Gyorgy Pfliegler

Debrecen, HB 4032, Hungary

Last Updated: 09/26/2026

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Found 24 publications

Clinical Relevance and Methodological Comparison of Anti-MDA5 Antibody Detection: A Five-Year Retrospective and Exploratory Pilot Study.

Clinical Relevance and Methodological Comparison of Anti-MDA5 Antibody Detection: A Five-Year Retrospective and Exploratory Pilot Study.

Journal: Biomolecules

Published: March 20, 2026

Management and Prognosis of Anti-MDA5 Dermatomyositis: Insights from a National Multicenter Cohort.

Management and Prognosis of Anti-MDA5 Dermatomyositis: Insights from a National Multicenter Cohort.

Journal: Biomedicines

Published: February 14, 2026

Antiangiogenic Treatment of Patients with Hereditary Hemorrhagic Telangiectasia: Experience of a Hungarian Center.

Antiangiogenic Treatment of Patients with Hereditary Hemorrhagic Telangiectasia: Experience of a Hungarian Center.

Journal: Journal of clinical medicine

Published: September 27, 2025

Case Report: Importance of high-throughput genetic investigations in the differential diagnosis of unexplained erythrocytosis.

Case Report: Importance of high-throughput genetic investigations in the differential diagnosis of unexplained erythrocytosis.

Journal: Pathology oncology research : POR

Published: November 21, 2024

Diagnostic challenges in patients with Castleman disease, a single center experience from Hungary.

Diagnostic challenges in patients with Castleman disease, a single center experience from Hungary.

Journal: Pathology oncology research : POR

Published: March 28, 2024

Clinical Investigation of Hereditary and Acquired Thrombophilic Factors in Patients with Venous and Arterial Thromboembolism.

Clinical Investigation of Hereditary and Acquired Thrombophilic Factors in Patients with Venous and Arterial Thromboembolism.

Journal: International journal of general medicine

Published: April 24, 2023

Rare disease education in Europe and beyond: time to act.

Rare disease education in Europe and beyond: time to act.

Journal: Orphanet journal of rare diseases

Published: December 17, 2021

Current Status of Clinical and Genetic Screening of Hereditary Hemorrhagic Telangiectasia Families in Hungary.

Current Status of Clinical and Genetic Screening of Hereditary Hemorrhagic Telangiectasia Families in Hungary.

Journal: Journal of clinical medicine

Published: June 23, 2021

Resolving Differential Diagnostic Problems in von Willebrand Disease, in Fibrinogen Disorders, in Prekallikrein Deficiency and in Hereditary Hemorrhagic Telangiectasia by Next-Generation Sequencing.

Resolving Differential Diagnostic Problems in von Willebrand Disease, in Fibrinogen Disorders, in Prekallikrein Deficiency and in Hereditary Hemorrhagic Telangiectasia by Next-Generation Sequencing.

Journal: Life (Basel, Switzerland)

Published: February 05, 2021

FBN1 gene mutations in 26 Hungarian patients with suspected Marfan syndrome or related fibrillinopathies.

FBN1 gene mutations in 26 Hungarian patients with suspected Marfan syndrome or related fibrillinopathies.

Journal: Journal of biotechnology

Published: January 31, 2019

Intravascular Occlusion by Leukemic Blast Cells Causing Multiplex Hand Necrosis in a Patient with Acute Myeloid Leukemia.

Intravascular Occlusion by Leukemic Blast Cells Causing Multiplex Hand Necrosis in a Patient with Acute Myeloid Leukemia.

Journal: Pathology oncology research : POR

Published: January 20, 2019

Clinical and laboratory characteristics of antithrombin deficiencies: A large cohort study from a single diagnostic center.

Clinical and laboratory characteristics of antithrombin deficiencies: A large cohort study from a single diagnostic center.

Journal: Thrombosis research

Published: July 27, 2017

Showing 1-12 of 24

Last Updated: 09/26/2026