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: 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
Scopus35
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
36
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
37
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
38
TITLE: Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemia Full Text
AUTHORS: Vulliamy, TJ; Kaeda, JS; Ait Chafa, D; Mangerini, R; Roper, D; Barbot, J; Mehta, AB; Athanassiou Metaxa, M; Luzzatto, L; Mason, PJ;
PUBLISHED: 1998, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 101, ISSUE: 4
AUTHORS: Vulliamy, TJ; Kaeda, JS; Ait Chafa, D; Mangerini, R; Roper, D; Barbot, J; Mehta, AB; Athanassiou Metaxa, M; Luzzatto, L; Mason, PJ;
PUBLISHED: 1998, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 101, ISSUE: 4
39
TITLE: Dominantly transmitted beta-thalassemia arising from the production of several aberrant mRNA species and one abnormal peptide
AUTHORS: Faustino, P ; Osorio Almeida, L; Romao, L ; Barbot, J; Fernandes, B; Justica, B; Lavinha, J;
PUBLISHED: 1998, SOURCE: BLOOD, VOLUME: 91, ISSUE: 2
AUTHORS: Faustino, P ; Osorio Almeida, L; Romao, L ; Barbot, J; Fernandes, B; Justica, B; Lavinha, J;
PUBLISHED: 1998, SOURCE: BLOOD, VOLUME: 91, ISSUE: 2
INDEXED IN: Scopus 
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