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Journal Articles

Loss-of-function mutations in PTPRJ cause a new form of inherited thrombocytopenia

Caterina Marconi, Christian A. Di Buduo, Kellie LeVine, Serena Barozzi, Michela Faleschini, Valeria Bozzi, Flavia Palombo, Spencer McKinstry, Giuseppe Lassandro, Paola Giordano, Patrizia Noris, Carlo L. Balduini, Anna Savoia, Alessandra Balduini, Tommaso Pippucci, Marco Seri, Nicholas Katsanis, Alessandro Pecci

Blood (2019) 133 (12): 1346–1357.

https://doi.org/10.1182/blood-2018-07-859496

Published: 2019

Includes: Supplemental data

Journal Articles

ACTN1 -related thrombocytopenia: identification of novel families for phenotypic characterization

Roberta Bottega, Caterina Marconi, Michela Faleschini, Gabriele Baj, Claudia Cagioni, Alessandro Pecci, Tommaso Pippucci, Ugo Ramenghi, Simonetta Pardini, Loretta Ngu, Carlo Baronci, Shinji Kunishima, Carlo L. Balduini, Marco Seri, Anna Savoia, Patrizia Noris

Blood (2015) 125 (5): 869–872.

https://doi.org/10.1182/blood-2014-08-594531

Published: 2015

Includes: Supplemental data

Journal Articles

Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders

Blood (2014) 124 (6): e4–e10.

https://doi.org/10.1182/blood-2014-03-564328

Published: 2014

Journal Articles

Small red blood cells mimicking platelets

Patrizia Noris, Carlo L. Balduini

Blood (2014) 123 (26): 4014.

https://doi.org/10.1182/blood-2014-04-569749

Published: 2014

Journal Articles

Desmopressin and super platelets

Alessandro Pecci, Carlo L. Balduini

Blood (2014) 123 (12): 1779–1780.

https://doi.org/10.1182/blood-2014-01-551242

Published: 2014

Journal Articles

ANKRD26 -related thrombocytopenia and myeloid malignancies

Blood (2013) 122 (11): 1987–1989.

https://doi.org/10.1182/blood-2013-04-499319

Published: 2013

Journal Articles

Efficacy of Thalidomide in the Treatment of Severe Recurrent Epistaxis in Hereditary Hemorrhagic Telangiectasia (HHT): Preliminary Results of an Ongoing Study

Carlo L Balduini, Francesca Bellistri, Fabio Pagella, Francesco Chu, Elina Matti, Giuseppe Spinozzi, Federica Ornati, Cecilia Canzonieri, Carla Olivieri, Cesare Danesino, Marco Benazzo, Rosangela Invernizzi

Blood (2012) 120 (21): 629.

https://doi.org/10.1182/blood.V120.21.629.629

Published: 2012

Journal Articles

Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families

Blood (2011) 117 (24): 6673–6680.

https://doi.org/10.1182/blood-2011-02-336537

Published: 2011

Journal Articles

Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations

Alessandro Pecci, Paolo Gresele, Catherine Klersy, Anna Savoia, Patrizia Noris, Tiziana Fierro, Valeria Bozzi, Anna Maria Mezzasoma, Federica Melazzini, Carlo L. Balduini

Blood (2010) 116 (26): 5832–5837.

https://doi.org/10.1182/blood-2010-08-304725

Published: 2010

Includes: Supplemental data

Journal Articles

Heterozygous Ala156Val Mutation in the GPIb Alpha (Heterozygous Bernard-Soulier Syndrome Type Bolzano) Induces Macrothrombocytopenia by Hampering Proplatelet Formation.

Alessandra Balduini, Alessandro Malara, Stefania Badalucco, Valeria Bozzi, Isabella Pallotta, Patrizia Noris, Mauro Torti, Carlo L Balduini, Alessandro Pecci

Blood (2008) 112 (11): 1233.

https://doi.org/10.1182/blood.V112.11.1233.1233

Published: 2008

Journal Articles

Why the disorder induced by GATA1 Arg216Gln mutation should be called “X-linked thrombocytopenia with thalassemia” rather than “X-linked gray platelet syndrome”

Carlo L. Balduini, Erica De Candia, Anna Savoia

Blood (2007) 110 (7): 2770–2771.

https://doi.org/10.1182/blood-2007-03-080978

Published: 2007

Journal Articles

Thrombopoietin (TPO) Levels in Inflammatory Disorders with or without Reactive Thrombocytosis.

Patrizia Noris, MD, Iride F. Ceresa, MD, Chiara Ambaglio, MD, Luca M. Dezzani, MD, Carlo L. Balduini, MD

Blood (2006) 108 (11): 1111.

https://doi.org/10.1182/blood.V108.11.1111.1111

Published: 2006

Journal Articles

Role of splenectomy in inherited thrombocytopenias

Carlo L. Balduini

Blood (2004) 104 (4): 1227.

https://doi.org/10.1182/blood-2004-03-0875

Published: 2004

Journal Articles

Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome

Anna Savoia, Carlo L. Balduini, Maria Savino, Patrizia Noris, Maria Del Vecchio, Silverio Perrotta, Simona Belletti, Vincenzo Poggi, Achille Iolascon

Blood (2001) 97 (5): 1330–1335.

https://doi.org/10.1182/blood.V97.5.1330

Published: 2001

Journal Articles

International Prognostic Scoring System and Other Prognostic Systems for Myelodysplastic Syndromes

Carlo L. Balduini, Roberta Guarnone, Alessandro Pecci, Esther Centenara, Edoardo Ascari

Blood (1997) 90 (10): 4232–4235.

https://doi.org/10.1182/blood.V90.10.4232

Published: 1997

NARROW

Loss-of-function mutations in PTPRJ cause a new form of inherited thrombocytopenia

ACTN1 -related thrombocytopenia: identification of novel families for phenotypic characterization

Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders

Small red blood cells mimicking platelets

Desmopressin and super platelets

ANKRD26 -related thrombocytopenia and myeloid malignancies

Efficacy of Thalidomide in the Treatment of Severe Recurrent Epistaxis in Hereditary Hemorrhagic Telangiectasia (HHT): Preliminary Results of an Ongoing Study

Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families

Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations

Heterozygous Ala156Val Mutation in the GPIb Alpha (Heterozygous Bernard-Soulier Syndrome Type Bolzano) Induces Macrothrombocytopenia by Hampering Proplatelet Formation.

Why the disorder induced by GATA1 Arg216Gln mutation should be called “X-linked thrombocytopenia with thalassemia” rather than “X-linked gray platelet syndrome”

Thrombopoietin (TPO) Levels in Inflammatory Disorders with or without Reactive Thrombocytosis.

Role of splenectomy in inherited thrombocytopenias

Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome

International Prognostic Scoring System and Other Prognostic Systems for Myelodysplastic Syndromes

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American Society of Hematology

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ASH Publications

American Society of Hematology

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