Hadzsiev K - Search Results

1

Hyponatremia and sensorineural hearing loss in preterm infants.

Ertl T, Hadzsiev K, Vincze O, Pytel J, Szabo I, Sulyok E. Ertl T, et al. Among authors: hadzsiev k. Biol Neonate. 2001 Feb;79(2):109-12. doi: 10.1159/000047076. Biol Neonate. 2001. PMID: 11223652

2

NGS-Based Identification of Two Novel PCDH19 Mutations in Female Patients with Early-Onset Epilepsy.

Szalai R, Hadzsiev K, Till A, Fogarasi A, Bodo T, Buki G, Banfai Z, Bene J. Szalai R, et al. Among authors: hadzsiev k. Int J Mol Sci. 2024 May 24;25(11):5732. doi: 10.3390/ijms25115732. Int J Mol Sci. 2024. PMID: 38891919 Free PMC article.

3

[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.

4

Overlapping Interstitial Deletions of the Region 9q22.33 to 9q33.3 of Three Patients Allow Pinpointing Candidate Genes for Epilepsy and Cleft Lip and Palate.

Szalai R, Till A, Szabo A, Melegh B, Hadzsiev K, Czako M. Szalai R, et al. Among authors: hadzsiev k. Mol Syndromol. 2023 Apr;14(2):109-122. doi: 10.1159/000525976. Epub 2022 Oct 27. Mol Syndromol. 2023. PMID: 37064343 Free PMC article.

5

Importance and application of WES in fetal genetic diagnostics: Identification of novel ASPM mutation in a fetus with microcephaly.

Szalai R, Till A, Gyenesei A, Bene J, Hadzsiev K. Szalai R, et al. Among authors: hadzsiev k. Mol Genet Metab Rep. 2024 Jan 18;38:101056. doi: 10.1016/j.ymgmr.2024.101056. eCollection 2024 Mar. Mol Genet Metab Rep. 2024. PMID: 38469100 Free PMC article.

6

Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases.

Komlósi K, Maász A, Kisfali P, Hadzsiev K, Bene J, Melegh BI, Melegh B, Ablonczy M, Németh K, Fekete G. Komlósi K, et al. Among authors: hadzsiev k. JIMD Rep. 2013;9:105-111. doi: 10.1007/8904_2012_187. Epub 2012 Nov 2. JIMD Rep. 2013. PMID: 23430555 Free PMC article.

7

Excess of malignancies in grandparents of children with malformations? Short communication.

Hadzsiev K, Tárnok A, Kosztolányi G, Méhes K. Hadzsiev K, et al. Acta Biol Hung. 2006 Mar;57(1):137-40. doi: 10.1556/ABiol.57.2006.1.14. Acta Biol Hung. 2006. PMID: 16646533

8

IL23R single nucleotide polymorphisms could be either beneficial or harmful in ulcerative colitis.

Fischer S, Kövesdi E, Magyari L, Csöngei V, Hadzsiev K, Melegh B, Hegyi P, Sarlós P. Fischer S, et al. Among authors: hadzsiev k. World J Gastroenterol. 2017 Jan 21;23(3):447-454. doi: 10.3748/wjg.v23.i3.447. World J Gastroenterol. 2017. PMID: 28210080 Free PMC article.

9

Mitochondrial DNA 11777C>A mutation associated Leigh syndrome: case report with a review of the previously described pedigrees.

Hadzsiev K, Maasz A, Kisfali P, Kalman E, Gomori E, Pal E, Berenyi E, Komlosi K, Melegh B. Hadzsiev K, et al. Neuromolecular Med. 2010 Sep;12(3):277-84. doi: 10.1007/s12017-010-8115-9. Epub 2010 May 26. Neuromolecular Med. 2010. PMID: 20502985

10

[Molecular genetic diagnosis of neurofibromatosis type I].

Polgár N, Komlósi K, Hadzsiev K, Illés T, Melegh B. Polgár N, et al. Among authors: hadzsiev k. Orv Hetil. 2011 Mar 13;152(11):415-9. doi: 10.1556/OH.2011.29059. Orv Hetil. 2011. PMID: 21362601 Hungarian.

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