Suchergebnisse - "Jacobson, Samuel G"

PubPharm (19)

1

Reserpine maintains photoreceptor survival in retinal ciliopathy by resolving proteostasis imbalance and ciliogenesis defects

enthalten in: eLife | 2023

von Chen, H. | Swaroop, M. | Papal, S. | +11

2

Mobility test to assess functional vision in dark-adapted patients with Leber congenital amaurosis

enthalten in: BMC ophthalmology | 2022

von Roman, A. | Cideciyan, A. | Wu, V. | +4

3

Intravitreal antisense oligonucleotide sepofarsen in Leber congenital amaurosis type 10 : a phase 1b/2 trial

enthalten in: Nature medicine | 2022

von Russell, S. | Drack, A. | Cideciyan, A. | +29

4

Durable vision improvement after a single treatment with antisense oligonucleotide sepofarsen : a case report

enthalten in: Nature medicine | 2021

von Cideciyan, A. | Jacobson, S. | Ho, A. | +7

5

Transient pupillary light reflex in CEP290- or NPHP5-associated Leber congenital amaurosis : Latency as a potential outcome measure of cone function

enthalten in: Vision research | 2020

von Krishnan, A. | Jacobson, S. | Roman, A. | +4

6

Treatment Potential for Macular Cone Vision in Leber Congenital Amaurosis Due to CEP290 or NPHP5 Mutations : Predictions From Artificial Intelligence

enthalten in: Investigative ophthalmology & visual science | 2019

von Sumaroka, A. | Garafalo, A. | Semenov, E. | +5

7

Leber Congenital Amaurosis (LCA) : Potential for Improvement of Vision

enthalten in: Investigative ophthalmology & visual science | 2019

von Cideciyan, A. | Jacobson, S.

8

Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defect

enthalten in: Nature medicine | 2019

von Cideciyan, A. | Jacobson, S. | Drack, A. | +24

CommentIn: Nat Med. 2019 Feb;25(2):198-199. - PMID 30718907

9

In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 Mutations

enthalten in: Cell reports | 2017

von Shimada, H. | Lu, Q. | Insinna-Kettenhofen, C. | +12

10

Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 Gene

enthalten in: Investigative ophthalmology & visual science | 2017

von Jacobson, S. | Cideciyan, A. | Sumaroka, A. | +10