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TITLE: Haplotype analysis of newly diagnosed Portuguese and Brazilian families with fibrinogen amyloidosis caused by the FGA p.Glu545Val variant
AUTHORS: Tavares, I ; Oliveira, ME; Maia, N; Moreira, L; Lacerda, PC; Santos, J; Santos, R; Costa, PP ; Lobato, L;
PUBLISHED: 2019, SOURCE: 16th International Symposium on Amyloidosis (ISA) in AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, VOLUME: 26, ISSUE: sup1
INDEXED IN: Scopus WOS CrossRef Handle
IN MY: ORCID
2
TITLE: Estrogen Metabolism-Associated CYP2D6 and IL6-174G/C Polymorphisms in Schistosoma haematobium Infection
AUTHORS: Cardoso, R ; Lacerda, PC; Costa, PP ; Machado, A; Carvalho, A; Bordalo, A; Fernandes, R; Soares, R ; Richter, J; Alves, H; Botelho, MC;
PUBLISHED: 2017, SOURCE: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, VOLUME: 18, ISSUE: 12
INDEXED IN: Scopus WOS CrossRef: 7 Handle
IN MY: ORCID
4
TITLE: Use of MALDI-TOF Mass Spectrometry to Assay the Transthyretin V30M Mutation in Serum From a Liver Transplant Donor: A Case Report. A Case Report
AUTHORS: Lacerda, PC; Moreira, L; Vitorino, R ; Costa, PP ;
PUBLISHED: 2015, SOURCE: TRANSPLANTATION, VOLUME: 99, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef Handle
IN MY: ORCID
5
TITLE: Inability of Mutant Transthyretin V30M to Cross the Blood-Eye Barrier
AUTHORS: Joao M Beirao ; Luciana V Moreira; Pedro C Lacerda; Rui P Vitorino ; Idalina B Beirao ; Paulo A Torres; Paulo P Costa ;
PUBLISHED: 2012, SOURCE: TRANSPLANTATION, VOLUME: 94, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 6
IN MY: ORCID
6
TITLE: Long-term follow-up of patients with hereditary fibrinogen A alpha-chain amyloidosis  Full Text
AUTHORS: Tavares, I ; Lobato, L; Moreira, L; Santos, J; Lacerda, P; Pinheiro, J; Costa, P;
PUBLISHED: 2011, SOURCE: Amyloid, VOLUME: 18, ISSUE: sup1
INDEXED IN: CrossRef: 2
IN MY: ORCID
7
TITLE: Genotyping Dombrock alleles in Portuguese blood donors by real-time PCR  Full Text
AUTHORS: Araujo, F ; Pereira, C; Monteiro, F; Henriques, I; Meireles, E; Lacerda, P; Cunha Ribeiro, LM; Reid, ME;
PUBLISHED: 2003, SOURCE: TRANSFUSION, VOLUME: 43, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef: 6
IN MY: ORCID
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TITLE: The clinical phenotype modulation of haemophilia by prothrombotic gene mutations  Full Text
AUTHORS: Araujo, F ; Fraga, M; Henriques, I; Monteiro, F; Meireles, E; Pereira, C; Lacerda, P; Cunha Ribeiro, LM;
PUBLISHED: 2003, SOURCE: HAEMOPHILIA, VOLUME: 9, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 5
IN MY: ORCID