Hawlina M - Search Results

1

SINGLE NUCLEOTIDE POLYMORPHISMS IN RETINAL DETACHMENT PATIENTS WITH AND WITHOUT PROLIFERATIVE VITREORETINOPATHY.

Lumi X, Jelen MM, Zupan A, Boštjančič E, Ravnik-Glavač M, Hawlina M, Glavač D. Lumi X, et al. Among authors: hawlina m. Retina. 2020 May;40(5):811-818. doi: 10.1097/IAE.0000000000002477. Retina. 2020. PMID: 30807515

2

Genotyping microarray (gene chip) for the ABCR (ABCA4) gene.

Jaakson K, Zernant J, Külm M, Hutchinson A, Tonisson N, Glavac D, Ravnik-Glavac M, Hawlina M, Meltzer MR, Caruso RC, Testa F, Maugeri A, Hoyng CB, Gouras P, Simonelli F, Lewis RA, Lupski JR, Cremers FP, Allikmets R. Jaakson K, et al. Among authors: hawlina m. Hum Mutat. 2003 Nov;22(5):395-403. doi: 10.1002/humu.10263. Hum Mutat. 2003. PMID: 14517951

3

Effect of tinted optical filters on visual acuity and contrast sensitivity in patients with inflammatory cystoid macular edema.

Valentincic NV, Berendschot TT, Hawlina M, Kraut A, Rothova A. Valentincic NV, et al. Among authors: hawlina m. Retina. 2007 Apr-May;27(4):483-9. doi: 10.1097/01.iae.0000243031.81022.a2. Retina. 2007. PMID: 17420703

4

Pattern electroretinography of larger stimulus field size and spectral-domain optical coherence tomography in patients with Stargardt disease.

Lenassi E, Jarc-Vidmar M, Glavac D, Hawlina M. Lenassi E, et al. Among authors: hawlina m. Br J Ophthalmol. 2009 Dec;93(12):1600-5. doi: 10.1136/bjo.2009.158725. Epub 2009 Jul 23. Br J Ophthalmol. 2009. PMID: 19628494

5

Absence of pathogenic mutations in VSX1 and SOD1 genes in patients with keratoconus.

Stabuc-Silih M, Strazisar M, Hawlina M, Glavac D. Stabuc-Silih M, et al. Among authors: hawlina m. Cornea. 2010 Feb;29(2):172-6. doi: 10.1097/ICO.0b013e3181aebf7a. Cornea. 2010. PMID: 20023586

6

Polymorphisms in COL4A3 and COL4A4 genes associated with keratoconus.

Stabuc-Silih M, Ravnik-Glavac M, Glavac D, Hawlina M, Strazisar M. Stabuc-Silih M, et al. Among authors: hawlina m. Mol Vis. 2009 Dec 20;15:2848-60. Mol Vis. 2009. PMID: 20029656 Free PMC article.

7

Genetics and clinical characteristics of keratoconus.

Stabuc-Silih M, Strazisar M, Ravnik-Glavac M, Hawlina M, Glavac D. Stabuc-Silih M, et al. Among authors: hawlina m. Acta Dermatovenerol Alp Pannonica Adriat. 2010;19(2):3-10. Acta Dermatovenerol Alp Pannonica Adriat. 2010. PMID: 20664914 Free article.

8

The value of two-field pattern electroretinogram in routine clinical electrophysiologic practice.

Lenassi E, Robson AG, Hawlina M, Holder GE. Lenassi E, et al. Among authors: hawlina m. Retina. 2012 Mar;32(3):588-99. doi: 10.1097/IAE.0b013e31822059ae. Retina. 2012. PMID: 21878848

9

Combination of retinitis pigmentosa and hearing loss caused by a novel mutation in PRPH2 and a known mutation in GJB2: importance for differential diagnosis of Usher syndrome.

Fakin A, Zupan A, Glavač D, Hawlina M. Fakin A, et al. Among authors: hawlina m. Vision Res. 2012 Dec 15;75:71-6. doi: 10.1016/j.visres.2012.07.011. Epub 2012 Jul 25. Vision Res. 2012. PMID: 22842402 Free article.

10

Fundus autofluorescence and optical coherence tomography in relation to visual function in Usher syndrome type 1 and 2.

Fakin A, Jarc-Vidmar M, Glavač D, Bonnet C, Petit C, Hawlina M. Fakin A, et al. Among authors: hawlina m. Vision Res. 2012 Dec 15;75:60-70. doi: 10.1016/j.visres.2012.08.017. Epub 2012 Sep 18. Vision Res. 2012. PMID: 23000274 Free article.

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