Search Results - "SCHILIRO, G"

Plasma Chitotriosidase Activity in Patients with β-Thalassemia by Barone, Rita, Di Gregorio, Felicia, Romeo, Maria A., Schilirò, Gino, Pavone, Lorenzo

“…Chitotriosidase, a macrophage marker, which is extremely increased in plasma of Gaucher patients, was measured in patients with β-thalassemia, an…”
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Application of a chemiluminescent methodology for detection of minimal residual disease in childhood acute lymphoblastic leukemia by Lo Nigro, L, Poli, A, Mirabile, E, Costantino, F, Schilirò, G

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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 by DIBENEDETTO, S. P, LO NIGRO, L, MAYER, S. P, ROVERA, G, SCHILIRO, G

“…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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Deletions in the mitochondrial DNA and decrease in the oxidative phosphorylation activity of children with fanconi syndrome secondary to antiblastic therapy by Di Cataldo, Andrea, Palumbo, Maddalena, Pittalà, Donatella, Renis, Marcella, Schilirò, Gino, Russo, Alessandra, Ragusa, Rosalia, Mollica, Florindo, Li Volti, Salvatore

“…The aim of this study is to verify whether there are deletions in mitochondrial DNA (mtDNA) and disorders in oxidative phosphorylation (Ox-phos) complexes in…”
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Association between high expression of natural killer related-genes (NCAM CD94) and early death during induction in children with acute myeloid leukemia by LoNigro, L, Mirabile, E, Munda, S, Barchitta, M, Bottino, D, Fazzio, A, Di Cataldo, A, Agodi, A, Schilirò, G

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Survey of sickle cell disease in Italy by Russo-Mancuso, G, Romeo, MA, Guardabasso, V, Schiliro, G

“…Divisione di Ematologia ed Oncologia Pediatrica, Universita, di Catania, Italy. diberuss@mbox.unict.it BACKGROUND AND OBJECTIVE: The present study was designed…”
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Dysmegakaryopoietic Thrombocytopenia in Patients With Distal Chromosome 11q Deletion by Gangarossa, Simone, Schiliró, Gino, Mattina, Teresa, Scardilli, Stefania, Mollica, Florindo, Cavallari, Vittorio

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VISCERAL LEISHMANIASIS IN THREE CHILDREN WITH LEUKEMIA by Di Cataldo, Andrea, Lo Nigro, Luca, Marino, Santo, Schilirò, Gino

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Growth and growth hormone in children during and after therapy for acute lymphoblastic leukaemia by CARUSO-NICOLETTI, M, MANCUSO, M, SPADARO, G, DIBENEDETTO, S. P, DICATALDO, A, SCHILIRO, G

“…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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Structural and ultrastructural study of the ovary in childhood leukemia after successful treatment by Marcello, M F, Nuciforo, G, Romeo, R, Di Dino, G, Russo, I, Russo, A, Palumbo, G, Schilirò, G

“…Ovarian biopsy specimens from ten girls (three postmenarcheal) who had undergone antiblastic treatment for acute lymphoblastic leukemia (ALL) and were in…”
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Molecular basis of α-thalassemia in Sicily by FICHERA, M, SPALLETTA, A, FIORENZA, F, LOMBARDO, T, SCHILIRO, G, TAMOUZA, R, LAPOUMKROULIE, C, LABIE, D, RAGUSA, A

“…To evaluate the allelic frequency and genetic diversity of alpha-thalassemia defects in Sicily, both epidemiological and patient-oriented studies were carried…”
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Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency in south-east Sicily by CITTADELLA, R., CIVITELLI, D., MANNA, I., AZZIA, N., DI CATALDO, A., SCHILIROA, G., BRANCATI, C.

“…In order to explore the nature of glucose-6-phosphate dehydrogenase (G6PD) deficiency in south-east Sicily, we have analysed the G6PD gene in 25 unrelated…”
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Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals by Merghoub, T, Maier-Redelsperger, M, Labie, D, Perichon, B, Feingold, N, Dibenedetto, S P, Schiliro, G, Samperi, P, Ducrocq, R, Elion, J, Krishnamoorthy, R

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DEPARTMENT OF PEDIATRIC HEMATOLOGY AND ONCOLOGY, UNIVERSITY OF CATANIA, ITALY by Ragusa, Rosalia, Schiliro, Gino

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Efficacy of an analysis of lymphocyte subsets in predicting the clinical response to alpha-interferon therapy in thalassaemia patients with chronic infection by hepatitis C virus: a pilot study by Russo-Mancuso, G, Di Gregorio, F, Passero, E, Sciotto, A, Mazzarino, M C, Malaponte, G, Schilirò, G

“…alpha-interferon (alpha-IFN) has been used to treat chronic non-A non-B hepatitis in thalassaemic patients with response rates from 45% to 83%. Unfortunately,…”
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Is intensive follow-up for early detection of tumors effective in children with Beckwith-Wiedemann syndrome? by Di Cataldo, A, Haupt, R, Fabietti, P, Schilirò, G

“…Two cases of Beckwith-Wiedemann syndrome who developed malignant tumor and eventually died are reported. The patients followed two different screening programs…”
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gamma-mRNA and Hb F levels in beta-thalassaemia by Efremov, D G, Dimovski, A J, Sukarova, E, Schilirò, G, Zisovski, N, Efremov, G D, Burrone, O R, Huisman, T H

“…The Hb F levels in beta-thalassaemia can be affected by factors both linked and unlinked to the beta-globin gene cluster. We have recently analysed a group of…”
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A mild form of Hb S-β-thalassemia syndrome is assured in Sicilian patients by β+mutant IVS-I nt 6(T→C) by Mirabile, Elena, Testa, Rosario, Samperi, Piera, Consalvo, Carmela, Romano, Vincenzo

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Presence of hemoglobinopathies in Sicily: A historic perspective by Schilirò, Gino, Mirabile, Elena, Testa, Rosario, Russo-Mancuso, Giovanna, Dibenedetto, Salvatore P.

“…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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Efficacy of oral administration of high-dose cobamamide in a patient with Imerslund-Gräsbeck syndrome by Gangarossa, S, Romano, V, Schilirò, G

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