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Detailed genetic characteristics of an international large cohort of patients with Stargardt disease: ProgStar study report 8.
Fujinami K, Strauss RW, Chiang JP, Audo IS, Bernstein PS, Birch DG, Bomotti SM, Cideciyan AV, Ervin AM, Marino MJ, Sahel JA, Mohand-Said S, Sunness JS, Traboulsi EI, West S, Wojciechowski R, Zrenner E, Michaelides M, Scholl HPN; ProgStar Study Group; ProgStar Study Group. Fujinami K, et al. Among authors: sahel ja. Br J Ophthalmol. 2019 Mar;103(3):390-397. doi: 10.1136/bjophthalmol-2018-312064. Epub 2018 Jun 20. Br J Ophthalmol. 2019. PMID: 29925512 Free PMC article.
A proposal for an updated staging system for LCHADD retinopathy.
Wongchaisuwat N, Gillingham MB, Yang P, Everett L, Gregor A, Harding CO, Sahel JA, Nischal KK, Scanga HL, Black D, Vockley J, Arnold G, Pennesi ME. Wongchaisuwat N, et al. Among authors: sahel ja. Ophthalmic Genet. 2024 Apr;45(2):140-146. doi: 10.1080/13816810.2024.2303682. Epub 2024 Jan 30. Ophthalmic Genet. 2024. PMID: 38288966 Free PMC article.
[Ophthalmological research in Germany: evaluation by an international expert panel].
Ader M, Cursiefen C, Fauser S, Gliem M, Helbig H, Lagrèze W, Marshall J, Roesky C, Sahel JA, Schlötzer-Schrehard U, Sieving P, Ueffing M. Ader M, et al. Among authors: sahel ja. Ophthalmologie. 2024 May 22. doi: 10.1007/s00347-024-02043-3. Online ahead of print. Ophthalmologie. 2024. PMID: 38775988 German.
Fully Automated OCT-based Tissue Screening System.
Pi S, Ganjee R, Wang L, Arbuckle RK, Zhao C, Sahel JA, Wang B, Chen Y. Pi S, et al. Among authors: sahel ja. ArXiv [Preprint]. 2024 May 15:arXiv:2405.09601v1. ArXiv. 2024. PMID: 38800655 Free PMC article. Preprint.
Oral 8-aminoguanine against age-related retinal degeneration.
Chen Y, Vats A, Xi Y, Wolf-Johnston A, Clinger O, Arbuckle R, Dermond C, Li J, Stolze D, Sahel JA, Jackson E, Birder L. Chen Y, et al. Among authors: sahel ja. Res Sq [Preprint]. 2024 May 6:rs.3.rs-4022389. doi: 10.21203/rs.3.rs-4022389/v1. Res Sq. 2024. PMID: 38765984 Free PMC article. Preprint.
Early diagnosis and treatment by newborn screening (NBS) or family history is associated with improved visual outcomes for long-chain 3-hydroxyacylCoA dehydrogenase deficiency (LCHADD) chorioretinopathy.
Gillingham MB, Choi D, Gregor A, Wongchaisuwat N, Black D, Scanga HL, Nischal KK, Sahel JA, Arnold G, Vockley J, Harding CO, Pennesi ME. Gillingham MB, et al. Among authors: sahel ja. J Inherit Metab Dis. 2024 Apr 16. doi: 10.1002/jimd.12738. Online ahead of print. J Inherit Metab Dis. 2024. PMID: 38623632
640 results