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Oral condition, chemistry of saliva, and salivary levels of Streptococcus mutans in thalassemic patients

Clinical oral investigations, 2002-12, Vol.6 (4), p.223-226

2002

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Marriage and parenthood among childhood cancer survivors: a report from the Italian AIEOP Off-Therapy Registry

Haematologica (Roma), 2011-05, Vol.96 (5), p.744-751

2011

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Osteonecrosis: An emerging complication of intensive chemotherapy for childhood acute lymphoblastic leukemia

Haematologica (Roma), 2003-07, Vol.88 (7), p.747

2003

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Growth hormone secretion in polytransfused prepubertal patients with homozygous β-thalassemia. Effect of long-term recombinant GH (recGH) therapy

Journal of endocrinological investigation, 2003-07, Vol.26 (7), p.623-628

2003

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Survival of children with cancer in Italy, 1989–98. A report from the hospital based registry of the Italian Association of Paediatric Haematology and Oncology (AIEOP)

European journal of cancer (1990), 2008-06, Vol.44 (9), p.1282-1289

2008

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Patterns of domestic migrations and access to childhood cancer care centres in Italy: A report from the hospital based registry of the Italian Association of Pediatric Hematology and Oncology (AIEOP)

European journal of cancer (1990), 2008-10, Vol.44 (15), p.2101-2105

2008

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Phlebotomy to Reduce Iron Overload in Patients Cured of Thalassemia by Bone Marrow Transplantation

Blood, 1997-08, Vol.90 (3), p.994-998

1997

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A PROMOTER MUTATION OF THE β-GLOBIN GENE (–101 C → T) HAS AN AGE-RELATED EXPRESSION PATTERN

Blood, 1993-05, Vol.81 (10), p.2818-2819

1993

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Endocrine functioning in multitransfused prepubertal patients with homozygous beta-thalassemia

The journal of clinical endocrinology and metabolism, 1984-04, Vol.58 (4), p.667-670

1984

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Deferasirox (Exjade®, ICL670) Demonstrates Iron Chelating Efficacy Related to Transfusional Iron Intake in Pediatric Patients

Blood, 2005-11, Vol.106 (11), p.2692-2692

2005

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Treatment reduction in highly selected standard-risk childhood acute lymphoblastic leukemia. The AIEOP ALL-9501 study

Haematologica (Roma), 2005-09, Vol.90 (9), p.1186-1191

2005

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High rate of human herpesvirus-8 seroprevalence in thalassemic patients in Italy

Journal of clinical virology, 2004-05, Vol.30 (1), p.106-109

2004

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The Incidence and Natural Course of Transfusion-Associated GB Virus C/Hepatitis G Virus Infection in a Cohort of Thalassemic Patients

Blood, 1998-02, Vol.91 (3), p.774-777

1998

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The Incidence and Natural Course of Transfusion-Associated GB Virus C/Hepatitis G Virus Infection in a Cohort of Thalassemic Patients

Blood, 1998-02, Vol.91 (3), p.774-777

1998

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Growth hormone secretion in polytransfused prepubertal patients with homozygous β-thalassemia. Effect of longterm recombinant GH (recGH) therapy

Journal of endocrinological investigation, 2003-07, Vol.26 (7), p.623-628

2003

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The Gamma Globin Chain Heterogeneity of the Sardinian Newborn Baby

Hemoglobin, 1986, Vol.10 (5), p.519-528

1986

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Free erythrocyte porphyrin (FEP) in the diagnosis of beta-thalassaemia trait and iron deficiency anaemia

Haematologica (Roma), 1982-06, Vol.67 (3), p.341

1982

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Prospective study of Yersinia enterocolitica infection in thalassemic patients

The Pediatric infectious disease journal, 1995-07, Vol.14 (7), p.579-583

1995

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Hemoglobin Hamilton [β11(A8)VAL →] in Sardinia

Hemoglobin, 1987, Vol.11 (2), p.161-167

1987

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Biochemical and Molecular Aspects of β-Thalassemia Types in Northern Sardinia

Hemoglobin, 1988, Vol.12 (5-6), p.661-671

1988

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Polymorphism of foetal haemoglobin in the Sardinian beta +-thalassaemia

Acta haematologica, 1986, Vol.76 (4), p.208-211

1986

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Neonatal screening for hemoglobinopathy in North Sardinia

European journal of pediatrics, 1981-10, Vol.137 (2), p.195-196

1981

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The unreliability of mean corpuscular volume and mean cellular hemoglobin determinations in the diagnosis of alpha-thalassemia in newborn infants

European journal of pediatrics, 1980-12, Vol.135 (2), p.165-167

1980

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The incidence and natural course of transfusion-associated GB virus C/hepatitis G virus infection in a cohort of thalassemic patients. The Cooleycare Cooperative Group

Blood, 1998-02, Vol.91 (3), p.774-777

1998

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Interferon-alpha therapy in Sicilian and Sardinian polytransfused thalassaemic patients with chronic hepatitis C

BioDrugs : clinical immunotherapeutics, biopharmaceuticals, and gene therapy, 1999-07, Vol.12 (1), p.55-63

1999

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Oral condition, chemistry of saliva, and salivary levels of Streptococcus mutans in thalassemic patients

Marriage and parenthood among childhood cancer survivors: a report from the Italian AIEOP Off-Therapy Registry

Osteonecrosis: An emerging complication of intensive chemotherapy for childhood acute lymphoblastic leukemia

Growth hormone secretion in polytransfused prepubertal patients with homozygous β-thalassemia. Effect of long-term recombinant GH (recGH) therapy

Survival of children with cancer in Italy, 1989–98. A report from the hospital based registry of the Italian Association of Paediatric Haematology and Oncology (AIEOP)

Patterns of domestic migrations and access to childhood cancer care centres in Italy: A report from the hospital based registry of the Italian Association of Pediatric Hematology and Oncology (AIEOP)

Phlebotomy to Reduce Iron Overload in Patients Cured of Thalassemia by Bone Marrow Transplantation

A PROMOTER MUTATION OF THE β-GLOBIN GENE (–101 C → T) HAS AN AGE-RELATED EXPRESSION PATTERN

Endocrine functioning in multitransfused prepubertal patients with homozygous beta-thalassemia

Deferasirox (Exjade®, ICL670) Demonstrates Iron Chelating Efficacy Related to Transfusional Iron Intake in Pediatric Patients

Treatment reduction in highly selected standard-risk childhood acute lymphoblastic leukemia. The AIEOP ALL-9501 study

High rate of human herpesvirus-8 seroprevalence in thalassemic patients in Italy

The Incidence and Natural Course of Transfusion-Associated GB Virus C/Hepatitis G Virus Infection in a Cohort of Thalassemic Patients

The Incidence and Natural Course of Transfusion-Associated GB Virus C/Hepatitis G Virus Infection in a Cohort of Thalassemic Patients

Growth hormone secretion in polytransfused prepubertal patients with homozygous β-thalassemia. Effect of longterm recombinant GH (recGH) therapy

The Gamma Globin Chain Heterogeneity of the Sardinian Newborn Baby

Free erythrocyte porphyrin (FEP) in the diagnosis of beta-thalassaemia trait and iron deficiency anaemia

Prospective study of Yersinia enterocolitica infection in thalassemic patients

Hemoglobin Hamilton [β11(A8)VAL →] in Sardinia

Biochemical and Molecular Aspects of β-Thalassemia Types in Northern Sardinia

Polymorphism of foetal haemoglobin in the Sardinian beta +-thalassaemia

Neonatal screening for hemoglobinopathy in North Sardinia

The unreliability of mean corpuscular volume and mean cellular hemoglobin determinations in the diagnosis of alpha-thalassemia in newborn infants

The incidence and natural course of transfusion-associated GB virus C/hepatitis G virus infection in a cohort of thalassemic patients. The Cooleycare Cooperative Group

Interferon-alpha therapy in Sicilian and Sardinian polytransfused thalassaemic patients with chronic hepatitis C

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