Molinari A - Search Results

1

Variant c.2262A>C in DOCK9 Leads to Exon Skipping in Keratoconus Family.

Karolak JA, Rydzanicz M, Ginter-Matuszewska B, Pitarque JA, Molinari A, Bejjani BA, Gajecka M. Karolak JA, et al. Among authors: molinari a. Invest Ophthalmol Vis Sci. 2015 Dec;56(13):7687-90. doi: 10.1167/iovs.15-17538. Invest Ophthalmol Vis Sci. 2015. PMID: 26641546

2

Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32.

Gajecka M, Radhakrishna U, Winters D, Nath SK, Rydzanicz M, Ratnamala U, Ewing K, Molinari A, Pitarque JA, Lee K, Leal SM, Bejjani BA. Gajecka M, et al. Among authors: molinari a. Invest Ophthalmol Vis Sci. 2009 Apr;50(4):1531-9. doi: 10.1167/iovs.08-2173. Epub 2008 Nov 14. Invest Ophthalmol Vis Sci. 2009. PMID: 19011015 Free PMC article.

3

Sequence variants in COL4A1 and COL4A2 genes in Ecuadorian families with keratoconus.

Karolak JA, Kulinska K, Nowak DM, Pitarque JA, Molinari A, Rydzanicz M, Bejjani BA, Gajecka M. Karolak JA, et al. Among authors: molinari a. Mol Vis. 2011 Mar 30;17:827-43. Mol Vis. 2011. PMID: 21527998 Free PMC article.

4

Novel mutation and three other sequence variants segregating with phenotype at keratoconus 13q32 susceptibility locus.

Czugala M, Karolak JA, Nowak DM, Polakowski P, Pitarque J, Molinari A, Rydzanicz M, Bejjani BA, Yue BY, Szaflik JP, Gajecka M. Czugala M, et al. Among authors: molinari a. Eur J Hum Genet. 2012 Apr;20(4):389-97. doi: 10.1038/ejhg.2011.203. Epub 2011 Nov 2. Eur J Hum Genet. 2012. PMID: 22045297 Free PMC article.

5

Substitution at IL1RN and deletion at SLC4A11 segregating with phenotype in familial keratoconus.

Nowak DM, Karolak JA, Kubiak J, Gut M, Pitarque JA, Molinari A, Bejjani BA, Gajecka M. Nowak DM, et al. Among authors: molinari a. Invest Ophthalmol Vis Sci. 2013 Mar 1;54(3):2207-15. doi: 10.1167/iovs.13-11592. Invest Ophthalmol Vis Sci. 2013. PMID: 23462747

6

Variants in SKP1, PROB1, and IL17B genes at keratoconus 5q31.1-q35.3 susceptibility locus identified by whole-exome sequencing.

Karolak JA, Gambin T, Pitarque JA, Molinari A, Jhangiani S, Stankiewicz P, Lupski JR, Gajecka M. Karolak JA, et al. Among authors: molinari a. Eur J Hum Genet. 2017 Jan;25(1):73-78. doi: 10.1038/ejhg.2016.130. Epub 2016 Oct 5. Eur J Hum Genet. 2017. PMID: 27703147 Free PMC article.

7

Cytochrome P4501B1 mutations cause only part of primary congenital glaucoma in Ecuador.

Curry SM, Daou AG, Hermanns P, Molinari A, Lewis RA, Bejjani BA. Curry SM, et al. Among authors: molinari a. Ophthalmic Genet. 2004 Mar;25(1):3-9. doi: 10.1076/opge.25.1.3.28999. Ophthalmic Genet. 2004. PMID: 15255109

8

[Crocodile tears and retraction syndrome].

Molinari A. Molinari A. Klin Monbl Augenheilkd. 1996 Jan;208(1):56-7. doi: 10.1055/s-2008-1035168. Klin Monbl Augenheilkd. 1996. PMID: 8839346 German.

9

Reducing the Global Burden of Myopia by Delaying the Onset of Myopia and Reducing Myopic Progression in Children: The Academy's Task Force on Myopia.

Modjtahedi BS, Abbott RL, Fong DS, Lum F, Tan D; Task Force on Myopia. Modjtahedi BS, et al. Ophthalmology. 2021 Jun;128(6):816-826. doi: 10.1016/j.ophtha.2020.10.040. Epub 2020 Dec 30. Ophthalmology. 2021. PMID: 33388160 Review.

10

Bilateral Symmetric and Asymmetric Superior Rectus Recession for Patients with Dissociated Vertical Deviation.

Tibrewal S, Nguyen PTT, Ganesh S, Molinari A. Tibrewal S, et al. Among authors: molinari a. Asia Pac J Ophthalmol (Phila). 2019 May-Jun;8(3):218-223. doi: 10.22608/APO.2018415. Epub 2019 May 15. Asia Pac J Ophthalmol (Phila). 2019. PMID: 31090282 Free article.

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