11
TITLE: Newborn screening for sickle cell disease in Europe: recommendations from a Pan-European Consensus Conference  Full Text
AUTHORS: Stephan Lobitz; Paul Telfer; Elena Cela; Bichr Allaf; Michael Angastiniotis; Carolina Backman Johansson; Catherine Badens; Celeste Bento; Marelle J Bouva; Duran Canatan; Matthew Charlton; Cathy Coppinger; Yvonne Daniel; Marianne de Montalembert; Patrick Ducoroy; Elena Dulin; Ralph Fingerhut; Claudia Froemmel; Marina Garcia Morin; Beatrice Gulbis; Ute Holtkamp; Baba Inusa; John James; Marina Kleanthous; Jeannette Klein; Joachim B Kunz; Lisa Langabeer; Claudine Lapoumeroulie; Ana Marcao; Jose L M Marin Soria; Corrina McMahon; Kwaku Ohene Frempong; Jean Marc Perini; Frederic B Piel; Giovanna Russo; Laura Sainati; Markus Schmugge; Allison Streetly; Leon Tshilolo; Charles Turner; Donatella Venturelli; Laura Vilarinho; Rachel Yahyaoui; Jacques Elion; Raffaella Colombatti; ...More
PUBLISHED: 2018, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 183, ISSUE: 4
INDEXED IN: Scopus WOS
12
TITLE: HAPPETYPES OF THE BETA-GLOBINIC CLUSTER ASSOCIATED WITH THE VARIATION OF THE HBF IN CARRIERS OF ETA-TALASEMIA OF PORTUGUESE ORIGIN  Full Text
AUTHORS: Manco, L; Bento, C; Relvas, L; Maia, T; Ribeiro, ML;
PUBLISHED: 2018, SOURCE: 60th National Congress of the Spanish-Society-of-Hematology-and-Hemotherapy in HAEMATOLOGICA, VOLUME: 103
INDEXED IN: WOS
13
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
INDEXED IN: Scopus
14
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
INDEXED IN: WOS
16
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
INDEXED IN: Scopus WOS CrossRef
17
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
INDEXED IN: WOS
18
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
INDEXED IN: Scopus WOS
19
TITLE: Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next-generation sequencing  Full Text
AUTHORS: Del Orbe Barreto, RD; Arrizabalaga, B; De la Hoz, AB; Garcia Orad, A; Tejada, MI; Garcia Ruiz, JC; Fidalgo, T; Bento, C; Manco, L; Ribeiro, ML;
PUBLISHED: 2016, SOURCE: INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, VOLUME: 38, ISSUE: 6
INDEXED IN: WOS
20
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
INDEXED IN: Scopus WOS CrossRef
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