Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

21 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Clinical and Molecular Characterization of Nine Novel Antithrombin Mutations.
Kállai J, Gindele R, Pénzes-Daku K, Balogh G, Bogáti R, Bécsi B, Katona É, Oláh Z, Ilonczai P, Boda Z, Róna-Tas Á, Nemes L, Marton I, Bereczky Z. Kállai J, et al. Among authors: gindele r. Int J Mol Sci. 2024 Mar 1;25(5):2893. doi: 10.3390/ijms25052893. Int J Mol Sci. 2024. PMID: 38474138 Free PMC article.
High penetrance of inferior vena cava system atresia in severe thrombophilia caused by homozygous antithrombin Budapest 3 variant: Description of a new syndrome.
de la Morena-Barrio ME, Gindele R, Bravo-Pérez C, Ilonczai P, Zuazu I, Speker M, Oláh Z, Rodríguez-Sevilla JJ, Entrena L, Infante MS, de la Morena-Barrio B, García JM, Schlammadinger Á, Cifuentes-Riquelme R, Mora-Casado A, Miñano A, Padilla J, Vicente V, Corral J, Bereczky Z. de la Morena-Barrio ME, et al. Among authors: gindele r. Am J Hematol. 2021 Nov 1;96(11):1363-1373. doi: 10.1002/ajh.26304. Epub 2021 Aug 12. Am J Hematol. 2021. PMID: 34324211 Free article.
Founder Effects in Hereditary Hemorrhagic Telangiectasia.
Major T, Gindele R, Balogh G, Bárdossy P, Bereczky Z. Major T, et al. Among authors: gindele r. J Clin Med. 2021 Apr 14;10(8):1682. doi: 10.3390/jcm10081682. J Clin Med. 2021. PMID: 33919892 Free PMC article. Review.
Resolving Differential Diagnostic Problems in von Willebrand Disease, in Fibrinogen Disorders, in Prekallikrein Deficiency and in Hereditary Hemorrhagic Telangiectasia by Next-Generation Sequencing.
Gindele R, Kerényi A, Kállai J, Pfliegler G, Schlammadinger Á, Szegedi I, Major T, Szabó Z, Bagoly Z, Kiss C, Kappelmayer J, Bereczky Z. Gindele R, et al. Life (Basel). 2021 Mar 5;11(3):202. doi: 10.3390/life11030202. Life (Basel). 2021. PMID: 33807613 Free PMC article.
Age and Origin of the Founder Antithrombin Budapest 3 (p.Leu131Phe) Mutation; Its High Prevalence in the Roma Population and Its Association With Cardiovascular Diseases.
Bereczky Z, Gindele R, Fiatal S, Speker M, Miklós T, Balogh L, Mezei Z, Szabó Z, Ádány R. Bereczky Z, et al. Among authors: gindele r. Front Cardiovasc Med. 2021 Feb 5;7:617711. doi: 10.3389/fcvm.2020.617711. eCollection 2020. Front Cardiovasc Med. 2021. PMID: 33614741 Free PMC article.
Pitfalls of delaying the diagnosis of hereditary haemorrhagic telangiectasia.
Major T, Csobay-Novák C, Gindele R, Szabó Z, Bora L, Jóni N, Rácz T, Karosi T, Bereczky Z. Major T, et al. Among authors: gindele r. J Int Med Res. 2020 Feb;48(2):300060519860971. doi: 10.1177/0300060519860971. Epub 2019 Sep 11. J Int Med Res. 2020. PMID: 31510822 Free PMC article.
21 results