Search research articles
Contact Us
Filters
Showing results (31-40 of 121) with videos related to
Page
of 13
Sort By:
Haematologica
|
August 13, 2016
Revealing eltrombopag's promotion of human megakaryopoiesis through AKT/ERK-dependent pathway activation
Christian A Di Buduo, Manuela Currao, Alessandro Pecci, et al.
Thrombosis Research
|
September 11, 2010
The irreversibility of platelet aggregation is regulated by myosin IIA, but is not compromised in MYH9-related disease
Silvia Catricalà, Gianni F Guidetti, Ilaria Canobbio, et al.
Genomics
|
June 5, 2004
Correlation between the clinical phenotype of MYH9-related disease and tissue distribution of class II nonmuscle myosin heavy chains
Valeria Marigo, Alessandra Nigro, Alessandro Pecci, et al.
European Journal of Medical Genetics
|
May 20, 2009
Identification of the first duplication in MYH9-related disease: a hot spot for unequal crossing-over within exon 24 of the MYH9 gene
Daniela De Rocco, Nuria Pujol-Moix, Alessandro Pecci, et al.
Haematologica
|
September 10, 2002
Defective expression of GPIb/IX/V complex in platelets from patients with May-Hegglin anomaly and Sebastian syndrome
Michele Di Pumpo, Patrizia Noris, Alessandro Pecci, et al.
Annals of Hematology
|
December 20, 2022
GP1BB c.179C > T is the most frequent cause of monoallelic Bernard-Soulier syndrome in the Italian population after the Bolzano variant: a report of two new families
Serena Barozzi, Alessandro Pecci, Maddalena Marinoni, et al.
European Journal of Haematology
|
July 11, 2012
Clonal chromosome anomalies affecting FLI1 mimic inherited thrombocytopenia of the Paris-Trousseau type
Patrizia Noris, Roberto Valli, Alessandro Pecci, et al.
International Journal of Molecular Medicine
|
August 4, 2005
Dissecting clinical findings: platelet defects segregate independently of deafness and cataract in a family affected by an apparent syndromic form of macrothrombocytopenia
Simone Gangarossa, Marco Seri, Alessandro Pecci, et al.
Haematologica
|
October 15, 2020
Pathogenetic and clinical study of a patient with thrombocytopenia due to the p.E527K gain-of-function variant of SRC
Serena Barozzi, Christian A Di Buduo, Caterina Marconi, et al.
Haematologica
|
October 14, 2011
A A386G biallelic GPIbα gene mutation with anomalous behavior: a new mechanism suggested for Bernard-Soulier syndrome pathogenesis
Silvia Vettore, Fabiana Tezza, Alessandro Malara, et al.
Page
of 13
Search research articles
Search
Showing results (31-40 of 121) with videos related to
Sort By:
Page
of 13
Haematologica
|
August 13, 2016
Revealing eltrombopag's promotion of human megakaryopoiesis through AKT/ERK-dependent pathway activation
Christian A Di Buduo, Manuela Currao, Alessandro Pecci, et al.
Thrombosis Research
|
September 11, 2010
The irreversibility of platelet aggregation is regulated by myosin IIA, but is not compromised in MYH9-related disease
Silvia Catricalà, Gianni F Guidetti, Ilaria Canobbio, et al.
Genomics
|
June 5, 2004
Correlation between the clinical phenotype of MYH9-related disease and tissue distribution of class II nonmuscle myosin heavy chains
Valeria Marigo, Alessandra Nigro, Alessandro Pecci, et al.
European Journal of Medical Genetics
|
May 20, 2009
Identification of the first duplication in MYH9-related disease: a hot spot for unequal crossing-over within exon 24 of the MYH9 gene
Daniela De Rocco, Nuria Pujol-Moix, Alessandro Pecci, et al.
Haematologica
|
September 10, 2002
Defective expression of GPIb/IX/V complex in platelets from patients with May-Hegglin anomaly and Sebastian syndrome
Michele Di Pumpo, Patrizia Noris, Alessandro Pecci, et al.
Annals of Hematology
|
December 20, 2022
GP1BB c.179C > T is the most frequent cause of monoallelic Bernard-Soulier syndrome in the Italian population after the Bolzano variant: a report of two new families
Serena Barozzi, Alessandro Pecci, Maddalena Marinoni, et al.
European Journal of Haematology
|
July 11, 2012
Clonal chromosome anomalies affecting FLI1 mimic inherited thrombocytopenia of the Paris-Trousseau type
Patrizia Noris, Roberto Valli, Alessandro Pecci, et al.
International Journal of Molecular Medicine
|
August 4, 2005
Dissecting clinical findings: platelet defects segregate independently of deafness and cataract in a family affected by an apparent syndromic form of macrothrombocytopenia
Simone Gangarossa, Marco Seri, Alessandro Pecci, et al.
Haematologica
|
October 15, 2020
Pathogenetic and clinical study of a patient with thrombocytopenia due to the p.E527K gain-of-function variant of SRC
Serena Barozzi, Christian A Di Buduo, Caterina Marconi, et al.
Haematologica
|
October 14, 2011
A A386G biallelic GPIbα gene mutation with anomalous behavior: a new mechanism suggested for Bernard-Soulier syndrome pathogenesis
Silvia Vettore, Fabiana Tezza, Alessandro Malara, et al.
Page
of 13