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Experimental Analysis of Tear Fluid and Its Processing for the Diagnosis of Multiple Sclerosis.
Sensors (Basel). 2023 Jun 1;23(11):5251. doi: 10.3390/s23115251.
Sensors (Basel). 2023.
PMID: 37299978
Free PMC article.
Native fluorescence of tear fluid as a tool for diagnostics of glaucoma.
Krajčíková K, Skirková M, Moravská M, Birková A, Tomečková V.
Krajčíková K, et al. Among authors: skirkova m.
RSC Adv. 2021 Mar 15;11(18):10842-10846. doi: 10.1039/d1ra00473e. eCollection 2021 Mar 10.
RSC Adv. 2021.
PMID: 35423590
Free PMC article.
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Associations of optical coherence tomography with disability and brain MRI volumetry in patients with multiple sclerosis.
Skirková M, Mikula P, Maretta M, Fedičová M, Vitková M, Frigová L, Szilasi J, Moravská M, Horňák M, Szilasiová J.
Skirková M, et al.
Neurol Neurochir Pol. 2022;56(4):326-332. doi: 10.5603/PJNNS.a2022.0022. Epub 2022 Mar 15.
Neurol Neurochir Pol. 2022.
PMID: 35289383
Free article.
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Answer to Finsterer about "Multisystem presentation of a homozygous POLG2 variant".
Dosekova P, Dubiel A, Karlowicz A, Zietkiewicz S, Rydzanicz M, Habalova V, Pienkowski VM, Skirkova M, Han V, Mosejova A, Gdovinova Z, Kaliszewska M, Tońska K, Szymanski MR, Skorvanek M, Ploski R.
Dosekova P, et al. Among authors: skirkova m.
Eur J Med Genet. 2020 May;63(5):103900. doi: 10.1016/j.ejmg.2020.103900. Epub 2020 Mar 9.
Eur J Med Genet. 2020.
PMID: 32165262
No abstract available.
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Whole exome sequencing identifies a homozygous POLG2 missense variant in an adult patient presenting with optic atrophy, movement disorders, premature ovarian failure and mitochondrial DNA depletion.
Dosekova P, Dubiel A, Karlowicz A, Zietkiewicz S, Rydzanicz M, Habalova V, Pienkowski VM, Skirkova M, Han V, Mosejova A, Gdovinova Z, Kaliszewska M, Tońska K, Szymanski MR, Skorvanek M, Ploski R.
Dosekova P, et al. Among authors: skirkova m.
Eur J Med Genet. 2020 Apr;63(4):103821. doi: 10.1016/j.ejmg.2019.103821. Epub 2019 Nov 26.
Eur J Med Genet. 2020.
PMID: 31778857
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