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

Year Number of Results
1993 23
1999 2
2000 4
2001 1
2002 1
2003 3
2004 2
2005 2
2007 1
2008 3
2009 1
2010 1
2011 1
2012 3
2013 3
2015 1
2017 4
2018 5
2019 2
2020 1
2021 4
2022 3
2023 3
2024 8
2025 0

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Related Articles by Review for PMID: 20301591

34 results

Results by year

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Page 1
Achromatopsia.
Kohl S, Jägle H, Wissinger B, Zobor D. Kohl S, et al. 2004 Jun 24 [updated 2018 Sep 20]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2004 Jun 24 [updated 2018 Sep 20]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 20301591 Free Books & Documents. Review.
Gene Therapy for Achromatopsia.
Baxter MF, Borchert GA. Baxter MF, et al. Int J Mol Sci. 2024 Sep 9;25(17):9739. doi: 10.3390/ijms25179739. Int J Mol Sci. 2024. PMID: 39273686 Free PMC article. Review.
Rod Monochromatism (Achromatopsia).
Tsang SH, Sharma T. Tsang SH, et al. Adv Exp Med Biol. 2018;1085:119-123. doi: 10.1007/978-3-319-95046-4_24. Adv Exp Med Biol. 2018. PMID: 30578497 Review.
Diagnosis and Treatment Options for Achromatopsia: A Review of the Literature.
Pascual-Camps I, Barranco-Gonzalez H, Aviñó-Martínez J, Silva E, Harto-Castaño M. Pascual-Camps I, et al. J Pediatr Ophthalmol Strabismus. 2018 Mar 1;55(2):85-92. doi: 10.3928/01913913-20171117-01. Epub 2017 Dec 19. J Pediatr Ophthalmol Strabismus. 2018. PMID: 29257187 Review.
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia.
Solaki M, Baumann B, Reuter P, Andreasson S, Audo I, Ayuso C, Balousha G, Benedicenti F, Birch D, Bitoun P, Blain D, Bocquet B, Branham K, Català-Mora J, De Baere E, Dollfus H, Falana M, Giorda R, Golovleva I, Gottlob I, Heckenlively JR, Jacobson SG, Jones K, Jägle H, Janecke AR, Kellner U, Liskova P, Lorenz B, Martorell-Sampol L, Messias A, Meunier I, Belga Ottoni Porto F, Papageorgiou E, Plomp AS, de Ravel TJL, Reiff CM, Renner AB, Rosenberg T, Rudolph G, Salati R, Sener EC, Sieving PA, Stanzial F, Traboulsi EI, Tsang SH, Varsanyi B, Weleber RG, Zobor D, Stingl K, Wissinger B, Kohl S. Solaki M, et al. Hum Mutat. 2022 Jul;43(7):832-858. doi: 10.1002/humu.24371. Epub 2022 Apr 14. Hum Mutat. 2022. PMID: 35332618 Review.
Hermansky-Pudlak Syndrome.
Introne WJ, Huizing M, Malicdan MCV, O'Brien KJ, Gahl WA. Introne WJ, et al. 2000 Jul 24 [updated 2023 May 25]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2000 Jul 24 [updated 2023 May 25]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 20301464 Free Books & Documents. Review.
Achromatopsia: Genetics and Gene Therapy.
Michalakis S, Gerhardt M, Rudolph G, Priglinger S, Priglinger C. Michalakis S, et al. Mol Diagn Ther. 2022 Jan;26(1):51-59. doi: 10.1007/s40291-021-00565-z. Epub 2021 Dec 3. Mol Diagn Ther. 2022. PMID: 34860352 Free PMC article. Review.
Gene therapy in color vision deficiency: a review.
El Moussawi Z, Boueiri M, Al-Haddad C. El Moussawi Z, et al. Int Ophthalmol. 2021 May;41(5):1917-1927. doi: 10.1007/s10792-021-01717-0. Epub 2021 Feb 2. Int Ophthalmol. 2021. PMID: 33528822 Review.
[Achromatopsia].
Poloschek CM, Kohl S. Poloschek CM, et al. Ophthalmologe. 2010 Jun;107(6):571-80; quiz 581-2. doi: 10.1007/s00347-010-2178-8. Ophthalmologe. 2010. PMID: 20533046 Review. German.
Oculocutaneous Albinism Type 4.
Hayashi M, Suzuki T. Hayashi M, et al. 2005 Nov 17 [updated 2017 Sep 7]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2005 Nov 17 [updated 2017 Sep 7]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 20301683 Free Books & Documents. Review.
34 results