Encontrados 2 documentos, a visualizar página 1 de 1

Ordenado por Data

PROP1 gene analysis in Portuguese patients with combined pituitary hormone defi...

Lemos, MC; Gomes, L; Bastos, M; Leite, V; Limbert, E; Carvalho, D; Bacelar, C; Monteiro, M; Fonseca, F; Agapito, A; Castro, JJ; Regateiro, FJ

OBJECTIVE: Mutations of the PROP1 gene lead to combined pituitary hormone deficiency (CPHD), which is characterized by a deficiency of GH, TSH, LH/FSH, PRL and, less frequently, ACTH. This study was undertaken to investigate the molecular defect in a cohort of patients with CPHD. DESIGN, PATIENTS AND MEASUREMENTS: A multicentric study involving 46 cases of CPHD (17 familial cases belonging to seven kindreds and...


Assay of thyroglobulin in the study of patients with differentiated thyroid car...

Limbert, E; Dinarés, J M; Santos, M A; Henriques, M M

Data: 1984   |   Origem: Acta Médica Portuguesa

2 Resultados

Texto Pesquisado

Refinar resultados

Autor











Data



Tipo de Documento


Recurso



Assunto








    Financiadores do RCAAP

Fundação para a Ciência e a Tecnologia Universidade do Minho   Governo Português Ministério da Educação e Ciência Programa Operacional da Sociedade do Conhecimento União Europeia