21
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
INDEXED IN: Scopus WOS CrossRef
22
TITLE: Polycythaemia-inducing mutations in the erythropoietin receptor (EPOR): mechanism and function as elucidated by epidermal growth factor receptor-EPOR chimeras  Full Text
AUTHORS: Mor Gross; Nathalie Ben Califa; Mary F McMullin; Melanie J Percy; Celeste Bento; Holger Cario; Milen Minkov; Drorit Neumann;
PUBLISHED: 2014, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 165, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef
23
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
24
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
26
TITLE: Erythrocytosis in Children and Adolescents-Classification, Characterization, and Consensus Recommendations for the Diagnostic Approach. Erythrocytosis in Children and Adolescents  Full Text
AUTHORS: Holger Cario; Mary Frances McMullin; Celeste Bento; Dagmar Pospisilova; Melanie J Percy; Kais Hussein; Jiri Schwarz; Maria Astrom; Sylvie Hermouet;
PUBLISHED: 2013, SOURCE: PEDIATRIC BLOOD & CANCER, VOLUME: 60, ISSUE: 11
INDEXED IN: Scopus WOS CrossRef
27
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
28
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
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