Márta Czakó - Search Results

Year	Number of Results
2002	3
2003	2
2004	3
2005	4
2006	3
2007	3
2008	1
2009	1
2012	1
2014	4
2015	3
2016	1
2017	1
2018	2
2019	3
2020	1
2021	2
2022	1
2023	1
2024	0

1

Mutation spectrum of the SCN1A gene in a Hungarian population with epilepsy.

Till Á, Zima J, Fekete A, Bene J, Czakó M, Szabó A, Melegh B, Hadzsiev K. Till Á, et al. Among authors: czako m. Seizure. 2020 Jan;74:8-13. doi: 10.1016/j.seizure.2019.10.019. Epub 2019 Nov 8. Seizure. 2020. PMID: 31765958 Free article.

2

Xp11.2 Duplication in Females: Unique Features of a Rare Copy Number Variation.

Czakó M, Till Á, Zima J, Zsigmond A, Szabó A, Maász A, Melegh B, Hadzsiev K. Czakó M, et al. Front Genet. 2021 Apr 14;12:635458. doi: 10.3389/fgene.2021.635458. eCollection 2021. Front Genet. 2021. PMID: 33936165 Free PMC article.

3

Genotype-Phenotype Associations in Patients With Type-1, Type-2, and Atypical NF1 Microdeletions.

Büki G, Zsigmond A, Czakó M, Szalai R, Antal G, Farkas V, Fekete G, Nagy D, Széll M, Tihanyi M, Melegh B, Hadzsiev K, Bene J. Büki G, et al. Among authors: czako m. Front Genet. 2021 Jun 8;12:673025. doi: 10.3389/fgene.2021.673025. eCollection 2021. Front Genet. 2021. PMID: 34168676 Free PMC article.

4

Alpha-thalassemia/mental retardation syndrome in a 45,X male.

Kellermayer R, Czakó M, Kiss-László Z, Gyuris P, Kozári A, Melegh B, Kosztolányi G. Kellermayer R, et al. Among authors: czako m. Am J Med Genet A. 2005 Feb 1;132A(4):431-3. doi: 10.1002/ajmg.a.30499. Am J Med Genet A. 2005. PMID: 15633163 Review.

5

Possible Phenotypic Consequences of Structural Differences in Idic(15) in a Small Cohort of Patients.

Czakó M, Till Á, Szabó A, Ripszám R, Melegh B, Hadzsiev K. Czakó M, et al. Int J Mol Sci. 2019 Oct 5;20(19):4935. doi: 10.3390/ijms20194935. Int J Mol Sci. 2019. PMID: 31590400 Free PMC article.

6

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: czako m. Mol Syndromol. 2023 Apr;14(2):109-122. doi: 10.1159/000525976. Epub 2022 Oct 27. Mol Syndromol. 2023. PMID: 37064343 Free PMC article.

7

Rubinstein-Taybi syndrome 2 with cerebellar abnormality and neural tube defect.

Hadzsiev K, Gyorsok Z, Till A, Czakó M, Bartsch O. Hadzsiev K, et al. Among authors: czako m. Clin Dysmorphol. 2019 Jul;28(3):137-141. doi: 10.1097/MCD.0000000000000262. Clin Dysmorphol. 2019. PMID: 30789376 Free PMC article.

8

Revealing the impact of the Caucasus region on the genetic legacy of Romani people from genome-wide data.

Bánfai Z, Ádám V, Pöstyéni E, Büki G, Czakó M, Miseta A, Melegh B. Bánfai Z, et al. Among authors: czako m. PLoS One. 2018 Sep 10;13(9):e0202890. doi: 10.1371/journal.pone.0202890. eCollection 2018. PLoS One. 2018. PMID: 30199533 Free PMC article.

9

Congenital chylothorax in Opitz G/BBB syndrome.

Funke S, Kellermayer R, Czakó M, So J, Kosztolányi G, Ertl T. Funke S, et al. Among authors: czako m. Am J Med Genet A. 2006 May 15;140(10):1119-21. doi: 10.1002/ajmg.a.31224. Am J Med Genet A. 2006. PMID: 16619207 No abstract available.

10

Severe dystrophy in DiGeorge syndrome.

Rózsai B, Kiss A, Csábi G, Czakó M, Decsi T. Rózsai B, et al. Among authors: czako m. World J Gastroenterol. 2009 Mar 21;15(11):1391-3. doi: 10.3748/wjg.15.1391. World J Gastroenterol. 2009. PMID: 19294771 Free PMC article.

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