Elisio Manuel Sousa Costa


AuthID: R-000-4J3

Confirmed Publications: 290



261
TITLE: A new case of (TA)8 allele in the UGT1A1 gene promoter in a Caucasian girl with Gilbert syndrome  Full Text
AUTHORS: Coelho, H; Costa, E ; Vieira, E; Branca, R; dos Santos, R; Barbot, J;
PUBLISHED: 2004, SOURCE: PEDIATRIC HEMATOLOGY AND ONCOLOGY, VOLUME: 21, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 8
IN MY: ORCID | ResearcherID
262
TITLE: Coexistence of congenital red cell pyruvate kinase and band 3 deficiency  Full Text
AUTHORS: Branca, R; Costa, E ; Rocha, S ; Coelho, H; Quintanilha, A ; Cabeda, JM ; Alice Santos-Silva ; Barbot, J;
PUBLISHED: 2004, SOURCE: CLINICAL AND LABORATORY HAEMATOLOGY, VOLUME: 26, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 5
IN MY: ORCID | ResearcherID
263
TITLE: Determination of neutrophil Fc gamma receptor IIIb antigens (HNA-1a, HNA-1b and HNA-1c) by fluorescence-primed allele-specific polymerase chain reaction  Full Text
AUTHORS: Costa, E ; Antunes, MB; Faria, S; Vieira, E; Branca, R; Barbot, J; Dos Santos, R;
PUBLISHED: 2004, SOURCE: CLINICAL AND LABORATORY HAEMATOLOGY, VOLUME: 26, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 1
IN MY: ORCID | ResearcherID
264
TITLE: Co-existence of congenital red cell pyruvate kinase and band 3 deficiency.
AUTHORS: Branca, R; Costa, E ; Rocha, S; Coelho, H; Quintanilha, A; Cabeda, JM; Alice Santos-Silva ; Barbot, J;
PUBLISHED: 2003, SOURCE: 45th Annual Meeting of the American-Society-of-Hematology in BLOOD, VOLUME: 102, ISSUE: 11
INDEXED IN: WOS
IN MY: ORCID | ResearcherID
265
TITLE: Determination of neutrophil Fc gamma receptor IIIb antigens (HNA-1a, HNA-1b and HNA-1c) by polymerase chain reaction with sequence-specific fluorochrome-labeled primers.
AUTHORS: Costa, E ; Antunes, M; Faria, S; Vieira, E; Branca, R; Barbot, J; dos Santos, R;
PUBLISHED: 2003, SOURCE: 45th Annual Meeting of the American-Society-of-Hematology in BLOOD, VOLUME: 102, ISSUE: 11
INDEXED IN: WOS
IN MY: ORCID | ResearcherID
266
TITLE: Inherited and acquired risk factors and their combined effects in pediatric stroke  Full Text
AUTHORS: Barreirinho, S; Ferro, A; Santos, M; Costa, E ; Pinto Basto, J; Sousa, A ; Sequeiros, J ; Maciel, P ; Barbot, C ; Barbot, J;
PUBLISHED: 2003, SOURCE: PEDIATRIC NEUROLOGY, VOLUME: 28, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 56
IN MY: ORCID | ResearcherID
267
TITLE: Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practice
AUTHORS: Costa, MD ; Magalhaes, P; Ferreirinha, F ; Guimaraes, L ; Januario, C; Gaspar, I; Loureiro, L; Vale, J; Garrett, C ; Regateiro, F; Magalhaes, M; Sousa, A ; Maciel, P ; Sequeiros, J ;
PUBLISHED: 2003, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 11, ISSUE: 11
INDEXED IN: Scopus WOS CrossRef: 15 Handle
IN MY: ORCID
268
TITLE: Pentanucleotide repeat (TTTTA)n polymorphism in the 5' control region of the apoliprotein (A) gene and atherothrombotic serum lipoprotein (A) concentration, in a pediatric population.
AUTHORS: Ferreira, H; Costa, E ; Vieira, E; Leao, A; Magalhães, R ; Gomes, JL; Barbot, J; dos Santos, R;
PUBLISHED: 2003, SOURCE: Haematologica, VOLUME: 88, ISSUE: 3
INDEXED IN: Scopus
IN MY: ORCID
269
TITLE: Glucose-6-phosphate dehydrogenase deficiency, neonatal hyperbilirubinemia and Gilbert's syndrome [Défice de glicose-6-fosfato desidrogenase, ictericia neonatal e sindroma de Gilbert]
AUTHORS: Costa, E ; Vieira, E; Cleto, E; Cabeda, JM ; Pinho, L; Coimbra, E; Dos Santos, R; Barbot, J;
PUBLISHED: 2002, SOURCE: Acta Medica Portuguesa, VOLUME: 15, ISSUE: 6
INDEXED IN: Scopus
IN MY: ORCID
270
Page 27 of 29. Total results: 290.

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