Jonathan Salvin
Alfred I. duPont Hospital for Children
14 Papers
29 Citations
Jonathan Salvin is an academic researcher from Alfred I. duPont Hospital for Children. The author has contributed to research in topics: Medicine & Strabismus. The author has an hindex of 7, co-authored 12 publications. Previous affiliations of Jonathan Salvin include Children's National Medical Center.
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Papers
Systematic approach to pediatric ocular trauma
TL;DR: This review broadens the understanding of the mechanisms, treatment, and prognostic indicators in pediatric ocular trauma to allow improved clinical care of these injuries.
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Update on retinopathy of prematurity: treatment options and outcomes.
TL;DR: This review offers an update on the screening and treatment guidelines, new treatment options, and short-term and long-term complications in ROP.
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Recessive GM3 synthase deficiency: Natural history, biochemistry, and therapeutic frontier.
Lauren E. Bowser,Millie Young,Olivia Wenger,Zineb Ammous,Karlla W. Brigatti,Vincent J Carson,Teresa Moser,James Deline,Kazuhiro Aoki,Thierry Morlet,Ethan M. Scott,Erik G. Puffenberger,Donna L. Robinson,Christine Hendrickson,Jonathan Salvin,Steven Gottlieb,Adam D. Heaps,Michael Tiemeyer,Kevin A. Strauss +18 more
TL;DR: These observations corroborate findings from transgenic mice which indicate that gangliosides might have a limited role in embryonic neurodevelopment but become vital for postnatal brain growth and function and have critical implications for the design and implementation ofganglioside restitution therapies.
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Ocular manifestations of Sturge-Weber syndrome.
TL;DR: The understanding of the pathogenesis and clinical manifestations of Sturge-Weber syndrome is presented and updated information on the treatment of SWS glaucoma and choroidal hemangioma is provided.
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Funduscopic examination and SD-OCT in detecting sickle cell retinopathy among pediatric patients.
Jing Jin,Robin E Miller,Jonathan Salvin,Sharon S. Lehman,Dorothy Hendricks,Amanda Friess,Lauren Libfraind +6 more
TL;DR: In this patient cohort SD-OCT showed that the severity of retinal change was associated with more severe sickle cell disease genotypes (SS and Sβ0), and the peripheral retina could be visualized on fundus examination but not easily imaged on SD- OCT, which had a higher detection rate and offered earlier diagnosis.
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