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of 44
pro vyhledávání: '"proto-oncogene ret"'
IMPLICAÇÕES CLÍNICAS DO DIAGNÓSTICO MOLECULAR NO MANEJO DO CARCINOMA MEDULAR DE TIREÓIDE HEREDITÁRIO
Publikováno v:
Clinical and Biomedical Research, Vol 23, Iss 1 - 2 (2022)
O carcinoma medular de tireóide (CMT) hereditário pode apresentar-se como componente das síndromes de Neoplasia Endócrina Múltipla (NEM 2A e 2B) ou Carcinoma Medular de Tireóide Familiar (CMTF). Diferentes mutações no RET foram identificadas
Externí odkaz:
https://doaj.org/article/38b3d9acc66b46dab905ba0691917be7
Akademický článek
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Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 44, Iss 4, Pp 535-539 (2016)
This article provides our own clinical observation of the patient with multiple endocrine neoplasia type 2B (MEN2B) associated with a germinal mutation in the RET proto-oncogene. Although there are highly informative laboratory methods available, in
Externí odkaz:
https://doaj.org/article/e32fa037f0a4481bae88bda500114e2d
Publikováno v:
Опухоли головы и шеи, Vol 0, Iss 4, Pp 23-28 (2015)
MEN 2B syndrome is a subtype of the multiple endocrine neoplasia type 2. It is characterized by the development of aggressive forms of medullary thyroid cancer at an early age, pheochromocytoma and hyperparathyroid syndrome. This article provides an
Externí odkaz:
https://doaj.org/article/b6455ad9a5344fcea50d283bb6a67fe0
IMPLICAÇÕES CLÍNICAS DO DIAGNÓSTICO MOLECULAR NO MANEJO DO CARCINOMA MEDULAR DE TIREÓIDE HEREDITÁRIO
Publikováno v:
Clinical & Biomedical Research; Vol. 23 No. 1-2 (2003): Revista HCPA
Clinical and Biomedical Research; v. 23 n. 1-2 (2003): Revista HCPA
Clinical and Biomedical Research
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Clinical and Biomedical Research; v. 23 n. 1-2 (2003): Revista HCPA
Clinical and Biomedical Research
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Hereditary MTC can occur either alone – familial MTC (FMTC) – or as the thyroid manifestation of multiple endocrine neoplasia type 2 (MEN 2) syndromes (MEN 2A and MEN 2B) or others. Three phenotypic subtypes have been reported. MEN 2A(1), MEN 2A(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0ac237dab880b802f8277d4824b8d4f6
https://seer.ufrgs.br/index.php/hcpa/article/view/126198
https://seer.ufrgs.br/index.php/hcpa/article/view/126198
Akademický článek
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Autor:
Sini, Valentina, DE IULIIS, Francesca, Rossi, Lorena, Lunardi, Gianluigi, Menghi, Antonello, Pecorella, Irene, Lanza, Rosina, Scarpa, Susanna
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3686::728f1176aa29a2b9e0bb05e08a18b3db
http://hdl.handle.net/11573/1197046
http://hdl.handle.net/11573/1197046
Akademický článek
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Autor:
Marco Aurélio Vamondes Kulcsar, Gláucia Maria Ferreira da Silva Mazeto, Alfio José Tincani, Débora Rodrigues Siqueira, Ana Luiza Maia, Léa Maria Zanini Maciel
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 58, Issue: 7, Pages: 667-700, Published: OCT 2014
SciELO
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Arquivos Brasileiros de Endocrinologia & Metabologia v.58 n.7 2014
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
SciELO
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Arquivos Brasileiros de Endocrinologia & Metabologia v.58 n.7 2014
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Made available in DSpace on 2015-02-02T12:39:11Z (GMT). No. of bitstreams: 0 Previous issue date: 2014-10-01Bitstream added on 2015-02-02T13:08:20Z : No. of bitstreams: 1 S0004-27302014000700667.pdf: 387060 bytes, checksum: fd70892aaed366def2b589f132
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4897e6c2b20a14c98b26526c5217afff
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302014000700667&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302014000700667&lng=en&tlng=en
Publikováno v:
Cancer Management and Research
Medullary thyroid carcinoma (MTC) is a rare malignant tumor originating from thyroid parafollicular C cells. This tumor accounts for 3%-4% of thyroid gland neoplasias. MTC may occur sporadically or be inherited. Hereditary MTC appears as part of the