Lišková P - Search Results

1

Case report: A rare variant m.4135T>C in the MT-ND1 gene leads to Leber hereditary optic neuropathy and altered respiratory chain supercomplexes.

Rákosníková T, Kelifová S, Štufková H, Lokvencová K, Lišková P, Kousal B, Honzík T, Hansíková H, Martínek V, Tesařová M. Rákosníková T, et al. Among authors: liskova p. Front Genet. 2023 May 18;14:1182288. doi: 10.3389/fgene.2023.1182288. eCollection 2023. Front Genet. 2023. PMID: 37274791 Free PMC article.

2

Immunohistochemical characterization of cytokeratins in the abnormal corneal endothelium of posterior polymorphous corneal dystrophy patients.

Jirsova K, Merjava S, Martincova R, Gwilliam R, Ebenezer ND, Liskova P, Filipec M. Jirsova K, et al. Among authors: liskova p. Exp Eye Res. 2007 Apr;84(4):680-6. doi: 10.1016/j.exer.2006.12.006. Epub 2006 Dec 15. Exp Eye Res. 2007. PMID: 17289024

3

[Retinitis pigmentosa mimicking uveitis. A case report].

Szabó E, Brichová M, Lišková P, Svozílková P, Ríhová E. Szabó E, et al. Among authors: liskova p. Cesk Slov Oftalmol. 2013 Mar;69(1):32-6. Cesk Slov Oftalmol. 2013. PMID: 23822599 Free article. Czech.

4

Phenotype associated with the H626P mutation and other changes in the TGFBI gene in Czech families.

Liskova P, Klintworth GK, Bowling BL, Filipec M, Jirsova K, Tuft SJ, Bhattacharya SS, Hardcastle AJ, Ebenezer ND. Liskova P, et al. Ophthalmic Res. 2008;40(2):105-8. doi: 10.1159/000115325. Epub 2008 Feb 6. Ophthalmic Res. 2008. PMID: 18259096

5

[Collagen in the human cornea--types, location and role].

Jirsová K, Merjavá S, Lisková P. Jirsová K, et al. Among authors: liskova p. Cesk Slov Oftalmol. 2008 Jul;64(4):167-70. Cesk Slov Oftalmol. 2008. PMID: 18780658 Review. Czech. No abstract available.

6

Descemet membrane endothelial keratoplasty with a stromal rim (DMEK-S).

Studeny P, Farkas A, Vokrojova M, Liskova P, Jirsova K. Studeny P, et al. Among authors: liskova p. Br J Ophthalmol. 2010 Jul;94(7):909-14. doi: 10.1136/bjo.2009.165134. Epub 2009 Oct 22. Br J Ophthalmol. 2010. PMID: 19850580

7

Molecular genetic cause of X-linked retinitis pigmentosa in a Czech family.

Liskova P, Colclough T, Hart-Holden N, Chakarova CF, O'Grady A, Kondrova L, Skalicka P, Diblik P, Hardcastle AJ. Liskova P, et al. Acta Ophthalmol. 2011 Mar;89(2):e213-5. doi: 10.1111/j.1755-3768.2009.01802.x. Acta Ophthalmol. 2011. PMID: 20064120 Free article. No abstract available.

8

[Treatment of severe caustic injuries of the anterior segment of the eye with limbal stem cell transplantation, penetrating keratoplasty and amnionic membrane transplantation].

Cernák A, Cernák M, Lísková P. Cernák A, et al. Among authors: liskova p. Cesk Slov Oftalmol. 2002 Jan;58(1):16-20. Cesk Slov Oftalmol. 2002. PMID: 11852548 Slovak.

9

Study of p.N247S KERA mutation in a British family with cornea plana.

Liskova P, Hysi PG, Williams D, Ainsworth JR, Shah S, de la Chapelle A, Tuft SJ, Bhattacharya SS. Liskova P, et al. Mol Vis. 2007 Jul 27;13:1339-47. Mol Vis. 2007. PMID: 17679937

10

Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. Online.

Ramprasad VL, Ebenezer ND, Aung T, Rajagopal R, Yong VH, Tuft SJ, Viswanathan D, El-Ashry MF, Liskova P, Tan DT, Bhattacharya SS, Kumaramanickavel G, Vithana EN. Ramprasad VL, et al. Among authors: liskova p. Hum Mutat. 2007 May;28(5):522-3. doi: 10.1002/humu.9487. Hum Mutat. 2007. PMID: 17397048

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