Kousal B - Search Results

1

Clinical and Genetic Study of X-Linked Juvenile Retinoschisis in the Czech Population.

Kousal B, Hlavata L, Vlaskova H, Dvorakova L, Brichova M, Dubska Z, Langrova H, Vincent AL, Dudakova L, Liskova P. Kousal B, et al. Genes (Basel). 2021 Nov 18;12(11):1816. doi: 10.3390/genes12111816. Genes (Basel). 2021. PMID: 34828422 Free PMC article.

2

[Minimal ocular findings in a patient with Best disease caused by the c.653G>A mutation in BEST1].

Kousal B, Chakarova F, Black GC, Ramsden S, Langrová H, Lisková P. Kousal B, et al. Cesk Slov Oftalmol. 2011 Nov-Dec;67(5-6):170-4. Cesk Slov Oftalmol. 2011. PMID: 22448417 Czech.

3

[Clinical findings in members of a Czech family with retinitis pigmentosa caused by the c.2426_2427delAG mutation in RPGR].

Kousal B, Skalická P, Diblík P, Kuthan P, Langrová H, Lišková P. Kousal B, et al. Cesk Slov Oftalmol. 2013 Mar;69(1):8-15. Cesk Slov Oftalmol. 2013. PMID: 23822596 Free article. Czech.

4

[Cytomegalovirus retinitis in HIV negative patients - retrospective study].

Beňová A, Brichová M, Svozílková P, Kousal B, Jeníčková D, Heissigerová J, Ríhová E. Beňová A, et al. Among authors: kousal b. Cesk Slov Oftalmol. 2013 Dec;69(6):227-34. Cesk Slov Oftalmol. 2013. PMID: 24697533 Free article. Czech.

5

Severe retinal degeneration in women with a c.2543del mutation in ORF15 of the RPGR gene.

Kousal B, Skalicka P, Valesova L, Fletcher T, Hart-Holden N, O'Grady A, Chakarova CF, Michaelides M, Hardcastle AJ, Liskova P. Kousal B, et al. Mol Vis. 2014 Sep 20;20:1307-17. eCollection 2014. Mol Vis. 2014. PMID: 25352739 Free PMC article.

6

[The molecular genetic and clinical findings in two probands with Stargardt disease].

Kousal B, Záhlava J, Vejvalková Š, Hejtmánková M, Lišková P. Kousal B, et al. Cesk Slov Oftalmol. 2014 Dec;70(6):228-33. Cesk Slov Oftalmol. 2014. PMID: 25640233 Free article. Czech.

7

[Clinical Tests Testing New Therapies for Stargardt Disease].

Kousal B, Ďuďáková Ľ, Hlavatá L, Lišková P. Kousal B, et al. Cesk Slov Oftalmol. 2016 Feb;72(1):293-7. Cesk Slov Oftalmol. 2016. PMID: 27041285 Free article. Review. Czech.

8

Phenotypic features of CRB1-associated early-onset severe retinal dystrophy and the different molecular approaches to identifying the disease-causing variants.

Kousal B, Dudakova L, Gaillyova R, Hejtmankova M, Diblik P, Michaelides M, Liskova P. Kousal B, et al. Graefes Arch Clin Exp Ophthalmol. 2016 Sep;254(9):1833-9. doi: 10.1007/s00417-016-3358-2. Epub 2016 Apr 25. Graefes Arch Clin Exp Ophthalmol. 2016. PMID: 27113771

9

[Gene Therapy for Inherited RETINAL AND OPTIC NERVE Disorders: Current Knowledge].

Ďuďáková Ľ, Kousal B, Kolářová H, Hlavatá L, Lišková P. Ďuďáková Ľ, et al. Among authors: kousal b. Cesk Slov Oftalmol. 2016 Fall;72(4):128-136. Cesk Slov Oftalmol. 2016. PMID: 27860478 Free article. Review. Czech.

10

[Preimplantation genetic diagnosis and monogenic inherited eye diseases].

Hlavatá L, Ďuďáková Ľ, Trková M, Soldátová I, Skalická P, Kousal B, Lišková P. Hlavatá L, et al. Among authors: kousal b. Cesk Slov Oftalmol. 2016 Fall;72(5):167-171. Cesk Slov Oftalmol. 2016. PMID: 28224801 Free article. Review. Czech.

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