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Levels of L-asparagine in CSF after intramuscular administration of asparaginase from Erwinia in children with acute lymphoblastic leukemia

Journal of clinical oncology, 1995-02, Vol.13 (2), p.339-344

1995

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Assessment of the value of treatment with granulocyte colony-stimulating factor in children with acute lymphoblastic leukemia: a randomized clinical trial

European journal of haematology, 1995-08, Vol.55 (2), p.93-96

1995

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Incidence and morbidity of infection by hepatitis C virus in children with acute lymphoblastic leukaemia

European journal of pediatrics, 1994-04, Vol.153 (4), p.271-275

1994

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Growth and growth hormone in children during and after therapy for acute lymphoblastic leukaemia

European journal of pediatrics, 1993-09, Vol.152 (9), p.730-733

1993

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Dissection of the association status of two polymorphisms in the β‐globin gene cluster with variations in F‐cell number in non‐anemic individuals

American journal of hematology, 1997-12, Vol.56 (4), p.239-243

1997

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Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals

Blood, 1996-03, Vol.87 (6), p.2607-2607

1996

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Detectable molecular residual disease at the beginning of maintenance therapy indicates poor outcome in children with T-cell acute lymphoblastic leukemia

Blood, 1997-08, Vol.90 (3), p.1226-1232

1997

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Presence of hemoglobinopathies in Sicily: A historic perspective

American journal of medical genetics, 1997-03, Vol.69 (2), p.200-206

1997

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Detection of Minimal Residual Disease: Methods and Relationship to Outcome in T-Lineage Acute Lymphoblastic Leukemia

Leukemia & lymphoma, 1998-12, Vol.32 (1-2), p.65-75

1998

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Reduction in the incidence of infection by hepatitis C virus in children with acute lymphoblastic leukemia after suspension of sampling from the finger

The Pediatric infectious disease journal, 1996-03, Vol.15 (3), p.265-266

1996

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Residual Clones in Childhood Leukemia

The New England journal of medicine, 1997-07, Vol.337 (1), p.50-51

1997

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A mild type of Hb S‐β+‐thalassemia [‐92(C→T)] in a sicilian family

American journal of hematology, 1993-02, Vol.42 (2), p.225-226

1993

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High performance liquid chromatography (HPLC): a simple method to quantify Hb C, O-Arab. Agenogi and F

Clinical and laboratory haematology, 1991-01, Vol.13 (2), p.169-175

1991

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Diabetes Insipidus 9 Years after Cessation of Therapy for Acute Lymphoblastic Leukemia

Pediatric hematology and oncology, 1991-01, Vol.8 (3), p.231-233

1991

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Six Rare Hemoglobin Variants Found in Sicily

Hemoglobin, 1991, Vol.15 (5), p.431-437

1991

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Hematological findings in 375 Sicilians with Hb S trait

Haematologica (Roma), 1990-03, Vol.75 (2), p.113

1990

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Increase with age in the prevalence of beta-thalassemia trait among Sicilians

The New England journal of medicine, 1989-09, Vol.321 (11), p.762-762

1989

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The effect of the beta thalassemia mutation on the clinical severity of the sickle beta thalassemia syndrome

Haematologica (Roma), 1989-07, Vol.74 (4), p.341

1989

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A comparative immunogenicity-reactogenicity dose-response study of influenza vaccine

Annals of allergy, 1990-09, Vol.65 (3), p.218

1990

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Non inherited hemoglobin anomalies

Haematologica (Roma), 1991-09, Vol.76 (5), p.414

1991

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Leucémie aiguë lymphoblastique de l'enfant : résultats du traitement en Sicile entre 1987 et 1992

La Presse médicale (1983), 1994, Vol.23 (28), p.1293-1298

1994

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6-Mercaptopurine Cumulative Dose: A Critical Factor of Maintenance Therapy in Average Risk Childhood Acute Lymphoblastic Leukemia

Pediatric hematology and oncology, 1994-01, Vol.11 (3), p.251-258

1994

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Acute lymphoblastic leukaemia in children. Results of treatment in Sicily from 1987 to 1992

La Presse médicale (1983), 1994-09, Vol.23 (28), p.1293-1298

1994

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Unusual sickle cell disease observed for the first time in Italy: Hb S-Hb D Los Angeles

Haematologica (Roma), 1990-09, Vol.75 (5), p.464

1990

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Increase with Age in the Prevalence of β-Thalassemia Trait among Sicilians

Annals of the New York Academy of Sciences, 1990-12, Vol.612 (1), p.504-507

1990

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Levels of L-asparagine in CSF after intramuscular administration of asparaginase from Erwinia in children with acute lymphoblastic leukemia

Assessment of the value of treatment with granulocyte colony-stimulating factor in children with acute lymphoblastic leukemia: a randomized clinical trial

Incidence and morbidity of infection by hepatitis C virus in children with acute lymphoblastic leukaemia

Growth and growth hormone in children during and after therapy for acute lymphoblastic leukaemia

Dissection of the association status of two polymorphisms in the β‐globin gene cluster with variations in F‐cell number in non‐anemic individuals

Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals

Detectable molecular residual disease at the beginning of maintenance therapy indicates poor outcome in children with T-cell acute lymphoblastic leukemia

Presence of hemoglobinopathies in Sicily: A historic perspective

Detection of Minimal Residual Disease: Methods and Relationship to Outcome in T-Lineage Acute Lymphoblastic Leukemia

Reduction in the incidence of infection by hepatitis C virus in children with acute lymphoblastic leukemia after suspension of sampling from the finger

Residual Clones in Childhood Leukemia

A mild type of Hb S‐β+‐thalassemia [‐92(C→T)] in a sicilian family

High performance liquid chromatography (HPLC): a simple method to quantify Hb C, O-Arab. Agenogi and F

Diabetes Insipidus 9 Years after Cessation of Therapy for Acute Lymphoblastic Leukemia

Six Rare Hemoglobin Variants Found in Sicily

Hematological findings in 375 Sicilians with Hb S trait

Increase with age in the prevalence of beta-thalassemia trait among Sicilians

The effect of the beta thalassemia mutation on the clinical severity of the sickle beta thalassemia syndrome

A comparative immunogenicity-reactogenicity dose-response study of influenza vaccine

Non inherited hemoglobin anomalies

Leucémie aiguë lymphoblastique de l'enfant : résultats du traitement en Sicile entre 1987 et 1992

6-Mercaptopurine Cumulative Dose: A Critical Factor of Maintenance Therapy in Average Risk Childhood Acute Lymphoblastic Leukemia

Acute lymphoblastic leukaemia in children. Results of treatment in Sicily from 1987 to 1992

Unusual sickle cell disease observed for the first time in Italy: Hb S-Hb D Los Angeles

Increase with Age in the Prevalence of β-Thalassemia Trait among Sicilians

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