Pikó H - Search Results

1

[Summary of the first Hungarian experiences with prenatal chromosomal microarray analysis and whole-exome sequencing].

Pikó H, Illés A, Nagy S, Beke A, Árvai K, Elekes T, Horváth E, Ferenczy M, Mosonyi P, Lukács V, Klujber V, Török O, Kiss Z, Tardy E, Tidrenczel Z, Tobiás B, Balla B, Lakatos P, Kósa J, Takács I. Pikó H, et al. Orv Hetil. 2024 Apr 7;165(14):523-530. doi: 10.1556/650.2024.33028. Print 2024 Apr 7. Orv Hetil. 2024. PMID: 38583142 Hungarian.

2

Genetic Factors Associated with the Development of Neuropathy in Type 2 Diabetes.

Tordai DZ, Hajdú N, Rácz R, Istenes I, Békeffy M, Vági OE, Kempler M, Körei AE, Tóbiás B, Illés A, Pikó H, Kósa JP, Árvai K, Papp M, Lakatos PA, Kempler P, Putz Z. Tordai DZ, et al. Among authors: piko h. Int J Mol Sci. 2024 Feb 2;25(3):1815. doi: 10.3390/ijms25031815. Int J Mol Sci. 2024. PMID: 38339094 Free PMC article.

3

Analysis of SIRT1 Gene SNPs and Clinical Characteristics in Medication-Related Osteonecrosis of the Jaw.

Bojtor B, Vaszilko M, Armos R, Tobias B, Podani J, Szentpeteri S, Balla B, Lengyel B, Piko H, Illes A, Kiss A, Putz Z, Takacs I, Kosa JP, Lakatos P. Bojtor B, et al. Among authors: piko h. Int J Mol Sci. 2024 Mar 25;25(7):3646. doi: 10.3390/ijms25073646. Int J Mol Sci. 2024. PMID: 38612458 Free PMC article.

4

Screening of premature ovarian insufficiency associated genes in Hungarian patients with next generation sequencing.

Illés A, Pikó H, Árvai K, Donka V, Szepesi O, Kósa J, Lakatos P, Beke A. Illés A, et al. Among authors: piko h. BMC Med Genomics. 2024 Apr 22;17(1):98. doi: 10.1186/s12920-024-01873-z. BMC Med Genomics. 2024. PMID: 38649916 Free PMC article.

5

Misfolding of fukutin-related protein (FKRP) variants in congenital and limb girdle muscular dystrophies.

Esapa CT, McIlhinney RAJ, Waite AJ, Benson MA, Mirzayan J, Piko H, Herczegfalvi Á, Horvath R, Karcagi V, Walter MC, Lochmüller H, Rizkallah PJ, Lu QL, Blake DJ. Esapa CT, et al. Among authors: piko h. Front Mol Biosci. 2023 Dec 7;10:1279700. doi: 10.3389/fmolb.2023.1279700. eCollection 2023. Front Mol Biosci. 2023. PMID: 38161385 Free PMC article.

6

Comparison of surgical strategies in the treatment of low-risk differentiated thyroid cancer.

Kiss A, Szili B, Bakos B, Ármós R, Putz Z, Árvai K, Kocsis-Deák B, Tobiás B, Balla B, Pikó H, Dank M, Kósa JP, Takács I, Lakatos P. Kiss A, et al. Among authors: piko h. BMC Endocr Disord. 2023 Jan 26;23(1):23. doi: 10.1186/s12902-023-01276-8. BMC Endocr Disord. 2023. PMID: 36703169 Free PMC article.

7

Clinical evaluation of rare copy number variations identified by chromosomal microarray in a Hungarian neurodevelopmental disorder patient cohort.

Lengyel A, Pinti É, Pikó H, Kristóf Á, Abonyi T, Némethi Z, Fekete G, Haltrich I. Lengyel A, et al. Among authors: piko h. Mol Cytogenet. 2022 Nov 1;15(1):47. doi: 10.1186/s13039-022-00623-z. Mol Cytogenet. 2022. PMID: 36320065 Free PMC article.

8

[Genotype-phenotype correlation in a newborn with de novo 3p25 deletion syndrome].

Sarkadi E, P Tardy E, Pikó H, Tidrenczel Z, Böjtös I, Kósa J, Simon J. Sarkadi E, et al. Among authors: piko h. Orv Hetil. 2022 Mar 20;163(12):478-483. doi: 10.1556/650.2022.32389. Print 2022 Mar 20. Orv Hetil. 2022. PMID: 35306482 Hungarian.

9

Chromosome 2q14.3 microdeletion encompassing CNTNAP5 gene in a patient carrying a complex chromosomal rearrangement.

Lengyel A, Pinti É, Nebral K, Pikó H, Ujfalusi A, Haas OA, Fekete G, Haltrich I. Lengyel A, et al. Among authors: piko h. J Genet. 2021;100:66. J Genet. 2021. PMID: 34553698 Free article.

10

[The significance of rare chromosomal abnormalities and fetoplacental mosaicism in prenatal diagnosis in the non-invasive prenatal testing era].

Tidrenczel Z, P Tardy E, Böjtös I, Sarkadi E, Simon J, Pikó H, Vermes G, Demeter J, Beke A. Tidrenczel Z, et al. Among authors: piko h. Orv Hetil. 2021 Jul 18;162(29):1156-1165. doi: 10.1556/650.2021.32098. Orv Hetil. 2021. PMID: 34274918 Hungarian.

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