Search Results - "Dibenedetto, S P"
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Levels of L-asparagine in CSF after intramuscular administration of asparaginase from Erwinia in children with acute lymphoblastic leukemia
Published in Journal of clinical oncology (01-02-1995)“…As part of a study on the pharmacokinetics associated with the administration of asparaginase (ASNase) from Erwinia to the CNS, we determined the levels of…”
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2
Assessment of the value of treatment with granulocyte colony-stimulating factor in children with acute lymphoblastic leukemia: a randomized clinical trial
Published in European journal of haematology (01-08-1995)“…The present trial was designed to test the effects of G-CSF on the duration of the second phase of induction chemotherapy in children with newly diagnosed…”
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3
Incidence and morbidity of infection by hepatitis C virus in children with acute lymphoblastic leukaemia
Published in European journal of pediatrics (01-04-1994)“…A group of 90 patients with acute lymphoblastic leukaemia (ALL) in first continuous complete remission (CCR), admitted in our hospital between January 1986 and…”
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4
Growth and growth hormone in children during and after therapy for acute lymphoblastic leukaemia
Published in European journal of pediatrics (01-09-1993)“…Growth impairment and growth hormone (GH) deficiency have been reported in children treated for acute lymphoblastic leukaemia (ALL). We have studied growth and…”
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5
Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals
Published in Blood (15-03-1996)Get full text
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6
Dissection of the association status of two polymorphisms in the β‐globin gene cluster with variations in F‐cell number in non‐anemic individuals
Published in American journal of hematology (01-12-1997)“…Expression of fetal hemoglobin (Hb F) is under polygenic control involving determinants both linked and unlinked to the β‐globin gene cluster on chromosome 11…”
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Detection of Minimal Residual Disease: Methods and Relationship to Outcome in T-Lineage Acute Lymphoblastic Leukemia
Published in Leukemia & lymphoma (01-12-1998)“…The molecular basis of acute lymphoblastic leukemia (ALL) of both B-cell and T-cell lineages seems better understood using polymerase chain reaction (PCR)…”
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8
A mild type of Hb S-beta(+)-thalassemia [-92(C-->T)] in a Sicilian family
Published in American journal of hematology (01-02-1993)“…Hematological data are presented for an adult Sicilian patient with a mild Hb S-beta(+)-thalassemia caused by a C-->T mutation at position -92 of the beta…”
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9
Presence of hemoglobinopathies in Sicily: A historic perspective
Published in American journal of medical genetics (17-03-1997)“…Sicily, at the center of the Mediterranean, has been the meeting place of Eastern and Western civilizations, and in the Sicilian population the presence of…”
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10
Reduction in the incidence of infection by hepatitis C virus in children with acute lymphoblastic leukemia after suspension of sampling from the finger
Published in The Pediatric infectious disease journal (01-03-1996)“…Advances in blood-banking techniques have reduced the incidence of infection by hepatitis C virus (HCV), which accounts for most cases of non-A non-B…”
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11
Residual Clones in Childhood Leukemia
Published in The New England journal of medicine (03-07-1997)“…To the Editor: Roberts and his colleagues (Jan. 30 issue) 1 do not emphasize that childhood acute lymphoblastic leukemia (ALL) is a heterogeneous disease with…”
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12
Detectable molecular residual disease at the beginning of maintenance therapy indicates poor outcome in children with T-cell acute lymphoblastic leukemia
Published in Blood (01-08-1997)“…The aims of this study were twofold: (1) to assess the marrow of patients with T-lineage acute lymphoblastic leukemia (T-ALL) for the presence of molecular…”
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13
High performance liquid chromatography (HPLC): a simple method to quantify Hb C, O-Arab, Agenogi and F
Published in Clinical and laboratory haematology (01-01-1991)“…Differentiation of some abnormal haemoglobins, such as Hb C, O-Arab, Agenogi, E, O-Indonesia, C-Harlem, and Siriraj, is difficult and quantitation of the…”
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Six rare hemoglobin variants found in Sicily
Published in Hemoglobin (1991)Get more information
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15
Diabetes insipidus 9 years after cessation of therapy for acute lymphoblastic leukemia
Published in Pediatric hematology and oncology (01-01-1991)“…A case of a 16-year-old who developed diabetes insipidus (DI) 9 years after cessation of therapy for ALL is reported. Because hereditary and traumatic factors…”
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Hematological findings in 375 Sicilians with Hb S trait
Published in Haematologica (Roma) (01-03-1990)“…We evaluated hematological parameters in 375 Sicilian adults with Hb S trait: Hb S levels were 41.91 +/- 2.65% in males and 40.92 +/- 2.8% in females. RBC,…”
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17
Increase with age in the prevalence of beta-thalassemia trait among Sicilians
Published in The New England journal of medicine (14-09-1989)Get more information
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18
The effect of the beta thalassemia mutation on the clinical severity of the sickle beta thalassemia syndrome
Published in Haematologica (Roma) (01-07-1989)“…In this study, we have defined the beta thalassemia mutation and characterized the beta globin haplotype and the alpha globin gene arrangement in a group of…”
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A comparative immunogenicity-reactogenicity dose-response study of influenza vaccine
Published in Annals of allergy (01-09-1990)“…This study examined the immunogenic and reactogenic responses of influenza vaccine in 29 healthy nonallergic adults at three vaccine dosages: 0.5 mL, 0.1 mL,…”
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20
Non inherited hemoglobin anomalies
Published in Haematologica (Roma) (01-09-1991)“…A number of genetic or acquired conditions in which hemoglobin anomalies occur without detectable modifications of globin genes are reviewed. They include…”
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