Search Results - Achille Iolascon

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  1. 1
    Advances in understanding the pathogenesis of red cell membrane disorders

    Advances in understanding the pathogenesis of red cell membrane disorders by Achille Iolascon, Immacolata Andolfo, Roberta Russo

    Published 2019
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  2. 2
    Congenital dyserythropoietic anemias

    Congenital dyserythropoietic anemias by Achille Iolascon, Immacolata Andolfo, Roberta Russo

    Published 2020
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  3. 3
    Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis

    Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis by Achille Iolascon, Luigia De Falco, C. Beaumont

    Published 2009
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  4. 4
    Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach

    Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach by Achille Iolascon, Maria Rosaria Esposito, Roberta Russo

    Published 2012
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  5. 5
    Congenital dyserythropoietic anemias: molecular insights and diagnostic approach

    Congenital dyserythropoietic anemias: molecular insights and diagnostic approach by Achille Iolascon, H. Heimpel, Anders Wåhlin, Hannah Tamary

    Published 2013
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  6. 6
    New insights on hereditary erythrocyte membrane defects

    New insights on hereditary erythrocyte membrane defects by Immacolata Andolfo, Roberta Russo, Antonella Gambale, Achille Iolascon

    Published 2016
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  7. 7
    Hereditary stomatocytosis: An underdiagnosed condition

    Hereditary stomatocytosis: An underdiagnosed condition by Immacolata Andolfo, Roberta Russo, Antonella Gambale, Achille Iolascon

    Published 2017
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  8. 8
    Genetic Analysis of the Coronavirus SARS-CoV-2 Host Protease TMPRSS2 in Different Populations

    Genetic Analysis of the Coronavirus SARS-CoV-2 Host Protease TMPRSS2 in Different Populations by Roberta Russo, Immacolata Andolfo, Vito Alessandro Lasorsa, Achille Iolascon, Mario Capasso

    Published 2020
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  9. 9
    Genetic Predisposition to Solid Pediatric Cancers

    Genetic Predisposition to Solid Pediatric Cancers by Mario Capasso, Annalaura Montella, Matilde Tirelli, Teresa Maiorino, Sueva Cantalupo, Achille Iolascon

    Published 2020
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  10. 10
    UGT1 Promoter Polymorphism Accounts for Increased Neonatal Appearance of Hereditary Spherocytosis

    UGT1 Promoter Polymorphism Accounts for Increased Neonatal Appearance of Hereditary Spherocytosis by Achille Iolascon, Maria Felicia Faienza, Arcangela Moretti, Silverio Perrotta, Emanuele Miraglia del Giudice

    Published 1998
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  11. 11
    Guidelines for the diagnosis and management of hereditary spherocytosis – 2011 update

    Guidelines for the diagnosis and management of hereditary spherocytosis – 2011 update by Paula Bolton‐Maggs, Jacob C. Langer, Achille Iolascon, Paul Tittensor, May‐Jean King

    Published 2011
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  12. 12
    Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2)

    Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2) by Achille Iolascon, Maria D’Apolito, Veronica Servedio, Flora Cimmino, Antonio Piga, Clara Camaschella

    Published 2005
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  13. 13
    Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients

    Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients by Immacolata Andolfo, Roberta Russo, Barbara Eleni Rosato, Francesco Manna, Antonella Gambale, Carlo Brugnara, Achille Iolascon

    Published 2018
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  14. 14
    Galectin-1 is a major effector of TrkB-mediated neuroblastoma aggressiveness

    Galectin-1 is a major effector of TrkB-mediated neuroblastoma aggressiveness by Flora Cimmino, Johannes H. Schulte, Massimo Zollo, Jan Köster, Rogier Versteeg, Achille Iolascon, Angelika Eggert, Alexander Schramm

    Published 2009
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  15. 15
    The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload

    The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload by Clara Camaschella, Alessandro Campanella, Luigia De Falco, Loredana Boschetto, Roberta Merlini, Laura Silvestri, Sonia Levi, Achille Iolascon

    Published 2007
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  16. 16
    Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d in erythroid cells

    Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d in erythroid cells by Immacolata Andolfo, Luigia De Falco, Ramazan Aşçı, Roberta Russo, Simona Colucci, Marisa Gorrese, Massimo Zollo, Achille Iolascon

    Published 2010
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  17. 17
    Localization of the Congenital Dyserythropoietic Anemia II Locus to Chromosome 20q11.2 by Genomewide Search

    Localization of the Congenital Dyserythropoietic Anemia II Locus to Chromosome 20q11.2 by Genomewide Search by Paolo Gasparini, Emanuele Miraglia del Giudice, J. Delaunay, Antonio Totaro, Matteo Granatiero, Salvatore Melchionda, L. Zelante, Achille Iolascon

    Published 1997
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  18. 18
    NCOA4 Deficiency Impairs Systemic Iron Homeostasis

    NCOA4 Deficiency Impairs Systemic Iron Homeostasis by Roberto Bellelli, Giorgia Federico, Alessandro Mattè, David Colecchia, Achille Iolascon, M Chiariello, Massimo Santoro, Lucia De Franceschi, Francesca Carlomagno

    Published 2016
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  19. 19
    Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome

    Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome by Anna Savoia, Carlo L. Balduini, Michelangelo Savino, Patrizia Noris, Maria Del Vecchio, Silverio Perrotta, Simona Belletti, Vincenzo Poggi, Achille Iolascon

    Published 2001
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  20. 20
    Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship

    Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship by Achille Iolascon, Roberta Russo, Maria Rosaria Esposito, Ramazan Aşçı, Carmelo Piscopo, Silverio Perrotta, Madeleine Fénéant‐Thibault, Loïc Garçon, J. Delaunay

    Published 2009
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