Works by Iolascon, Achille

Results: 160
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    Genetic counseling during COVID‐19 pandemic: Tuscany experience.

    Published in:
    Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 10, p. 1, doi. 10.1002/mgg3.1433
    By:
    • Pagliazzi, Angelica;
    • Mancano, Giorgia;
    • Forzano, Giulia;
    • Giovanni, Fabiana;
    • Gori, Giulia;
    • Traficante, Giovanna;
    • Iolascon, Achille;
    • Giglio, Sabrina
    Publication type:
    Article
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    Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy.

    Published in:
    Nephrology Dialysis Transplantation, 2014, v. 29, n. suppl_4, p. iv80, doi. 10.1093/ndt/gfu071
    By:
    • Caridi, Gianluca;
    • Lugani, Francesca;
    • Dagnino, Monica;
    • Gigante, Maddalena;
    • Iolascon, Achille;
    • Falco, Mariateresa;
    • Graziano, Claudio;
    • Benetti, Elisa;
    • Dugo, Mauro;
    • Del Prete, Dorella;
    • Granata, Antonio;
    • Borracelli, Donella;
    • Moggia, Elisabetta;
    • Quaglia, Marco;
    • Rinaldi, Rita;
    • Gesualdo, Loreto;
    • Ghiggeri, Gian Marco
    Publication type:
    Article
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    A multidisciplinary approach to inherited retinal dystrophies from diagnosis to initial care: a narrative review with inputs from clinical practice.

    Published in:
    Orphanet Journal of Rare Diseases, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13023-023-02798-z
    By:
    • Murro, Vittoria;
    • Banfi, Sandro;
    • Testa, Francesco;
    • Iarossi, Giancarlo;
    • Falsini, Benedetto;
    • Sodi, Andrea;
    • Signorini, Sabrina;
    • Iolascon, Achille;
    • Russo, Roberta;
    • Mucciolo, Dario Pasquale;
    • Caputo, Roberto;
    • Bacci, Giacomo Maria;
    • Bargiacchi, Sara;
    • Turco, Simona;
    • Fortini, Stefania;
    • Simonelli, Francesca
    Publication type:
    Article
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    Association of PARP1 polymorphisms with response to chemotherapy in patients with high‐risk neuroblastoma.

    Published in:
    Journal of Cellular & Molecular Medicine, 2020, v. 24, n. 7, p. 4072, doi. 10.1111/jcmm.15058
    By:
    • Avitabile, Marianna;
    • Lasorsa, Vito Alessandro;
    • Cantalupo, Sueva;
    • Cardinale, Antonella;
    • Cimmino, Flora;
    • Montella, Annalaura;
    • Capasso, Dalila;
    • Haupt, Riccardo;
    • Amoroso, Loredana;
    • Garaventa, Alberto;
    • Quattrone, Alessandro;
    • Corrias, Maria Valeria;
    • Iolascon, Achille;
    • Capasso, Mario
    Publication type:
    Article
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    GENETIC CHARACTERIZATION OF A COHORT OF PATIENTS AFFECTED BY SCHIZOPHRENIA. THE ROLE FOR RARE STRUCTURAL VARIANTS IN MODULATING TREATMENT RESISTANT ENDOPHENOTYPES: PRELIMINARY DATA.

    Published in:
    Schizophrenia Bulletin, 2020, v. 46, p. S201, doi. 10.1093/schbul/sbaa030.482
    By:
    • Barone, Annarita;
    • Iasevoli, Felice;
    • Matrone, Marta;
    • Buonaguro, Elisabetta Filomena ;
    • Falco, Mariateresa;
    • Genesio, Rita;
    • Pignataro, Piero;
    • Capasso, Mario;
    • Gambale, Antonella;
    • Avagliano, Camilla;
    • Razzino, Eugenio;
    • Notar Francesco, Danilo;
    • Ciccarelli, Mariateresa;
    • Vitiello, Giuseppina;
    • Andolfo, Immacolata;
    • Nitsch, Lucio;
    • Iolascon, Achille;
    • de Bartolomeis, Andrea
    Publication type:
    Article
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    Unveiling the genetic landscape of suspected congenital dyserythropoietic anemia type I: A retrospective cohort study of 36 patients.

    Published in:
    American Journal of Hematology, 2024, v. 99, n. 8, p. 1511, doi. 10.1002/ajh.27350
    By:
    • Marra, Roberta;
    • Nostroso, Antonella;
    • Rosato, Barbara Eleni;
    • Esposito, Federica Maria;
    • D'Onofrio, Vanessa;
    • Iscaro, Anthony;
    • Gambale, Antonella;
    • Bruschi, Barbara;
    • Coccia, Paola;
    • Poloni, Antonella;
    • Unal, Sule;
    • Romano, Alberto;
    • Iolascon, Achille;
    • Andolfo, Immacolata;
    • Russo, Roberta
    Publication type:
    Article
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    PIEZO1 mutations impact on early clinical manifestations of myelodysplastic syndromes.

    Published in:
    American Journal of Hematology, 2023, v. 98, n. 4, p. E72, doi. 10.1002/ajh.26863
    By:
    • Attardi, Enrico;
    • Andolfo, Immacolata;
    • Russo, Roberta;
    • Tiberi, Lucia;
    • Raddi, Marco Gabriele;
    • Rosato, Barbara Eleni;
    • Marra, Roberta;
    • Formicola, Daniela;
    • Del Giudice, Federica;
    • Brogi, Alice;
    • Consagra, Angela;
    • Amato, Cristina;
    • Sanna, Alessandro;
    • Artuso, Rosangela;
    • Iolascon, Achille;
    • Santini, Valeria
    Publication type:
    Article
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    Recommendations for diagnosis and treatment of methemoglobinemia.

    Published in:
    American Journal of Hematology, 2021, v. 96, n. 12, p. 1666, doi. 10.1002/ajh.26340
    By:
    • Iolascon, Achille;
    • Bianchi, Paola;
    • Andolfo, Immacolata;
    • Russo, Roberta;
    • Barcellini, Wilma;
    • Fermo, Elisa;
    • Toldi, Gergely;
    • Ghirardello, Stefano;
    • Rees, Davis;
    • Van Wijk, Richard;
    • Kattamis, Antonis;
    • Gallagher, Patrick G.;
    • Roy, Noemi;
    • Taher, Ali;
    • Mohty, Razan;
    • Kulozik, Andreas;
    • De Franceschi, Lucia;
    • Gambale, Antonella;
    • De Montalembert, Mariane;
    • Forni, Gian Luca
    Publication type:
    Article
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    Fyn kinase is a novel modulator of erythropoietin signaling and stress erythropoiesis.

    Published in:
    American Journal of Hematology, 2019, v. 94, n. 1, p. 10, doi. 10.1002/ajh.25295
    By:
    • Beneduce, Elisabetta;
    • Matte, Alessandro;
    • De Falco, Luigia;
    • Mbiandjeu, Serge;
    • Chiabrando, Deborah;
    • Tolosano, Emanuela;
    • Federti, Enrica;
    • Petrillo, Sara;
    • Mohandas, Narla;
    • Siciliano, Angela;
    • Babu, Wilson;
    • Menon, Vijay;
    • Ghaffari, Saghi;
    • Iolascon, Achille;
    • De Franceschi, Lucia
    Publication type:
    Article
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    Hereditary xerocytosis revisited.

    Published in:
    American Journal of Hematology, 2014, v. 89, n. 12, p. 1142, doi. 10.1002/ajh.23799
    By:
    • Archer, Natasha M.;
    • Shmukler, Boris E.;
    • Andolfo, Immacolata;
    • Vandorpe, David H.;
    • Gnanasambandam, Radhakrishnan;
    • Higgins, John M.;
    • Rivera, Alicia;
    • Fleming, Mark D.;
    • Sachs, Frederick;
    • Gottlieb, Philip A.;
    • Iolascon, Achille;
    • Brugnara, Carlo;
    • Alper, Seth L.;
    • Nathan, David G.
    Publication type:
    Article
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    Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1.

    Published in:
    Nature Genetics, 2005, v. 37, n. 11, p. 1258, doi. 10.1038/ng1656
    By:
    • Bruce, Lesley J.;
    • C. Robinson, Hannah;
    • Guizouarn, Hélène;
    • Borgese, Franck;
    • Harrison, Penny;
    • King, May-Jean;
    • Goede, Jeroen S.;
    • Coles, Suzanne E.;
    • Gore, Daniel M.;
    • Lutz, Hans U.;
    • Ficarella, Romina;
    • Layton, D. Mark;
    • Iolascon, Achille;
    • Ellory, J. Clive;
    • Stewart, Gordon W.
    Publication type:
    Article
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    FGFR1 is a potential therapeutic target in neuroblastoma.

    Published in:
    Cancer Cell International, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12935-022-02587-x
    By:
    • Cimmino, Flora;
    • Montella, Annalaura;
    • Tirelli, Matilde;
    • Avitabile, Marianna;
    • Lasorsa, Vito Alessandro;
    • Visconte, Feliciano;
    • Cantalupo, Sueva;
    • Maiorino, Teresa;
    • De Angelis, Biagio;
    • Morini, Martina;
    • Castellano, Aurora;
    • Locatelli, Franco;
    • Capasso, Mario;
    • Iolascon, Achille
    Publication type:
    Article