Maldonado Ramiro S (Ramiro S Maldonado)

Publication Activity (10 Years)

Years Active: 2021-2022
Publications (10 Years): 6

Top Topics

Metastatic Colorectal Cancer

Optical Coherence Tomography

Vascular Endothelial Growth Factor

Top Venues

Ophthalmic genetics

Retinal cases & brief reports

International journal of retina and vitreous

This page only lists publications with an associated author ORCID identifier.

Publications

Hailey Mair, Nicholas Fowler, Maria E Papatzanaki, Padmaja Sudhakar, Maldonado Ramiro S
Novel missense WFS1 variant causing autosomal dominant atypical Wolfram syndrome. Ophthalmic genetics 43 (4) (2022)
Christopher A Turski, Mitchell A Jacobs, Michelle M Abou-Jaoude, Nicholas H Fowler, Ryan Harpole, Emily Altman, John B Chadwell, Gabriel Kindl, Hayley R James, Shivani V Reddy, Maldonado Ramiro S
Short-term outcomes in patients with center-involving diabetic macular edema after a single dose of intravitreal bevacizumab. International journal of retina and vitreous 8 (1) (2022)
Jacobs Mitchell, May El-Rashedy, Nicholas Fowler, Belinda Shirkey, John Kitchens, Maldonado Ramiro S
Anatomical and functional outcomes of bevacizumab treatment in pediatric autosomal recessive bestrophinopathy. Retinal cases & brief reports (2022)
Mitchell Jacobs, El-Rashedy May, Fowler Nicholas, Shirkey Belinda, Kitchens John, Maldonado Ramiro S
Anatomical and functional outcomes of bevacizumab treatment in pediatric autosomal recessive bestrophinopathy. Retinal cases & brief reports (2022)
Nicholas H Fowler, May I El-Rashedy, Emad A Chishti, Craig W Vander Kooi, Maldonado Ramiro S
Multimodal imaging and genetic findings in a case of ARSG-related atypical Usher syndrome. Ophthalmic genetics 42 (3) (2021)
Austin D Igelman, Cristy Ku, Mariana Matioli da Palma, Michalis Georgiou, Elena R Schiff, Byron L Lam, Eeva-Marja Sankila, Jeeyun Ahn, Lindsey Pyers, Ajoy Vincent, Juliana Maria Ferraz Sallum, Wadih M Zein, Jin Kyun Oh, Maldonado Ramiro S, Joseph Ryu, Stephen H Tsang, Michael B Gorin, Andrew R Webster, Michel Michaelides, Paul Yang, Mark E Pennesi
Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome. Ophthalmic genetics 42 (6) (2021)