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Journal Articles

The Use of Recombinant FXIII in a Major Acute Bleeding Episode of a Patient with Congenital FXIII Deficiency – the First Experience

Zoltan Boda, MD PhD DSc, Anita Arokszallasi, MD, Adrienne Kerenyi, MDPhD, Zsuzsanna Bereczky, MDPhD, Laszlo Muszbek, MDPhDDSc, Gyorgy Pfliegler, MD PhD, Agota Schlammadinger, MDPhD

Blood (2014) 124 (21): 5065.

https://doi.org/10.1182/blood.V124.21.5065.5065

Published: 2014

Journal Articles

Interaction of factor XIII subunits

Éva Katona, Krisztina Pénzes, Andrea Csapó, Ferenc Fazakas, Miklós L. Udvardy, Zsuzsa Bagoly, Zsuzsanna Z. Orosz, László Muszbek

Blood (2014) 123 (11): 1757–1763.

https://doi.org/10.1182/blood-2013-10-533596

Published: 2014

Includes: Supplemental data

Journal Articles

Severe bleeding complications caused by an autoantibody against the B subunit of plasma factor XIII: a novel form of acquired factor XIII deficiency

Éva Ajzner, Ágota Schlammadinger, Adrienne Kerényi, Zsuzsanna Bereczky, Éva Katona, Gizella Haramura, Zoltán Boda, László Muszbek

Blood (2009) 113 (3): 723–725.

https://doi.org/10.1182/blood-2008-09-179333

Published: 2009

Journal Articles

Establishment of an International Registry of Patients with Inherited FXIII Deficiency.

Vytautas Ivaskevicius, MD, Rainer Seitz, MD, PhD, Hans P. Kohler, MD, PhD, Laszlo Muszbek, PhD, Robert A.S. Ariens, PhD, Erhard Seifried, MD, PhD, Akitada Ichinose, PhD, Diane J. Nugent, MD, PhD, Johannes Oldenburg, MD, PhD

Blood (2007) 110 (11): 2149.

https://doi.org/10.1182/blood.V110.11.2149.2149

Published: 2007

Journal Articles

The mystery of FXIII-A Val34Leu polymorphism

Laszlo Muszbek

Blood (2003) 101 (8): 2904.

https://doi.org/10.1182/blood-2003-02-0597

Published: 2003

Journal Articles

Molecular Mechanism of a Mild Phenotype in Coagulation Factor XIII (FXIII) Deficiency: A Splicing Mutation Permitting Partial Correct Splicing of FXIII A-Subunit mRNA

Hanna Mikkola, Laszlo Muszbek, Elina Laiho, Martti Syrjälä, Eija Hämäläinen, Gizela Haramura, Toivo Salmi, Leena Peltonen, Aarno Palotie

Blood (1997) 89 (4): 1279–1287.

https://doi.org/10.1182/blood.V89.4.1279

Published: 1997

NARROW

The Use of Recombinant FXIII in a Major Acute Bleeding Episode of a Patient with Congenital FXIII Deficiency – the First Experience

Interaction of factor XIII subunits

Severe bleeding complications caused by an autoantibody against the B subunit of plasma factor XIII: a novel form of acquired factor XIII deficiency

Establishment of an International Registry of Patients with Inherited FXIII Deficiency.

The mystery of FXIII-A Val34Leu polymorphism

Molecular Mechanism of a Mild Phenotype in Coagulation Factor XIII (FXIII) Deficiency: A Splicing Mutation Permitting Partial Correct Splicing of FXIII A-Subunit mRNA

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ASH Publications

American Society of Hematology

The Use of Recombinant FXIII in a Major Acute Bleeding Episode of a Patient with Congenital FXIII Deficiency – the First Experience

Interaction of factor XIII subunits

Severe bleeding complications caused by an autoantibody against the B subunit of plasma factor XIII: a novel form of acquired factor XIII deficiency

Establishment of an International Registry of Patients with Inherited FXIII Deficiency.

The mystery of FXIII-A Val34Leu polymorphism

Molecular Mechanism of a Mild Phenotype in Coagulation Factor XIII (FXIII) Deficiency: A Splicing Mutation Permitting Partial Correct Splicing of FXIII A-Subunit mRNA

Email alerts

ASH Publications

American Society of Hematology

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