Maria Leticia Sousa Ribeiro
AuthID: R-000-KT0
21
TITLE: Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells
AUTHORS: Zita Garate; Oscar Quintana Bustamante; Ana M Crane; Emmanuel Olivier; Laurent Poirot; Roman Galetto; Penelope Kosinski; Collin Hill; Charles Kung; Xabi Agirre; Israel Orman; Laura Cerrato; Omaira Alberquilla; Fatima Rodriguez Fornes; Noemi Fusaki; Felix Garcia Sanchez; Tabita M Maia; Maria L Ribeiro; Julian Sevilla; Felipe Prosper; ...More
PUBLISHED: 2015, SOURCE: STEM CELL REPORTS, VOLUME: 5, ISSUE: 6
AUTHORS: Zita Garate; Oscar Quintana Bustamante; Ana M Crane; Emmanuel Olivier; Laurent Poirot; Roman Galetto; Penelope Kosinski; Collin Hill; Charles Kung; Xabi Agirre; Israel Orman; Laura Cerrato; Omaira Alberquilla; Fatima Rodriguez Fornes; Noemi Fusaki; Felix Garcia Sanchez; Tabita M Maia; Maria L Ribeiro; Julian Sevilla; Felipe Prosper; ...More
PUBLISHED: 2015, SOURCE: STEM CELL REPORTS, VOLUME: 5, ISSUE: 6
22
TITLE: Convergence, similarities and distinctions in management across media industries
AUTHORS: Faustino, P; Ribeiro, L;
PUBLISHED: 2015, SOURCE: Managing Media Firms and Industries: What's So Special About Media Management?
AUTHORS: Faustino, P; Ribeiro, L;
PUBLISHED: 2015, SOURCE: Managing Media Firms and Industries: What's So Special About Media Management?
INDEXED IN: 
Scopus 
CrossRef
Scopus CrossRef23
TITLE: Genetic Basis of Congenital Erythrocytosis: Mutation Update and Online Databases Full Text
AUTHORS: Celeste Bento; Melanie J Percy; Betty Gardie; Tabita Magalhães Maia; Richard van Wijk; Silverio Perrotta; Fulvio Della Ragione; Helena Almeida; Cedric Rossi; François Girodon; Maria Åström; Drorit Neumann; Susanne Schnittger; Britta Landin; Milen Minkov; Maria Luigia Randi; Stéphane Richard; Nicole Casadevall; William Vainchenker; Susana Rives; ...More
PUBLISHED: 2014, SOURCE: HUMAN MUTATION, VOLUME: 35, ISSUE: 1
AUTHORS: Celeste Bento; Melanie J Percy; Betty Gardie; Tabita Magalhães Maia; Richard van Wijk; Silverio Perrotta; Fulvio Della Ragione; Helena Almeida; Cedric Rossi; François Girodon; Maria Åström; Drorit Neumann; Susanne Schnittger; Britta Landin; Milen Minkov; Maria Luigia Randi; Stéphane Richard; Nicole Casadevall; William Vainchenker; Susana Rives; ...More
PUBLISHED: 2014, SOURCE: HUMAN MUTATION, VOLUME: 35, ISSUE: 1
24
TITLE: JAK2V617F allele burden is associated with thrombotic mechanisms activation in polycythemia vera and essential thrombocythemia patients Full Text
AUTHORS: Margarida Coucelo; Goncalo Caetano; Teresa Sevivas; Susana Almeida Santos; Teresa Fidalgo; Celeste Bento; Manuela Fortuna; Marta Duarte; Cristina Menezes; Leticia Ribeiro, ML;
PUBLISHED: 2014, SOURCE: INTERNATIONAL JOURNAL OF HEMATOLOGY, VOLUME: 99, ISSUE: 1
AUTHORS: Margarida Coucelo; Goncalo Caetano; Teresa Sevivas; Susana Almeida Santos; Teresa Fidalgo; Celeste Bento; Manuela Fortuna; Marta Duarte; Cristina Menezes; Leticia Ribeiro, ML;
PUBLISHED: 2014, SOURCE: INTERNATIONAL JOURNAL OF HEMATOLOGY, VOLUME: 99, ISSUE: 1
25
TITLE: beta thalassemia major due to acquired uniparental disomy in a previously healthy adolescent Full Text
AUTHORS: Celeste Bento; Tabita M Maia; Jelena D Milosevic; Isabel M Carreira ; Robert Kralovics; Leticia L Ribeiro;
PUBLISHED: 2013, SOURCE: HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, VOLUME: 98, ISSUE: 1
AUTHORS: Celeste Bento; Tabita M Maia; Jelena D Milosevic; Isabel M Carreira ; Robert Kralovics; Leticia L Ribeiro;
PUBLISHED: 2013, SOURCE: HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, VOLUME: 98, ISSUE: 1
26
TITLE: Molecular diagnosis of haemophilia A at Centro Hospitalar de Coimbra in Portugal: study of 103 families-15 new mutations Full Text
AUTHORS: Silva Pinto, CS; Fidalgo, T; Salvado, R; Marques, D; Goncalves, E; Martinho, P; Markoff, A; Martins, N; Leticia Ribeiro, ML;
PUBLISHED: 2012, SOURCE: HAEMOPHILIA, VOLUME: 18, ISSUE: 1
AUTHORS: Silva Pinto, CS; Fidalgo, T; Salvado, R; Marques, D; Goncalves, E; Martinho, P; Markoff, A; Martins, N; Leticia Ribeiro, ML;
PUBLISHED: 2012, SOURCE: HAEMOPHILIA, VOLUME: 18, ISSUE: 1
INDEXED IN: Scopus 
WOS
Scopus WOS27
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
28
TITLE: Nonsense-mediated mRNA decay (NMD) blockage promotes nonsense mRNA stabilization in protein 4.1R deficient cells carrying the 4.1R Coimbra variant of hereditary elliptocytosis Full Text
AUTHORS: Madeleine Morinière; François Delhommeau; Alain Calender; Leticia Ribeiro; Jean Delaunay; Faouzi Baklouti;
PUBLISHED: 2010, SOURCE: Blood Cells, Molecules, and Diseases, VOLUME: 45, ISSUE: 4
AUTHORS: Madeleine Morinière; François Delhommeau; Alain Calender; Leticia Ribeiro; Jean Delaunay; Faouzi Baklouti;
PUBLISHED: 2010, SOURCE: Blood Cells, Molecules, and Diseases, VOLUME: 45, ISSUE: 4
29
TITLE: Novel human pathological mutations. Gene symbol: PKLR. Disease: pyruvate kinase deficiency.
AUTHORS: Manco, L ; Ribeiro, ML;
PUBLISHED: 2009, SOURCE: Human genetics, VOLUME: 125, ISSUE: 3
AUTHORS: Manco, L ; Ribeiro, ML;
PUBLISHED: 2009, SOURCE: Human genetics, VOLUME: 125, ISSUE: 3
INDEXED IN: Scopus
Scopus30
TITLE: Novel human pathological mutations. Gene symbol: PKLR. Disease: pyruvate kinase deficiency.
AUTHORS: Manco, L ; Trovoada, MJ; Ribeiro, ML;
PUBLISHED: 2009, SOURCE: Human genetics, VOLUME: 125, ISSUE: 3
AUTHORS: Manco, L ; Trovoada, MJ; Ribeiro, ML;
PUBLISHED: 2009, SOURCE: Human genetics, VOLUME: 125, ISSUE: 3
INDEXED IN: Scopus
Scopus