AAAAAA

   
Results: 1-11 |
Results: 11
Iron chelation: New therapies
Authors: Galanello, R
Citation: R. Galanello, Iron chelation: New therapies, SEM HEMATOL, 38(1), 2001, pp. 73-76
Identification of three rare beta-thalassemia mutations in the Pakistani population
Authors: Khan, SN Riazuddin, S Galanello, R
Citation: Sn. Khan et al., Identification of three rare beta-thalassemia mutations in the Pakistani population, HEMOGLOBIN, 24(1), 2000, pp. 15-22
Hb Sallanches [alpha 104(G11)Cys -> Tyr]: a rare alpha 2-globin chain variant found in the homozygous state in three members of a Pakistani family
Authors: Khan, SN Butt, FI Riazuddin, S Galanello, R
Citation: Sn. Khan et al., Hb Sallanches [alpha 104(G11)Cys -> Tyr]: a rare alpha 2-globin chain variant found in the homozygous state in three members of a Pakistani family, HEMOGLOBIN, 24(1), 2000, pp. 31-35
Safety profile of the oral iron chelator deferiprone: a multicentre study
Authors: Cohen, AR Galanello, R Piga, A DiPalma, A Vullo, C Tricta, F
Citation: Ar. Cohen et al., Safety profile of the oral iron chelator deferiprone: a multicentre study, BR J HAEM, 108(2), 2000, pp. 305-312
Co-inherited Gilbert's syndrome: a factor determining hyperbilirubinemia in homozygous beta-thalassemia
Authors: Galanello, R Cipollina, MD Dessi, C Giagu, N Lai, E Cao, A
Citation: R. Galanello et al., Co-inherited Gilbert's syndrome: a factor determining hyperbilirubinemia in homozygous beta-thalassemia, HAEMATOLOG, 84(2), 1999, pp. 103-105
C -> T mutation at -158 (G)gamma HPFH associated with 4 bp deletion (-225-222) in the promoter region of the (A)gamma gene in homozygous beta(0) 39 nonsense thalassemia
Authors: Gonzalez, FA Ropero, P Sanchez, J Rosatelli, C Galanello, R Villegas, A
Citation: Fa. Gonzalez et al., C -> T mutation at -158 (G)gamma HPFH associated with 4 bp deletion (-225-222) in the promoter region of the (A)gamma gene in homozygous beta(0) 39 nonsense thalassemia, HAEMATOLOG, 84(1), 1999, pp. 90-92
Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome
Authors: Galanello, R Cipollina, MD Carboni, G Perseu, L Barella, S Corrias, A Cao, A
Citation: R. Galanello et al., Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome, EUR J PED, 158(11), 1999, pp. 914-916
Posttranslational deamidation of proteins: The case of hemoglobin J Sardegna [alpha 50(CD8)His -> Asn -> Asp]
Authors: Paleari, R Paglietti, E Mosca, A Mortarino, M Maccioni, L Satta, S Cao, A Galanello, R
Citation: R. Paleari et al., Posttranslational deamidation of proteins: The case of hemoglobin J Sardegna [alpha 50(CD8)His -> Asn -> Asp], CLIN CHEM, 45(1), 1999, pp. 21-28
Soluble transferrin receptor as a potential determinant of iron loading incongenital anaemias due to ineffective erythropoiesis
Authors: Cazzola, M Beguin, Y Bergamaschi, G Guarnone, R Cerani, P Barella, S Cao, A Galanello, R
Citation: M. Cazzola et al., Soluble transferrin receptor as a potential determinant of iron loading incongenital anaemias due to ineffective erythropoiesis, BR J HAEM, 106(3), 1999, pp. 752-755
Prenatal diagnosis and screening of the haemoglobinopathies
Authors: Cao, A Galanello, R Rosatelli, MC
Citation: A. Cao et al., Prenatal diagnosis and screening of the haemoglobinopathies, BAIL CLIN H, 11(1), 1998, pp. 215-238
Globin chain synthesis analysis by high performance liquid chromatography in the screening of thalassemia syndromes
Authors: Galanello, R Satta, S Pirroni, MG Travi, M Maccioni, L
Citation: R. Galanello et al., Globin chain synthesis analysis by high performance liquid chromatography in the screening of thalassemia syndromes, HEMOGLOBIN, 22(5-6), 1998, pp. 501-508
Risultati: 1-11 |