Jose Manuel Baptista Cabeda


AuthID: R-002-1GF

Confirmed Publications: 35



21
TITLE: T-lymphocyte expression and function in hemochromatosis
AUTHORS: Maria de Sousa; Graça Porto; Fernando A Arosa; Carla Cardoso; Cabeda, JM ; Rosa Lacerda; José Fraga;
PUBLISHED: 2000, SOURCE: Hemochromatosis
INDEXED IN: CrossRef: 7
IN MY: ORCID
22
TITLE: Glucose-6-phosphate dehydrogenase deficiency in 2 girls [Défice de glicose-6-fosfato desidrogenase em duas crianças do sexo feminino.]
AUTHORS: Costa, E ; Cabeda, JM ; Abreu, ME; Silva, A; Morais, L; Alexandrino, AM; Justica, B; Barbot, J;
PUBLISHED: 1999, SOURCE: Acta medica portuguesa, VOLUME: 12, ISSUE: 7-11
INDEXED IN: Scopus
IN MY: ORCID
23
TITLE: T cell numbers relate to bone involvement in Gaucher disease  Full Text
AUTHORS: Lacerda, L; Arosa, FA ; Lacerda, R; Cabeda, JM ; Porto, G ; Amaral, O; Fortuna, A; Pinto, R; Oliveira, P ; McLaren, CE; Miranda, CS; de Sousa, M ;
PUBLISHED: 1999, SOURCE: BLOOD CELLS MOLECULES AND DISEASES, VOLUME: 25, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 40
IN MY: ORCID
24
TITLE: Unexpected pattern of beta-globin mutations in beta-thalassaemia patients from northern Portugal  Full Text
AUTHORS: Cabeda, JM ; Cristina Correia; Alexandra Estevinho; Carla Simoes; Maria Luis Amorim; Luciana Pinho; Benvindo JusticA;
PUBLISHED: 1999, SOURCE: British Journal of Haematology - Br J Haematol, VOLUME: 105, ISSUE: 1
INDEXED IN: CrossRef: 1
25
TITLE: Unexpected pattern of beta-globin mutations in beta-thalassaemia patients from northern Portugal  Full Text
AUTHORS: Cabeda, JM ; Correia, C; Estevinho, A; Simoes, C; Amorim, ML; Pinho, L; Justica, B;
PUBLISHED: 1999, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 105, ISSUE: 1
INDEXED IN: Scopus WOS
26
TITLE: HFE mutations in patients with hereditary haemochromatosis in Sweden. HFE MUTATIONS IN PATIENTS WITH HH IN SWEDEN  Full Text
AUTHORS: Cardoso, ; Stål, ; Hagen, ; Cabeda, JM ; Cabeda, ; Esin, ; De Sousa, ; Hultcrantz, ;
PUBLISHED: 1998, SOURCE: JOURNAL OF INTERNAL MEDICINE, VOLUME: 243, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 70
IN MY: ORCID
27
TITLE: Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA-A29, and non-classical forms of hemochromatosis  Full Text
AUTHORS: Porto, G ; Alves, H; Rodrigues, P ; Cabeda, JM ; Portal, C; Ruivo, A; Justica, B; Wolff, R; De Sousa, M ;
PUBLISHED: 1998, SOURCE: IMMUNOGENETICS, VOLUME: 47, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 49
IN MY: ORCID
28
TITLE: MHC class-I associations in iron overload: new link between the H63D mutation, HLA-A29 and “non-classical” haemochromatosis
AUTHORS: Porto, G; Alves, H; Rodrigues, P ; Cabeda, JM ; Portal, C; Ruivo, A; Justiça, B; Wolff, R; De Sousa, M;
PUBLISHED: 1998, SOURCE: Journal of Hepatology, VOLUME: 28
INDEXED IN: CrossRef
IN MY: ORCID
29
TITLE: Prevalence of the C282Y and H63D mutations in the HFE gene in patients with hereditary haemochromatosis and in control subjects from Northern Germany  Full Text
AUTHORS: Nielsen, P; Carpinteiro, S; Fischer, R; Cabeda, JM ; Porto, G ; Gabbe, EE;
PUBLISHED: 1998, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 103, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 57
IN MY: ORCID
30
TITLE: Pure red cell aplasia associated to clonal CD8+ T-cell large granular lymphocytosis: Dependence on cyclosporin A therapy
AUTHORS: Coutinho, J; Lima, M ; Teixeira, MD; Cabeda, JM ; Leite, F; Justica, B;
PUBLISHED: 1998, SOURCE: ACTA HAEMATOLOGICA, VOLUME: 100, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 7
IN MY: ORCID
Page 3 of 4. Total results: 35.

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