Szaflik JP - Search Results

1

Evidence against RAB40AL being the locus for Martin-Probst X-linked deafness-intellectual disability syndrome.

Ołdak M, Ścieżyńska A, Młynarski W, Borowiec M, Ruszkowska E, Szulborski K, Pollak A, Kosińska J, Mueller-Malesińska M, Stawiński P, Szaflik JP, Płoski R. Ołdak M, et al. Among authors: szaflik jp. Hum Mutat. 2014 Oct;35(10):1171-4. doi: 10.1002/humu.22620. Epub 2014 Aug 7. Hum Mutat. 2014. PMID: 25044830

2

Genetics of Meesmann corneal dystrophy: a novel mutation in the keratin 3 gene in an asymptomatic family suggests genotype-phenotype correlation.

Szaflik JP, Ołdak M, Maksym RB, Kamińska A, Pollak A, Udziela M, Płoski R, Szaflik J. Szaflik JP, et al. Among authors: szaflik j. Mol Vis. 2008 Sep 15;14:1713-8. Mol Vis. 2008. PMID: 18806880 Free PMC article.

3

Optical coherence tomography and in vivo confocal microscopy features of obstetric injury of the cornea.

Szaflik JP, Ołdak M, Kwiecień S, Udziela M, Szaflik J. Szaflik JP, et al. Among authors: szaflik j. Cornea. 2008 Oct;27(9):1070-3. doi: 10.1097/ICO.0b013e318172fbff. Cornea. 2008. PMID: 18812775

4

OCT and in vivo confocal microscopy of a pigmented corneal tumor-like lesion.

Szaflik JP, Oldak M, Ulinska M, Tesla P, Szaflik J. Szaflik JP, et al. Among authors: szaflik j. Ophthalmic Surg Lasers Imaging. 2009 Nov-Dec;40(6):586-8. doi: 10.3928/15428877-20091030-09. Ophthalmic Surg Lasers Imaging. 2009. PMID: 19928725

5

Phacoemulsification with corneal astigmatism correction with the use of a toric intraocular lens in a case of megalocornea.

Rękas M, Pawlik R, Kluś A, Różycki R, Szaflik JP, Ołdak M. Rękas M, et al. Among authors: szaflik jp. J Cataract Refract Surg. 2011 Aug;37(8):1546-50. doi: 10.1016/j.jcrs.2011.04.023. J Cataract Refract Surg. 2011. PMID: 21782100

6

Late-onset lattice corneal dystrophy without typical lattice lines caused by a novel mutation in the TGFBI gene.

Ołdak M, Szaflik JP, Ścieżyńska A, Udziela M, Maksym RB, Rymgayłło-Jankowska B, Hofmann-Rummelt C, Menzel-Severing J, Płoski R, Żarnowski T, Kruse FE, Szaflik J. Ołdak M, et al. Among authors: szaflik j, szaflik jp. Cornea. 2014 Mar;33(3):294-9. doi: 10.1097/ICO.0000000000000062. Cornea. 2014. PMID: 24473223

7

[Not only optic neuropathy: new molecular and clinical aspects of OPA1 gene mutations].

Ołdak M, Sciezyńska A, Szulborski K, Szaflik JP, Szaflik J. Ołdak M, et al. Among authors: szaflik j, szaflik jp. Klin Oczna. 2014;116(1):52-8. Klin Oczna. 2014. PMID: 25137924 Review. Polish.

8

Fuchs Endothelial Corneal Dystrophy: Strong Association with rs613872 Not Paralleled by Changes in Corneal Endothelial TCF4 mRNA Level.

Ołdak M, Ruszkowska E, Udziela M, Oziębło D, Bińczyk E, Ścieżyńska A, Płoski R, Szaflik JP. Ołdak M, et al. Among authors: szaflik jp. Biomed Res Int. 2015;2015:640234. doi: 10.1155/2015/640234. Epub 2015 Sep 16. Biomed Res Int. 2015. PMID: 26451375 Free PMC article.

9

Next-generation sequencing of ABCA4: High frequency of complex alleles and novel mutations in patients with retinal dystrophies from Central Europe.

Ścieżyńska A, Oziębło D, Ambroziak AM, Korwin M, Szulborski K, Krawczyński M, Stawiński P, Szaflik J, Szaflik JP, Płoski R, Ołdak M. Ścieżyńska A, et al. Among authors: szaflik j, szaflik jp. Exp Eye Res. 2016 Apr;145:93-99. doi: 10.1016/j.exer.2015.11.011. Epub 2015 Nov 22. Exp Eye Res. 2016. PMID: 26593885

10

[Fuchs endothelial corneal dystrophy and trinucleotide repeat expansion in TCF4--implications for diagnostics and therapy].

Oziębło D, Szaflik JP, Ołdak M. Oziębło D, et al. Among authors: szaflik jp. Klin Oczna. 2015;117(3):200-3. Klin Oczna. 2015. PMID: 26999947 Review. Polish.

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