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51. Simultaneous Automated Determination of Glucose 6-Phosphate Dehydrogenase and 6-Phosphogluconate Dehydrogenase Activities in Whole Blood

52. Somatic deletion of the normal β-globin gene leading to thalassaemia intermedia in heterozygous β-thalassaemic patients

53. Relationship between transfusion regimen and suppression of erythropoiesis in β-thalassaemia major

54. First detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in an Italian child

55. A new β chain hemoglobin variant with increased oxygen affinity: Hb Santa Giusta Sardegna [β93(F9)Cys→Trp; HBB c.282TG]

56. Serum erythropoietin and erythropoiesis in high- and low-fetal hemoglobin beta-thalassemia intermedia patients

57. A pilot trial of deferiprone for neurodegeneration with brain iron accumulation

58. Cholelithiasis and Gilbert's syndrome in homozygous β-thalassaemia

59. Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome

61. Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patients

62. 25 Three years follow-up outcome of deferiprone for pantothenate kinase-associated neurodegeneration (PKAN)

63. Genotype of subjects with borderline hemoglobin A2 levels: Implication for, β-thalassemia carrier screening

64. HB A2-SANT' antioco [α2δ293(F9)CYS→GLY]: A new δ chain variant identified by sequencing of amplified DNA

66. Homozygosity for nondeletion delta-beta(0) thalassemia resulting in a silent clinical phenotype

67. H63D mutation in the HFE gene increases iron overload in beta-thalassemia carriers

68. Normal individuals with high Hb A2levels

69. Use of Neutrophil Cell Population Data for the Detection of Neutrophil Hypergranulation and Other Neutrophil Inclusions As Dohle Bodies, Cytoplasm Vacuolation

70. DAO-2, a New Software Tool for Multiple Differential Diagnoses with Probability. Application for the Screening of Rare Anemias in Sardinia

71. No evidence of cardiac iron in 20 never- or minimally-transfused patients with thalassemia intermedia

72. Limits to the use of the glucose 6-phosphate dehydrogenase/6-phosphogluconate dehydrogenase index for the detection of glucose 6-phosphate dehydrogenase deficiency

73. Evaluation of an automatic HPLC analyser for thalassemia and haemoglobin variants screening

74. Hereditary Spherocytosis: How the New Information Provided by the Routine Hematology Analysers May Help in Its Differential Diagnosis or Flagging

75. Beta Thalassemia Trait: How the New Information Provided by the Routine Hematology Analysers May Help in Its Differential Diagnosis or Flagging

76. Alfa Thalassemia Intermedia (HbH disease): How the New Information Provided by the Routine Hematology Analysers May Help in Its Differential Diagnosis or Flagging

77. Homozygosity for nondeletion δ-β0 thalassemia resulting in a silent clinical phenotype

78. HbH disease in Sardinia: molecular, hematological and clinical aspects

79. Lack of Heart Iron Overload in Patients with Thalassemia Intermedia

80. Lack of Correlation between Serum Ferritin and Liver Iron Concentration in Beta-Zero Thalassemia Intermedia

81. Erythropoiesis following bone marrow transplantation from donors heterozygous for β-thalassaemia

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