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DC Field | Value | Language |
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dc.contributor | Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP | - |
dc.contributor.author | TOLEDO, Sergio P. A. | - |
dc.contributor.author | LOURENCO JR., Delmar M. | - |
dc.contributor.author | TOLEDO, Rodrigo A. | - |
dc.date.accessioned | 2014-01-28T22:17:25Z | - |
dc.date.available | 2014-01-28T22:17:25Z | - |
dc.date.issued | 2013 | - |
dc.identifier.citation | CLINICS, v.68, n.7, p.1039-1056, 2013 | - |
dc.identifier.issn | 1807-5932 | - |
dc.identifier.uri | https://observatorio.fm.usp.br/handle/OPI/3936 | - |
dc.description.abstract | 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 could add helpful information and clues for performing an early differential diagnosis to distinguish between these conditions. The early diagnosis of patients with inherited endocrine tumors may be performed either clinically or by mutation analysis in at-risk individuals. Early detection usually has a large impact in tumor management, allowing preventive clinical or surgical therapy in most cases. Advice for the clinical and surgical management of inherited endocrine tumors is also discussed. In addition, recent clinical and genetic advances for 17 different forms of inherited endocrine tumors are briefly reviewed. | - |
dc.description.sponsorship | National Research Council (CNPq) [401990/2010-9] | - |
dc.description.sponsorship | State Research Foundation (FAPESP) | - |
dc.description.sponsorship | CNPq | - |
dc.description.sponsorship | FAPESP | - |
dc.language.iso | eng | - |
dc.publisher | HOSPITAL CLINICAS, UNIV SAO PAULO | - |
dc.relation.ispartof | Clinics | - |
dc.rights | openAccess | - |
dc.subject.other | medullary-thyroid carcinoma | - |
dc.subject.other | neoplasia type-1 men1 | - |
dc.subject.other | genotype-phenotype correlation | - |
dc.subject.other | isolated pituitary-adenomas | - |
dc.subject.other | hippel-lindau syndrome | - |
dc.subject.other | pancreatic neuroendocrine tumors | - |
dc.subject.other | pediatric adrenocortical tumor | - |
dc.subject.other | adrenal-cortical carcinoma | - |
dc.subject.other | interacting protein gene | - |
dc.subject.other | neurofibromatosis type-i | - |
dc.title | A differential diagnosis of inherited endocrine tumors and their tumor counterparts | - |
dc.type | article | - |
dc.rights.holder | Copyright HOSPITAL CLINICAS, UNIV SAO PAULO | - |
dc.identifier.doi | 10.6061/clinics/2013(07)24 | - |
dc.identifier.pmid | 23917672 | - |
dc.subject.wos | Medicine, General & Internal | - |
dc.type.category | review | - |
dc.type.version | publishedVersion | - |
hcfmusp.author.external | TOLEDO, Rodrigo A.:Univ Texas Hlth Sci Ctr San Antonio, San Antonio, TX 78229 USA | - |
hcfmusp.description.beginpage | 1039 | - |
hcfmusp.description.endpage | 1056 | - |
hcfmusp.description.issue | 7 | - |
hcfmusp.description.volume | 68 | - |
hcfmusp.origem | WOS | - |
hcfmusp.origem.id | 2-s2.0-84881243586 | - |
hcfmusp.origem.id | WOS:000322601600024 | - |
hcfmusp.origem.id | SCIELO:S1807-59322013000701039 | - |
hcfmusp.publisher.city | SAO PAULO | - |
hcfmusp.publisher.country | BRAZIL | - |
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dc.description.index | MEDLINE | - |
hcfmusp.remissive.sponsorship | CNPq | - |
hcfmusp.remissive.sponsorship | FAPESP | - |
hcfmusp.citation.scopus | 13 | - |
hcfmusp.scopus.lastupdate | 2024-04-12 | - |
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