22
TITLE: Hereditary spherocytosis and the (TA)(n)TAA polymorphism of UGT1A1 gene promoter region-A comparison of the bilirubin plasmatic levels in the different clinical forms  Full Text
AUTHORS: Susana Rocha ; Elisio Costa ; Luis Belo; Alice Santos-Silva ; Petronila Rocha Pereira; Alexandre Quintanilha; Elisio Costa; Luis Belo ; Alice Santos Silva; Susana Rocha; Elisio Costa; Fatima Ferreira; Esmeralda Cleto; Jose Barbot; Petronila Rocha Pereira; Alexandre Quintanilha;
PUBLISHED: 2010, SOURCE: BLOOD CELLS MOLECULES AND DISEASES, VOLUME: 44, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 6
24
TITLE: Single nucleotide polymorphisms in the apo(a) kringle IV type 8 domain are not associated with atherothrombotic serum lipoprotein (a) concentration, in a portuguese paediatric population  Full Text
AUTHORS: Ferreira, H; Costa, E ; Vieira, E; Barbot, J; Dos Santos, R;
PUBLISHED: 2008, SOURCE: INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, VOLUME: 30, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef
25
TITLE: Audiologic abnormalities of Fanconi anaemia  Full Text
AUTHORS: Maria Jose Vale; Maria Jose Dinis; Marika Bini Antunes; Beatriz Porto ; Jose Barbot; Miguel B Coutinho;
PUBLISHED: 2008, SOURCE: ACTA OTO-LARYNGOLOGICA, VOLUME: 128, ISSUE: 9
INDEXED IN: Scopus WOS CrossRef
26
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
27
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
28
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
29
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
30
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
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