Search Results - "Schiliró, Gino"

The Changing Profile of Sickle Cell Disease in Italy by Russo-Mancuso, Giovanna, La Spina, Milena, Schiliro, Gino

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Use of PEG-interferon alfa-2a plus ribavirin as treatment for chronic HCV hepatitis in a child cured of ALL by Lo Nigro, Luca, Guardo, Paola, La Spina, Milena, Mirabile, Elena, Pisana, Paola, Schilirò, Gino

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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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Prognostic impact of t(9;11) in childhood acute myeloid leukemia (AML) by Lo Nigro, Luca, Bottino, Daria, Panarello, Claudio, Morerio, Cristina, Mirabile, Elena, Rapella, Anna Maria, Di Cataldo, Andrea, Schiliro, Gino

“…Leukemia (2003) 17, 636. doi:10.1038/sj.leu.2402846…”
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Art therapy as support for children with leukemia during painful procedures by Favara-Scacco, Cinzia, Smirne, Giuseppina, Schilirò, Gino, Di Cataldo, Andrea

“…Background Children with leukemia undergo painful procedures such as lumbar puncture and bone marrow aspiration. To overcome pain, certain units offer total…”
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Road Traffic Pollution and Childhood Leukemia: A Nationwide Case-control Study in Italy by Magnani, Corrado, Ranucci, Alessandra, Badaloni, Chiara, Cesaroni, Giulia, Ferrante, Daniela, Miligi, Lucia, Mattioli, Stefano, Rondelli, Roberto, Bisanti, Luigi, Zambon, Paola, Cannizzaro, Santina, Michelozzi, Paola, Cocco, Pierluigi, Celentano, Egidio, Assennato, Giorgio, Merlo, Domenico Franco, Mosciatti, Paola, Minelli, Liliana, Cuttini, Marina, Torregrossa, Maria Valeria, Lagorio, Susanna, Haupt, Riccardo, Forastiere, Francesco

“…Background The association of childhood leukemia with traffic pollution was considered in a number of studies from 1989 onwards, with results not entirely…”
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Low serum levels of interleukin-6 in children with post-infective acute thrombocytopenic purpura by Gangarossa, S, Romano, V, Munda, S E, Sciotto, A, Schilirò, G

“…Interleukin-6 plays an important role in host defense mechanisms and it appears to be a major mediator of the acute-phase response. IL-6 is also an important…”
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Correlation between High Expression of Natural Killer Related-Genes (NCAM/CD94) and Early Death during Induction in Children with Acute Myeloid Leukemia by Nigro, Luca Lo, Mirabile, Elena, Munda, Silvana, Bottino, Daria, Manuela, Tumino, Gino, Schiliro

“…Death early (DE) during the induction phase of therapy is a rare but dramatic event in children with acute myeloid leukemia (AML). Recent reports emphasize…”
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Antioxidant enzymatic systems and oxidative stress in erythrocytes with G6PD deficiency: effect of deferoxamine by Vanella, A, Campisi, A, Castorina, C, Sorrenti, V, Attaguile, G, Samperi, P, Azzia, N, Di Giacomo, C, Schilirò, G

“…In the present study we have assayed the effect of divicine in G6PD-deficient red blood cells in the presence of deferoxamine (iron-chelating drug) and NaN3…”
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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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Prolylhydroxylase and procollagen type III in long-term survivors of acute lymphoblastic leukemia (ALL): A biochemical approach to HCV-related liver disease by Leonardi, Salvatore, La Spina, Milena, La Rosa, Mario, Schilirò, Gino

“…Background We examined two proteins, prolylhydroxylase (hPH) and procollagen type III (PIIIP), as possible non‐invasive HCV‐related markers of liver disease…”
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Occurrence of a FAB-M1 AML in a child during treatment of APL: emergence of an immature clone or a therapy related-AML? by Lo Nigro, Luca, Schiliro, Gino

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

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Reflection about communication of diagnosis and informed consent in pediatric oncology by Schilirò, Gino, Di Cataldo, Andrea

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Evidence for the molecular heterogeneity of sickle cell anemia chromosomes bearing the betaS/Benin haplotype by Patrinos, George P, Samperi, Piera, Lo Nigro, Luca, Kollia, Panagoula, Schiliro, Gino, Papadakis, Manoussos N

“…There are at least four distinct African and one Asian chromosomal backgrounds (haplotypes) on which the sickle cell mutation has arisen. Additionally,…”
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LETTER TO THE EDITOR: The changing profile of sickle cell disease in Italy by Russo-Mancuso, Giovanna, La Spina, Milena, Schiliro, Gino

“…Sickle cell disease is the most frequent haemoglobinopathy in Italy. A national survey was conducted to evaluate the changes in the distribution of the cases…”
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Increase of F cells during acute hemolysis in glucose-6-phosphate dehydrogenase-deficient males by SCHILIRÓ, G, RUSSO, A, ROMEO, M. A, TESTA, R, MUSUMECI, S, MANCUSO, G. R, RUSSO, G

“…Five male Sicilian children with glucose-6-phosphate dehydrogenase deficiency were studied shortly after hemolytic crisis in order to evaluate the immediate…”
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Evidence for the molecular heterogeneity of sickle cell anemia chromosomes bearing the b super(S)/Benin haplotype by Patrinos, George P, Samperi, Piera, Nigro, Luca lo, Kollia, Panagoula, Schiliro, Gino, Papadakis, Manoussos N

“…There are at least four distinct African and one Asian chromosomal backgrounds (haplotypes) on which the sickle cell mutation has arisen. Additionally,…”
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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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Detectable Molecular Residual Disease at the Beginning of Maintenance Therapy Indicates Poor Outcome in Children With T-Cell Acute Lymphoblastic Leukemia by Dibenedetto, Salvatore P., Lo Nigro, Luca, Pine Mayer, Sharon, Rovera, Giovanni, Schilirò, Gino

“…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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