Maria Celeste Sena São Miguel Bento Lago de Queiroz
AuthID: R-001-F38
31
TITLE: Chronic haemolytic anaemia because of pyruvate kinase (PK) deficiency in a child heterozygous for haemoglobin S and no clinical features of sickle cell disease. Letter to the Editor Full Text
AUTHORS: Licinio Manco ; Jose M Manuel Vagace; Luis Relvas; Umbelina Rebelo; Celeste Bento; Ana Villegas; Maria Leticia Ribeiro;
PUBLISHED: 2010, SOURCE: EUROPEAN JOURNAL OF HAEMATOLOGY, VOLUME: 84, ISSUE: 1
AUTHORS: Licinio Manco ; Jose M Manuel Vagace; Luis Relvas; Umbelina Rebelo; Celeste Bento; Ana Villegas; Maria Leticia Ribeiro;
PUBLISHED: 2010, SOURCE: EUROPEAN JOURNAL OF HAEMATOLOGY, VOLUME: 84, ISSUE: 1
32
TITLE: Complex inheritance of chronic haemolytic anaemia Full Text
AUTHORS: Rita Coutinho; Celeste Bento; Helena Almeida; Elisabete Cunha; Licinio Manco ; Fatima Ferreira; Leticia L Ribeiro ;
PUBLISHED: 2009, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 144, ISSUE: 4
AUTHORS: Rita Coutinho; Celeste Bento; Helena Almeida; Elisabete Cunha; Licinio Manco ; Fatima Ferreira; Leticia L Ribeiro ;
PUBLISHED: 2009, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 144, ISSUE: 4
33
TITLE: The use of capillary blood samples in a large scale screening approach for the detection of beta-thalassemia and hemoglobin variants Full Text
AUTHORS: Celeste Bento; Luis Relvas; Helena Vazao ; Joana Campos; Umbelina Rebelo; Maria Leticia Ribeiro ;
PUBLISHED: 2006, SOURCE: HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, VOLUME: 91, ISSUE: 11
AUTHORS: Celeste Bento; Luis Relvas; Helena Vazao ; Joana Campos; Umbelina Rebelo; Maria Leticia Ribeiro ;
PUBLISHED: 2006, SOURCE: HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, VOLUME: 91, ISSUE: 11
INDEXED IN: 
Scopus 
WOS
Scopus WOS34
TITLE: Gene symbol: NT5C3. Disease: haemolytic anemia.
AUTHORS: Manco, L ; Pereira, J; Bento, MC; Ribeiro, ML;
PUBLISHED: 2005, SOURCE: Human genetics., VOLUME: 118, ISSUE: 3-4
AUTHORS: Manco, L ; Pereira, J; Bento, MC; Ribeiro, ML;
PUBLISHED: 2005, SOURCE: Human genetics., VOLUME: 118, ISSUE: 3-4
INDEXED IN: Scopus
Scopus35
TITLE: Gene symbol: HBA1. Disease: Haemoglobin alpha 1.
AUTHORS: Vazao, H; Bento, C; Ribeiro, L;
PUBLISHED: 2005, SOURCE: Human genetics, VOLUME: 117, ISSUE: 2-3
AUTHORS: Vazao, H; Bento, C; Ribeiro, L;
PUBLISHED: 2005, SOURCE: Human genetics, VOLUME: 117, ISSUE: 2-3
INDEXED IN: Scopus
Scopus36
TITLE: Consequences at mRNA level of the PKLR gene splicing mutations IVS10(+1) G -> C and IVS8(+2) T -> G causing pyruvate kinase deficiency Full Text
AUTHORS: Manco, L ; Bento, C; Ribeiro, ML ; Tamagnini, G;
PUBLISHED: 2002, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 118, ISSUE: 3
AUTHORS: Manco, L ; Bento, C; Ribeiro, ML ; Tamagnini, G;
PUBLISHED: 2002, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 118, ISSUE: 3
37
TITLE: Hb vila real [beta 36(C2)Pro -> His]: a newly discovered high oxygen affinity variant
AUTHORS: Bento, MC; Ribeiro, ML ; Cunha, E; Rebelo, U; Granjo, E; Granado, C; Tamagnini, GP;
PUBLISHED: 2000, SOURCE: HEMOGLOBIN, VOLUME: 24, ISSUE: 1
AUTHORS: Bento, MC; Ribeiro, ML ; Cunha, E; Rebelo, U; Granjo, E; Granado, C; Tamagnini, GP;
PUBLISHED: 2000, SOURCE: HEMOGLOBIN, VOLUME: 24, ISSUE: 1
38
TITLE: Genetic heterogeneity of beta-thalassemia in populations of the Iberian Peninsula
AUTHORS: Ribeiro, ML; Goncalves, P; Cunha, E; Bento, C; Almeida, H; Pereira, J; Nunez, GM; Tamagnini, GP;
PUBLISHED: 1997, SOURCE: HEMOGLOBIN, VOLUME: 21, ISSUE: 3
AUTHORS: Ribeiro, ML; Goncalves, P; Cunha, E; Bento, C; Almeida, H; Pereira, J; Nunez, GM; Tamagnini, GP;
PUBLISHED: 1997, SOURCE: HEMOGLOBIN, VOLUME: 21, ISSUE: 3
INDEXED IN: WOS 
CrossRef
WOS CrossRef