Barbazetto I - Search Results

1

Atypical unilateral maculopathy associated with acute exudative polymorphous vitelliform maculopathy-like yellowish deposits.

Bruè C, Barbazetto I, Markomichelakis NN, Yannuzzi LA, Bailey Freund K, Kotsolis AI. Bruè C, et al. Among authors: barbazetto i. Retin Cases Brief Rep. 2012 Spring;6(2):135-8. doi: 10.1097/ICB.0b013e318234ccab. Retin Cases Brief Rep. 2012. PMID: 25390943

2

Peculiar manifestation of macular telangiectasia type 2.

Bruè C, Tseng JJ, Barbazetto I, Lima LH, Yannuzzi LA. Bruè C, et al. Among authors: barbazetto i. Retin Cases Brief Rep. 2011 Fall;5(4):309-12. doi: 10.1097/ICB.0b013e3181f66b8c. Retin Cases Brief Rep. 2011. PMID: 25390421

3

Long-term follow-up in enhanced s-cone syndrome.

Pachydaki SI, Bhatnagar PA, Barbazetto IA, Klaver CC, Freund BK, Yannuzzi LA. Pachydaki SI, et al. Among authors: barbazetto ia. Retin Cases Brief Rep. 2009 Spring;3(2):118-20. doi: 10.1097/ICB.0b013e31816c687e. Retin Cases Brief Rep. 2009. PMID: 25391051

4

Central serous chorioretinopathy and peripheral retinal neovascularization.

Barbazetto IA, Cinquini M, Takahashi BS, Yannuzzi LA. Barbazetto IA, et al. Retin Cases Brief Rep. 2009 Spring;3(2):224-7. doi: 10.1097/ICB.0b013e31816b31e3. Retin Cases Brief Rep. 2009. PMID: 25391082

5

Idiopathic Acute Exudative Polymorphous Vitelliform Maculopathy: Clinical Spectrum and Multimodal Imaging Characteristics.

Barbazetto I, Dansingani KK, Dolz-Marco R, Giovannini A, Piccolino FC, Agarwal A, Lima LH, Vianna RN, Yannuzzi LA. Barbazetto I, et al. Ophthalmology. 2018 Jan;125(1):75-88. doi: 10.1016/j.ophtha.2017.07.020. Epub 2017 Aug 23. Ophthalmology. 2018. PMID: 28844323

6

Autofluorescence of basal laminar drusen.

Meyerle CB, Smith RT, Barbazetto IA, Yannuzzi LA. Meyerle CB, et al. Retina. 2007 Oct;27(8):1101-6. doi: 10.1097/IAE.0b013e3181451617. Retina. 2007. PMID: 18040253 Free PMC article.

7

Pseudo-vitelliform macular detachment and cuticular drusen: exclusion of 6 candidate genes.

Barbazetto IA, Yannuzzi NA, Klais CM, Merriam JE, Zernant J, Peiretti E, Yannuzzi LA, Allikmets R. Barbazetto IA, et al. Ophthalmic Genet. 2007 Dec;28(4):192-7. doi: 10.1080/13816810701538596. Ophthalmic Genet. 2007. PMID: 18161617

8

Macular dystrophy in Heimler syndrome.

Lima LH, Barbazetto IA, Chen R, Yannuzzi LA, Tsang SH, Spaide RF. Lima LH, et al. Ophthalmic Genet. 2011 Jun;32(2):97-100. doi: 10.3109/13816810.2010.551797. Epub 2011 Mar 2. Ophthalmic Genet. 2011. PMID: 21366429 Free PMC article.

9

Phenotypic features of patients with NR2E3 mutations.

Pachydaki SI, Klaver CC, Barbazetto IA, Roy MS, Gouras P, Allikmets R, Yannuzzi LA. Pachydaki SI, et al. Among authors: barbazetto ia. Arch Ophthalmol. 2009 Jan;127(1):71-5. doi: 10.1001/archophthalmol.2008.534. Arch Ophthalmol. 2009. PMID: 19139342

10

Elastin rs2301995 polymorphism is not associated with polypoidal choroidal vasculopathy in caucasians.

Lima LH, Merriam JE, Freund KB, Barbazetto IA, Spaide RF, Yannuzzi LA, Allikmets R. Lima LH, et al. Ophthalmic Genet. 2011 Jun;32(2):80-2. doi: 10.3109/13816810.2010.544362. Epub 2011 Mar 10. Ophthalmic Genet. 2011. PMID: 21391811

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