Hadzsiev K - Search Results

1

Increased prevalence of functional minor allele variants of drug metabolizing CYP2B6 and CYP2D6 genes in Roma population samples.

Weber A, Szalai R, Sipeky C, Magyari L, Melegh M, Jaromi L, Matyas P, Duga B, Kovesdi E, Hadzsiev K, Melegh B. Weber A, et al. Among authors: hadzsiev k. Pharmacol Rep. 2015 Jun;67(3):460-4. doi: 10.1016/j.pharep.2014.11.006. Epub 2014 Nov 27. Pharmacol Rep. 2015. PMID: 25933954

2

Identification of an NF1 Microdeletion with Optical Genome Mapping.

Büki G, Bekő A, Bödör C, Urbán P, Németh K, Hadzsiev K, Fekete G, Kehrer-Sawatzki H, Bene J. Büki G, et al. Among authors: hadzsiev k. Int J Mol Sci. 2023 Sep 1;24(17):13580. doi: 10.3390/ijms241713580. Int J Mol Sci. 2023. PMID: 37686382 Free PMC article.

3

Superimposed Mosaicism in the Form of Extremely Extended Segmental Plexiform Neurofibroma Caused by a Novel Pathogenic Variant in the NF1 Gene.

Veres K, Bene J, Hadzsiev K, Garami M, Pálla S, Happle R, Medvecz M, Szalai ZZ. Veres K, et al. Among authors: hadzsiev k. Int J Mol Sci. 2023 Jul 29;24(15):12154. doi: 10.3390/ijms241512154. Int J Mol Sci. 2023. PMID: 37569527 Free PMC article.

4

Microhomology-Mediated Break-Induced Replication: A Possible Molecular Mechanism of the Formation of a Large CNV in FBN1 Gene in a Patient with Marfan Syndrome.

Buki G, Hadzsiev K, Bene J. Buki G, et al. Among authors: hadzsiev k. Curr Mol Med. 2023;23(5):433-441. doi: 10.2174/1566524022666220428111943. Curr Mol Med. 2023. PMID: 37038253

5

Three-Year Follow-Up after Intrauterine mTOR Inhibitor Administration for Fetus with TSC-Associated Rhabdomyoma.

Maász A, Bodó T, Till Á, Molnár G, Masszi G, Labossa G, Herbert Z, Bene J, Hadzsiev K. Maász A, et al. Among authors: hadzsiev k. Int J Mol Sci. 2023 Aug 17;24(16):12886. doi: 10.3390/ijms241612886. Int J Mol Sci. 2023. PMID: 37629066 Free PMC article.

6

Observation of a Possible Successful Treatment of DEPDC5-Related Epilepsy with mTOR Inhibitor.

Hadzsiev K, Hegyi M, Fogarasi A, Bodó-Baltavári T, Zsigmond A, Maász A, Szabó A, Till Á. Hadzsiev K, et al. Neuropediatrics. 2023 Oct;54(5):344-346. doi: 10.1055/a-2104-1614. Epub 2023 Jun 1. Neuropediatrics. 2023. PMID: 37263295 Free PMC article.

7

[Neurofibromatosis-1 microdeletion syndrome.].

Büki G, Till Á, Zsigmond A, Bene J, Hadzsiev K. Büki G, et al. Among authors: hadzsiev k. Orv Hetil. 2022 Dec 18;163(51):2041-2051. doi: 10.1556/650.2022.32673. Print 2022 Dec 18. Orv Hetil. 2022. PMID: 36528827 Review. Hungarian.

8

Cognitive functioning and clinical characteristics of children with non-syndromic orofacial clefts: A case-control study.

Sándor-Bajusz KA, Dergez T, Molnár E, Hadzsiev K, Till Á, Zsigmond A, Vástyán A, Csábi G. Sándor-Bajusz KA, et al. Among authors: hadzsiev k. Front Psychol. 2023 Feb 28;14:1115304. doi: 10.3389/fpsyg.2023.1115304. eCollection 2023. Front Psychol. 2023. PMID: 36925595 Free PMC article.

9

The Importance of Genetic Testing in the Differential Diagnosis of Atypical TSC2-PKD1 Contiguous Gene Syndrome-Case Series.

Orosz P, Kollák Z, Pethő Á, Fogarasi A, Reusz G, Hadzsiev K, Szabó T. Orosz P, et al. Among authors: hadzsiev k. Children (Basel). 2023 Feb 22;10(3):420. doi: 10.3390/children10030420. Children (Basel). 2023. PMID: 36979978 Free PMC article.

10

Co-occurrence of neurofibromatosis type 1 and pseudoachondroplasia - a first case report.

Pálla S, Anker P, Farkas K, Plázár D, Kiss S, Marschalkó P, Szalai Z, Bene J, Hadzsiev K, Maróti Z, Kalmár T, Medvecz M. Pálla S, et al. Among authors: hadzsiev k. BMC Pediatr. 2023 Mar 8;23(1):110. doi: 10.1186/s12887-023-03920-7. BMC Pediatr. 2023. PMID: 36890482 Free PMC article.

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