M. A. T. Ferreira

Ophthalmologic Impairment and Intellectual Disability in a Girl Presenting Kenny-Caffey Syndrome Type 2

R. Ligabue-Braun, M. Fiegenbaum, R. Rosa, 2020, Journal of Pediatric Genetics.

WAGRO syndrome: a rare genetic condition associated with aniridia and additional ophthalmologic abnormalities.

R. Rosa, P. Zen, Y. Ferrão, 2019, Arquivos brasileiros de oftalmologia.

Retinal vascular tortuosity: Mechanisms and measurements

M. Vilela, C. E. Amaral, M. B. Ferreira, 2020, European journal of ophthalmology.

Increased levels of chitotriosidase in a patient with Alagille syndrome: association or coincidence?

R. Rosa, P. Zen, M. Floriani, 2018 .

Unusual features in a child with Marshall-Smith syndrome due to a novel NFIX variant: Evidence for an abnormal protein function

R. Ligabue-Braun, S. Rogatto, M. Fiegenbaum, 2021 .

Visual loss as first clinical manifestation of X-linked adrenoleukodystrophy

R. Rosa, P. Zen, R. C. Rosa, 2019 .