Page 1 | Search Results | Blood | American Society of Hematology

1-18 of 18

Sort by

Sort Order Select

Journal Articles

Biochemical and Metabolomic Analysis of Glycolytic Activity in Red Blood Cells from Low-Risk Myelodysplastic Syndromes (LR-MDS) Patients and in-Vitro Effect of the Pyruvate Kinase Activator AG-946

Bruno Fattizzo, Cristina Vercellati, Anna Marcello, Parija Patel, Megan Wind-Rotolo, Loredana Pettine, Marcella Bonanomi, Daniela Gaglio, Claudia Leoni, Elisa Fermo, Paola Bianchi, Anna Zaninoni, Wilma Barcellini

Blood (2023) 142 (Supplement 1): 6456.

https://doi.org/10.1182/blood-2023-188316

Published: 2023

Journal Articles

Evaluation of Red Blood Cell Metabolism in Patients with Low-Risk Myelodysplastic Syndrome (LR-MDS): A Proof-of-Concept Study

Bruno Fattizzo, Cristina Vercellati, Anna Marcello, Marta Bortolotti, Anna Zaninoni, Elisa Fermo, Paola Bianchi, Wilma Barcellini

Blood (2022) 140 (Supplement 1): 4016–4017.

https://doi.org/10.1182/blood-2022-159938

Published: 2022

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

Iron Overload and Cytokine Serum Levels in Congenital Hemolytic Anemias

Wilma Barcellini, Anna Ines Gregorini, MD, Giulia Soverini, Anna Zaninoni, Juri A Giannotta, Cristina Vercellati, Valeria Ferri, Paola Bianchi, Agostino Cortelezzi, MD, Maria Domenica Cappellini

Blood (2016) 128 (22): 2458.

https://doi.org/10.1182/blood.V128.22.2458.2458

Published: 2016

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

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

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

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

An Unusual Case of ‘Delayed‘ Febrile Non Hemolytic Transfusion Reaction in a Thalassemia Major Patient with Asymptomatic Plasmodium Falciparum Infection.

Carla Boschetti, Franca Radaelli, Mariangela Colombi, Cristina Vercellati, Luisa Caspani, Romualdo Grande, Maria Domenica Cappellini, Alberto Zanella

Blood (2009) 114 (22): 4186.

https://doi.org/10.1182/blood.V114.22.4186.4186

Published: 2009

Journal Articles

Identification of SEC23B as the Gene Responsible for Congenital Dyserythropoietic Anemia Type II using a Proteomic-Genomic Approach.

Paola Bianchi, Elisa Fermo, Cristina Vercellati, Carla Boschetti, Wilma Barcellini, Alessandra Iurlo, Anna Paola Marcello, Pier Giorgio Righetti, Alberto Zanella

Blood (2009) 114 (22): 4028.

https://doi.org/10.1182/blood.V114.22.4028.4028

Published: 2009

Journal Articles

Two Atypical Severe Cda Forms Presenting as Hydrops Foetalis Are Caused by Mutations in the SEC23B Gene.

Elisa Fermo, Paola Bianchi, Cristina Vercellati, Wilma Barcellini, Carla Boschetti, Anna Paola Marcello, Alberto Zanella

Blood (2009) 114 (22): 1981.

https://doi.org/10.1182/blood.V114.22.1981.1981

Published: 2009

Journal Articles

Clinical and Haematologic Features of 300 Patients Affected by Hereditary Spherocytosis as a Function of the Type of the Membrane Protein Defect.

Wilma Barcellini, MD, Mariagabriella Mariani, PhD, Cristina Vercellati, PhD, Anna P. Marcello, PhD, Elisa Fermo, PhD, Paola Pedotti, Carla Boschetti, MD, Alberto Zanella, MD

Blood (2007) 110 (11): 1724.

https://doi.org/10.1182/blood.V110.11.1724.1724

Published: 2007

Journal Articles

Coexistence of Congenital Red Cell Pyruvate Kinase Deficiency and Hereditary Stomatocytosis.

Anna P. Marcello, PhD, Cristina Vercellati, PhD, Elisa Fermo, PhD, Paola Bianchi, PhD, Wilma Barcellini, MD, Alberto Zanella, MD

Blood (2007) 110 (11): 1738.

https://doi.org/10.1182/blood.V110.11.1738.1738

Published: 2007

Journal Articles

Recessive Congenital Methaemoglobinaemia: Three New Mutations in the NADH-Cytochrome b5 Reductase Gene.

Elisa Fermo, PhD, Paola Bianchi, PhD, Cristina Vercellati, PhD, Anna P. Marcello, PhD, Wilma Barcellini, MD, Ornella Marangoni, MD, Massimo Garatti, MD, Alberto Zanella, MD

Blood (2006) 108 (11): 1576.

https://doi.org/10.1182/blood.V108.11.1576.1576

Published: 2006

Journal Articles

Red Cell Pyruvate Kinase Deficiency: Molecular Characterization of 10 New Variants.

Elisa Fermo, Paola Bianchi, Cristina Vercellati, Frederic Cotton, Alberto Zanella

Blood (2004) 104 (11): 1590.

https://doi.org/10.1182/blood.V104.11.1590.1590

Published: 2004

Journal Articles

Three New Mutations of Glucose-6-Phosphate Isomerase Associated with Chronic Hemolytic Anemia.

Cristina Vercellati, Elisa Fermo, Anna Marcello, Mariagabriella Mariani, Paola Bianchi, Wilma Barcellini, Saverio Ladogana, Alessandro De Fanti, Alberto Zanella

Blood (2004) 104 (11): 3673.

https://doi.org/10.1182/blood.V104.11.3673.3673

Published: 2004

Journal Articles

Molecular Characterization of PK-LR Gene in Pyruvate Kinase–Deficient Italian Patients

Alberto Zanella, Paola Bianchi, Luciano Baronciani, Manuela Zappa, Elena Bredi, Cristina Vercellati, Fiorella Alfinito, Giovanni Pelissero, Girolamo Sirchia

Blood (1997) 89 (10): 3847–3852.

https://doi.org/10.1182/blood.V89.10.3847

Published: 1997

NARROW

Biochemical and Metabolomic Analysis of Glycolytic Activity in Red Blood Cells from Low-Risk Myelodysplastic Syndromes (LR-MDS) Patients and in-Vitro Effect of the Pyruvate Kinase Activator AG-946

Evaluation of Red Blood Cell Metabolism in Patients with Low-Risk Myelodysplastic Syndrome (LR-MDS): A Proof-of-Concept Study

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

Iron Overload and Cytokine Serum Levels in Congenital Hemolytic Anemias

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

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

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

Molecular characterization of the First Italian Variant of Phosphoglycerate Kinase Deficiency

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

An Unusual Case of ‘Delayed‘ Febrile Non Hemolytic Transfusion Reaction in a Thalassemia Major Patient with Asymptomatic Plasmodium Falciparum Infection.

Identification of SEC23B as the Gene Responsible for Congenital Dyserythropoietic Anemia Type II using a Proteomic-Genomic Approach.

Two Atypical Severe Cda Forms Presenting as Hydrops Foetalis Are Caused by Mutations in the SEC23B Gene.

Clinical and Haematologic Features of 300 Patients Affected by Hereditary Spherocytosis as a Function of the Type of the Membrane Protein Defect.

Coexistence of Congenital Red Cell Pyruvate Kinase Deficiency and Hereditary Stomatocytosis.

Recessive Congenital Methaemoglobinaemia: Three New Mutations in the NADH-Cytochrome b5 Reductase Gene.

Red Cell Pyruvate Kinase Deficiency: Molecular Characterization of 10 New Variants.

Three New Mutations of Glucose-6-Phosphate Isomerase Associated with Chronic Hemolytic Anemia.

Molecular Characterization of PK-LR Gene in Pyruvate Kinase–Deficient Italian Patients

Email alerts

ASH Publications

American Society of Hematology

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only