Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Nicholas Fowler"'
Autor:
Mitchell Jacobs, Nicholas Demas, Angela Hemesath, Christopher Turski, Nicholas Fowler, John Benjamin Chadwell, Alec Dupont, Victoria Kupper, Kishor Acharya, Sarah Robbins, Kory Heier, Ramiro Maldonado
Publikováno v:
Journal of Ophthalmology, Vol 2024 (2024)
Conclusion: In conclusion, 200 mg of caffeine elevated blood pressure after 2 h but did not impact the retinal VD. This underscores the intricate relationship between caffeine, blood pressure, and retinal vascular dynamics, prompting further explorat
Externí odkaz:
https://doaj.org/article/d705f12f5774414d86273ec37b5d8e8d
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 23, Iss , Pp 101136- (2021)
Purpose: We report the case of a 33-year-old male who presented with unilateral central serous retinopathy three days after the injection of a COVID-19 vaccine. Observations: A 33-year-old healthy Hispanic male referred to the ophthalmology service d
Externí odkaz:
https://doaj.org/article/0b6b1cd80ce64c6ab98bdc0baf5067ae
Publikováno v:
Journal of Clinical and Translational Science, Vol 3, Pp 16-17 (2019)
OBJECTIVES/SPECIFIC AIMS: The study aims to track and correlate ocular neuropathic symptoms, corneal sensitivity and dry-eye like pain, after scleral buckle and posterior vitrectomy surgeries. The goal is to identify a population of patients that rec
Externí odkaz:
https://doaj.org/article/beafbb1ae1044721945623091d4c8d55
Publikováno v:
Ophthalmic Genetics. 43:567-572
Autor:
Jacobs Mitchell, May El-Rashedy, Nicholas Fowler, Belinda Shirkey, John Kitchens, Ramiro S Maldonado
Publikováno v:
RETINAL Cases & Brief Reports.
Publikováno v:
Ophthalmic genetics. 43(4)
In contrast to the classic autosomal recessive Wolfram syndrome, Wolfram-like syndrome (WLS) is an autosomal dominant disease caused by heterozygous variants in the WFS1 gene. Here, we present deep phenotyping of a mother and son with a WFS1 variant
Autor:
Nicholas Fowler, Michael P. Williamson
Publikováno v:
SSRN Electronic Journal.
Publikováno v:
American Journal of Ophthalmology Case Reports
American Journal of Ophthalmology Case Reports, Vol 23, Iss, Pp 101136-(2021)
American Journal of Ophthalmology Case Reports, Vol 23, Iss, Pp 101136-(2021)
Purpose: We report the case of a 33-year-old male who presented with unilateral central serous retinopathy three days after the injection of a COVID-19 vaccine. Observations: A 33-year-old healthy Hispanic male referred to the ophthalmology service d
Publikováno v:
Ophthalmic Genet
BACKGROUND: Atypical Usher syndrome has recently been associated with arylsulfatase G (ARSG) variants. In these cases, characteristic findings include progressive sensorineural hearing loss (SNHL) without vestibular involvement and ring-shaped late-o
Publikováno v:
Journal of Clinical and Translational Science
OBJECTIVES/SPECIFIC AIMS: The study aims to track and correlate ocular neuropathic symptoms, corneal sensitivity and dry-eye like pain, after scleral buckle and posterior vitrectomy surgeries. The goal is to identify a population of patients that rec