Mark E Pennesi (M E Pennesi)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 6

Top Topics

Optical Coherence Tomography

Molecularly Imprinted

Top Venues

Ophthalmic genetics

Current eye research

BMC ophthalmology

Documenta ophthalmologica. Advances in ophthalmology

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

Publications

A Amato, W Tschetter, L Everett, S T Bailey, A K Lauer, P Yang, Mark E Pennesi
Partial rescue of the full-field electroretinogram in patients with RPE65-related retinal dystrophy following gene augmentation therapy with voretigene neparvovec-rzyl. Documenta ophthalmologica. Advances in ophthalmology (2024)
Mariana Matioli da Palma, Cristy Ku, Austin D Igelman, Amanda Burr, Liliya Shevchenko Sutherland, Celide Koerner, David Valle, Mark E Pennesi, Paul Yang
A possible ocular biomarker for response to hyperornithinemia in gyrate atrophy: the effect of pyridoxine, lysine, and arginine-restricted diet in a patient with advanced disease. Ophthalmic genetics (2022)
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)
Katie M Litts, Michalis Georgiou, Christopher S Langlo, Emily J Patterson, Rebecca R Mastey, Angelos Kalitzeos, Rachel E Linderman, Byron L Lam, Gerald A Fishman, Mark E Pennesi, Christine N Kay, William W Hauswirth, Michel Michaelides, Joseph Carroll
Interocular Symmetry of Foveal Cone Topography in Congenital Achromatopsia. Current eye research 45 (10) (2020)
Huber Martins Vasconcelos, Mauricio Enrique Vargas, Mark E Pennesi
Multimodal imaging of ring 14 syndrome associated maculopathy. Ophthalmic genetics 40 (6) (2019)
Maria F Shurygina, Maria A Parker, Catie L Schlechter, Rui Chen, Yumei Li, Richard G Weleber, Paul Yang, Mark E Pennesi
A case report of two siblings with Alstrom syndrome without hearing loss associated with two new ALMS1 variants. BMC ophthalmology 19 (1) (2019)