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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 3
2003 2
2004 4
2005 12
2006 7
2007 9
2008 5
2009 7
2010 19
2011 26
2012 24
2013 35
2014 40
2015 39
2016 35
2017 33
2018 31
2019 41
2020 44
2021 59
2022 44
2023 40
2024 14

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507 results

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Page 1
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
Retinal Disorders.
Sahel JA, Banin E, Bennett J, Duncan JL, Roska B. Sahel JA, et al. Cold Spring Harb Perspect Med. 2024 Apr 2:a041728. doi: 10.1101/cshperspect.a041728. Online ahead of print. Cold Spring Harb Perspect Med. 2024. PMID: 38565268
Three-dimensional choroidal contour mapping in healthy population.
Arora S, Singh SR, Rosario B, Ibrahim MN, Selvam A, Zarnegar A, Harihar S, Sant V, Sahel JA, Vupparaboina KK, Chhablani J. Arora S, et al. Among authors: sahel ja. Sci Rep. 2024 Mar 14;14(1):6210. doi: 10.1038/s41598-024-56376-9. Sci Rep. 2024. PMID: 38485744 Free PMC article.
RAR Inhibitors Display Photo-Protective and Anti-Inflammatory Effects in A2E Stimulated RPE Cells In Vitro through Non-Specific Modulation of PPAR or RXR Transactivation.
Fontaine V, Boumedine T, Monteiro E, Fournié M, Gersende G, Sahel JA, Picaud S, Veillet S, Lafont R, Latil M, Dilda PJ, Camelo S. Fontaine V, et al. Among authors: sahel ja. Int J Mol Sci. 2024 Mar 6;25(5):3037. doi: 10.3390/ijms25053037. Int J Mol Sci. 2024. PMID: 38474284 Free PMC article.
Coding and non-coding variants in the ciliopathy gene CFAP410 cause early-onset non-syndromic retinal degeneration.
Sangermano R, Gupta P, Price C, Han J, Navarro J, Condroyer C, Place EM, Antonio A, Mukai S, Zanlonghi X, Sahel JA, Duncan JL, Pierce EA, Zeitz C, Audo I, Huckfeldt RM, Bujakowska KM. Sangermano R, et al. Among authors: sahel ja. Res Sq [Preprint]. 2024 Feb 9:rs.3.rs-3871956. doi: 10.21203/rs.3.rs-3871956/v1. Res Sq. 2024. PMID: 38405922 Free PMC article. Preprint.
Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophy.
Zeitz C, Navarro J, Azizzadeh Pormehr L, Méjécase C, Neves LM, Letellier C, Condroyer C, Albadri S, Amprou A, Antonio A, Ben-Yacoub T, Wohlschlegel J, Andrieu C, Serafini M, Bianco L, Antropoli A, Nassisi M, El Shamieh S, Chantot-Bastaraud S, Mohand-Saïd S, Smirnov V, Sahel JA, Del Bene F, Audo I. Zeitz C, et al. Among authors: sahel ja. Genet Med. 2024 Jan 28:101081. doi: 10.1016/j.gim.2024.101081. Online ahead of print. Genet Med. 2024. PMID: 38293907 Free article.
507 results