Elisio Manuel Sousa Costa


AuthID: R-000-4J3

Confirmed Publications: 290



251
TITLE: Molecular study of Portuguese patients with clinical diagnosis of Shwachman-Diamond syndrome  Full Text
AUTHORS: Costa, E ; Oliveira, J; Vieira, E; Duque, F; Garcia, P; Goncalves, I; Diego, L; Barbot, J; Santos, R;
PUBLISHED: 2007, SOURCE: 12th Congress of the European-Hematology-Association in HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, VOLUME: 92
INDEXED IN: WOS
IN MY: ORCID | ResearcherID
252
TITLE: Neutrophilactivation markers in chronic renal failure patients under haemodialysis and recombinant human erythropoietin  Full Text
AUTHORS: Costa, F ; Rocha, S ; Rocha Pereira, P; Castro, E; Miranda, V; Sameiro S Faria; Loureiro, A; Quintanilha, A; Belo, L ; Alice Santos-Silva ;
PUBLISHED: 2007, SOURCE: 12th Congress of the European-Hematology-Association in HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, VOLUME: 92
INDEXED IN: WOS
IN MY: ORCID | ResearcherID
253
TITLE: Platelet indices in chronic alcoholic liver disease patients with thrombocytopenia [Índices plaquetários em indivíduos com doença hepática alcoólica crónica]
AUTHORS: Costa, AC; Ribeiro, B; Costa, E ;
PUBLISHED: 2007, SOURCE: Arquivos de Gastroenterologia, VOLUME: 44, ISSUE: 3
INDEXED IN: Scopus
IN MY: ORCID
254
TITLE: Analysis of the UDP-glucuronosyltransferase gene in Portuguese patients with a clinical diagnosis of Gilbert and Crigler-Najjar syndromes  Full Text
AUTHORS: Costa, E ; Vieira, E; Martins, M; Saraiva, J; Cancela, E; Costa, M; Bauerle, R; Freitas, T; Carvalho, JR; Santos Silva, E; Barbot, J; dos Santos, R;
PUBLISHED: 2006, SOURCE: BLOOD CELLS MOLECULES AND DISEASES, VOLUME: 36, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 27
IN MY: ORCID | ResearcherID
255
TITLE: Hematologically important mutations: Bilirubin UDP-glucuronosyltransferase gene mutations in gilbert and Crigler-Najjar syndromes  Full Text
AUTHORS: Costa, E ;
PUBLISHED: 2006, SOURCE: BLOOD CELLS MOLECULES AND DISEASES, VOLUME: 36, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 27
IN MY: ORCID | ResearcherID
256
TITLE: Erythropoietin levels in the different clinical forms of hereditary spherocytosis  Full Text
AUTHORS: Rocha, S ; Costa, E ; Catarino, C ; Belo, L ; Castro, EMB; Barbot, J; Quintanilha, A ; Alice Santos-Silva ;
PUBLISHED: 2005, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 131, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 13
IN MY: ORCID | ResearcherID
257
TITLE: Molecular characterization of a Portuguese patient with Shwachman-Diamond syndrome
AUTHORS: Lima, RM; Costa, T ; Rocha, C; Vieira, E; dos Santos, R; Barbot, J; Rocha, H;
PUBLISHED: 2005, SOURCE: JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, VOLUME: 41, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 3
IN MY: ORCID | ResearcherID
258
TITLE: Protein deficiency balance as a predictor of clinical outcome in hereditary spherocytosis  Full Text
AUTHORS: Rocha, S ; Rebelo, I ; Costa, E ; Catarino, C ; Belo, L ; Castro, EMB; Cabeda, JM ; Barbot, J; Quintanilha, A ; Alice Santos-Silva ;
PUBLISHED: 2005, SOURCE: EUROPEAN JOURNAL OF HAEMATOLOGY, VOLUME: 74, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 14 Handle
IN MY: ORCID
259
TITLE: The identification of multiple thrombophilic risk factors in an infant with cerebrovascular accident
AUTHORS: Neves, J; Costa, E ; Branca, R; Carrilho, I; Barbot, J; Barbot, C ;
PUBLISHED: 2005, SOURCE: REVISTA DE NEUROLOGIA, VOLUME: 40, ISSUE: 8
INDEXED IN: Scopus WOS
IN MY: ORCID | ResearcherID
260
Page 26 of 29. Total results: 290.

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