José Alberto Barcelos de Morais Barbot
AuthID: R-000-PJP
31
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
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
32
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
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
33
TITLE: Neutrophil dysfunction in a case of glucose-6-phosphate dehydrogenase deficiency
AUTHORS: Costa, E ; Vasconcelos, J; Santos, E; Laranjeira, A; Melo, JC; Barbot, J;
PUBLISHED: 2002, SOURCE: JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, VOLUME: 24, ISSUE: 2
AUTHORS: Costa, E ; Vasconcelos, J; Santos, E; Laranjeira, A; Melo, JC; Barbot, J;
PUBLISHED: 2002, SOURCE: JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, VOLUME: 24, ISSUE: 2
34
TITLE: Influence of Gilbert's syndrome on serum bilirubin levels and gallstone formation in children with chronic hemolytic disease [Influencia del síndrome de Gilbert en los valores de bilirrubina sérica y presencia de litiasis vesicular en pacientes con hemólisis crónica congénita]
AUTHORS: Costa, E ; Pinto, R; Vieira, E; Polo, S; Sarmento, AM; Oliveira, I; Pimenta, R; dos Santos, R; Barbot, J;
PUBLISHED: 2002, SOURCE: Anales Espanoles de Pediatria, VOLUME: 57, ISSUE: 6
AUTHORS: Costa, E ; Pinto, R; Vieira, E; Polo, S; Sarmento, AM; Oliveira, I; Pimenta, R; dos Santos, R; Barbot, J;
PUBLISHED: 2002, SOURCE: Anales Espanoles de Pediatria, VOLUME: 57, ISSUE: 6
INDEXED IN: 
Scopus
Scopus35
TITLE: TATA-Box polymorphism in the uridine diphosphate glucuronosyl transferase gene in Portuguese patients with clinical diagnosis of Gilbert Syndrome.
AUTHORS: Costa, E ; Vieira, E; Santos Silva, E; Barbot, J; dos Santos, R;
PUBLISHED: 2002, SOURCE: Haematologica, VOLUME: 87, ISSUE: 4
AUTHORS: Costa, E ; Vieira, E; Santos Silva, E; Barbot, J; dos Santos, R;
PUBLISHED: 2002, SOURCE: Haematologica, VOLUME: 87, ISSUE: 4
INDEXED IN: Scopus
Scopus36
TITLE: Ten years of prophylactic treatment with fresh-frozen plasma in a child with chronic relapsing thrombotic thrombocytopenic purpura as a result of a congenital deficiency of von Willebrand factor-cleaving protease Full Text
AUTHORS: Barbot, J; Costa, E ; Guerra, M; Barreirinho, MS; Isvarlal, P; Robles, R; Gerritsen, HE; Lammle, B; Furlan, M;
PUBLISHED: 2001, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 113, ISSUE: 3
AUTHORS: Barbot, J; Costa, E ; Guerra, M; Barreirinho, MS; Isvarlal, P; Robles, R; Gerritsen, HE; Lammle, B; Furlan, M;
PUBLISHED: 2001, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 113, ISSUE: 3
37
TITLE: A new PKLR gene mutation in the R-type promoter region affects the gene transcription causing pyruvate kinase deficiency Full Text
AUTHORS: Manco, L ; Ribeiro, ML ; Maximo, V ; Almeida, H; Costa, A; Freitas, O; Barbot, J; Abade, A; Tamagnini, G;
PUBLISHED: 2000, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 110, ISSUE: 4
AUTHORS: Manco, L ; Ribeiro, ML ; Maximo, V ; Almeida, H; Costa, A; Freitas, O; Barbot, J; Abade, A; Tamagnini, G;
PUBLISHED: 2000, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 110, ISSUE: 4
38
TITLE: Hydrops fetalis associated with erythrocyte pyruvate kinase deficiency Full Text
AUTHORS: Ferreira, P; Morais, L; Costa, R; Resende, C; Dias, CP; Araujo, F; Costa, E ; Barbot, J; Vilarinho, A;
PUBLISHED: 2000, SOURCE: EUROPEAN JOURNAL OF PEDIATRICS, VOLUME: 159, ISSUE: 7
AUTHORS: Ferreira, P; Morais, L; Costa, R; Resende, C; Dias, CP; Araujo, F; Costa, E ; Barbot, J; Vilarinho, A;
PUBLISHED: 2000, SOURCE: EUROPEAN JOURNAL OF PEDIATRICS, VOLUME: 159, ISSUE: 7
39
TITLE: Glucose-6-phosphate dehydrogenase Aveiro: a de novo mutation associated with chronic nonspherocytic hemolytic anemia
AUTHORS: Costa, E ; Cabeda, JM ; Vieira, E; Pinto, R; Pereira, SA; Ferraz, L; Santos, R; Barbot, J;
PUBLISHED: 2000, SOURCE: BLOOD, VOLUME: 95, ISSUE: 4
AUTHORS: Costa, E ; Cabeda, JM ; Vieira, E; Pinto, R; Pereira, SA; Ferraz, L; Santos, R; Barbot, J;
PUBLISHED: 2000, SOURCE: BLOOD, VOLUME: 95, ISSUE: 4
INDEXED IN: Scopus 
WOS
Scopus WOS40
TITLE: Glucose-6-phosphate dehydrogenase deficiency in 2 girls [Défice de glicose-6-fosfato desidrogenase em duas crianças do sexo feminino.]
AUTHORS: Costa, E ; Cabeda, JM ; Abreu, ME; Silva, A; Morais, L; Alexandrino, AM; Justica, B; Barbot, J;
PUBLISHED: 1999, SOURCE: Acta medica portuguesa, VOLUME: 12, ISSUE: 7-11
AUTHORS: Costa, E ; Cabeda, JM ; Abreu, ME; Silva, A; Morais, L; Alexandrino, AM; Justica, B; Barbot, J;
PUBLISHED: 1999, SOURCE: Acta medica portuguesa, VOLUME: 12, ISSUE: 7-11
INDEXED IN: Scopus
Scopus