41
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
INDEXED IN: Scopus Handle
42
TITLE: Band 3 profile as a marker of oxidative stress in hereditary spherocytosis.
AUTHORS: Granjo, E; Alice Santos-Silva ; Rebelo, I ; Novoa, A; Costa, E ; Barbot, J; Ribeiro, MM; Quintanilha, A;
PUBLISHED: 1998, SOURCE: BLOOD, VOLUME: 92, ISSUE: 10
INDEXED IN: WOS Handle
43
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
INDEXED IN: Scopus WOS CrossRef
44
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
INDEXED IN: Scopus WOS
Page 5 of 5. Total results: 44.