I. Bodó

发表

Type 1 von Willebrand disease mutation Cys1149Arg causes intracellular retention and degradation of heterodimers: a possible general mechanism for dominant mutations of oligomeric proteins.

J. Eikenboom, J. Sadler, E. Tuley, 2001, Blood.

Von Willebrand factor propeptide and pathophysiological mechanisms in European and Iranian patients with type 3 von Willebrand disease enrolled in the 3WINTERS‐IPS study

F. Rosendaal, P. Mannucci, A. Tosetto, 2022, Journal of thrombosis and haemostasis : JTH.

An Alu‐mediated novel large deletion is the most frequent cause of type 3 von Willebrand disease in Hungary

R. Marschalek, T. Masszi, R. Schneppenheim, 2008, Journal of thrombosis and haemostasis : JTH.

Platelet‐dependent von Willebrand factor activity. Nomenclature and methodology: communication from the SSC of the ISTH

J. Eikenboom, R. Montgomery, J. Di Paola, 2015, Journal of thrombosis and haemostasis : JTH.

dominant mutations of oligomeric proteins retention and degradation of heterodimers: a possible general mechanism for Type 1 von Willebrand disease mutation Cys1149Arg causes intracellular

J. Eikenboom, J. Sadler, E. Tuley, 2013 .

Fundamentals for a Systematic Approach to Mild and Moderate Inherited Bleeding Disorders: An EHA Consensus Report

P. Noris, A. Srivastava, V. Blanchette, 2019, HemaSphere.

von Willebrand disease and platelet disorders

S. Israels, E. Favaloro, S. Brown, 2014, Haemophilia : the official journal of the World Federation of Hemophilia.

Clinical Utilization and Cost of Thrombophilia Testing in Patients with Venous Thromboembolism

M. Gaddh, I. Bodó, E. Cheng, 2020, TH Open.

Rituximab leads to early elimination of circulating CD20+ T and B lymphocytes in patients with iTTP despite ongoing TPEx.

S. Stowell, R. Kudchadkar, M. Gaddh, 2020, Blood advances.

Radioguided lymph node biopsy of a chemoresistant lymph node detected on interim FDG PET-CT in Hodgkin lymphoma

V. Bérczi, T. Masszi, I. Garai, 2011, International journal of hematology.

Armillifer-Infected Snakes Sold at Congolese Bushmeat Markets Represent an Emerging Zoonotic Threat

M. Sulyok, D. Tappe, I. Bodó, 2017, EcoHealth.

Accelerated clearance alone explains ultra‐large multimers in von Willebrand disease Vicenza

I. Deák, T. Masszi, A. Gézsi, 2010, Journal of thrombosis and haemostasis : JTH.

Ruxolitinib: a steroid sparing agent in chronic graft-versus-host disease

J. Dipersio, H. Khoury, D. Roberts, 2018, Bone Marrow Transplantation.

Common large partial VWF gene deletion does not cause alloantibody formation in the Hungarian type 3 von Willebrand disease population

H. Losonczy, L. Nemes, T. Masszi, 2011, Journal of thrombosis and haemostasis : JTH.

Combined immunosuppression for acquired hemophilia A: CyDRi is a highly effective low-toxicity regimen

T. Masszi, R. Horvath, M. Gaddh, 2022, Blood.

Low-Dose Combined Immunosuppression Results In Rapid Remission In Patients With Acquired Hemophilia A

K. Pap, T. Masszi, K. Szabó, 2013 .

Comparison of von Willebrand factor platelet‐binding activity assays: ELISA overreads type 2B with loss of HMW multimers

R. Montgomery, G. Castaman, F. Peyvandi, 2020, Journal of thrombosis and haemostasis : JTH.

An international collaborative study to compare different von Willebrand factor glycoprotein Ib binding activity assays: the COMPASS‐VWF study

R. Montgomery, G. Castaman, F. Peyvandi, 2018, Journal of thrombosis and haemostasis : JTH.

Bleeding symptoms in patients diagnosed as type 3 von Willebrand disease: Results from 3WINTERS‐IPS, an international and collaborative cross‐sectional study

P. Mannucci, J. Oldenburg, M. Morfini, 2020, Journal of thrombosis and haemostasis : JTH.

Genotypes of European and Iranian patients with type 3 von Willebrand disease enrolled in 3WINTERS-IPS.

P. Mannucci, A. Tosetto, J. Goudemand, 2021, Blood advances.

Co-infections in Visceral Pentastomiasis, Democratic Republic of the Congo

C. Schoen, M. Sulyok, D. Tappe, 2016, Emerging infectious diseases.

Ocular Pentastomiasis in the Democratic Republic of the Congo

M. Sulyok, D. Tappe, I. Bodó, 2014, PLoS neglected tropical diseases.

Localization of Disulfide Bonds in the Cystine Knot Domain of Human von Willebrand Factor*

J. Sadler, E. Tuley, I. Bodó, 2000, The Journal of Biological Chemistry.

The evolutionary logic of sepsis.

V. Müller, M. Sulyok, Péter Apari, 2017, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

Successful treatment with rivaroxaban of an extended superficial vein thrombosis in a patient with acquired antithrombin deficiency due to Peg-asparaginase treatment

J. Iványi, I. Bodó, M. Plander, 2015, Annals of Hematology.

Use of thrombopoietin receptor agonists in adults with immune thrombocytopenia: a systematic review and Central European expert consensus

T. Lissitchkov, D. Pulanić, I. Bodó, 2023, Annals of Hematology.

Peripheral Blood Stem Cell Mobilization and Engraftment after Autologous Stem Cell Transplantation with Biosimilar rhG-CSF

Z. Borbényi, T. Masszi, P. Reményi, 2014, Advances in Therapy.

Effect of vitamin A treatment on the immune reactivity of patients with systemic lupus erythematosus.

P. Gergely, I. Bodó, R. González-Cabello, 1988, Journal of clinical & laboratory immunology.

D-dimer determination as a screening tool to exclude atrial thrombi in atrial fibrillation.

A. Bezzegh, I. Bodó, J. Tomcsányi, 2003, The American journal of cardiology.

Does the frequency of molecular monitoring after tyrosine kinase inhibitor discontinuation affect outcomes of patients with chronic myeloid leukemia?

Zhengjia Chen, H. Khoury, M. Arellano, 2017, Cancer.

Complement Inhibition in Paroxysmal Nocturnal Hemoglobinuria (PNH): A Systematic Review and Expert Opinion from Central Europe on Special Patient Populations

J. Čermák, J. Windyga, A. Piekarska, 2023, Advances in therapy.

Inflammation and oxidative stress caused by nitric oxide synthase uncoupling might lead to left ventricular diastolic and systolic dysfunction in patients with hypertension

Melinda Kiss, A. Patócs, Z. Prohászka, 2015, Journal of geriatric cardiology : JGC.

[Transthyretin familial amyloid polyneuropathy - three Hungarian cases with rare mutations (His88Arg and Phe33Leu)].

I. Balogh, I. Bodó, Z. Arányi, 2016, Ideggyogyaszati szemle.

Thrombosis risk in systemic lupus erythematosus: the role of thrombophilic risk factors

P. Gergely, E. Nagy, I. Bodó, 2007, Scandinavian journal of rheumatology.

Fundamentals for a Systematic Approach to Mild and Moderate Inherited Bleeding Disorders: A EHA Consensus Report

P. Noris, A. Tosetto, F. Leebeek, 2019 .

The evolutionary logic of sepsis.

V. Müller, M. Sulyok, Péter Apari, 2017, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.