Found: 10
Select item for more details and to access through your institution.
In Vivo Quasi-Elastic Light Scattering Eye Scanner Detects Molecular Aging in Humans.
- Published in:
- 2020
- By:
- Publication type:
- journal article
IN VIVO ASSESSMENT OF MOLECULAR AGING BY QUASI-ELASTIC LIGHT SCATTERING IN HUMAN LENS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P1039, doi. 10.1016/j.jalz.2016.06.2156
- By:
- Publication type:
- Article
Detection of Alzheimer’s disease-linked changes in the lens by quasi-elastic light scattering ophthalmoscopy in young subjects with down syndrome.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P645, doi. 10.1016/j.jalz.2015.06.941
- By:
- Publication type:
- Article
Noninvasive detection of Alzheimer's disease Aβ pathology in the lenses of human subjects with Down syndrome
- Published in:
- 2012
- By:
- Publication type:
- Abstract
Down syndrome: a review of ocular manifestations.
- Published in:
- Therapeutic Advances in Ophthalmology, 2022, p. 1, doi. 10.1177/25158414221101718
- By:
- Publication type:
- Article
Down syndrome: a review of ocular manifestations.
- Published in:
- Therapeutic Advances in Ophthalmology, 2022, v. 14, p. 1, doi. 10.1177/25158414221101718
- By:
- Publication type:
- Article
Neuroimaging Findings in Patients With Down Syndrome and Nystagmus.
- Published in:
- 2016
- By:
- Publication type:
- Letter to the Editor
Optic Nerve Appearance in Patients With Down Syndrome.
- Published in:
- Journal of Pediatric Ophthalmology & Strabismus, 2013, v. 50, n. 1, p. 60, doi. 10.3928/01913913-20121214-01
- By:
- Publication type:
- Article
What's Your Diagnosis?
- Published in:
- Journal of Pediatric Ophthalmology & Strabismus, 2008, v. 45, n. 2, p. 76, doi. 10.3928/01913913-20080301-05
- By:
- Publication type:
- Article
Recessive variants in COL25A1 gene as novel cause of arthrogryposis multiplex congenita with ocular congenital cranial dysinnervation disorder.
- Published in:
- Human Mutation, 2022, v. 43, n. 4, p. 487, doi. 10.1002/humu.24333
- By:
- Publication type:
- Article