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Silvia La Marca

Showing results (1-10 of 21) with videos related to

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Platelets|June 27, 2019
Acquired platelet dysfunction and overproduction of platelet cyclic AMP in two patients with myeloid malignanciesAnna Lecchi, Eti A Femia, Silvia La Marca, et al.
Blood Transfusion = Trasfusione Del Sangue|February 16, 2023
Flow-chamber device (T-TAS) to diagnose patients suspected of platelet function defectsAnna Lecchi, Silvia La Marca, Lidia Padovan, et al.
Internal and Emergency Medicine|August 27, 2020
Ferric carboxymaltose for sub-acute and chronic iron deficiency anemia in inherited platelet function defectsNatalia Scaramellini, Marco Capecchi, Andrea Artoni, et al.
Haematologica|July 18, 2009
Platelet morphological changes in 2 patients with von Willebrand disease type 3 caused by large homozygous deletions of the von Willebrand factor genePaquita Nurden, Alan T Nurden, Silvia La Marca, et al.
International Journal of Laboratory Hematology|May 4, 2023
Use of total thrombus-formation analysis system in detecting acquired platelet function defects: A case reportFederico Boggio, Anna Lecchi, Silvia La Marca, et al.
Blood Transfusion = Trasfusione Del Sangue|February 5, 2024
Evaluation of an automated platelet aggregation method for detection of congenital or acquired platelet function defectsAnna Lecchi, Marco Capecchi, Lidia Padovan, et al.
American Journal of Hematology|June 2, 2011
Circulating and progenitor endothelial cells are abnormal in patients with different types of von Willebrand disease and correlate with markers of angiogenesisGiuseppe Gritti, Agostino Cortelezzi, Paolo Bucciarelli, et al.
Platelets|December 28, 2019
Novel variant in HPS3 gene in a patient with Hermansky Pudlak syndrome (HPS) type 3Anna Lecchi, Silvia La Marca, Eti A Femia, et al.
Haematologica|September 24, 2009
Premature termination codon mutations in the von Willebrand factor gene are associated with allele-specific and position-dependent mRNA decayManuela Platè, Stefano Duga, Luciano Baronciani, et al.
American Journal of Hematology|June 8, 2012
Molecular characterization, recombinant protein expression, and mRNA analysis of type 3 von Willebrand disease: Studies of an Italian cohort of 10 patientsMaria Solimando, Luciano Baronciani, Silvia La Marca, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Platelets|June 27, 2019
Acquired platelet dysfunction and overproduction of platelet cyclic AMP in two patients with myeloid malignanciesAnna Lecchi, Eti A Femia, Silvia La Marca, et al.
Blood Transfusion = Trasfusione Del Sangue|February 16, 2023
Flow-chamber device (T-TAS) to diagnose patients suspected of platelet function defectsAnna Lecchi, Silvia La Marca, Lidia Padovan, et al.
Internal and Emergency Medicine|August 27, 2020
Ferric carboxymaltose for sub-acute and chronic iron deficiency anemia in inherited platelet function defectsNatalia Scaramellini, Marco Capecchi, Andrea Artoni, et al.
Haematologica|July 18, 2009
Platelet morphological changes in 2 patients with von Willebrand disease type 3 caused by large homozygous deletions of the von Willebrand factor genePaquita Nurden, Alan T Nurden, Silvia La Marca, et al.
International Journal of Laboratory Hematology|May 4, 2023
Use of total thrombus-formation analysis system in detecting acquired platelet function defects: A case reportFederico Boggio, Anna Lecchi, Silvia La Marca, et al.
Blood Transfusion = Trasfusione Del Sangue|February 5, 2024
Evaluation of an automated platelet aggregation method for detection of congenital or acquired platelet function defectsAnna Lecchi, Marco Capecchi, Lidia Padovan, et al.
American Journal of Hematology|June 2, 2011
Circulating and progenitor endothelial cells are abnormal in patients with different types of von Willebrand disease and correlate with markers of angiogenesisGiuseppe Gritti, Agostino Cortelezzi, Paolo Bucciarelli, et al.
Platelets|December 28, 2019
Novel variant in HPS3 gene in a patient with Hermansky Pudlak syndrome (HPS) type 3Anna Lecchi, Silvia La Marca, Eti A Femia, et al.
Haematologica|September 24, 2009
Premature termination codon mutations in the von Willebrand factor gene are associated with allele-specific and position-dependent mRNA decayManuela Platè, Stefano Duga, Luciano Baronciani, et al.
American Journal of Hematology|June 8, 2012
Molecular characterization, recombinant protein expression, and mRNA analysis of type 3 von Willebrand disease: Studies of an Italian cohort of 10 patientsMaria Solimando, Luciano Baronciani, Silvia La Marca, et al.
Pageof 3