Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1979 1
1988 1
1989 2
1991 1
1994 1
1995 1
1996 2
1997 1
1998 2
1999 2
2000 1
2001 8
2002 2
2003 4
2004 3
2005 3
2006 2
2007 2
2008 4
2009 6
2010 11
2011 8
2012 7
2013 9
2014 10
2015 7
2016 18
2017 11
2018 13
2019 8
2020 6
2021 13
2022 13
2023 9
2024 12

Text availability

Article attribute

Article type

Publication date

Search Results

180 results

Results by year

Filters applied: . Clear all
Page 1
Stargardt Disease.
Tsang SH, Sharma T. Tsang SH, et al. Adv Exp Med Biol. 2018;1085:139-151. doi: 10.1007/978-3-319-95046-4_27. Adv Exp Med Biol. 2018. PMID: 30578500 Review.
Stargardt disease (STGD) is one of the most common macular dystrophies in young adults. ...Some flecks are surrounded by a ring of decreased AF. Peripapillary sparing is one the characteristics of Stargardt disease, but this area can be involved in abo …
Stargardt disease (STGD) is one of the most common macular dystrophies in young adults. ...Some flecks are surrounded by a rin …
Therapy Approaches for Stargardt Disease.
Piotter E, McClements ME, MacLaren RE. Piotter E, et al. Biomolecules. 2021 Aug 9;11(8):1179. doi: 10.3390/biom11081179. Biomolecules. 2021. PMID: 34439845 Free PMC article. Review.
Despite being the most prevalent cause of inherited blindness in children, Stargardt disease is yet to achieve the same clinical trial success as has been achieved for other inherited retinal diseases. With an early age of onset and continual progression of disea …
Despite being the most prevalent cause of inherited blindness in children, Stargardt disease is yet to achieve the same clinic …
Stargardt disease: clinical features, molecular genetics, animal models and therapeutic options.
Tanna P, Strauss RW, Fujinami K, Michaelides M. Tanna P, et al. Br J Ophthalmol. 2017 Jan;101(1):25-30. doi: 10.1136/bjophthalmol-2016-308823. Epub 2016 Aug 4. Br J Ophthalmol. 2017. PMID: 27491360 Free PMC article. Review.
Stargardt disease (STGD1; MIM 248200) is the most prevalent inherited macular dystrophy and is associated with disease-causing sequence variants in the gene ABCA4 Significant advances have been made over the last 10 years in our understanding of both the clin …
Stargardt disease (STGD1; MIM 248200) is the most prevalent inherited macular dystrophy and is associated with disease- …
Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations.
Cremers FPM, Lee W, Collin RWJ, Allikmets R. Cremers FPM, et al. Prog Retin Eye Res. 2020 Nov;79:100861. doi: 10.1016/j.preteyeres.2020.100861. Epub 2020 Apr 9. Prog Retin Eye Res. 2020. PMID: 32278709 Free PMC article. Review.
The corresponding gene, ABCA4, was cloned in 1997, and variants were identified as the cause of autosomal recessive Stargardt disease (STGD1). Over the next two decades, variation in ABCA4 has been attributed to phenotypes other than the classically defined STGD1 or …
The corresponding gene, ABCA4, was cloned in 1997, and variants were identified as the cause of autosomal recessive Stargardt dise …
Gene therapy for inherited retinal diseases: progress and possibilities.
Hu ML, Edwards TL, O'Hare F, Hickey DG, Wang JH, Liu Z, Ayton LN. Hu ML, et al. Clin Exp Optom. 2021 May;104(4):444-454. doi: 10.1080/08164622.2021.1880863. Epub 2021 Mar 2. Clin Exp Optom. 2021. PMID: 33689657 Free article. Review.
Important photoreceptor IRDs include retinitis pigmentosa and Leber congenital amaurosis. Macular dystrophies include Stargardt and Best disease. Currently, IRDs are largely incurable but the landscape of treatment options is rapidly changing for these diseases whic …
Important photoreceptor IRDs include retinitis pigmentosa and Leber congenital amaurosis. Macular dystrophies include Stargardt and B …
Stargardt macular dystrophy and therapeutic approaches.
Fujinami K, Waheed N, Laich Y, Yang P, Fujinami-Yokokawa Y, Higgins JJ, Lu JT, Curtiss D, Clary C, Michaelides M. Fujinami K, et al. Br J Ophthalmol. 2024 Mar 20;108(4):495-505. doi: 10.1136/bjo-2022-323071. Br J Ophthalmol. 2024. PMID: 37940365 Free PMC article. Review.
Stargardt macular dystrophy (Stargardt disease; STGD1; OMIM 248200) is the most prevalent inherited macular dystrophy. ...Major advances in understanding both the clinical and molecular features, as well as the underlying pathophysiology, have culminated in m …
Stargardt macular dystrophy (Stargardt disease; STGD1; OMIM 248200) is the most prevalent inherited macular dystrophy. …
Macular dystrophies: clinical and imaging features, molecular genetics and therapeutic options.
Rahman N, Georgiou M, Khan KN, Michaelides M. Rahman N, et al. Br J Ophthalmol. 2020 Apr;104(4):451-460. doi: 10.1136/bjophthalmol-2019-315086. Epub 2019 Nov 8. Br J Ophthalmol. 2020. PMID: 31704701 Free PMC article. Review.
The developments in high-resolution multimodal retinal imaging have also transformed our ability to make accurate and more timely diagnoses and more sensitive quantitative assessment of disease progression, and allowed the design of optimised clinical trial endpoints for n …
The developments in high-resolution multimodal retinal imaging have also transformed our ability to make accurate and more timely diagnoses …
Structure and function of ABCA4 and its role in the visual cycle and Stargardt macular degeneration.
Molday RS, Garces FA, Scortecci JF, Molday LL. Molday RS, et al. Prog Retin Eye Res. 2022 Jul;89:101036. doi: 10.1016/j.preteyeres.2021.101036. Epub 2021 Dec 23. Prog Retin Eye Res. 2022. PMID: 34954332 Review.
Loss-of-function mutations in the gene encoding ABCA4 cause autosomal recessive Stargardt macular degeneration, also known as Stargardt disease (STGD1), and related autosomal recessive retinopathies characterized by impaired central vision and an accumulation …
Loss-of-function mutations in the gene encoding ABCA4 cause autosomal recessive Stargardt macular degeneration, also known as Star …
Stemming retinal regeneration with pluripotent stem cells.
Jin ZB, Gao ML, Deng WL, Wu KC, Sugita S, Mandai M, Takahashi M. Jin ZB, et al. Prog Retin Eye Res. 2019 Mar;69:38-56. doi: 10.1016/j.preteyeres.2018.11.003. Epub 2018 Nov 9. Prog Retin Eye Res. 2019. PMID: 30419340 Free article. Review.
Cell replacement therapy is a promising treatment for irreversible retinal cell death in diverse diseases, such as age-related macular degeneration (AMD), Stargardt's disease, retinitis pigmentosa (RP) and glaucoma. These diseases are all characterized by the degene …
Cell replacement therapy is a promising treatment for irreversible retinal cell death in diverse diseases, such as age-related macular degen …
Stargardt disease masquerades.
Ricca AM, Han IC, Sohn EH. Ricca AM, et al. Curr Opin Ophthalmol. 2021 May 1;32(3):214-224. doi: 10.1097/ICU.0000000000000750. Curr Opin Ophthalmol. 2021. PMID: 33653979 Review.
PURPOSE OF REVIEW: Stargardt disease is the most common inherited macular dystrophy but has a wide clinical spectrum, and several inherited macular dystrophies have phenotypic similarities that can make clinical diagnosis challenging. ...RECENT FINDINGS: Multimodal …
PURPOSE OF REVIEW: Stargardt disease is the most common inherited macular dystrophy but has a wide clinical spectrum, and seve …
180 results