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

Autor: Brúgós B; Division of Hematology, Department of Internal Medicine, University of Debrecen, Debrecen, Hungary.; Center of Expertise of Rare Diseases, University of Debrecen, Debrecen, Hungary., Simon Z; Division of Hematology, Department of Internal Medicine, University of Debrecen, Debrecen, Hungary., Méhes G; Department of Pathology, University of Debrecen, Debrecen, Hungary., Illés Á; Division of Hematology, Department of Internal Medicine, University of Debrecen, Debrecen, Hungary., Pfliegler G; Division of Hematology, Department of Internal Medicine, University of Debrecen, Debrecen, Hungary.; Center of Expertise of Rare Diseases, University of Debrecen, Debrecen, Hungary.

Publikováno v: Pathology oncology research : POR [Pathol Oncol Res] 2024 Aug 26; Vol. 30, pp. 1611785. Date of Electronic Publication: 2024 Aug 26 (Print Publication: 2024).

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

Autor: Tumiene B; Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania., Peters H; Dieter Scheffner Center for Medical Education and Educational Research, Dean's Office of Study Affairs, Charité - Universitätsmedizin, Berlin, Germany.; Association of Medical Schools in Europe e.V., Berlin, Germany., Melegh B; Department of Medical Genetics, and Szentagothai Research Center, University of Pecs, School of Medicine, Pecs, Hungary., Peterlin B; Clinical Institute of Genomic Medicine, University Medical Center Ljubljana, Ljubljana, Slovenia., Utkus A; Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.; Association of Medical Schools in Europe e.V., Berlin, Germany., Fatkulina N; Institute of Health Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania., Pfliegler G; Centre for Rare Diseases, Faculty of Medicine, University of Debrecen, Debrecen, Hungary., Graessner H; Institute for Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.; Centre for Rare Diseases, University Hospital Tübingen, Tübingen, Germany., Hermanns S; Institute for Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.; Centre for Rare Diseases, University Hospital Tübingen, Tübingen, Germany., Scarpa M; Regional Center for Rare Diseases, University Hospital of Udine, Udine, Italy., Blay JY; Centre Léon Berard, University Claude Bernard Lyon 1& Unicancer Lyon, Lyon, France., Ashton S; EURORDIS - Rare Diseases Europe, Paris, France., McKay L; Medics4RareDiseases, High Wycombe, England, UK., Baynam G; Telethon Kids Institute and the Faculty of Health and Medical Sciences, Division of Paediatrics, He University of Western Australia, Nedlands, WA, Australia. Gareth.Baynam@health.wa.gov.au.; Western Australian Register of Developmental Anomalies and Genetic Services of Western Australia, Perth, WA, Australia. Gareth.Baynam@health.wa.gov.au.; Rare Care Centre, Child and Adolescent Health Service, Perth, WA, Australia. Gareth.Baynam@health.wa.gov.au.

Publikováno v: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2022 Dec 19; Vol. 17 (1), pp. 441. Date of Electronic Publication: 2022 Dec 19.

[Interview with Dr. György Pfliegler by B. Király Györgyi].

Autor: Pfliegler G

Publikováno v: Orvosi hetilap [Orv Hetil] 2008 Apr 20; Vol. 149 (16), pp. 767.

Desmopressin And Bleeding Time In Patients With Cirrhosis

Autor: Rak, K., Harsfalvi, J., Tornai, I., Pfliegler, G., Boda, Z., Misz, M.

Publikováno v: British Medical Journal (Clinical Research Edition), 1986 Jan 01. 292(6513), 138-138.

Externí odkaz: https://www.jstor.org/stable/29521862

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

Autor: Gindele R; Division of Clinical Laboratory Science and Specialist Clinical Hemostasis Laboratory, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary., Kerényi A; Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.; Department of Laboratory Medicine, Faculty of Pharmacy, University of Debrecen, 4032 Debrecen, Hungary., Kállai J; Division of Clinical Laboratory Science and Specialist Clinical Hemostasis Laboratory, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary., Pfliegler G; Center of Expertise for Rare Diseases, Clinical Center, University of Debrecen, 4032 Debrecen, Hungary., Schlammadinger Á; Department of Internal Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary., Szegedi I; Division of Pediatric Hematology and Oncology, Department of Pediatrics, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary., Major T; Otorhinolaryngology and Head-Neck Surgery Division, Kenézy Gyula Teaching Hospital, University of Debrecen, 4032 Debrecen, Hungary., Szabó Z; Division of Clinical Laboratory Science and Specialist Clinical Hemostasis Laboratory, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary., Bagoly Z; Division of Clinical Laboratory Science and Specialist Clinical Hemostasis Laboratory, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary., Kiss C; Division of Pediatric Hematology and Oncology, Department of Pediatrics, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary., Kappelmayer J; Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary., Bereczky Z; Division of Clinical Laboratory Science and Specialist Clinical Hemostasis Laboratory, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.

Publikováno v: Life (Basel, Switzerland) [Life (Basel)] 2021 Mar 05; Vol. 11 (3). Date of Electronic Publication: 2021 Mar 05.