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Journal Articles

A Mild DBA Phenotype Associated with a Non-Canonical Splice Site Mutation in RPS26

Elisa Fermo, Marta la Vecchia, Alberto Zanella, Irma Dianzani, Paola Bianchi

Blood (2023) 142 (Supplement 1): 5673.

https://doi.org/10.1182/blood-2023-180118

Published: 2023

Journal Articles

Red cell–bound antibodies and transfusion requirements in hospitalized patients with COVID-19

Alessandra Berzuini, Cristiana Bianco, Cinzia Paccapelo, Francesco Bertolini, Giuliana Gregato, Alessandra Cattaneo, Elisa Erba, Alessandra Bandera, Andrea Gori, Giuseppe Lamorte, Maria Manunta, Laura Porretti, Nicoletta Revelli, Francesca Truglio, Giacomo Grasselli, Alberto Zanella, Stefania Villa, Luca Valenti, Daniele Prati

Blood (2020) 136 (6): 766–768.

https://doi.org/10.1182/blood.2020006695

Published: 2020

Journal Articles

Prognostic and Predictive Impact of Small PNH Clones in a Large Cohort of Patients with Myelodysplastic Syndromes and Aplastic Anemia: A Single-Center Experience

Bruno Fattizzo, MD, Alan Dunlop, Robin M. Ireland, FRCP, Shireen Kassam, MD, Dario Consonni, MD, Deborah Yallop, MBBS FRCP FRCPath PhD, Ghulam J. Mufti, Judith Marsh, Alberto Zanella, MD, Wilma Barcellini, MD, Austin G. Kulasekararaj, MBBS, MD MRCP, FRCPath

Blood (2018) 132 (Supplement 1): 3870.

https://doi.org/10.1182/blood-2018-99-116772

Published: 2018

Journal Articles

Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study

Blood (2018) 131 (20): 2183–2192.

https://doi.org/10.1182/blood-2017-10-810796

Published: 2018

Includes: Supplemental data

Journal Articles

Prevalence of Bone Marrow Fibrosis in 47 Cases of Autoimmune Hemolytic Anemia Patients: Clinical and Biologic Relationships

Bruno Fattizzo, MD, Anna Zaninoni, BS, Umberto Gianelli, Alberto Zanella, MD, Agostino Cortelezzi, Prof, Wilma Barcellini, MD

Blood (2017) 130 (Supplement 1): 3491.

https://doi.org/10.1182/blood.V130.Suppl_1.3491.3491

Published: 2017

Journal Articles

Healthcare Resource Utilization in Autoimmune Hemolytic Anemia Patients: Analysis of 190 Cases from a Single Center

Wilma Barcellini, MD, Bruno Fattizzo, MD, Anna Zaninoni, BS, juri A. Giannotta, Valeria Ferri, Alberto Zanella, MD, Agostino Cortelezzi, Prof

Blood (2017) 130 (Supplement 1): 3370.

https://doi.org/10.1182/blood.V130.Suppl_1.3370.3370

Published: 2017

Journal Articles

Use of Next Generation Sequencing Panel to Clarify Undiagnosed Cases of Hereditary Hemolytic Anemias

Elisa Fermo, PhD, Cristina Vercellati, PhD, Anna Paola Marcello, PhD, Ebru Yilmaz Keskin, MD, Aurora Feliu Torres, MD, Silverio Perrotta, Tekin Aksu, MD, Anna Zaninoni, BS, Valentina Brancaleoni, MSc, Richard van Wijk, PhD, Sultan Aydin Koker, MD, Alberto Zanella, MD, Agostino Cortelezzi, Prof, Wilma Barcellini, MD, Paola Bianchi, BSc, PhD

Blood (2017) 130 (Supplement 1): 3480.

https://doi.org/10.1182/blood.V130.Suppl_1.3480.3480

Published: 2017

Journal Articles

Brain MRI Findings and Neuro-Psychiatric Involvement in Paroxysmal Nocturnal Hemoglobinuria (PNH)

Wilma Barcellini, Elisa Scola, Silvia Lanfranconi, Marika Grottaroli, Francesca Binda, Bruno Fattizzo, MD, Anna Zaninoni, Gloria Valcamonica, Carla Boschetti, Massimiliano Buoli, Carlo Alfredo Altamura, Nereo Bresolin, Fabio Triulzi, Alberto Zanella, Agostino Cortelezzi, MD

Blood (2016) 128 (22): 4800.

https://doi.org/10.1182/blood.V128.22.4800.4800

Published: 2016

Journal Articles

Gardos Channel Mutation Is Associated with Hereditary Dehydrate Stomatocytosis: a Complex Channelopathy

Elisa Fermo, PhD, Anna Yu. Bogdanova, Dr PhD, Polina Petkova-Kirova, PhD, Anna Zaninoni, BSc, PhD, Anna Paola Marcello, PhD, Asya Makhro, PhD, Pascal Hänggi, PhD, Laura Hertz, PhD, Jens Danielczok, Nadia Mirra, MD, Alberto Zanella, MD, Wilma Barcellini, MD, Kaestner Lars, PhD, Paola Bianchi, PhD

Blood (2015) 126 (23): 3333.

https://doi.org/10.1182/blood.V126.23.3333.3333

Published: 2015

Journal Articles

Diagnostic Power of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) Evaluated in 118 Patients Affected By Hereditary Hemolytic Anemias

Paola Bianchi, PhD, Anna Zaninoni, BSc, PhD, Elisa Fermo, PhD, Cristina Vercellati, BSc, Marcello Anna Paola, BSc, Alberto Zanella, MD, Agostino Cortelezzi, MD, Wilma Barcellini, MD

Blood (2015) 126 (23): 942.

https://doi.org/10.1182/blood.V126.23.942.942

Published: 2015

Journal Articles

Biallelic Mutations in PARP4 Are Linked to a Variant Form of Congenital Dyserythropoietic Anemia

Paola Bianchi, PhD, Elisa Fermo, PhD, Jennifer C Eng, Jacob C Ulirsch, Cristina Vercellati, BSc, Paola Braidotti, MD, Gordon Hildick-Smith, Timothy J Satchwell, PhD, Stephanie Pellegrin, PhD, Alberto Zanella, MD, Wilma Barcellini, MD, Barry H. Paw, MD, PhD, Ashley Mark Toye, PhD, Vijay G Sankaran, MD PhD

Blood (2015) 126 (23): 272.

https://doi.org/10.1182/blood.V126.23.272.272

Published: 2015

Journal Articles

Predictors of Outcome and Response to Therapy in Primary Autoimmune Hemolytic Anemia: A Gimema Study of 307 Patients

Blood (2014) 124 (21): 1346.

https://doi.org/10.1182/blood.V124.21.1346.1346

Published: 2014

Journal Articles

Clinical heterogeneity and predictors of outcome in primary autoimmune hemolytic anemia: a GIMEMA study of 308 patients

Blood (2014) 124 (19): 2930–2936.

https://doi.org/10.1182/blood-2014-06-583021

Published: 2014

Includes: Supplemental data

Journal Articles

Clinical Heterogeneity Of Autoimmune Hemolytic Anemia: A 35-Years Retrospective Study Of 157 Patients

Wilma Barcellini, MD, Bruno Fattizzo, MD, Tommaso Radice, MD, Anna Zaninoni, BS, Nicoletta Revelli, Maria Antonietta Villa, Carla Boschetti, MD, Agostino Cortelezzi, MD, Alberto Zanella, M.D.

Blood (2013) 122 (21): 3428.

https://doi.org/10.1182/blood.V122.21.3428.3428

Published: 2013

Journal Articles

Low-dose rituximab in adult patients with idiopathic autoimmune hemolytic anemia: clinical efficacy and biologic studies

Wilma Barcellini, Francesco Zaja, Anna Zaninoni, Francesca Guia Imperiali, Marta Lisa Battista, Eros Di Bona, Bruno Fattizzo, Dario Consonni, Agostino Cortelezzi, Renato Fanin, Alberto Zanella

Blood (2012) 119 (16): 3691–3697.

https://doi.org/10.1182/blood-2011-06-363556

Published: 2012

Journal Articles

A Case of Congenital Red Cell Pyruvate Kinase Deficiency Associated with Hereditary Spherocytosis

Cristina Vercellati, PhD, Anna Paola Maria Luisa Marcello, PhD, Elisa Fermo, PhD, Paola Bianchi, PhD, Carla Boschetti, Alessandra Iurlo, M.D., Alberto Zanella, M.D., Wilma Barcellini, MD

Blood (2011) 118 (21): 5272.

https://doi.org/10.1182/blood.V118.21.5272.5272

Published: 2011

Journal Articles

Molecular characterization of the First Italian Variant of Phosphoglycerate Kinase Deficiency

Paola Bianchi, M Sc, Elisa Fermo, M Sc, Luana Mandarà, M.D., Cristina Vercellati, PhD, Anna Paola Maria Luisa Marcello, PhD, Agostino Cortelezzi, MD, Wilma Barcellini, MD, Alberto Zanella, M.D.

Blood (2011) 118 (21): 5270.

https://doi.org/10.1182/blood.V118.21.5270.5270

Published: 2011

Journal Articles

Expression of TLRs in B-CLL: Relationship with Disease Activity

Wilma Barcellini, MD, Francesca Guia Imperiali, Anna Zaninoni, Gianluigi Reda, MD, Bruno Fattizzo, Alberto Zanella, M.D., Agostino Cortelezzi, MD

Blood (2011) 118 (21): 4597.

https://doi.org/10.1182/blood.V118.21.4597.4597

Published: 2011

Journal Articles

Molecular Analysis of the SEC23B Gene In Patients Affected by Congenital Dyserythropoietic Anemia Type II (CDAII)

Paola Bianchi, PhD, Klaus Schwarz, MD, Elisa Fermo, PhD, Katja Heinrich, MD, Cristina Vercellati, PhD, Anna Paola Maria Luisa Marcello, PhD, Richard van Wijk, PhD, Rob van Zwieten, MD, Laura Banov, MD, Antonella Sau, MD, Walter A. Wuillemin, MD, Stephen Opat, MD, Wilma Barcellini, MD, Hermann Heimpel, MD, Prof., Alberto Zanella, MD

Blood (2010) 116 (21): 4227.

https://doi.org/10.1182/blood.V116.21.4227.4227

Published: 2010

Journal Articles

Low-Dose Rituximab In Idiopathic Autoimmune Hemolytic Anemia: Biological Studies

Wilma Barcellini, Francesco Zaja, Anna Zaninoni, Francesca Guia Imperiali, Marta Lisa Battista, Eros Di Bona, Dario Consonni, Alberto Zanella, MD

Blood (2010) 116 (21): 3206.

https://doi.org/10.1182/blood.V116.21.3206.3206

Published: 2010

NARROW

A Mild DBA Phenotype Associated with a Non-Canonical Splice Site Mutation in RPS26

Red cell–bound antibodies and transfusion requirements in hospitalized patients with COVID-19

Prognostic and Predictive Impact of Small PNH Clones in a Large Cohort of Patients with Myelodysplastic Syndromes and Aplastic Anemia: A Single-Center Experience

Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study

Prevalence of Bone Marrow Fibrosis in 47 Cases of Autoimmune Hemolytic Anemia Patients: Clinical and Biologic Relationships

Healthcare Resource Utilization in Autoimmune Hemolytic Anemia Patients: Analysis of 190 Cases from a Single Center

Use of Next Generation Sequencing Panel to Clarify Undiagnosed Cases of Hereditary Hemolytic Anemias

Brain MRI Findings and Neuro-Psychiatric Involvement in Paroxysmal Nocturnal Hemoglobinuria (PNH)

Gardos Channel Mutation Is Associated with Hereditary Dehydrate Stomatocytosis: a Complex Channelopathy

Diagnostic Power of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) Evaluated in 118 Patients Affected By Hereditary Hemolytic Anemias

Biallelic Mutations in PARP4 Are Linked to a Variant Form of Congenital Dyserythropoietic Anemia

Predictors of Outcome and Response to Therapy in Primary Autoimmune Hemolytic Anemia: A Gimema Study of 307 Patients

Clinical heterogeneity and predictors of outcome in primary autoimmune hemolytic anemia: a GIMEMA study of 308 patients

Clinical Heterogeneity Of Autoimmune Hemolytic Anemia: A 35-Years Retrospective Study Of 157 Patients

Low-dose rituximab in adult patients with idiopathic autoimmune hemolytic anemia: clinical efficacy and biologic studies

A Case of Congenital Red Cell Pyruvate Kinase Deficiency Associated with Hereditary Spherocytosis

Molecular characterization of the First Italian Variant of Phosphoglycerate Kinase Deficiency

Expression of TLRs in B-CLL: Relationship with Disease Activity

Molecular Analysis of the SEC23B Gene In Patients Affected by Congenital Dyserythropoietic Anemia Type II (CDAII)

Low-Dose Rituximab In Idiopathic Autoimmune Hemolytic Anemia: Biological Studies

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American Society of Hematology

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ASH Publications

American Society of Hematology

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