RB1CC1 duplication and aberrant overexpression in a patient with schizophrenia: further phenotype delineation and proposal of a pathogenetic mechanism by Edoardo Errichiello, Roberto Giorda, Antonella Gambale, Achille Iolascon, Orsetta Zuffardi, Sabrina Giglio

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Novel PKLR missense mutation (A300P) causing pyruvate kinase deficiency in an Omani Kindred—PK deficiency masquerading as congenital dyserythropoietic anemia by Naglaa Fawaz, Ismail Beshlawi, Alauldeen Alqasim, Mathew Zachariah, Roberta Russo, Immacolata Andolfo, Antonella Gambale, Anil Pathare, Achille Iolascon

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Corrigendum: Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein by Roberta Russo, Roberta Russo, Roberta Marra, Roberta Marra, Immacolata Andolfo, Immacolata Andolfo, Gianluca De Rosa, Gianluca De Rosa, Barbara Eleni Rosato, Barbara Eleni Rosato, Francesco Manna, Antonella Gambale, Antonella Gambale, Maddalena Raia, Sule Unal, Susanna Barella, Achille Iolascon, Achille Iolascon

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Genetic predictors of response to treatment of chronic hepatitis C virus infection in patients from southern Italy by Mario Masarone, Roberta Russo, Antonella Gambale, Concetta Langella, Ferdinando Carlo Sasso, Luca Fontanella, Marco Romano, Achille Iolascon, Marcello Persico

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Complex Modes of Inheritance in Hereditary Red Blood Cell Disorders: A Case Series Study of 155 Patients by Immacolata Andolfo, Stefania Martone, Barbara Eleni Rosato, Roberta Marra, Antonella Gambale, Gian Luca Forni, Valeria Pinto, Magnus Göransson, Vasiliki Papadopoulou, Mathilde Gavillet, Mohsen Elalfy, Antonella Panarelli, Giovanna Tomaiuolo, Achille Iolascon, Roberta Russo

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DICER1 Syndrome: A Multicenter Surgical Experience and Systematic Review by Claudio Spinelli, Marco Ghionzoli, Linda Idrissi Sahli, Carla Guglielmo, Silvia Frascella, Silvia Romano, Carlo Ferrari, Fabrizio Gennari, Giovanni Conzo, Riccardo Morganti, Luigi De Napoli, Lucia Quaglietta, Lucia De Martino, Stefania Picariello, Anna Grandone, Caterina Luongo, Antonella Gambale, Armando Patrizio, Poupak Fallahi, Alessandro Antonelli, Silvia Martina Ferrari

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Summary of Joint European Hematology Association (EHA) and EuroBloodNet Recommendations on Diagnosis and Treatment of Methemoglobinemia by Achille Iolascon, Immacolata Andolfo, Roberta Russo, Wilma Barcellini, Elisa Fermo, Gergely Toldi, Stefano Ghirardello, Davis Rees, Richard Van Wijk, Antonis Kattamis, Patrick G. Gallagher, Noemi Roy, Ali Taher, Razan Mohty, Andreas Kulozik, Lucia De Franceschi, Antonella Gambale, Mariane De Montalembert, Gian Luca Forni, Cornelis L. Harteveld, Josef Prchal, Paola Bianchi, on behalf of SWG of Red Cell and Iron of EHA and EuroBloodNet

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