Maria Celeste Sena São Miguel Bento Lago de Queiroz
AuthID: R-001-F38
31
TITLE: Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?) Full Text
AUTHORS: Celeste Bento; Helena Almeida; Tabita M Maia; Luis Relvas; Ana C Oliveira; Cedric Rossi; Francois Girodon; Carlos Fernandez Lago; Ascension Aguado Diaz; Cristina Fraga; Ricardo M Costa; Ana L Araujo; Joao Silva; Helena Vitoria; Natalina Miguel; Maria Pedro Silveira; Guillermo Martin Nunez; Maria Leticia Ribeiro ;
PUBLISHED: 2013, SOURCE: EUROPEAN JOURNAL OF HAEMATOLOGY, VOLUME: 91, ISSUE: 4
AUTHORS: Celeste Bento; Helena Almeida; Tabita M Maia; Luis Relvas; Ana C Oliveira; Cedric Rossi; Francois Girodon; Carlos Fernandez Lago; Ascension Aguado Diaz; Cristina Fraga; Ricardo M Costa; Ana L Araujo; Joao Silva; Helena Vitoria; Natalina Miguel; Maria Pedro Silveira; Guillermo Martin Nunez; Maria Leticia Ribeiro ;
PUBLISHED: 2013, SOURCE: EUROPEAN JOURNAL OF HAEMATOLOGY, VOLUME: 91, ISSUE: 4
32
TITLE: Primary familial congenital erythrocytosis: two novel EPOR mutations found in Spain Full Text
AUTHORS: Bento, C; Almeida, H; Fernandez Lago, C; Ribeiro, ML ;
PUBLISHED: 2013, SOURCE: INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, VOLUME: 35, ISSUE: 5
AUTHORS: Bento, C; Almeida, H; Fernandez Lago, C; Ribeiro, ML ;
PUBLISHED: 2013, SOURCE: INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, VOLUME: 35, ISSUE: 5
33
TITLE: Hb IBERIA [alpha 104(G11)Cys -> Arg, TGC > CGC (alpha 2) (HBA2:c.313T > C)], A NEW alpha-THALASSEMIC HEMOGLOBIN VARIANT FOUND IN THE IBERIAN PENINSULA: REPORT OF SIX CASES Full Text
AUTHORS: Celeste Bento; Ana Catarina Oliveira; Joana Neves; Mariline Gameiro; Elizabete Cunha ; Margarida Coucelo; Ricardo Marques Costa; Jose Barbot; Emilia Costa; Carlos Fernandez Lago; Leticia L Ribeiro ;
PUBLISHED: 2012, SOURCE: HEMOGLOBIN, VOLUME: 36, ISSUE: 6
AUTHORS: Celeste Bento; Ana Catarina Oliveira; Joana Neves; Mariline Gameiro; Elizabete Cunha ; Margarida Coucelo; Ricardo Marques Costa; Jose Barbot; Emilia Costa; Carlos Fernandez Lago; Leticia L Ribeiro ;
PUBLISHED: 2012, SOURCE: HEMOGLOBIN, VOLUME: 36, ISSUE: 6
34
TITLE: HIGH PREVALENCE OF HEMOGLOBIN DISORDERS AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE (G6PD) DEFICIENCY IN THE REPUBLIC OF GUINEA (WEST AFRICA) Full Text
AUTHORS: Tamba S Millimono; Kovana M Loua; Silvia L Rath; Luis Relvas; Celeste Bento; Mandiou Diakite; Martin Jarvis; Nathalie Daries; Leticia M Ribeiro ; Licinio Manco ; Jaspal S Kaeda;
PUBLISHED: 2012, SOURCE: HEMOGLOBIN, VOLUME: 36, ISSUE: 1
AUTHORS: Tamba S Millimono; Kovana M Loua; Silvia L Rath; Luis Relvas; Celeste Bento; Mandiou Diakite; Martin Jarvis; Nathalie Daries; Leticia M Ribeiro ; Licinio Manco ; Jaspal S Kaeda;
PUBLISHED: 2012, SOURCE: HEMOGLOBIN, VOLUME: 36, ISSUE: 1
35
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
36
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
37
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 WOS38
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
Scopus39
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
Scopus40
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
