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Uncovering accurate prognostic markers for high-risk uveal melanoma through DNA methylation profiling.
Clin Transl Med. 2023 Jul;13(7):e1317. doi: 10.1002/ctm2.1317.
Clin Transl Med. 2023.
PMID: 37478301
Free PMC article.
No abstract available.
Admixed phenotype of NEDD4L associated periventricular nodular heterotopia: A case report.
Pecimonova M, Radvanszky J, Smolak D, Budis J, Lichvar M, Kristinova D, Rozova I, Turna J, Szemes T.
Pecimonova M, et al.
Medicine (Baltimore). 2021 Jun 4;100(22):e26136. doi: 10.1097/MD.0000000000026136.
Medicine (Baltimore). 2021.
PMID: 34087865
Free PMC article.
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Structural and Functional Impact of Seven Missense Variants of Phenylalanine Hydroxylase.
Pecimonova M, Kluckova D, Csicsay F, Reblova K, Krahulec J, Procházkova D, Skultety L, Kadasi L, Soltysova A.
Pecimonova M, et al.
Genes (Basel). 2019 Jun 15;10(6):459. doi: 10.3390/genes10060459.
Genes (Basel). 2019.
PMID: 31208052
Free PMC article.
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Functional and structural characterisation of 5 missense mutations of the phenylalanine hydroxylase.
Pecimonova M, Polak E, Csicsay F, Reblova K, Stojiljkovic M, Levarski Z, Skultety L, Kadasi L, Soltysova A.
Pecimonova M, et al.
Gen Physiol Biophys. 2017 Oct;36(4):361-371. doi: 10.4149/gpb_2017003. Epub 2017 Jun 27.
Gen Physiol Biophys. 2017.
PMID: 28653649
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