Adelhardt, Tina

Evaluation of Individualized Physiotherapy in Pediatric Patients with Severe Bleeding Disorders

Adolf, Daniela

Dokumentationsqualität und Therapieadhärenz: Daten der Haemoassist-Community

Aebi-Huber, Isabella

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Akhter, Mohammad Suhail

Alpha-2 Macroglobulin: A Novel Putative Interacting Partner of FXIII/FXIIIB Subunit?

Albert, Thilo

AIM-Active-Studie – Hintergrund – Ziel – Design

LumiTope: Toward Improving the Performance of Identification of Antifactor VIII Antibodies in Congenital and Acquired Hemophilia A

Albisetti, Manuela

Erste Daten aus dem Schweizer Hämophilie-Register

Allerkamp, Hanna

Einfluss des Von-Willebrand-Faktors auf die porcine Angiogenese über das TIE-System

Al-Rifai, Rawya

Molecular Profiling of Fetal and Adult Liver Sinusoidal Endothelial Cells: A F8 Secreting Cell

Over Expression of Specific Transcription Factors to Boost FVIII Expression

Analyzing intracellular F8 mRNA and Protein of a Methionine Missense Mutation (c.[2T>G];[0]) in a Patient-Specific IPS Cell Model

Althaus, Karina

Combined Acquired Alpha- and Delta-Storage Pool Disease in Endstage Renal

Flow Cytometric Assessment of AKT Signaling in Platelet Activation: An Alternative Diagnostic Tool for Small Volumes of Blood

Apoptosis Inhibition: A Promising Approach for Cold Storage of Apheresis Platelet Concentrates

Autoantibody-Mediated Desialylation Impairs Human Thrombopoiesis and Platelet Life Span

Amling, Michael

Impact of Hepatitis C Infection on Bone Microstructure of Patients with Hemophilia

Anna, Pavlova

NGS for Diagnosing Inherited Bleeding, Thrombotic and Platelet Disorders: Points to Consider by Reporting Results—Primum Non Nocere, Secundum Cavere, Tertium Sanare

Diagnostic of Large Genetic Defects in Blood Coagulation Genes: NGS vs. MLPA

Ay, Cihan

Das Österreichische Hämophilie-Register

Bakchoul, Tamam

Combined Acquired Alpha- and Delta-Storage Pool Disease in Endstage Renal

Flow Cytometric Assessment of AKT Signaling in Platelet Activation: An Alternative Diagnostic Tool for Small Volumes of Blood

Autoantibody-Mediated Changes in Platelets Sialic Pattern: Potential Impact on Platelet Functionality and Lifespan in Immune Thrombocytopenia

Apoptosis Inhibition: A Promising Approach for Cold Storage of Apheresis Platelet Concentrates

Autoantibody-Mediated Desialylation Impairs Human Thrombopoiesis and Platelet Life Span

Barbara, Preisler

Diagnostic of Large Genetic Defects in Blood Coagulation Genes: NGS vs. MLPA

Barvencik, Florian

Impact of Hepatitis C Infection on Bone Microstructure of Patients with Hemophilia

Baumann, S.

Randomisiert-kontrollierte Cross-Over Studie zur Effektivität der manuellen Lymphdrainage bei Patienten mit schwerer Hämophilie

Behnaz, Pezeshkpoor

NGS for Diagnosing Inherited Bleeding, Thrombotic and Platelet Disorders: Points to Consider by Reporting Results—Primum Non Nocere, Secundum Cavere, Tertium Sanare

Diagnostic of Large Genetic Defects in Blood Coagulation Genes: NGS vs. MLPA

Berkemeier, Ann-Cristin

LumiTope: Toward Improving the Performance of Identification of Antifactor VIII Antibodies in Congenital and Acquired Hemophilia A

Berlin, Claudia

Emicizumab – Erfahrungen zur Anwendung bei Kindern mit Hämophilie und Hemmkörpern

Bethge, Wolfgang

Autoantibody-Mediated Desialylation Impairs Human Thrombopoiesis and Platelet Life Span

Beutel, Manfred

Influence of Thrombotic Thrombocytopenic Purpura on Depressivity, Cognitive Conduction, Quality of Life, and Resilience of Patients

Bidlingmaier, Christoph

Emicizumab – Erfahrungen zur Anwendung bei Kindern mit Hämophilie und Hemmkörpern

Biswas, Arijit

Alpha-2 Macroglobulin: A Novel Putative Interacting Partner of FXIII/FXIIIB Subunit?

Impact of Novel Missense Mutation (p. Arg510Cys) in the FGA Gene Resulting in Dysfibrinogenemia

Böhm, Peter

Fit for Life Fitness-App – sicheres und effektives Training in Fitnesseinrichtungen

Bönigk, Hagen

Vollautomatisierte Hemmkörperbestimmung

Bosher, Stephen

Combined Acquired Alpha- and Delta-Storage Pool Disease in Endstage Renal

Brehm, Maria A.

Degradation of VWD Type 2B Variants by ADAMTS-13 in Simulated Circulation

Functional and Structural Properties of the 2nd Gain-of-Function Variant in the C4 Domain of von Willebrand Factor

Bütikofer, Lukas

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Cadamuro, J.

Messungen von rVWF – Vonicog alpha (Veyvondi) in gespikten humanen Plasmaproben - erste Ergebnisse einer multizentrischen Studie der ÖGLMKC und ÖQUASTA in Österreich

Cermakova, Zuzana

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Dayo, J.

Randomisiert-kontrollierte Cross-Over Studie zur Effektivität der manuellen Lymphdrainage bei Patienten mit schwerer Hämophilie

Desch, K.

Randomisiert-kontrollierte Cross-Over Studie zur Effektivität der manuellen Lymphdrainage bei Patienten mit schwerer Hämophilie

Detering, Carsten

Einfluss des Von-Willebrand-Faktors auf die porcine Angiogenese über das TIE-System

Dodt, Johannes

Alpha-2 Macroglobulin: A Novel Putative Interacting Partner of FXIII/FXIIIB Subunit?

Eberl, Wolfgang

Subkutane Applikation eines plasmatischen FVII – Konzentrates zur Blutungsprophylaxe bei schwerem FVII - Mangel

Ekhlasi-Hundrieser, Mahnaz

Einfluss des Von-Willebrand-Faktors auf die porcine Angiogenese über das TIE-System

El-Maarri, Osman

Molecular Profiling of Fetal and Adult Liver Sinusoidal Endothelial Cells: A F8 Secreting Cell

Over Expression of Specific Transcription Factors to Boost FVIII Expression

Analyzing intracellular F8 mRNA and Protein of a Methionine Missense Mutation (c.[2T>G];[0]) in a Patient-Specific IPS Cell Model

Analysis of Single-Cell Expression Data of Liver Sinusoidal Endothelial Cells Reveals Strong Variability of F8 Expression Associated with Specific Expression Profile

Inversions at Xq28 Causing Hemophilia A Are Associated with Specific

Etzweiler, Denise

Age Effect on Pressure Pain Threshold of Asymptomatic Ankles and Knees in Young Individuals with and without Hemophilia: A Cross-Sectional Study

Faul, Christoph

Autoantibody-Mediated Desialylation Impairs Human Thrombopoiesis and Platelet Life Span

Fraunberger, P.

Messungen von rVWF – Vonicog alpha (Veyvondi) in gespikten humanen Plasmaproben - erste Ergebnisse einer multizentrischen Studie der ÖGLMKC und ÖQUASTA in Österreich

Friedman, Kenneth D.

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Fujimura, Yoshihiro

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

George, James N.

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Gerlach, N.

Randomisiert-kontrollierte Cross-Over Studie zur Effektivität der manuellen Lymphdrainage bei Patienten mit schwerer Hämophilie

Gessner, Michaela

Combined Acquired Alpha- and Delta-Storage Pool Disease in Endstage Renal

Gold, Georg

Dokumentationsqualität und Therapieadhärenz: Daten der Haemoassist-Community

Goldmann, G.

FXIII Protein Inhibitor against the FXIII-A Subunit in an 8-Year-Old Boy with Inherited Severe Factor XIII Deficiency Complicated by Multiple Intracerebral Cavernomas

Goldmann, Georg

Provision of Psychological Services in Hemophilia Treatment Postulated under the Guidelines of the WFH and the GTH—But Also in Demand? Experiences from the Hemophilia Center Bonn

Hämophilietherapie im Wandel: Auswirkungen auf das Gerinnungslabor

Successful Embryo Transfer and Pregnancy with Donated Egg in a Female with Severe FXIII Deficiency and Climacterium Praecox

AIM-Active-Studie – Hintergrund – Ziel – Design

Gottstein, Saskia

Recombinant Porcine Factor VIII in Patients with Acquired Hemophilia A: Single-Center Experience and Dosing Strategy

Griesmacher, A.

Messungen von rVWF – Vonicog alpha (Veyvondi) in gespikten humanen Plasmaproben - erste Ergebnisse einer multizentrischen Studie der ÖGLMKC und ÖQUASTA in Österreich

Grübel, H.

Randomisiert-kontrollierte Cross-Over Studie zur Effektivität der manuellen Lymphdrainage bei Patienten mit schwerer Hämophilie

Halimeh, Susan

Dokumentationsqualität und Therapieadhärenz: Daten der Haemoassist-Community

Hammer, Stefanie

Autoantibody-Mediated Desialylation Impairs Human Thrombopoiesis and Platelet Life Span

Hauer, R.

Messungen von rVWF – Vonicog alpha (Veyvondi) in gespikten humanen Plasmaproben - erste Ergebnisse einer multizentrischen Studie der ÖGLMKC und ÖQUASTA in Österreich

Haushofer, AC

Messungen von rVWF – Vonicog alpha (Veyvondi) in gespikten humanen Plasmaproben - erste Ergebnisse einer multizentrischen Studie der ÖGLMKC und ÖQUASTA in Österreich

Heimbach, Andre

Inversions at Xq28 Causing Hemophilia A Are Associated with Specific

Heller, Christine

Characterization of FVIII Pharmacokinetics in Hemophilia A Patients with or without Nonneutralizing FVIII Antibodies

Signature of the Antibody Response to FVIII

Nonneutralizing Factor VIII Antibodies as a Marker for Inhibitor Development in a Longitudinal Cohort of Hemophilia A Patients

Herzig, Marie

AIM-Active-Studie – Hintergrund – Ziel – Design

Hilberg, Thomas

AIM-Active-Studie – Hintergrund – Ziel – Design

Holstein, Katharina

Impact of Hepatitis C Infection on Bone Microstructure of Patients with Hemophilia

Holzer, Ursula

Autoantibody-Mediated Desialylation Impairs Human Thrombopoiesis and Platelet Life Span

Hoppe, Berthold

Ersteinstellung und Umstellung auf Emicizumab

Horneff, S.

FXIII Protein Inhibitor against the FXIII-A Subunit in an 8-Year-Old Boy with Inherited Severe Factor XIII Deficiency Complicated by Multiple Intracerebral Cavernomas

Horneff, Silvia

Provision of Psychological Services in Hemophilia Treatment Postulated under the Guidelines of the WFH and the GTH—But Also in Demand? Experiences from the Hemophilia Center Bonn

Hämophilietherapie im Wandel: Auswirkungen auf das Gerinnungslabor

Successful Embryo Transfer and Pregnancy with Donated Egg in a Female with Severe FXIII Deficiency and Climacterium Praecox

Hovinga, Johanna A. Kremer

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Hrachovinova, Ingrid

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Huck, Volker

Functional and Structural Properties of the 2nd Gain-of-Function Variant in the C4 Domain of von Willebrand Factor

Hukauf, Martin

Dokumentationsqualität und Therapieadhärenz: Daten der Haemoassist-Community

Inge, Scharrer

Influence of Thrombotic Thrombocytopenic Purpura on Depressivity, Cognitive Conduction, Quality of Life, and Resilience of Patients

Iris, Radermacher

Diagnostic of Large Genetic Defects in Blood Coagulation Genes: NGS vs. MLPA

Irsara, C.

Messungen von rVWF – Vonicog alpha (Veyvondi) in gespikten humanen Plasmaproben - erste Ergebnisse einer multizentrischen Studie der ÖGLMKC und ÖQUASTA in Österreich

Ivaskevicius, Vytautas

Successful Embryo Transfer and Pregnancy with Donated Egg in a Female with Severe FXIII Deficiency and Climacterium Praecox

Impact of Novel Missense Mutation (p. Arg510Cys) in the FGA Gene Resulting in Dysfibrinogenemia

Jamil, Muhammad Ahmer

Molecular Profiling of Fetal and Adult Liver Sinusoidal Endothelial Cells: A F8 Secreting Cell

Over Expression of Specific Transcription Factors to Boost FVIII Expression

Analyzing intracellular F8 mRNA and Protein of a Methionine Missense Mutation (c.[2T>G];[0]) in a Patient-Specific IPS Cell Model

Analysis of Single-Cell Expression Data of Liver Sinusoidal Endothelial Cells Reveals Strong Variability of F8 Expression Associated with Specific Expression Profile

Inversions at Xq28 Causing Hemophilia A Are Associated with Specific

Joeres, Jan

Fit for Life Fitness-App – sicheres und effektives Training in Fitnesseinrichtungen

Johannes, Oldenburg

NGS for Diagnosing Inherited Bleeding, Thrombotic and Platelet Disorders: Points to Consider by Reporting Results—Primum Non Nocere, Secundum Cavere, Tertium Sanare

Diagnostic of Large Genetic Defects in Blood Coagulation Genes: NGS vs. MLPA

Juranek, Sabrina

Emicizumab – Erfahrungen zur Anwendung bei Kindern mit Hämophilie und Hemmkörpern

Jutta, Beckedahl

Diagnostic of Large Genetic Defects in Blood Coagulation Genes: NGS vs. MLPA

Kahle, Jörg

Nonneutralizing Factor VIII Antibodies as a Marker for Inhibitor Development in a Longitudinal Cohort of Hemophilia A Patients

Kahre, Elisabeth

Evaluation of Individualized Physiotherapy in Pediatric Patients with Severe Bleeding Disorders

Kaiser, Katharina

Einfluss des Von-Willebrand-Faktors auf die porcine Angiogenese über das TIE-System

Karl, Lackner

Influence of Thrombotic Thrombocytopenic Purpura on Depressivity, Cognitive Conduction, Quality of Life, and Resilience of Patients

Kaya, Esra

Characterization of FVIII Pharmacokinetics in Hemophilia A Patients with or without Nonneutralizing FVIII Antibodies

Keipert, Christine

Das neue DHR

Kemkes-Matthes, Bettina

Familial Multiple Coagulation Factor Deficiencies: Follow-up Analyses

Kerstan, A.

FXIII Protein Inhibitor against the FXIII-A Subunit in an 8-Year-Old Boy with Inherited Severe Factor XIII Deficiency Complicated by Multiple Intracerebral Cavernomas

Kersten, Alexa

Hämophilietherapie im Wandel: Auswirkungen auf das Gerinnungslabor

Kiesewetter, Holger

Ersteinstellung und Umstellung auf Emicizumab

Klamroth, Robert

Recombinant Porcine Factor VIII in Patients with Acquired Hemophilia A: Single-Center Experience and Dosing Strategy

Klein, C.

FXIII Protein Inhibitor against the FXIII-A Subunit in an 8-Year-Old Boy with Inherited Severe Factor XIII Deficiency Complicated by Multiple Intracerebral Cavernomas

Klein, Claudia

Provision of Psychological Services in Hemophilia Treatment Postulated under the Guidelines of the WFH and the GTH—But Also in Demand? Experiences from the Hemophilia Center Bonn

Hämophilietherapie im Wandel: Auswirkungen auf das Gerinnungslabor

Successful Embryo Transfer and Pregnancy with Donated Egg in a Female with Severe FXIII Deficiency and Climacterium Praecox

Klingebiel, Thomas

Signature of the Antibody Response to FVIII

Nonneutralizing Factor VIII Antibodies as a Marker for Inhibitor Development in a Longitudinal Cohort of Hemophilia A Patients

Knöbl, Paul N.

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Knöfler, Ralf

Evaluation of Individualized Physiotherapy in Pediatric Patients with Severe Bleeding Disorders

Kokame, Koichi

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

König, Gesa

Degradation of VWD Type 2B Variants by ADAMTS-13 in Simulated Circulation

Functional and Structural Properties of the 2nd Gain-of-Function Variant in the C4 Domain of von Willebrand Factor

Königs, C.

Responsiveness of PBMCs Isolated from Healthy Individuals toward rFVIII and rFVIIIFc

Königs, Christoph

Characterization of FVIII Pharmacokinetics in Hemophilia A Patients with or without Nonneutralizing FVIII Antibodies

Signature of the Antibody Response to FVIII

Nonneutralizing Factor VIII Antibodies as a Marker for Inhibitor Development in a Longitudinal Cohort of Hemophilia A Patients

Kopf, L.

Randomisiert-kontrollierte Cross-Over Studie zur Effektivität der manuellen Lymphdrainage bei Patienten mit schwerer Hämophilie

Kragh, T.

Ongoing Effect of Therapeutic rVWF in Patients with Severe VWD

Kramer, Sonja

Emicizumab – Erfahrungen zur Anwendung bei Kindern mit Hämophilie und Hemmkörpern

Krettler, Christoph

Alpha-2 Macroglobulin: A Novel Putative Interacting Partner of FXIII/FXIIIB Subunit?

Krüger, Steffen

AIM-Active-Studie – Hintergrund – Ziel – Design

Kubicek-Hofmann, Cornelia

Recombinant Porcine Factor VIII in Patients with Acquired Hemophilia A: Single-Center Experience and Dosing Strategy

Kurme, Anatol

Fit for Life Fitness-App – sicheres und effektives Training in Fitnesseinrichtungen

Kurnik, Karin

Emicizumab – Erfahrungen zur Anwendung bei Kindern mit Hämophilie und Hemmkörpern

Lambeck, Katharina

Unusual Bleeding in a Patient after Bone Marrow Transplantation Caused by Acquired Deficiency of Coagulation Factors IX and XI

Lämmle, Bernhard

Influence of Thrombotic Thrombocytopenic Purpura on Depressivity, Cognitive Conduction, Quality of Life, and Resilience of Patients

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Langer, Elisabeth

Recombinant Porcine Factor VIII in Patients with Acquired Hemophilia A: Single-Center Experience and Dosing Strategy

Langer, Florian

Impact of Hepatitis C Infection on Bone Microstructure of Patients with Hemophilia

Largiadèr, Carlo R.

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Lehner, Stefanie

Einfluss des Von-Willebrand-Faktors auf die porcine Angiogenese über das TIE-System

Male-Dressler, Christoph

Das Österreichische Hämophilie-Register

Marini, Irene

Autoantibody-Mediated Changes in Platelets Sialic Pattern: Potential Impact on Platelet Functionality and Lifespan in Immune Thrombocytopenia

Apoptosis Inhibition: A Promising Approach for Cold Storage of Apheresis Platelet Concentrates

Autoantibody-Mediated Desialylation Impairs Human Thrombopoiesis and Platelet Life Span

Marquardt, N.

FXIII Protein Inhibitor against the FXIII-A Subunit in an 8-Year-Old Boy with Inherited Severe Factor XIII Deficiency Complicated by Multiple Intracerebral Cavernomas

Marquardt, Natascha

Provision of Psychological Services in Hemophilia Treatment Postulated under the Guidelines of the WFH and the GTH—But Also in Demand? Experiences from the Hemophilia Center Bonn

Hämophilietherapie im Wandel: Auswirkungen auf das Gerinnungslabor

Successful Embryo Transfer and Pregnancy with Donated Egg in a Female with Severe FXIII Deficiency and Climacterium Praecox

Matsumoto, Masanori

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Matysiak, Anna

Impact of Hepatitis C Infection on Bone Microstructure of Patients with Hemophilia

Melanie, Rath

Over Expression of Specific Transcription Factors to Boost FVIII Expression

Michael, Krause

Familial Multiple Coagulation Factor Deficiencies: Follow-up Analyses

Miesbach, W.

Randomisiert-kontrollierte Cross-Over Studie zur Effektivität der manuellen Lymphdrainage bei Patienten mit schwerer Hämophilie

Miriam, Wagner

Flow Cytometric Assessment of AKT Signaling in Platelet Activation: An Alternative Diagnostic Tool for Small Volumes of Blood

Miyata, Toshiyuki

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Möhnle, P.

Ongoing Effect of Therapeutic rVWF in Patients with Severe VWD

Moldenhauer, Anja

Familial Multiple Coagulation Factor Deficiencies: Follow-up Analyses

Müller, Jens

Hämophilietherapie im Wandel: Auswirkungen auf das Gerinnungslabor

Nadalin, Silvio

Combined Acquired Alpha- and Delta-Storage Pool Disease in Endstage Renal

Neimanis, Sonja

Nonneutralizing Factor VIII Antibodies as a Marker for Inhibitor Development in a Longitudinal Cohort of Hemophilia A Patients

Nitze, Claudia

Evaluation of Individualized Physiotherapy in Pediatric Patients with Severe Bleeding Disorders

Nowak-Harnau, Stefanie

Apoptosis Inhibition: A Promising Approach for Cold Storage of Apheresis Platelet Concentrates

Nuesgen, Nicole

Inversions at Xq28 Causing Hemophilia A Are Associated with Specific

Nüsgen, Nicole

LumiTope: Toward Improving the Performance of Identification of Antifactor VIII Antibodies in Congenital and Acquired Hemophilia A

Obser, Tobias

Degradation of VWD Type 2B Variants by ADAMTS-13 in Simulated Circulation

Functional and Structural Properties of the 2nd Gain-of-Function Variant in the C4 Domain of von Willebrand Factor

Ochs, Sebastian

Fit for Life Fitness-App – sicheres und effektives Training in Fitnesseinrichtungen

Oldenburg, J.

FXIII Protein Inhibitor against the FXIII-A Subunit in an 8-Year-Old Boy with Inherited Severe Factor XIII Deficiency Complicated by Multiple Intracerebral Cavernomas

Oldenburg, Johannes

Provision of Psychological Services in Hemophilia Treatment Postulated under the Guidelines of the WFH and the GTH—But Also in Demand? Experiences from the Hemophilia Center Bonn

Hämophilietherapie im Wandel: Auswirkungen auf das Gerinnungslabor

Successful Embryo Transfer and Pregnancy with Donated Egg in a Female with Severe FXIII Deficiency and Climacterium Praecox

Alpha-2 Macroglobulin: A Novel Putative Interacting Partner of FXIII/FXIIIB Subunit?

Dokumentationsqualität und Therapieadhärenz: Daten der Haemoassist-Community

Molecular Profiling of Fetal and Adult Liver Sinusoidal Endothelial Cells: A F8 Secreting Cell

AIM-Active-Studie – Hintergrund – Ziel – Design

LumiTope: Toward Improving the Performance of Identification of Antifactor VIII Antibodies in Congenital and Acquired Hemophilia A

AHEAD International and German Studies: Effectiveness, Safety, and Quality of Life Outcomes in Patients with Hemophilia A Treated with Antihemophilic Factor (Recombinant) in a Real-World Setting Over 5 Years

Inversions at Xq28 Causing Hemophilia A Are Associated with Specific

Impact of Novel Missense Mutation (p. Arg510Cys) in the FGA Gene Resulting in Dysfibrinogenemia

Oldenburg, Johannnes

Over Expression of Specific Transcription Factors to Boost FVIII Expression

Analyzing intracellular F8 mRNA and Protein of a Methionine Missense Mutation (c.[2T>G];[0]) in a Patient-Specific IPS Cell Model

Olivieri, Martin

Emicizumab – Erfahrungen zur Anwendung bei Kindern mit Hämophilie und Hemmkörpern

Familial Multiple Coagulation Factor Deficiencies: Follow-up Analyses

on behalf of the ABIRISK consortium,

Signature of the Antibody Response to FVIII

on behalf of the ABIRISK Consortium,

Nonneutralizing Factor VIII Antibodies as a Marker for Inhibitor Development in a Longitudinal Cohort of Hemophilia A Patients

Orlowski, A.

Responsiveness of PBMCs Isolated from Healthy Individuals toward rFVIII and rFVIIIFc

Orlowski, Aleksander

Characterization of FVIII Pharmacokinetics in Hemophilia A Patients with or without Nonneutralizing FVIII Antibodies

Signature of the Antibody Response to FVIII

Nonneutralizing Factor VIII Antibodies as a Marker for Inhibitor Development in a Longitudinal Cohort of Hemophilia A Patients

Pabinger-Fasching, Ingrid

Das Österreichische Hämophilie-Register

Pavlova, Anna

Familial Multiple Coagulation Factor Deficiencies: Follow-up Analyses

Impact of Novel Missense Mutation (p. Arg510Cys) in the FGA Gene Resulting in Dysfibrinogenemia

Pavlova, Anne

Inversions at Xq28 Causing Hemophilia A Are Associated with Specific

Pekrul, I.

Ongoing Effect of Therapeutic rVWF in Patients with Severe VWD

Pelzl, Lisann

Autoantibody-Mediated Changes in Platelets Sialic Pattern: Potential Impact on Platelet Functionality and Lifespan in Immune Thrombocytopenia

Apoptosis Inhibition: A Promising Approach for Cold Storage of Apheresis Platelet Concentrates

Autoantibody-Mediated Desialylation Impairs Human Thrombopoiesis and Platelet Life Span

Petros, Sirak

Quantifizierung der Diskrepanz zwischen Ein- und Zweistufen-Assays für Faktor IX- Präparate mit verlängerter Halbwertszeit

Pezeshkpoor, Behnaz

Familial Multiple Coagulation Factor Deficiencies: Follow-up Analyses

LumiTope: Toward Improving the Performance of Identification of Antifactor VIII Antibodies in Congenital and Acquired Hemophilia A

Inversions at Xq28 Causing Hemophilia A Are Associated with Specific

Pfarrer, Christiane

Einfluss des Von-Willebrand-Faktors auf die porcine Angiogenese über das TIE-System

Pfrepper, Christian

Quantifizierung der Diskrepanz zwischen Ein- und Zweistufen-Assays für Faktor IX- Präparate mit verlängerter Halbwertszeit

Pollich, Christiane

Recombinant Porcine Factor VIII in Patients with Acquired Hemophilia A: Single-Center Experience and Dosing Strategy

Pötzsch, Bernd

Hämophilietherapie im Wandel: Auswirkungen auf das Gerinnungslabor

Prondzinski, Mario von Depka

Einfluss des Von-Willebrand-Faktors auf die porcine Angiogenese über das TIE-System

Prüller, F.

Messungen von rVWF – Vonicog alpha (Veyvondi) in gespikten humanen Plasmaproben - erste Ergebnisse einer multizentrischen Studie der ÖGLMKC und ÖQUASTA in Österreich

Quehenberger, P.

Messungen von rVWF – Vonicog alpha (Veyvondi) in gespikten humanen Plasmaproben - erste Ergebnisse einer multizentrischen Studie der ÖGLMKC und ÖQUASTA in Österreich

Radek, J.

Messungen von rVWF – Vonicog alpha (Veyvondi) in gespikten humanen Plasmaproben - erste Ergebnisse einer multizentrischen Studie der ÖGLMKC und ÖQUASTA in Österreich

Range, Ursula

Evaluation of Individualized Physiotherapy in Pediatric Patients with Severe Bleeding Disorders

Rath, Melanie

Analyzing intracellular F8 mRNA and Protein of a Methionine Missense Mutation (c.[2T>G];[0]) in a Patient-Specific IPS Cell Model

Reichmann, Jan

Dokumentationsqualität und Therapieadhärenz: Daten der Haemoassist-Community

Reinhart, Christoph

Alpha-2 Macroglobulin: A Novel Putative Interacting Partner of FXIII/FXIIIB Subunit?

Rejtö, Judith

Das Österreichische Hämophilie-Register

Reuter, Andreas

Alpha-2 Macroglobulin: A Novel Putative Interacting Partner of FXIII/FXIIIB Subunit?

Rigoni, Flaviana

Flow Cytometric Assessment of AKT Signaling in Platelet Activation: An Alternative Diagnostic Tool for Small Volumes of Blood

Rigoni, Flavianna

Autoantibody-Mediated Changes in Platelets Sialic Pattern: Potential Impact on Platelet Functionality and Lifespan in Immune Thrombocytopenia

Apoptosis Inhibition: A Promising Approach for Cold Storage of Apheresis Platelet Concentrates

Rolvien, Tim

Impact of Hepatitis C Infection on Bone Microstructure of Patients with Hemophilia

Roth, S.

Randomisiert-kontrollierte Cross-Over Studie zur Effektivität der manuellen Lymphdrainage bei Patienten mit schwerer Hämophilie

Sakai, Kazuya

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Schlagenhauf, A.

Messungen von rVWF – Vonicog alpha (Veyvondi) in gespikten humanen Plasmaproben - erste Ergebnisse einer multizentrischen Studie der ÖGLMKC und ÖQUASTA in Österreich

Schleithoff, Elisabeth Schulze

Provision of Psychological Services in Hemophilia Treatment Postulated under the Guidelines of the WFH and the GTH—But Also in Demand? Experiences from the Hemophilia Center Bonn

Schmidt, A.

Responsiveness of PBMCs Isolated from Healthy Individuals toward rFVIII and rFVIIIFc

Schmidt, Anja

Signature of the Antibody Response to FVIII

Nonneutralizing Factor VIII Antibodies as a Marker for Inhibitor Development in a Longitudinal Cohort of Hemophilia A Patients

Schneider, Stefan W.

Functional and Structural Properties of the 2nd Gain-of-Function Variant in the C4 Domain of von Willebrand Factor

Schneppenheim, Reinhard

Degradation of VWD Type 2B Variants by ADAMTS-13 in Simulated Circulation

Functional and Structural Properties of the 2nd Gain-of-Function Variant in the C4 Domain of von Willebrand Factor

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Scholz, Ute

Familial Multiple Coagulation Factor Deficiencies: Follow-up Analyses

Schultze-Strasser, S.

Responsiveness of PBMCs Isolated from Healthy Individuals toward rFVIII and rFVIIIFc

Schultze-Strasser, Stephan

Characterization of FVIII Pharmacokinetics in Hemophilia A Patients with or without Nonneutralizing FVIII Antibodies

Signature of the Antibody Response to FVIII

Nonneutralizing Factor VIII Antibodies as a Marker for Inhibitor Development in a Longitudinal Cohort of Hemophilia A Patients

Schwabe, Dirk

Nonneutralizing Factor VIII Antibodies as a Marker for Inhibitor Development in a Longitudinal Cohort of Hemophilia A Patients

Schwarte, Sabine

Subkutane Applikation eines plasmatischen FVII – Konzentrates zur Blutungsprophylaxe bei schwerem FVII - Mangel

Seier, J.

Messungen von rVWF – Vonicog alpha (Veyvondi) in gespikten humanen Plasmaproben - erste Ergebnisse einer multizentrischen Studie der ÖGLMKC und ÖQUASTA in Österreich

Seuser, Axel

Fit for Life Fitness-App – sicheres und effektives Training in Fitnesseinrichtungen

Handschriftanalyse und EMG der oberen Extremität bei Kindern mit Hämophilie

Sharma, Amit

Inversions at Xq28 Causing Hemophilia A Are Associated with Specific

Sibylle, Böschen

Influence of Thrombotic Thrombocytopenic Purpura on Depressivity, Cognitive Conduction, Quality of Life, and Resilience of Patients

Siegemund, Annelie

Quantifizierung der Diskrepanz zwischen Ein- und Zweistufen-Assays für Faktor IX- Präparate mit verlängerter Halbwertszeit

Vollautomatisierte Hemmkörperbestimmung

Siegemund, Thomas

Quantifizierung der Diskrepanz zwischen Ein- und Zweistufen-Assays für Faktor IX- Präparate mit verlängerter Halbwertszeit

Vollautomatisierte Hemmkörperbestimmung

Singer, Heike

Molecular Profiling of Fetal and Adult Liver Sinusoidal Endothelial Cells: A F8 Secreting Cell

Analyzing intracellular F8 mRNA and Protein of a Methionine Missense Mutation (c.[2T>G];[0]) in a Patient-Specific IPS Cell Model

Singh, Sneha

Alpha-2 Macroglobulin: A Novel Putative Interacting Partner of FXIII/FXIIIB Subunit?

Impact of Novel Missense Mutation (p. Arg510Cys) in the FGA Gene Resulting in Dysfibrinogenemia

Sleiman, Hanan

Over Expression of Specific Transcription Factors to Boost FVIII Expression

Spannagl, M.

Ongoing Effect of Therapeutic rVWF in Patients with Severe VWD

Sparber-Sauer, Monika

Dokumentationsqualität und Therapieadhärenz: Daten der Haemoassist-Community

Stapel, Iris

Subkutane Applikation eines plasmatischen FVII – Konzentrates zur Blutungsprophylaxe bei schwerem FVII - Mangel

Stichel, Diana

Characterization of FVIII Pharmacokinetics in Hemophilia A Patients with or without Nonneutralizing FVIII Antibodies

Signature of the Antibody Response to FVIII

Nonneutralizing Factor VIII Antibodies as a Marker for Inhibitor Development in a Longitudinal Cohort of Hemophilia A Patients

Streif, Werner

Das Österreichische Hämophilie-Register

Sussitz-Rack, S.

Messungen von rVWF – Vonicog alpha (Veyvondi) in gespikten humanen Plasmaproben - erste Ergebnisse einer multizentrischen Studie der ÖGLMKC und ÖQUASTA in Österreich

Sykora, Karl-Walter

Unusual Bleeding in a Patient after Bone Marrow Transplantation Caused by Acquired Deficiency of Coagulation Factors IX and XI

Taleghani, Magnus Mansouri

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Tanja, Falter

Influence of Thrombotic Thrombocytopenic Purpura on Depressivity, Cognitive Conduction, Quality of Life, and Resilience of Patients

Terrell, Deirdra R.

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Tiede, Andreas

Dokumentationsqualität und Therapieadhärenz: Daten der Haemoassist-Community

Tomasits, J.

Messungen von rVWF – Vonicog alpha (Veyvondi) in gespikten humanen Plasmaproben - erste Ergebnisse einer multizentrischen Studie der ÖGLMKC und ÖQUASTA in Österreich

Trunz-Carlisi, Elmar

Fit for Life Fitness-App – sicheres und effektives Training in Fitnesseinrichtungen

Ursula, Schmitt

Familial Multiple Coagulation Factor Deficiencies: Follow-up Analyses

Ute, Scholz

Diagnostic of Large Genetic Defects in Blood Coagulation Genes: NGS vs. MLPA

van Dorland, Hendrika A.

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Vesely, Sara K.

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Vitkus, Martynas

Impact of Novel Missense Mutation (p. Arg510Cys) in the FGA Gene Resulting in Dysfibrinogenemia

Volkers, Peter

Alpha-2 Macroglobulin: A Novel Putative Interacting Partner of FXIII/FXIIIB Subunit?

von Krogh, Anne Sophie

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

von Mackensen, Sylvia

Evaluation of Individualized Physiotherapy in Pediatric Patients with Severe Bleeding Disorders

Wieland, Ivonne

Unusual Bleeding in a Patient after Bone Marrow Transplantation Caused by Acquired Deficiency of Coagulation Factors IX and XI

Wimmer, E.

Messungen von rVWF – Vonicog alpha (Veyvondi) in gespikten humanen Plasmaproben - erste Ergebnisse einer multizentrischen Studie der ÖGLMKC und ÖQUASTA in Österreich

Winkler, Alexander

Fit for Life Fitness-App – sicheres und effektives Training in Fitnesseinrichtungen

Witt, Leonora

Impact of Hepatitis C Infection on Bone Microstructure of Patients with Hemophilia

Wolfgang, Eberl

Familial Multiple Coagulation Factor Deficiencies: Follow-up Analyses

Yagi, Hideo

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Zerlik, M.

Randomisiert-kontrollierte Cross-Over Studie zur Effektivität der manuellen Lymphdrainage bei Patienten mit schwerer Hämophilie

Zieger, Barbara

Familial Multiple Coagulation Factor Deficiencies: Follow-up Analyses

Zlamal, Jan

Autoantibody-Mediated Changes in Platelets Sialic Pattern: Potential Impact on Platelet Functionality and Lifespan in Immune Thrombocytopenia

Autoantibody-Mediated Desialylation Impairs Human Thrombopoiesis and Platelet Life Span