Maria Leticia Sousa Ribeiro


AuthID: R-000-KT0

Confirmed Publications: 39



21
TITLE: Two new glucose-6-phosphate dehydrogenase mutations causing chronic hemolysis  Full Text
AUTHORS: Manco, L ; Goncalves, P; Macedo Ribeiro, S ; Seabra, C; Melo, P; Ribeiro, ML ;
PUBLISHED: 2005, SOURCE: HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, VOLUME: 90, ISSUE: 8
INDEXED IN: Scopus WOS
IN MY: ORCID
22
TITLE: Onset of X-linked sideroblastic anemia in the fourth decade  Full Text
AUTHORS: Cortesao, E; Vidan, J; Pereira, J; Goncalves, P; Ribeiro, ML ; Tamagnini, G;
PUBLISHED: 2004, SOURCE: HAEMATOLOGICA, VOLUME: 89, ISSUE: 10
INDEXED IN: Scopus WOS
IN MY: ORCID
23
TITLE: A band 3-based macrocomplex of integral and peripheral proteins in the RBC membrane
AUTHORS: Bruce, LJ; Beckmann, R; Ribeiro, ML ; Peters, LL; Chasis, JA; Delaunay, J; Mohandas, N; Anstee, DJ; Tanner, MJA;
PUBLISHED: 2003, SOURCE: BLOOD, VOLUME: 101, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
24
TITLE: Abnormal NK cell lymphocytosis detected after splenectomy: Association with repeated infections, relapsing neutropenia, and persistent polyclonal B-cell proliferation  Full Text
AUTHORS: Granjo, E; Lima, M ; Fraga, M; Santos, F; Magalhaes, C; Queiros, ML; Moreira, I; Rocha, S; Alice Santos-Silva ; Rebelo, I ; Quintanilha, A ; Ribeiro, ML ; Candeias, J; Orfao, A;
PUBLISHED: 2002, SOURCE: INTERNATIONAL JOURNAL OF HEMATOLOGY, VOLUME: 75, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
25
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
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
26
TITLE: A new PKLR gene mutation in the R-type promoter region affects the gene transcription causing pyruvate kinase deficiency  Full Text
AUTHORS: Manco, L ; Ribeiro, ML ; Maximo, V ; Almeida, H; Costa, A; Freitas, O; Barbot, J; Abade, A; Tamagnini, G;
PUBLISHED: 2000, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 110, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 43
IN MY: ORCID
27
TITLE: beta-thalassemia intermedia resulting from compound heterozygosity for an IVSI-1 (G-A) and a silent 5 ' UTR+33 (C-G) mutation  Full Text
AUTHORS: Bento, MC; Ribeiro, ML ; Cunha, E; Goncalves, P; Martin Nunez, G; Tamagnini, G;
PUBLISHED: 2000, SOURCE: HAEMATOLOGICA, VOLUME: 85, ISSUE: 4
INDEXED IN: Scopus WOS
IN MY: ORCID
28
TITLE: Elliptocytosis in patients with C-terminal domain mutations of protein 4.1 correlates with encoded messenger RNA levels rather than with alterations in primary protein structure
AUTHORS: Moriniere, M; Ribeiro, L ; Dalla Venezia, N; Deguillien, M; Maillet, P; Cynober, T; Delhommeau, F; Almeida, H; Tamagnini, G; Delaunay, J; Baklouti, F;
PUBLISHED: 2000, SOURCE: BLOOD, VOLUME: 95, ISSUE: 5
INDEXED IN: Scopus WOS
IN MY: ORCID
29
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
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
30
TITLE: Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3
AUTHORS: Ribeiro, ML ; Alloisio, N; Almeida, H; Gomes, C; Texier, P; Lemos, C; Mimoso, G; Morle, L; Bey Cabet, F; Rudigoz, RC; Delaunay, J; Tamagnini, G;
PUBLISHED: 2000, SOURCE: BLOOD, VOLUME: 96, ISSUE: 4
INDEXED IN: Scopus WOS
IN MY: ORCID
Page 3 of 4. Total results: 39.

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