Maria Leticia Sousa Ribeiro


AuthID: R-000-KT0

Confirmed Publications: 39



31
TITLE: PK-LR gene mutations in pyruvate kinase deficient Portuguese patients  Full Text
AUTHORS: Manco, L ; Ribeiro, ML ; Almeida, H; Freitas, O; Abade, A; Tamagnini, G;
PUBLISHED: 1999, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 105, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 20
IN MY: ORCID
32
TITLE: Hemoglobin disorders in Macao
AUTHORS: Ribeiro, ML ; Tamagnini, GP;
PUBLISHED: 1997, SOURCE: HEMOGLOBIN, VOLUME: 21, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
33
TITLE: Hh Lepore-Baltimore (delta(68Leu)-beta(84Thr)) and Hh Lepore-Washington-Boston (delta(87Gln)-delta(IVS-II-8)) in Central Portugal and Spanish Alta Extremadura  Full Text
AUTHORS: Ribeiro, ML ; Cunha, E; Goncalves, P; Nunez, GM; Galan, MAF; Tamagnini, GP; Smetanina, NS; Gu, LH; Huisman, THJ;
PUBLISHED: 1997, SOURCE: HUMAN GENETICS, VOLUME: 99, ISSUE: 5
INDEXED IN: Scopus WOS
IN MY: ORCID
34
TITLE: Modulation of clinical expression and band 3 deficiency in hereditary spherocytosis
AUTHORS: Alloisio, N; Texier, P; Vallier, A; Ribeiro, ML ; Morle, L; Bozon, M; Bursaux, E; Maillet, P; Goncalves, P; Tanner, MJA; Tamagnini, G; Delaunay, J;
PUBLISHED: 1997, SOURCE: American-Society-of-Haematology Annual Meeting in BLOOD, VOLUME: 90, ISSUE: 1
INDEXED IN: Scopus WOS
IN MY: ORCID
35
TITLE: A VARIANT OF SPECTRIN LOW-EXPRESSION ALLELE ALPHA(LELY) CARRYING A HEREDITARY ELLIPTOCYTOSIS MUTATION IN CODON-28
AUTHORS: RANDON, J; BOULANGER, L; MARECHAL, J; GARBARZ, M; VALLIER, A; RIBEIRO, L ; TAMAGNINI, G; DHERMY, D; DELAUNAY, J;
PUBLISHED: 1994, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 88, ISSUE: 3
INDEXED IN: Scopus WOS
IN MY: ORCID
36
TITLE: POSSIBLE FACTORS INFLUENCING THE HEMOGLOBIN AND FETAL HEMOGLOBIN LEVELS IN PATIENTS WITH BETA-THALASSEMIA DUE TO A HOMOZYGOSITY FOR THE IVS-I-6 (T-]C) MUTATION
AUTHORS: EFREMOV, DG; DIMOVSKI, AJ; BAYSAL, E; YE, Z; ADEKILE, AD; RIBEIRO, MLS ; SCHILIRO, G; ALTAY, C; GURGEY, A; EFREMOV, GD; HUISMAN, THJ;
PUBLISHED: 1994, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 86, ISSUE: 4
INDEXED IN: WOS
37
TITLE: BETA-THALASSEMIA MUTATIONS IN THE PORTUGUESE - HIGH-FREQUENCIES OF 2 ALLELES IN RESTRICTED POPULATIONS
AUTHORS: TAMAGNINI, GP; GONCALVES, P; RIBEIRO, MLS ; KAEDA, J; KUTLAR, F; BAYSAL, E; HUISMAN, THJ;
PUBLISHED: 1993, SOURCE: HEMOGLOBIN, VOLUME: 17, ISSUE: 1
INDEXED IN: Scopus WOS
IN MY: ORCID
38
TITLE: A NOVEL BETA-DEGREES-THALASSEMIA MUTATION (CODON-15, TGG-]TGA) IS PREVALENT IN A POPULATION OF CENTRAL PORTUGAL
AUTHORS: RIBEIRO, MLS ; BAYSAL, E; KUTLAR, F; TAMAGNINI, GP; GONCALVES, P; LOPES, D; HUISMAN, THJ;
PUBLISHED: 1992, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 80, ISSUE: 4
INDEXED IN: Scopus WOS
IN MY: ORCID
39
TITLE: HB-COIMBRA OR ALPHA-2-BETA-299(G1)ASP-]GLU, A NEWLY DISCOVERED HIGH OXYGEN-AFFINITY VARIANT
AUTHORS: TAMAGNINI, GP; RIBEIRO, ML ; VALENTE, V; RAMACHANDRAN, M; WILSON, JB; BAYSAL, E; GU, LH; HUISMAN, THJ;
PUBLISHED: 1991, SOURCE: HEMOGLOBIN, VOLUME: 15, ISSUE: 6
INDEXED IN: Scopus WOS
IN MY: ORCID
Page 4 of 4. Total results: 39.

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