Maria Leticia Sousa Ribeiro


AuthID: R-000-KT0

Confirmed Publications: 39



1
TITLE: Hb PLASENCIA [alpha 125(H8)Leu -> Arg (alpha 2)] IS A FREQUENT CAUSE OF alpha(+)-THALASSEMIA IN THE PORTUGUESE POPULATION  Full Text
AUTHORS: Elizabete Cunha ; Celeste Bento; Ana Oliveira; Luis Relvas; Joana Neves; Mariline Gameiro; Cristina Barros; Ana Araujo; Ana Macedo; Paula Rocha; Ricardo Costa; Tabita Maia; Leticia Ribeiro, ML ;
PUBLISHED: 2013, SOURCE: HEMOGLOBIN, VOLUME: 37, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 1
IN MY: ORCID
2
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
INDEXED IN: Scopus WOS CrossRef: 3
IN MY: ORCID
3
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
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
4
TITLE: Transient Neonatal Cyanosis Associated With a New Hb F Variant: Hb F Viseu. Hb F Viseu
AUTHORS: Celeste Bento; Tabita Magalhaes Maia; Ines Carvalhais; Filipa Moita; Gabriela Abreu; Luis Relvas; Alexandra Pereira; Jose Farela Neves; Maria L Ribeiro ;
PUBLISHED: 2013, SOURCE: JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, VOLUME: 35, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
5
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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
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
7
TITLE: Pyruvate Kinase Deficiency in Sub-Saharan Africa: Identification of a Highly Frequent Missense Mutation (G829A; Glu277Lys) and Association with Malaria  Full Text
AUTHORS: Patricia Machado; Licinio Manco ; Claudia Gomes; Cristina Mendes; Natercia Fernandes; Graca Salome; Luis Sitoe; Sergio Chibute; Jose Langa; Leticia Ribeiro ; Juliana Miranda; Jorge Cano; Joao Pinto ; Amorim, Antonio ; Virgilio E do Rosario; Ana Paula Arez ;
PUBLISHED: 2012, SOURCE: PLOS ONE, VOLUME: 7, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef: 24
IN MY: ORCID
8
TITLE: Chronic hemolytic anemia is associated with a new glucose-6-phosphate dehydrogenase in-frame deletion in an older woman  Full Text
AUTHORS: Licinio Manco ; Janet Pereira; Luis Relvas; Umbelina Rebel; Ana Isabel Crisostomo; Celeste Bento; Leticia Ribeiro ;
PUBLISHED: 2011, SOURCE: BLOOD CELLS MOLECULES AND DISEASES, VOLUME: 46, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
9
TITLE: RhD variant caused by an in-frame triplet duplication in the RHD gene. IN-FRAME TRIPLET DUPLICATION IN RHD  Full Text
AUTHORS: Janet C Pereira; Maria J Rodrigues; Louise Tilley; Joyce Poole; Teresa Chabert; Maria L Ribeiro ;
PUBLISHED: 2011, SOURCE: TRANSFUSION, VOLUME: 51, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 6
IN MY: ORCID
10
Page 1 of 4. Total results: 39.

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