlm.nih.gov/19169500

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