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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

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

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

NT-ProBNP and VEGF Serum Evaluation In AL Amyloidosis

Francesca Saltarelli, PhD, Alessandro Moscetti, PhD, Maria Paola Bianchi, PhD, Guglielmo Bruno, PhD, Gerardo Salerno, PhD, Maria Teresa Corsetti, PhD, Patrizia Cardelli, PhD, Giovanna Ferranti, PhD, Giacinto La Verde, PhD

Blood (2010) 116 (21): 5008.

https://doi.org/10.1182/blood.V116.21.5008.5008

Published: 2010

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

Presence of JAK2 V617F Mutation in Peripheral Blood of Blood Donors with Upper-Limit Hematocrit and Platelet Values.

Paola Bianchi, PhD, Elisa Fermo, PhD, Fulvio Mozzi, M.D., Maurizio Marconi, M.D., Alberto Zanella, M.D.

Blood (2007) 110 (11): 2533.

https://doi.org/10.1182/blood.V110.11.2533.2533

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

Analysis of JAK2 V167F Mutation in Myelodysplastic Syndromes.

Elisa Fermo, PhD, Anna Zaninoni, PhD, Francesca G. Imperiali, PhD, Paola Bianchi, PhD, Mariangela Colombi, MD, Wilma Barcellini, MD, Alberto Zanella, MD

Blood (2007) 110 (11): 4591.

https://doi.org/10.1182/blood.V110.11.4591.4591

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

Early-Polycythemia Vera (e-PV) with Thrombocytosis: Clinical Characteristics, Morphological Features and JAK2 V617F Mutational Status Contributing to the Differential Diagnosis with Essential Thrombocythemia.

Alessandra Iurlo, MD, Umberto Gianelli, MD, Alessia Moro, Paola Bianchi, PhD, Elisa Fermo, PhD, Claudia Vener, MD, Federica Savi, Radaelli Franca, MD, Silvano Bosari, Alberto Zanella, MD

Blood (2006) 108 (11): 3628.

https://doi.org/10.1182/blood.V108.11.3628.3628

Published: 2006

Journal Articles

Pyrimidine 5′ Nucleotidase Deficiency: Clinical and Molecular Characterization of Two New Italian Patients.

Elisa Fermo, PhD, Anna Marcello, PhD, Paola Bianchi, PhD, Simona Viglio, Laurent R. Chiarelli, Giovanna Valentini, Alberto Zanella, MD

Blood (2005) 106 (11): 3711.

https://doi.org/10.1182/blood.V106.11.3711.3711

Published: 2005

NARROW

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

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

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

NT-ProBNP and VEGF Serum Evaluation In AL Amyloidosis

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

Presence of JAK2 V617F Mutation in Peripheral Blood of Blood Donors with Upper-Limit Hematocrit and Platelet Values.

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

Analysis of JAK2 V167F Mutation in Myelodysplastic Syndromes.

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

Early-Polycythemia Vera (e-PV) with Thrombocytosis: Clinical Characteristics, Morphological Features and JAK2 V617F Mutational Status Contributing to the Differential Diagnosis with Essential Thrombocythemia.

Pyrimidine 5′ Nucleotidase Deficiency: Clinical and Molecular Characterization of Two New Italian Patients.

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American Society of Hematology

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ASH Publications

American Society of Hematology

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