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Alessandro Pecci

Showing results (111-120 of 121) with videos related to

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Blood|July 4, 2014
Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disordersPatrizia Noris, Ginevra Biino, Alessandro Pecci, et al.
Hemasphere|September 3, 2021
The EHA Research Roadmap: Platelet DisordersCarlo Balduini, Kathleen Freson, Andreas Greinacher, et al.
Haematologica|February 16, 2023
ANKRD26 is a new regulator of type I cytokine receptor signaling in normal and pathological hematopoiesisFrancesca Basso-Valentina, Alessandro Donada, Vladimir T Manchev, et al.
Medicine|June 7, 2003
MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illnessMarco Seri, Alessandro Pecci, Filomena Di Bari, et al.
Human Mutation|December 7, 2007
Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related diseaseAlessandro Pecci, Emanuele Panza, Núria Pujol-Moix, et al.
Blood|September 14, 2013
ANKRD26-related thrombocytopenia and myeloid malignanciesPatrizia Noris, Remi Favier, Marie-Christine Alessi, et al.
Nature Genetics|March 26, 2015
Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemiaLeila Noetzli, Richard W Lo, Alisa B Lee-Sherick, et al.
Haematologica|April 8, 2017
Bleeding risk of surgery and its prevention in patients with inherited platelet disordersSara Orsini, Patrizia Noris, Loredana Bury, et al.
Human Mutation|June 18, 2014
Spectrum of the mutations in Bernard-Soulier syndromeAnna Savoia, Shinji Kunishima, Daniela De Rocco, et al.
Human Mutation|November 5, 2013
MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlationsAlessandro Pecci, Catherine Klersy, Paolo Gresele, et al.
Pageof 13

Showing results (111-120 of 121) with videos related to

Sort By:
Pageof 13
Blood|July 4, 2014
Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disordersPatrizia Noris, Ginevra Biino, Alessandro Pecci, et al.
Hemasphere|September 3, 2021
The EHA Research Roadmap: Platelet DisordersCarlo Balduini, Kathleen Freson, Andreas Greinacher, et al.
Haematologica|February 16, 2023
ANKRD26 is a new regulator of type I cytokine receptor signaling in normal and pathological hematopoiesisFrancesca Basso-Valentina, Alessandro Donada, Vladimir T Manchev, et al.
Medicine|June 7, 2003
MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illnessMarco Seri, Alessandro Pecci, Filomena Di Bari, et al.
Human Mutation|December 7, 2007
Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related diseaseAlessandro Pecci, Emanuele Panza, Núria Pujol-Moix, et al.
Blood|September 14, 2013
ANKRD26-related thrombocytopenia and myeloid malignanciesPatrizia Noris, Remi Favier, Marie-Christine Alessi, et al.
Nature Genetics|March 26, 2015
Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemiaLeila Noetzli, Richard W Lo, Alisa B Lee-Sherick, et al.
Haematologica|April 8, 2017
Bleeding risk of surgery and its prevention in patients with inherited platelet disordersSara Orsini, Patrizia Noris, Loredana Bury, et al.
Human Mutation|June 18, 2014
Spectrum of the mutations in Bernard-Soulier syndromeAnna Savoia, Shinji Kunishima, Daniela De Rocco, et al.
Human Mutation|November 5, 2013
MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlationsAlessandro Pecci, Catherine Klersy, Paolo Gresele, et al.
Pageof 13