Pierrache LH - Search Results

1

The efficacy of microarray screening for autosomal recessive retinitis pigmentosa in routine clinical practice.

van Huet RA, Pierrache LH, Meester-Smoor MA, Klaver CC, van den Born LI, Hoyng CB, de Wijs IJ, Collin RW, Hoefsloot LH, Klevering BJ. van Huet RA, et al. Among authors: pierrache lh. Mol Vis. 2015 Apr 28;21:461-76. eCollection 2015. Mol Vis. 2015. PMID: 25999674 Free PMC article.

2

Mutations in AGBL5, Encoding α-Tubulin Deglutamylase, Are Associated With Autosomal Recessive Retinitis Pigmentosa.

Astuti GD, Arno G, Hull S, Pierrache L, Venselaar H, Carss K, Raymond FL, Collin RW, Faradz SM, van den Born LI, Webster AR, Cremers FP. Astuti GD, et al. Invest Ophthalmol Vis Sci. 2016 Nov 1;57(14):6180-6187. doi: 10.1167/iovs.16-20148. Invest Ophthalmol Vis Sci. 2016. PMID: 27842159

3

Visual Prognosis in USH2A-Associated Retinitis Pigmentosa Is Worse for Patients with Usher Syndrome Type IIa Than for Those with Nonsyndromic Retinitis Pigmentosa.

Pierrache LH, Hartel BP, van Wijk E, Meester-Smoor MA, Cremers FP, de Baere E, de Zaeytijd J, van Schooneveld MJ, Cremers CW, Dagnelie G, Hoyng CB, Bergen AA, Leroy BP, Pennings RJ, van den Born LI, Klaver CC. Pierrache LH, et al. Ophthalmology. 2016 May;123(5):1151-60. doi: 10.1016/j.ophtha.2016.01.021. Epub 2016 Feb 27. Ophthalmology. 2016. PMID: 26927203

4

Whole-Exome Sequencing Identifies Biallelic IDH3A Variants as a Cause of Retinitis Pigmentosa Accompanied by Pseudocoloboma.

Pierrache LHM, Kimchi A, Ratnapriya R, Roberts L, Astuti GDN, Obolensky A, Beryozkin A, Tjon-Fo-Sang MJH, Schuil J, Klaver CCW, Bongers EMHF, Haer-Wigman L, Schalij N, Breuning MH, Fischer GM, Banin E, Ramesar RS, Swaroop A, van den Born LI, Sharon D, Cremers FPM. Pierrache LHM, et al. Ophthalmology. 2017 Jul;124(7):992-1003. doi: 10.1016/j.ophtha.2017.03.010. Epub 2017 Apr 13. Ophthalmology. 2017. PMID: 28412069 Free PMC article.

5

Antisense Oligonucleotide-Based Splicing Correction in Individuals with Leber Congenital Amaurosis due to Compound Heterozygosity for the c.2991+1655A>G Mutation in CEP290.

Duijkers L, van den Born LI, Neidhardt J, Bax NM, Pierrache LHM, Klevering BJ, Collin RWJ, Garanto A. Duijkers L, et al. Among authors: pierrache lhm. Int J Mol Sci. 2018 Mar 7;19(3):753. doi: 10.3390/ijms19030753. Int J Mol Sci. 2018. PMID: 29518907 Free PMC article.

6

Extending the Spectrum of EYS-Associated Retinal Disease to Macular Dystrophy.

Pierrache LHM, Messchaert M, Thiadens AAHJ, Haer-Wigman L, de Jong-Hesse Y, van Zelst-Stams WAG, Collin RWJ, Klaver CCW, van den Born LI. Pierrache LHM, et al. Invest Ophthalmol Vis Sci. 2019 May 1;60(6):2049-2063. doi: 10.1167/iovs.18-25531. Invest Ophthalmol Vis Sci. 2019. PMID: 31074760

7

Straylight as an Indicator for Cataract Extraction in Patients with Retinal Dystrophy.

van Bree MCJ, Pierrache L, Zijlmans BLM, Reus NJ, van den Born LI, van den Berg TJTP. van Bree MCJ, et al. Ophthalmol Retina. 2017 Nov-Dec;1(6):531-544. doi: 10.1016/j.oret.2017.02.010. Epub 2017 Apr 5. Ophthalmol Retina. 2017. PMID: 31047448

8

LONGITUDINAL STUDY OF RPE65-ASSOCIATED INHERITED RETINAL DEGENERATIONS.

Pierrache LHM, Ghafaryasl B, Khan MI, Yzer S, van Genderen MM, Schuil J, Boonstra FN, Pott JWR, de Faber JTHN, Tjon-Fo-Sang MJH, Vermeer KA, Cremers FPM, Klaver CCW, van den Born LI. Pierrache LHM, et al. Retina. 2020 Sep;40(9):1812-1828. doi: 10.1097/IAE.0000000000002681. Retina. 2020. PMID: 32032261

9

Method for segmentation of the layers in the outer retina.

Novosel J, Vermeer KA, Pierrache L, Klaver CC, van den Born LI, van Vliet LJ. Novosel J, et al. Annu Int Conf IEEE Eng Med Biol Soc. 2015 Aug;2015:5646-9. doi: 10.1109/EMBC.2015.7319673. Annu Int Conf IEEE Eng Med Biol Soc. 2015. PMID: 26737573

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