D. Habart

发表

Thirty‐four novel mutations detected in factor VIII gene by multiplex CSGE: modeling of 13 novel amino acid substitutions

M. Novotny, D. Habart, D. Kalábová, 2003, Journal of thrombosis and haemostasis : JTH.

Lipasin/betatrophin is differentially expressed in liver and white adipose tissue without association with insulin resistance in Wistar and Goto-Kakizaki rats.

D. Habart, F. Saudek, Z. Berková, 2017, Physiological research.

Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM‐1VWD study

J. Goudemand, S. Lethagen, J. Eikenboom, 2009, Journal of Thrombosis and Haemostasis.

Identification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the European study: molecular and clinical markers for the diagnosis and management of type 1 VWD (MCMDM-1VWD).

J. Goudemand, S. Lethagen, J. Eikenboom, 2008, Blood.

Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM‐1VWD)

J. Goudemand, S. Lethagen, J. Eikenboom, 2008, Journal of thrombosis and haemostasis : JTH.

Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD).

J. Goudemand, C. Halldén, S. Lethagen, 2007, Blood.

Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD

J. Goudemand, S. Lethagen, J. Eikenboom, 2006, Journal of thrombosis and haemostasis : JTH.

Detection of pancreatic islet allograft impairment in advance of functional failure using magnetic resonance imaging

D. Jirák, M. Hájek, V. Herynek, 2012, Transplant international : official journal of the European Society for Organ Transplantation.

[Molecular diagnosis of haemophilia A in clinical practice].

D. Habart, 2005, Casopis lekaru ceskych.

Synthetic mRNA is a more reliable tool for the delivery of DNA-targeting proteins into the cell nucleus than fusion with a protein transduction domain

J. Kříž, D. Habart, F. Saudek, 2017, PloS one.

The Modifier of hemostasis (Mh) locus on chromosome 4 controls in vivo hemostasis of Gp6-/- mice.

José A Fernández, T. Wiltshire, M. Cooke, 2008, Blood.

Conditional Knockout of Integrin α2β1 in Murine Megakaryocytes Leads to Reduced Mean Platelet Volume

D. Habart, Z. Ruggeri, T. Kunicki, 2013, PloS one.

Recombinant coagulation factor VIIa in the management of bleeding in patients with von Willebrand disease type 2A.

D. Habart, M. Matýšková, A. Buliková, 2004, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): results from the European Study MCMDM-1VWD.

A. Tosetto, J. Goudemand, S. Lethagen, 2008, Blood.

Significant prevalence of the intron 1 factor VIII gene inversion among patients with severe hemophilia A in the Czech Republic

D. Habart, D. Kalábová, Z. Vorlová, 2003, Journal of thrombosis and haemostasis : JTH.

Transplantation of Pancreatic Islets Into the Omentum Using a Biocompatible Plasma-Thrombin Gel: First Experience at the Institute for Clinical and Experimental Medicine in Prague.

D. Habart, J. Fronek, Z. Berková, 2022, Transplantation proceedings.

Combining Donor Characteristics with Immunohistological Data Improves the Prediction of Islet Isolation Success

L. Voska, T. Neškudla, D. Habart, 2016, Journal of diabetes research.

A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM‐1 VWD)

A. Tosetto, J. Goudemand, S. Lethagen, 2006, Journal of thrombosis and haemostasis : JTH.

The impact of bleeding history, von Willebrand factor and PFA–100® on the diagnosis of type 1 von Willebrand disease: results from the European study MCMDM‐1VWD

A. Tosetto, J. Goudemand, S. Lethagen, 2010, British journal of haematology.

Impact of plasma von Willebrand factor levels in the diagnosis of type 1 von Willebrand disease: results from a multicenter European study (MCMDM‐1VWD)

A. Tosetto, J. Goudemand, S. Lethagen, 2007, Journal of thrombosis and haemostasis : JTH.

Replicate real‐time PCR testing of DNA in maternal plasma increases the sensitivity of non‐invasive fetal sex determination

David Habart, D. Habart, V. Komrska, 2003, Prenatal diagnosis.

The Potential of Pancreatic Organoids for Diabetes Research and Therapy

D. Habart, F. Saudek, T. Koblas, 2021, Islets.

Characterization of large in-frame von Willebrand factor deletions highlights differing pathogenic mechanisms.

D. Hampshire, J. Goudemand, C. Halldén, 2020, Blood advances.

The Molecular Pathogenesis of Hemophilia A

D. Habart, D Habart, 2005 .

European Study MCMDM-1VWD phenotype in type 1 von Willebrand disease (VWD): results from the Response to desmopressin is influenced by the genotype and

A. Tosetto, J. Goudemand, S. Lethagen, 2013 .

Automated Analysis of Microscopic Images of Isolated Pancreatic Islets

Jan Švihlík, Jan Kybic, Jan Schier, 2016, Cell transplantation.

Benefits of Islet Transplantation as an Alternative to Pancreas Transplantation: Retrospective Study of More Than 10 Ten Years of Experience in a Single Center.

T. Neškudla, D. Habart, F. Saudek, 2017, The review of diabetic studies : RDS.

Supervised and unsupervised segmentation using superpixels, model estimation, and graph cut

Jan Kybic, Jan Svihlík, David Habart, 2017, J. Electronic Imaging.

Factor XI gene mutations in factor XI deficient patients of the Czech Republic

S. Duga, F. Rodeghiero, G. Castaman, 2008, American journal of hematology.

Simultaneous and Semi-Automated Evaluation of Three Variable Tandem Repeats within von Willebrand Factor Gene by Capillary Electrophoresis with Multicolour Fluorescent Detection

D. Habart, Z. Vorlová, 2003, Acta Haematologica.

Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): results from the European Study MCMDM-1VWD.

A. Tosetto, J. Goudemand, S. Lethagen, 2008, Blood.

IsletSwipe, a mobile platform for expert opinion exchange on islet graft images

Dirk-Jan Cornelissen, M. Capek, D. Habart, 2023, Islets.