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Society of Dermatology Hospitalists supportive care guidelines for the management of Stevens-Johnson syndrome/toxic epidermal necrolysis in adults
Seminario-Vidal, Lucia, Daniela Kroshinsky, Stephen Malachowski, James Sun, Alina Markova, Thomas Beachkofsky, Benjamin Kaffenberger, et al. 2020. “Society of Dermatology Hospitalists Supportive Care Guidelines for the Management of Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis in Adults”. J Am Acad Dermatol 82 (6): 1553-67.
Reliability of Conjunctival Biopsy for Diagnosis of Ocular Mucous Membrane Pemphigoid: Redetermination of the Standard for Diagnosis and Outcomes of Previously Biopsy-Negative Patients
Anesi, Stephen, Laura Eggenschwiler, Mariantonia Ferrara, Pichaporn Artornsombudh, Marisa Walsh, and Stephen Foster. 2020. “Reliability of Conjunctival Biopsy for Diagnosis of Ocular Mucous Membrane Pemphigoid: Redetermination of the Standard for Diagnosis and Outcomes of Previously Biopsy-Negative Patients”. Ocul Immunol Inflamm, 1-8.
Nr2e3 is a genetic modifier that rescues retinal degeneration and promotes homeostasis in multiple models of retinitis pigmentosa
Li, Sujun, Shyamtanu Datta, Emily Brabbit, Zoe Love, Victoria Woytowicz, Kyle Flattery, Jessica Capri, et al. 2021. “Nr2e3 Is a Genetic Modifier That Rescues Retinal Degeneration and Promotes Homeostasis in Multiple Models of Retinitis Pigmentosa”. Gene Ther 28 (5): 223-41.
Low-carbohydrate-diet scores and the risk of primary open-angle glaucoma: data from three US cohorts
Hanyuda, Akiko, Bernard Rosner, Janey Wiggs, Walter Willett, Kazuo Tsubota, Louis Pasquale, and Jae Kang. 2020. “Low-Carbohydrate-Diet Scores and the Risk of Primary Open-Angle Glaucoma: Data from Three US Cohorts”. Eye (Lond) 34 (8): 1465-75.
Copy-number variation contributes 9% of pathogenicity in the inherited retinal degenerations
Zampaglione, Erin, Benyam Kinde, Emily Place, Daniel Navarro-Gomez, Matthew Maher, Farzad Jamshidi, Sherwin Nassiri, et al. 2020. “Copy-Number Variation Contributes 9% of Pathogenicity in the Inherited Retinal Degenerations”. Genet Med 22 (6): 1079-87.
MULTIMODAL IMAGING IN ACUTE RETINAL NECROSIS PRESENTING WITH MACULAR INVOLVEMENT
Wang, Jay, Yifan Lu, Lucia Sobrin, and Deeba Husain. 2022. “MULTIMODAL IMAGING IN ACUTE RETINAL NECROSIS PRESENTING WITH MACULAR INVOLVEMENT”. Retin Cases Brief Rep 16 (3): 347-50.
Expanding the phenotypic spectrum in RDH12-associated retinal disease
Scott, Hilary, Emily Place, Kevin Ferenchak, Erin Zampaglione, Naomi Wagner, Katherine Chao, Stephanie DiTroia, et al. 2020. “Expanding the Phenotypic Spectrum in RDH12-Associated Retinal Disease”. Cold Spring Harb Mol Case Stud 6 (1).
A combined RNA-seq and whole genome sequencing approach for identification of non-coding pathogenic variants in single families
Bronstein, Revital, Elizabeth Capowski, Sudeep Mehrotra, Alex Jansen, Daniel Navarro-Gomez, Mathew Maher, Emily Place, et al. 2020. “A Combined RNA-Seq and Whole Genome Sequencing Approach for Identification of Non-Coding Pathogenic Variants in Single Families”. Hum Mol Genet 29 (6): 967-79.
Prevalence and risk factors for visual impairment among elderly residents in 'homes for the aged' in India: the Hyderabad Ocular Morbidity in Elderly Study (HOMES)
Marmamula, Srinivas, Navya Rekha Barrenakala, Rajesh Challa, Thirupathi Reddy Kumbham, Satya Brahmanandam Modepalli, Ratnakar Yellapragada, Madhuri Bhakki, Rohit Khanna, and David Friedman. 2021. “Prevalence and Risk Factors for Visual Impairment Among Elderly Residents in ’homes for the Aged’ in India: The Hyderabad Ocular Morbidity in Elderly Study (HOMES)”. Br J Ophthalmol 105 (1): 32-36.