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L Baronciani

Showing results (41-50 of 50) with videos related to

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Blood Cells, Molecules & Diseases|January 1, 1995
Study of the molecular defects in pyruvate kinase deficient patients affected by nonspherocytic hemolytic anemiaL Baronciani, I Q Magalhães, D H Mahoney, et al.
Journal of Thrombosis and Haemostasis : JTH|July 25, 2015
Evaluation of an heterogeneous group of patients with von Willebrand disease using an assay alternative to ristocetin induced platelet agglutinationF Stufano, L Baronciani, M T Pagliari, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 11, 2008
Expression studies of missense mutations p.D141Y, p.C275S located in the propeptide of von Willebrand factor in patients with type 3 von Willebrand diseaseL Baronciani, A B Federici, G Cozzi, et al.
Journal of Thrombosis and Haemostasis : JTH|April 30, 2013
A synonymous (c.3390C>T) or a splice-site (c.3380-2A>G) mutation causes exon 26 skipping in four patients with von Willebrand disease (2A/IIE)M T Pagliari, L Baronciani, I Garcìa Oya, et al.
Journal of Thrombosis and Haemostasis : JTH|May 9, 2009
Type 2A (IIH) von Willebrand disease is due to mutations that affect von Willebrand factor multimerizationL Baronciani, A B Federici, M Punzo, et al.
British Journal of Haematology|August 1, 1997
A variant of the EPB3 gene of the anti-Lepore type in hereditary spherocytosisP Bianchi, A Zanella, N Alloisio, et al.
Journal of Thrombosis and Haemostasis : JTH|January 18, 2006
An association of candidate gene haplotypes and bleeding severity in von Willebrand disease type 2A, 2B, and 2M pedigreesT J Kunicki, L Baronciani, M T Canciani, et al.
Journal of Thrombosis and Haemostasis : JTH|June 14, 2018
An international collaborative study to compare different von Willebrand factor glycoprotein Ib binding activity assays: the COMPASS-VWF studyA Szederjesi, L Baronciani, U Budde, et al.
Journal of Thrombosis and Haemostasis : JTH|November 27, 2014
Predictors of von Willebrand disease diagnosis in individuals with borderline von Willebrand factor plasma levelsP Bucciarelli, S M Siboni, F Stufano, et al.
Journal of Thrombosis and Haemostasis : JTH|July 4, 2013
The type 2B p.R1306W natural mutation of von Willebrand factor dramatically enhances the multimer sensitivity to shear stressG L Scaglione, S Lancellotti, M Papi, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Blood Cells, Molecules & Diseases|January 1, 1995
Study of the molecular defects in pyruvate kinase deficient patients affected by nonspherocytic hemolytic anemiaL Baronciani, I Q Magalhães, D H Mahoney, et al.
Journal of Thrombosis and Haemostasis : JTH|July 25, 2015
Evaluation of an heterogeneous group of patients with von Willebrand disease using an assay alternative to ristocetin induced platelet agglutinationF Stufano, L Baronciani, M T Pagliari, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 11, 2008
Expression studies of missense mutations p.D141Y, p.C275S located in the propeptide of von Willebrand factor in patients with type 3 von Willebrand diseaseL Baronciani, A B Federici, G Cozzi, et al.
Journal of Thrombosis and Haemostasis : JTH|April 30, 2013
A synonymous (c.3390C>T) or a splice-site (c.3380-2A>G) mutation causes exon 26 skipping in four patients with von Willebrand disease (2A/IIE)M T Pagliari, L Baronciani, I Garcìa Oya, et al.
Journal of Thrombosis and Haemostasis : JTH|May 9, 2009
Type 2A (IIH) von Willebrand disease is due to mutations that affect von Willebrand factor multimerizationL Baronciani, A B Federici, M Punzo, et al.
British Journal of Haematology|August 1, 1997
A variant of the EPB3 gene of the anti-Lepore type in hereditary spherocytosisP Bianchi, A Zanella, N Alloisio, et al.
Journal of Thrombosis and Haemostasis : JTH|January 18, 2006
An association of candidate gene haplotypes and bleeding severity in von Willebrand disease type 2A, 2B, and 2M pedigreesT J Kunicki, L Baronciani, M T Canciani, et al.
Journal of Thrombosis and Haemostasis : JTH|June 14, 2018
An international collaborative study to compare different von Willebrand factor glycoprotein Ib binding activity assays: the COMPASS-VWF studyA Szederjesi, L Baronciani, U Budde, et al.
Journal of Thrombosis and Haemostasis : JTH|November 27, 2014
Predictors of von Willebrand disease diagnosis in individuals with borderline von Willebrand factor plasma levelsP Bucciarelli, S M Siboni, F Stufano, et al.
Journal of Thrombosis and Haemostasis : JTH|July 4, 2013
The type 2B p.R1306W natural mutation of von Willebrand factor dramatically enhances the multimer sensitivity to shear stressG L Scaglione, S Lancellotti, M Papi, et al.
Pageof 5