Koczok K - Search Results

1

Genetic counselling legislation and practice in cancer in EU Member States.

McCrary JM, Van Valckenborgh E, Poirel HA, de Putter R, van Rooij J, Horgan D, Dierks ML, Antonova O, Brunet J, Chirita-Emandi A, Colas C, Dalmas M, Ehrencrona H, Grima C, Janavičius R, Klink B, Koczok K, Krajc M, Lace B, Leitsalu L, Mistrik M, Paneque M, Primorac D, Roetzer KM, Ronez J, Slámová L, Spanou E, Stamatopoulos K, Stoklosa T, Strang-Karlsson S, Szakszon K, Szczałuba K, Turner J, van Dooren MF, van Zelst-Stams WAG, Vassallo LM, Wadt KAW, Žigman T, Ripperger T, Genuardi M, Van den Bulcke M, Bergmann AK. McCrary JM, et al. Among authors: koczok k. Eur J Public Health. 2024 Aug 1;34(4):666-675. doi: 10.1093/eurpub/ckae093. Eur J Public Health. 2024. PMID: 38905592 Free PMC article.

2

Helsmoortel-Van der Aa Syndrome-Cardiothoracic and Ectodermal Manifestations in Two Patients as Further Support of a Previous Observation on Phenotypic Overlap with RASopathies.

Szabó TM, Balogh I, Ujfalusi A, Szűcs Z, Madar L, Koczok K, Bessenyei B, Csürke I, Szakszon K. Szabó TM, et al. Among authors: koczok k. Genes (Basel). 2022 Dec 15;13(12):2367. doi: 10.3390/genes13122367. Genes (Basel). 2022. PMID: 36553633 Free PMC article.

3

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

Madar L, Szakszon K, Pfliegler G, Szabó GP, Brúgós B, Ronen N, Papp J, Zahuczky K, Szakos E, Fekete G, Oláh É, Koczok K, Balogh I. Madar L, et al. Among authors: koczok k. J Biotechnol. 2019 Aug 10;301:105-111. doi: 10.1016/j.jbiotec.2019.05.012. Epub 2019 Jun 1. J Biotechnol. 2019. PMID: 31163209

4

Interfering effect of maternal cell contamination on invasive prenatal molecular genetic testing.

Koczok K, Gombos É, Madar L, Török O, Balogh I. Koczok K, et al. Prenat Diagn. 2018 Aug;38(9):713-719. doi: 10.1002/pd.5319. Epub 2018 Jul 11. Prenat Diagn. 2018. PMID: 29935118

5

Cytogenetic Investigation of Infertile Patients in Hungary: A 10-Year Retrospective Study.

Andó S, Koczok K, Bessenyei B, Balogh I, Ujfalusi A. Andó S, et al. Among authors: koczok k. Genes (Basel). 2022 Nov 10;13(11):2086. doi: 10.3390/genes13112086. Genes (Basel). 2022. PMID: 36360324 Free PMC article.

6

Molecular Analysis of Cystic Fibrosis Patients in Hungary - An Update to the Mutational Spectrum.

Ivády G, Koczok K, Madar L, Gombos E, Toth I, Gyori K, Balogh I. Ivády G, et al. Among authors: koczok k. J Med Biochem. 2015 Jan;34(1):46-51. doi: 10.2478/jomb-2014-0055. Epub 2014 Oct 8. J Med Biochem. 2015. PMID: 28356823 Free PMC article.

7

Mutational spectrum of smith-lemli-opitz syndrome patients in hungary.

Balogh I, Koczok K, Szabó GP, Török O, Hadzsiev K, Csábi G, Balogh L, Dzsudzsák E, Ajzner E, Szabó L, Csákváry V, Oláh AV. Balogh I, et al. Among authors: koczok k. Mol Syndromol. 2012 Nov;3(5):215-22. doi: 10.1159/000343923. Epub 2012 Nov 9. Mol Syndromol. 2012. PMID: 23293579 Free PMC article.

8

Detection of internal tandem duplications in the FLT3 gene by different electrophoretic methods.

Bubán T, Koczok K, Földesi R, Szabó G, Sümegi A, Tanyi M, Szerafin L, Udvardy M, Kappelmayer J, Antal-Szalmás P. Bubán T, et al. Among authors: koczok k. Clin Chem Lab Med. 2011 Nov 4;50(2):301-10. doi: 10.1515/CCLM.2011.762. Clin Chem Lab Med. 2011. PMID: 22053959

9

An Ultra-Rare Manifestation of an X-Linked Recessive Disorder: Duchenne Muscular Dystrophy in a Female Patient.

Szűcs Z, Pinti É, Haltrich I, Szén OP, Nagy T, Barta E, Méhes G, Bidiga L, Török O, Ujfalusi A, Koczok K, Balogh I. Szűcs Z, et al. Among authors: koczok k. Int J Mol Sci. 2022 Oct 28;23(21):13076. doi: 10.3390/ijms232113076. Int J Mol Sci. 2022. PMID: 36361862 Free PMC article.

10

Double Heterozygosity for Rare Deleterious Variants in the BRCA1 and BRCA2 Genes in a Hungarian Patient with Breast Cancer.

Madar L, Majoros V, Szűcs Z, Nagy O, Babicz T, Butz H, Patócs A, Balogh I, Koczok K. Madar L, et al. Among authors: koczok k. Int J Mol Sci. 2023 Oct 18;24(20):15334. doi: 10.3390/ijms242015334. Int J Mol Sci. 2023. PMID: 37895014 Free PMC article.

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