Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Guilhermina Cantinho"'
Autor:
Aline Silva Barreto, António J.A. Nogueira, P. Vaz, Manuela Vieira, C. Barros, B. Martins, Ricardo Dias de Castro, R. Parafita, Lucília Salgado, D. Neves, Jorge Pereira, Pedro Almeida, Guilhermina Cantinho, I. Conde, C. Gaspar, T. Lucio, E Rodrigues, P. Simaozinho, Carla Oliveira, J. Vale, Gabriela R. Cardoso, Ana Santos, Pedro Teles, Aurora Carvalho, F. R. C. Costa, J.A.M. Santos, M. T. Rézio, Durval C. Costa, S. Pintao, F. Godinho, Francisco Alves, T. Reis, J. Isidoro
Publikováno v:
Revista Española de Medicina Nuclear e Imagen Molecular (English Edition). 34:1-8
© 2014 Elsevier España, S.L.U. and SEMNIM. All rights reserved.
Objectives: In 2009-2010 a Portuguese consortium was created to implement the methodologies proposed by the Dose Datamed II (DDM2) project, aiming to collect data from diagnostic
Objectives: In 2009-2010 a Portuguese consortium was created to implement the methodologies proposed by the Dose Datamed II (DDM2) project, aiming to collect data from diagnostic
Autor:
Maria da Conceição, Azevedo Coutinho, Nuno, Cortez-Dias, Guilhermina, Cantinho, Isabel, Conceição, Tatiana, Guimarães, Gustavo, Lima da Silva, Miguel, Nobre Menezes, Ana Rita, Francisco, Rui, Plácido, Fausto J, Pinto
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. 36(5)
Familial amyloid polyneuropathy (FAP) is a rare disease caused by systemic deposition of amyloidogenic variants of the transthyretin (TTR) protein. The TTR-V30M mutation is caused by the substitution of valine by methionine at position 30 and mainly
Autor:
Antonio Gouveia Oliveira, Mamede de Carvalho, Susana Gonçalves, Guilhermina Cantinho, Maria C. Azevedo Coutinho, António Nunes Diogo, Isabel Conceição, Nuno Cortez-Dias, Armando L. Bordalo e Sá, Ana G. Almeida
Publikováno v:
Circulation: Cardiovascular Imaging
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
© American Heart Association, Inc. All rights reserved. Unauthorized use prohibited.
Background: Transthyretin familial amyloid polyneuropathy is a hereditary form of amyloidosis characterized by sensorimotor and autonomic neuropathy, cardiac c
Background: Transthyretin familial amyloid polyneuropathy is a hereditary form of amyloidosis characterized by sensorimotor and autonomic neuropathy, cardiac c
Autor:
Isabel Santos, H. Pena, Rui Moreira, Célia Fernandes, Paula C. Campello, L. Patricio, Guilhermina Cantinho
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Novel mixed ligand oxotechnetium complexes of the type [(TcO)-Tc-99m(SSS)(SR)], in which the SR monodentate ligand is derived from dipeptides gly-gly, phe-gly and ala-gly, have been synthesized. These complexes, which have a molecular weight above 30