Zobrazeno 1 - 8
of 8
pro vyhledávání: '"M. J. Bugalho"'
Autor:
A. P. Santos, J. Vinagre, P. Soares, I. Claro, A. C. Sanches, L. Gomes, I. Fernandes, A. L. Catarino, J. Preto, B. D. Pereira, A. P. Marques, F. Rodrigues, C. Amaral, G. Rocha, J. C. Mellidez, H. Simões, J. M. Lopes, M. J. Bugalho, On behalf of the NETs Study Group of the Portuguese Society of Endocrinology, Diabetes and Metabolism
Publikováno v:
International Journal of Endocrinology, Vol 2020 (2020)
Externí odkaz:
https://doaj.org/article/b89833f2959a4043a64786c1afb816b3
Autor:
A. P. Santos, J. Vinagre, P. Soares, I. Claro, A. C. Sanches, L. Gomes, I. Fernandes, A. L. Catarino, J. Preto, B. D. Pereira, A. P. Marques, F. Rodrigues, C. Amaral, G. Rocha, J. C. Mellidez, H. Simões, J. M. Lopes, M. J. Bugalho, On behalf of the NETs Study Group of the Portuguese Society of Endocrinology, Diabetes and Metabolism
Publikováno v:
International Journal of Endocrinology, Vol 2019 (2019)
Background. The incidence of gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs) has been increasing in the last five decades, but there is no large-scale data regarding these tumours in Portugal. We conducted a cross-sectional, multicentric s
Externí odkaz:
https://doaj.org/article/b06279028dfd4a7d9ad9e7f12debeb9b
Autor:
M J Bugalho, L G Sobrinho
Publikováno v:
Acta Médica Portuguesa, Vol 8, Iss 7-8 (1995)
Multiple endocrine neoplasia type 2 (MEN 2) is an autosomal dominant cancer syndrome. Clinical features and diagnostic aspects of this syndrome are reviewed with a focus on progress biochemical screening to genetic analysis of those at risk. The clin
Externí odkaz:
https://doaj.org/article/3f565c618e3d4fc1a04912a300a6c8fe
Publikováno v:
Journal of endocrinological investigation. 35(11)
Extra-adrenal paragangliomas (PGL) are rare neoplasms occurring in sporadic and familial forms, the latter mostly in association with germline mutations of SD- HB, SDHC or SDHD genes.Characterize frequency and spectrum of germline mutations among a c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9c9ffdd87c408b26a43a39a472063eff
https://pubmed.ncbi.nlm.nih.gov/22293219
https://pubmed.ncbi.nlm.nih.gov/22293219
Autor:
M J, Correia, L O, Lopes, M J, Bugalho, L, Cristina, A I, Santos, A D, Bordalo, B, Pinho, H L, da Silva, M D, Gonçalves, C, Ribeiro, J L, Tuna
Publikováno v:
Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology. 19(1)
Pheochromocytomas (Pheo) can occur sporadically, isolated or in association with other neuroendocrine lesions. In multiple endocrine neoplasia type 2A (MEN-2A), Pheo is associated to medullary thyroid carcinoma (MTC) or its precursor, C-cell hyperpla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fb2d54cde15fa31868852e5bdd8c7f89
https://pubmed.ncbi.nlm.nih.gov/10731789
https://pubmed.ncbi.nlm.nih.gov/10731789
Autor:
Nelson Wohllk, Pamela N. Schultz, Sangeeta Khorana, Carolyn Sue Richards, Gilbert J. Cote, Nelson G. Ordóñez, Helmuth Goepfert, Douglas B. Evans, M. M. J. Bugalho, Robert F. Gagel
Publikováno v:
The Journal of clinical endocrinology and metabolism. 81(10)
Analysis of peripheral blood or tumor DNA samples from 101 patients with apparent sporadic medullary thyroid carcinoma (MTC) was performed to assess the frequency of RET proto-oncogene mutations in this patient population. Peripheral blood and/or tum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::274306eacfafd4b84d5494d91240cdcb
https://pubmed.ncbi.nlm.nih.gov/8855832
https://pubmed.ncbi.nlm.nih.gov/8855832
Autor:
M J, Bugalho, L G, Sobrinho
Publikováno v:
Acta medica portuguesa. 8(7-8)
Multiple endocrine neoplasia type 2 (MEN 2) is an autosomal dominant cancer syndrome. Clinical features and diagnostic aspects of this syndrome are reviewed with a focus on progress biochemical screening to genetic analysis of those at risk. The clin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::52d2a222823bbd43c74d88f3e040694d
https://pubmed.ncbi.nlm.nih.gov/7484255
https://pubmed.ncbi.nlm.nih.gov/7484255
Autor:
M J, Bugalho, E, Limbert, L G, Sobrinho, A L, Clode, J, Soares, J F, Nunes, M C, Pereira, M A, Santos
Publikováno v:
Cancer. 70(11)
A kindred affected by multiple endocrine neoplasia type 2A (MEN 2A), associated with symmetric, bilateral, scapular pruritic skin lesions (PSL), is reported.There were 21 members, including the propositus, in four generations. Screening of 10 family
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::380ea16f57fc88f5e91915b963ca9c1d
https://pubmed.ncbi.nlm.nih.gov/1358428
https://pubmed.ncbi.nlm.nih.gov/1358428