S. Finzi

发表

Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity.

Xiaorong Liu, S. Maurer-Stroh, D. Mackey, 2016, The Journal of clinical investigation.

Founder mutations of CYP1B1 gene in patients with congenital glaucoma from the United States and Brazil

J. Haines, J. Wiggs, E. D. del Bono, 2004, Journal of Medical Genetics.

Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil

V. P. Costa, M. B. de Melo, S. Senthil, 2015, PloS one.

Multimodal image analysis of the retina in Hunter syndrome (mucopolysaccharidosis type II): Case report

C. Kim, M. Oyamada, S. L. Pimentel, 2018, Ophthalmic genetics.

Surgical Resection of Giant Papillae and Autologous Conjunctival Graft in Patients With Severe Vernal Keratoconjunctivitis and Giant Papillae

P. E. Dantas, M. Nishiwaki-Dantas, S. Finzi, 2000, Ophthalmic plastic and reconstructive surgery.

Impact of ERT and follow-up of 17 patients from the same family with a mild form of MPS II

C. Kim, C. G. Matas, D. Bertola, 2021, Clinics.

Molecular and clinical characterization of a patient with a chromosome 4p deletion, Wolf-Hirschhorn syndrome, and congenital glaucoma

J. Wiggs, S. Finzi, C. Pinto, 2001, Ophthalmic genetics.

Angiopoietin-1 is required for Schlemm’s canal development in mice and humans

Xiaorong Liu, D. Mackey, A. Hewitt, 2017, The Journal of clinical investigation.

Rho kinase inhibitors for glaucoma treatment

P. Challa, Remo Susanna Júnior, S. Finzi, 2015 .

Retinitis pigmentosa and nanophthalmos in a patient with attenuated Hunter’s syndrome

M. Oyamada, Thiago Gonçalves dos Santos Martins, Ana Luiza Fontes de Azevedo Costa, 2023, Documenta Ophthalmologica.

Efficacy of topical dorzolamide therapy for cystoid macular edema in a patient with MFRP-related nanophthalmos-retinitis pigmentosa-foveoschisis-optic disk drusen syndrome.

R. Susanna, W. Takahashi, Bianca N. Susanna, 2015, Retinal cases & brief reports.

Posterior Polar Cataract: Genetic Analysis of a Large Family

I. Maumenee, J. Sallum, O. Sundin, 2005, Ophthalmic genetics.

Hypotrichosis with juvenile macular dystrophy: a case report with molecular study.

R. Susanna, T. Young, S. Finzi, 2017, Arquivos brasileiros de oftalmologia.

[Efficacy study in vitro: assessment of the properties of resveratrol and resveratrol + N-acetyl-cysteine on proliferation and inhibition of collagen activity].

G. Zavattini, F. Marzatico, S. Giardina, 2010, Minerva ginecologica.

Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity.

Xiaorong Liu, S. Maurer-Stroh, D. Mackey, 2016, The Journal of clinical investigation.