Michael B Gorin
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Explore the profile of Michael B Gorin including associated specialties, affiliations and a list of published articles.
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104
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4010
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Recent Articles
1.
Miller J, Thompson B, Handa J, Luthert P, Chakravarthy U, Csaky K, et al.
Exp Eye Res
. 2025 Feb;
254:110304.
PMID: 39983974
Clinicians recognize the heterogeneity of age-related macular degeneration (AMD) in presentation, progression, and treatment response, as well as the challenges in distinguishing it from other macular degenerations. As part of...
2.
Good S, Adamus G, Gorin M, Jacquez J, Grossman J, Matsuura I, et al.
ACR Open Rheumatol
. 2024 Nov;
7(1):e11743.
PMID: 39511790
Objective: Autoimmune retinopathy and hydroxychloroquine (HCQ)-related retinal toxicity share many similarities, raising the possibility autoimmunity plays a role in HCQ retinopathy. The objective of this study is to determine whether...
3.
Pediatric patients with von Hippel-Lindau and hemangioblastomas treated successfully with belzutifan
Duan E, Robinson M, Davis C, Pruthi S, Shin C, Lewis M, et al.
Pediatr Blood Cancer
. 2024 Oct;
72(1):e31371.
PMID: 39415342
Hemangioblastoma is the most common tumor associated with von Hippel-Lindau (VHL), and are a leading cause of mortality. We present five pediatric patients with VHL-associated hemangioblastomas treated with belzutifan, a...
4.
Ramo J, Gorman B, Weng L, Jurgens S, Singhanetr P, Tieger M, et al.
medRxiv
. 2024 May;
PMID: 38766240
Central serous chorioretinopathy (CSC) is a fluid maculopathy whose etiology is not well understood. Abnormal choroidal veins in CSC patients have been shown to have similarities with varicose veins. To...
5.
Hitti-Malin R, Panneman D, Corradi Z, Boonen E, Astuti G, Dhaenens C, et al.
Biomolecules
. 2024 Mar;
14(3).
PMID: 38540785
Inherited macular dystrophies (iMDs) are a group of genetic disorders, which affect the central region of the retina. To investigate the genetic basis of iMDs, we used single-molecule Molecular Inversion...
6.
Brock D, Wang M, Hussain H, Rauch D, Marra M, Pennesi M, et al.
Hum Mol Genet
. 2024 Mar;
33(11):945-957.
PMID: 38453143
Inherited retinal diseases (IRDs) are a group of rare genetic eye conditions that cause blindness. Despite progress in identifying genes associated with IRDs, improvements are necessary for classifying rare autosomal...
7.
Daniels A, Chang E, Chew E, Gombos D, Gorin M, Shields C, et al.
Ophthalmology
. 2023 Dec;
131(5):622-633.
PMID: 38092079
Purpose: To develop guidelines for ocular surveillance and early intervention for individuals with von Hippel-Lindau (VHL) disease. Design: Systematic review of the literature. Participants: Expert panel of retina specialists and...
8.
Ng E, Kady N, Hu J, Dave A, Jiang Z, Pei J, et al.
Cells
. 2022 Nov;
11(21).
PMID: 36359858
Recessive Stargardt disease (STGD1) is an inherited retinopathy caused by mutations in the gene. The ABCA4 protein is a phospholipid-retinoid flippase in the outer segments of photoreceptors and the internal...
9.
10.
den Hollander A, Mullins R, Orozco L, Voigt A, Chen H, Strunz T, et al.
Exp Eye Res
. 2022 Sep;
225:109248.
PMID: 36108770
Genomic studies in age-related macular degeneration (AMD) have identified genetic variants that account for the majority of AMD risk. An important next step is to understand the functional consequences and...