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Genotype and phenotype correlation in glucose-6-phosphate dehydrogenase deficiency

Haematologica (Roma), 2001-01, Vol.86 (1), p.30

2001

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HFE Gene Mutations an Apulian Population: Allele Frequencies

European journal of epidemiology, 2003-01, Vol.18 (7), p.685-689

2003

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Analysis of HLA–DRB1★-A★ and -B★ alleles in prenatal diagnosis for determination of maternal contamination in fetal DNA

Molecular human reproduction, 2002-06, Vol.8 (6), p.586-588

2002

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Lymphocyte subset reconstitution after HLA-identical placental blood transplantation (PBT) or PBT plus bone marrow transplantation (BMT) in three children with beta-thalassemia major

Bone marrow transplantation (Basingstoke), 2000-10, Vol.26 (7), p.743-747

2000

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Influence of factor VIII/von Willebrand complex on the activated protein C-resistance phenotype and on the risk for venous thromboembolism in heterozygous carriers of the factor V Leiden mutation

Blood coagulation & fibrinolysis, 1999-10, Vol.10 (7), p.409

1999

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Influence of factor VIII/von Willebrand complex on the activated protein C-resistance phenotype and on the risk for venous thromboembolism in heterozygous carriers of the factor V Leiden mutation

Blood coagulation & fibrinolysis, 1999-10, Vol.10 (7), p.416

1999

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Prenatal diagnosis of β-thalassaemia using fetal erythroblasts enriched from maternal blood by a novel gradient

Molecular human reproduction, 2000-06, Vol.6 (6), p.571-574

2000

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Ontogeny of human lymphocytes. Two-color fluorescence analysis of circulating lymphocyte subsets in fetuses in the second trimester of pregnancy

Fetal diagnosis and therapy, 1991, Vol.6 (3-4), p.101

1991

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Study of the Molecular Defects in Glucose Phosphate Isomerase-Deficient Patients Affected by Chronic Hemolytic Anemia

Blood, 1996-09, Vol.88 (6), p.2306-2310

1996

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Molecular basis of beta-thalassemia intermedia in a southern Italian region (Puglia)

Acta haematologica, 1991-01, Vol.86 (4), p.174-178

1991

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Lymphocyte subset reconstitution after HLA-identical placental blood transplantation (PBT) or PBT plus bone marrow transplantation (BMT) in three children with [beta]-thalassemia major

Bone marrow transplantation (Basingstoke), 2000-10, Vol.26 (7), p.743

2000

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Lymphocyte subset reconstitution after HLA-identical placental blood transplantation (PBT) or pbt plus bone marrow transplantation (BMT) in three children with /3-thalassemia major

Bone marrow transplantation (Basingstoke), 2000, Vol.26 (7), p.743-747

2000

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alpha-Thalassaemia in Apulia: biosynthetic studies

Journal of medical genetics, 1983-06, Vol.20 (3), p.206-209

1983

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Chronic viral hepatitis in patients with beta-thalassaemia minor

Haematologica (Roma), 1982-11, Vol.67 (6), p.867

1982

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Chronic Viral Hepatitis in Thalassemic Liver Disease: A Long-Term Study in Patients with Acute Hepatitis with Nontransfusion-Dependent Thalassemia Minor

Vox sanguinis, 1983-01, Vol.44 (1), p.14-24

1983

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Erythrocytic glycolysis and autohemolysis in thalassemia

Il Progresso medico, 1962-01, Vol.18, p.12

1962

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Promoter mutations producing mild β‐thalassaemia in the Italian population

British journal of haematology, 1992-02, Vol.80 (2), p.222-226

1992

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On a case of association of thalassemia and "hereditary persistence of fetal hemoglobin"

Haematologica (Roma), 1962, Vol.47, p.353

1962

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Frequency and meaning of some red blood cells and haemoglobin abnormalities in a sample of the population from Apulia (South Eastern Italy)

Blut, 1966-08, Vol.13 (5), p.305-312

1966

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The glucose content of thalassemic, fetal and neonatal erythrocytes

Bollettino della Societa italiana di biologia sperimentale, 1961-05, Vol.37, p.378

1961

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Beta-thalassemia intermedia in Apulia (southern Italy)

Birth defects original article series, 1987, Vol.23 (5A), p.297

1987

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A new delta-chain variant hemoglobin A2-Puglia or alpha 2 delta 2 26 Glu-->Asp (B8), detected by DNA analysis in a family of southern Italian origin

Human mutation, 1993, Vol.2 (4), p.327-329

1993

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Thalassemia types in Puglia

Birth defects original article series, 1982, Vol.18 (7), p.195

1982

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(α)20.5 is the most frequent large deletion in the Puglia Region of Italy

Hemoglobin, 1994-09, Vol.18 (4-5), p.353-357

1994

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Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease

Genotype and phenotype correlation in glucose-6-phosphate dehydrogenase deficiency

HFE Gene Mutations an Apulian Population: Allele Frequencies

Analysis of HLA–DRB1★-A★ and -B★ alleles in prenatal diagnosis for determination of maternal contamination in fetal DNA

Lymphocyte subset reconstitution after HLA-identical placental blood transplantation (PBT) or PBT plus bone marrow transplantation (BMT) in three children with beta-thalassemia major

Influence of factor VIII/von Willebrand complex on the activated protein C-resistance phenotype and on the risk for venous thromboembolism in heterozygous carriers of the factor V Leiden mutation

Influence of factor VIII/von Willebrand complex on the activated protein C-resistance phenotype and on the risk for venous thromboembolism in heterozygous carriers of the factor V Leiden mutation

Prenatal diagnosis of β-thalassaemia using fetal erythroblasts enriched from maternal blood by a novel gradient

Ontogeny of human lymphocytes. Two-color fluorescence analysis of circulating lymphocyte subsets in fetuses in the second trimester of pregnancy

Study of the Molecular Defects in Glucose Phosphate Isomerase-Deficient Patients Affected by Chronic Hemolytic Anemia

Molecular basis of beta-thalassemia intermedia in a southern Italian region (Puglia)

Lymphocyte subset reconstitution after HLA-identical placental blood transplantation (PBT) or PBT plus bone marrow transplantation (BMT) in three children with [beta]-thalassemia major

Lymphocyte subset reconstitution after HLA-identical placental blood transplantation (PBT) or pbt plus bone marrow transplantation (BMT) in three children with /3-thalassemia major

alpha-Thalassaemia in Apulia: biosynthetic studies

Chronic viral hepatitis in patients with beta-thalassaemia minor

Chronic Viral Hepatitis in Thalassemic Liver Disease: A Long-Term Study in Patients with Acute Hepatitis with Nontransfusion-Dependent Thalassemia Minor

Erythrocytic glycolysis and autohemolysis in thalassemia

Promoter mutations producing mild β‐thalassaemia in the Italian population

On a case of association of thalassemia and "hereditary persistence of fetal hemoglobin"

Frequency and meaning of some red blood cells and haemoglobin abnormalities in a sample of the population from Apulia (South Eastern Italy)

The glucose content of thalassemic, fetal and neonatal erythrocytes

Beta-thalassemia intermedia in Apulia (southern Italy)

A new delta-chain variant hemoglobin A2-Puglia or alpha 2 delta 2 26 Glu-->Asp (B8), detected by DNA analysis in a family of southern Italian origin

Thalassemia types in Puglia

(α)20.5 is the most frequent large deletion in the Puglia Region of Italy

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