Maria Celeste Sena São Miguel Bento Lago de Queiroz
AuthID: R-001-F38
11
TITLE: Delirium: nursing interventions directed to the hospitalized adult patient– a bibliographic review Full Text
AUTHORS: Bento, MSPM; Marques, RMD; Sousa, PP;
PUBLISHED: 2018, SOURCE: Enfermeria Global, VOLUME: 17, ISSUE: 4
AUTHORS: Bento, MSPM; Marques, RMD; Sousa, PP;
PUBLISHED: 2018, SOURCE: Enfermeria Global, VOLUME: 17, ISSUE: 4
INDEXED IN: 
Scopus
Scopus12
TITLE: Detection of a homozygosity of a new nonsense mutation in the P5 ' N-1 coding gene in a case of pyrimidine-5-nucleotidase deficiency after thorough cytological diagnostic
AUTHORS: Kirschner, MMJ; Koschmieder, S; Manco, L; Bento, C; Kurth, I; Eggermann, T; Herwartz, R; Jost, E; Bruemmendorf, TH; Fuchs, R;
PUBLISHED: 2017, SOURCE: ONCOLOGY RESEARCH AND TREATMENT, VOLUME: 40
AUTHORS: Kirschner, MMJ; Koschmieder, S; Manco, L; Bento, C; Kurth, I; Eggermann, T; Herwartz, R; Jost, E; Bruemmendorf, TH; Fuchs, R;
PUBLISHED: 2017, SOURCE: ONCOLOGY RESEARCH AND TREATMENT, VOLUME: 40
INDEXED IN: 
WOS
WOS13
TITLE: Congenital dyserythropoietic anemia associated to a GATA1 mutation aggravated by pyruvate kinase deficiency Full Text
AUTHORS: Janet Pereira; Celeste Bento; Licinio Manco; Ataulfo Gonzalez; Jose Vagace; Maria Leticia Ribeiro;
PUBLISHED: 2016, SOURCE: ANNALS OF HEMATOLOGY, VOLUME: 95, ISSUE: 9
AUTHORS: Janet Pereira; Celeste Bento; Licinio Manco; Ataulfo Gonzalez; Jose Vagace; Maria Leticia Ribeiro;
PUBLISHED: 2016, SOURCE: ANNALS OF HEMATOLOGY, VOLUME: 95, ISSUE: 9
14
TITLE: "SEPARATING THE WHEAT FROM THE CHAFF" CONGENITAL HEMOLYTIC ANEMIA STUDY WITH A TARGETED NEXT GENERATION SEQUENCING PANEL Full Text
AUTHORS: Bento, C; Magalhaes Maia, TM; Oliveira, AC; Relvas, L; Almeida, H; Pereira, J; Cunha, E; Manco, L; Ribeiro, L;
PUBLISHED: 2016, SOURCE: 21st Congress of the European-Hematology-Association in HAEMATOLOGICA, VOLUME: 101
AUTHORS: Bento, C; Magalhaes Maia, TM; Oliveira, AC; Relvas, L; Almeida, H; Pereira, J; Cunha, E; Manco, L; Ribeiro, L;
PUBLISHED: 2016, SOURCE: 21st Congress of the European-Hematology-Association in HAEMATOLOGICA, VOLUME: 101
INDEXED IN: WOS
WOS15
TITLE: Gene panel sequencing improves the diagnostic work-up of patients with idiopathic erythrocytosis and identifies new mutations Full Text
AUTHORS: Carme Camps; Nayia Petousi; Celeste Bento; Holger Cario; Richard R Copley; Mary Frances McMullin; Richard van Wijk; Peter J Ratcliffe; Peter A Robbins; Jenny C Taylor;
PUBLISHED: 2016, SOURCE: HAEMATOLOGICA, VOLUME: 101, ISSUE: 11
AUTHORS: Carme Camps; Nayia Petousi; Celeste Bento; Holger Cario; Richard R Copley; Mary Frances McMullin; Richard van Wijk; Peter J Ratcliffe; Peter A Robbins; Jenny C Taylor;
PUBLISHED: 2016, SOURCE: HAEMATOLOGICA, VOLUME: 101, ISSUE: 11
INDEXED IN: Scopus WOS
Scopus WOS16
TITLE: Clinical relevance of erythrocyte ferritin in microcytic anemias Full Text
AUTHORS: Jose M Vagace; Antonio Pecas; Jorge Groiss; Celeste Bento; Maria Leticia Ribeiro; Guillermo Gervasini;
PUBLISHED: 2015, SOURCE: CLINICA CHIMICA ACTA, VOLUME: 442
AUTHORS: Jose M Vagace; Antonio Pecas; Jorge Groiss; Celeste Bento; Maria Leticia Ribeiro; Guillermo Gervasini;
PUBLISHED: 2015, SOURCE: CLINICA CHIMICA ACTA, VOLUME: 442
17
TITLE: Polymorphic variations influencing fetal hemoglobin levels: Association study in beta-thalassemia carriers and in normal individuals of Portuguese origin Full Text
AUTHORS: Clara Pereira; Luis Relvas; Celeste Bento; Augusto Abade; Leticia Ribeiro, ML; Licinio Manco;
PUBLISHED: 2015, SOURCE: BLOOD CELLS MOLECULES AND DISEASES, VOLUME: 54, ISSUE: 4
AUTHORS: Clara Pereira; Luis Relvas; Celeste Bento; Augusto Abade; Leticia Ribeiro, ML; Licinio Manco;
PUBLISHED: 2015, SOURCE: BLOOD CELLS MOLECULES AND DISEASES, VOLUME: 54, ISSUE: 4
18
TITLE: Outcomes of pregnancy in patients with congenital erythrocytosis Full Text
AUTHORS: Mary F McMullin; Celeste Bento; Cedric Rossi; Glenn G Rainey; Francois Girodon; Holger Cario;
PUBLISHED: 2015, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 170, ISSUE: 4
AUTHORS: Mary F McMullin; Celeste Bento; Cedric Rossi; Glenn G Rainey; Francois Girodon; Holger Cario;
PUBLISHED: 2015, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 170, ISSUE: 4
INDEXED IN: WOS 
CrossRef
WOS CrossRef19
TITLE: HEREDITARY HEMOLYTIC ANEMIA BY GPI DEFICIENCY: TWO NEW MUTATIONS IN A PORTUGUESE MALE Full Text
AUTHORS: Manco, L; Bento, C; Relvas, L; Seabra, C; Ribeiro, ML;
PUBLISHED: 2015, SOURCE: 57th National Congress of the Spanish-Society-of-Hematology-and-Hemotherapy in HAEMATOLOGICA, VOLUME: 100
AUTHORS: Manco, L; Bento, C; Relvas, L; Seabra, C; Ribeiro, ML;
PUBLISHED: 2015, SOURCE: 57th National Congress of the Spanish-Society-of-Hematology-and-Hemotherapy in HAEMATOLOGICA, VOLUME: 100
INDEXED IN: WOS
WOS20
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
