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Journal Articles

Second Generation Tyrosine Kinase Inhibitors (2G-TKI) in the Frontline Treatment of Elderly Patients with Chronic Myeloid Leukemia

Blood (2017) 130 (Supplement 1): 1606.

https://doi.org/10.1182/blood.V130.Suppl_1.1606.1606

Published: 2017

Journal Articles

Efficacy and Safety of Nilotinib in First Line Therapy in a Real Life Cohort of Chronic Myeloid Leukemia Patients

Luigia Luciano, MD, Mario Annunziata, MD, Maria Rosaria Esposito, MD, Palmieri Francesco, MD, Maria Iovine, MD, Paolo Danise, MD, Simona Pagliuca, MD, Giovanna Giagnuolo, MD, Antonello Sica, MD, Roberto Vallone, MD, Marilena Spiezia, MD, Fabrizio Pane, MD

Blood (2014) 124 (21): 5531.

https://doi.org/10.1182/blood.V124.21.5531.5531

Published: 2014

Journal Articles

Thrombosis History and Relationship With Low Thrombocytosis, Leukocytosis, and Other Characteristics At Diagnosis In 977 Essential Thrombocythemia Patients A Multivariate Analysis Of The Registro Italiano Trombocitemie (RIT)

Luigi Gugliotta, MD, Alessandra Iurlo, MD, Alessia Tieghi, MD, Gabriele Gugliotta, MD, Anna Candoni, MD, Elisa Rumi, MD, Elisabetta Antonioli, MD, Alessandra Ricco, Monica Lunghi, MD, Rosario Potito Scalzulli, MD, Anna Rita Scortechini, MD, Katia Codeluppi, Bruno Martino, MD, Alfredo Dragani, MD, Andrea Patriarca, MD, Vincenzo Martinelli, MD, Giorgia Battipaglia, MD, Maria Luigia Randi, MD, Elisabetta Cosi, MD, Anna Marina Liberati, MD, Viviana Appolloni, MD, Nilla Maschio, MD, Lucia Mastrullo, MD, Maria Rosaria Villa, MD, Maria Rosaria Esposito, MD, Nicola Cantore, MD, Fausto Palmieri, MD, Maria Langella, MD, Flavia Rivellini, MD, Maria Gabriella Mazzucconi, MD, Cristina Santoro, MD, Ercole De Biasi, MD, Angela Rago, MD, Nicola Polverelli, MD, Pierangelo Spedini, MD, Emma Cacciola, MD, Rossella R Cacciola, MD, Ivana Pierri, MD, Laura Mitsheunig, MD, Marzia Salvucci, Ferdinando Porretto, MD, Andrea Piccin, MD, Umberto Santoro, Gianluca Gaidano, Giuseppe Cimino, MD, Francesco Lanza, MD, Agostino Cortelezzi, MD, Giuseppe Tagariello, MD, Serena Rupoli, MD, Giorgina Specchia, Francesco Passamonti, MD, Alessandro M. Vannucchi, MD, Fabrizio Pane, Nicola Vianelli, MD, Rossella Miglio, Paola Monari

Blood (2013) 122 (21): 2829.

https://doi.org/10.1182/blood.V122.21.2829.2829

Published: 2013

Journal Articles

Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1

Blood (2013) 121 (19): 3925–3935.

https://doi.org/10.1182/blood-2013-02-482489

Published: 2013

Includes: Supplemental data

Journal Articles

Missense Mutations in the ABCB6 Transporter Cause Dominant Familial Pseudohyperkalemia

Immacolata Andolfo, Seth Alper, MD, PhD, Jean Delaunay, Carla Auriemma, Roberta Russo, Maria Rosaria Esposito, Alok K. Sharma, Boris E Shmukler, David H Vandorpe, Carlo Brugnara, M.D., Lucia De Franceschi, MD, Achille Iolascon, MD, PhD

Blood (2012) 120 (21): 3184.

https://doi.org/10.1182/blood.V120.21.3184.3184

Published: 2012

Journal Articles

In Vitro Characterization of R14W Mutation in SEC23B , the CDAII Causative Gene

Maria Rosaria Esposito, Roberta Russo, Annaelena Troiano, Immacolata Andolfo, Roberta Asci, Achille Iolascon, MD, PhD

Blood (2011) 118 (21): 2098.

https://doi.org/10.1182/blood.V118.21.2098.2098

Published: 2011

Journal Articles

Allelic Distribution Assessment of SEC23B Mutations In Cda II Patients From Italy: Towards the Identification of Possible Founder Mutations

Roberta Russo, Maria Rosaria Esposito, Antonella Gambale, Annaelena Troiano, Maria Luisa Serra, Ilaria De Maggio, Achille Iolascon

Blood (2010) 116 (21): 1005.

https://doi.org/10.1182/blood.V116.21.1005.1005

Published: 2010

Journal Articles

COPII Complex Characterization During Erythroid Differentiation and Its Involvement in CDAII Disease.

Roberta Russo, Maria Rosaria Esposito, Daniela Spano, Luigia De Falco, Roberta Asci, Carmelo Piscopo, Immacolata Andolfo, Achille Iolascon, MD, PhD

Blood (2009) 114 (22): 3009.

https://doi.org/10.1182/blood.V114.22.3009.3009

Published: 2009

Journal Articles

BAND 3CEINGE (Gly796Arg) Mutation Causes Dehydrated Hereditary Stomatocytosis (DHS) with Dyserythropoietic Phenotype

Luigia De Falco, Lucia De Franceschi, Frank Borgese, Carmelo Piscopo, Maria Rosaria Esposito, Rosa Anna Avvisati, Pietro Izzo, Helene Guizouarn, Andrea Biondani, Achille Iolascon, MD, PhD

Blood (2008) 112 (11): 2874.

https://doi.org/10.1182/blood.V112.11.2874.2874

Published: 2008

NARROW

Second Generation Tyrosine Kinase Inhibitors (2G-TKI) in the Frontline Treatment of Elderly Patients with Chronic Myeloid Leukemia

Efficacy and Safety of Nilotinib in First Line Therapy in a Real Life Cohort of Chronic Myeloid Leukemia Patients

Thrombosis History and Relationship With Low Thrombocytosis, Leukocytosis, and Other Characteristics At Diagnosis In 977 Essential Thrombocythemia Patients A Multivariate Analysis Of The Registro Italiano Trombocitemie (RIT)

Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1

Missense Mutations in the ABCB6 Transporter Cause Dominant Familial Pseudohyperkalemia

In Vitro Characterization of R14W Mutation in SEC23B , the CDAII Causative Gene

Allelic Distribution Assessment of SEC23B Mutations In Cda II Patients From Italy: Towards the Identification of Possible Founder Mutations

COPII Complex Characterization During Erythroid Differentiation and Its Involvement in CDAII Disease.

BAND 3CEINGE (Gly796Arg) Mutation Causes Dehydrated Hereditary Stomatocytosis (DHS) with Dyserythropoietic Phenotype

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American Society of Hematology

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American Society of Hematology

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