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Nanomedicine in Ophthalmology: From Bench to Bedside.
- Published in:
- Journal of Clinical Medicine, 2024, v. 13, n. 24, p. 7651, doi. 10.3390/jcm13247651
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- Publication type:
- Article
Characterization of the Interaction of Human γS Crystallin with Metal Ions and Its Effect on Protein Aggregation.
- Published in:
- Biomolecules (2218-273X), 2024, v. 14, n. 12, p. 1644, doi. 10.3390/biom14121644
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- Publication type:
- Article
Causes of visual impairment and blindness among Yemenis with diabetes: a hospital-based study.
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- Eastern Mediterranean Health Journal, 2011, v. 17, n. 11, p. 831, doi. 10.26719/2011.17.11.831
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- Publication type:
- Article
Causes of blindness in people aged 50 years and over: community-based versus hospital-based study.
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- Eastern Mediterranean Health Journal, 2010, v. 16, n. 9, p. 942, doi. 10.26719/2010.16.9.942
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- Publication type:
- Article
PDCA 循环管理联合延续护理在老年 白内障病人中的应用.
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- Chinese Nursing Research, 2023, v. 37, n. 14, p. 2643, doi. 10.12102/j.issn.1009-6493.2023.14.031
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- Publication type:
- Article
PUBLIC HEALTH EDUCATION USING SUPERCOURSE: A COMPUTER-BASED LEARNING RESOURCE FOR HEALTHCARE PROFESSIONALS IN THE SOUTHERN PROVINCE OF ZAMBIA.
- Published in:
- Public Health Reports, 2014, v. 129, n. 1, p. 100, doi. 10.1177/003335491412900116
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- Publication type:
- Article
Comparison of modification sites in glycated crystallin in vitro and in vivo.
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- Analytical & Bioanalytical Chemistry, 2015, v. 407, n. 9, p. 2557, doi. 10.1007/s00216-015-8487-7
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- Publication type:
- Article
A 16.7 kb deletion in Sipa1l3 is associated with juvenile cataract in mice.
- Published in:
- Mammalian Genome, 2017, v. 28, n. 11/12, p. 515, doi. 10.1007/s00335-017-9720-9
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- Publication type:
- Article
A novel spontaneous mutation of BCAR3 results in extrusion cataracts in CF#1 mouse strain.
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- Mammalian Genome, 2016, v. 27, n. 9/10, p. 451, doi. 10.1007/s00335-016-9653-8
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- Publication type:
- Article
A novel locus on canine chromosome 13 is associated with cataract in the Australian Shepherd breed of domestic dog.
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- Mammalian Genome, 2015, v. 26, n. 5/6, p. 257, doi. 10.1007/s00335-015-9562-2
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- Publication type:
- Article
Lens density tracking in mice by Scheimpflug imaging.
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- Mammalian Genome, 2013, v. 24, n. 7/8, p. 295, doi. 10.1007/s00335-013-9470-2
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- Publication type:
- Article
A spontaneous mutation in Srebf2 leads to cataracts and persistent skin wounds in the lens opacity 13 ( lop13) mouse.
- Published in:
- Mammalian Genome, 2011, v. 22, n. 11/12, p. 661, doi. 10.1007/s00335-011-9354-2
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- Publication type:
- Article
A deletion in a cis element of Foxe3 causes cataracts and microphthalmia in rct mice.
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- Mammalian Genome, 2011, v. 22, n. 11/12, p. 693, doi. 10.1007/s00335-011-9358-y
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- Publication type:
- Article
A 1-bp deletion in the γC-crystallin leads to dominant cataracts in mice.
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- Mammalian Genome, 2010, v. 21, n. 7/8, p. 361, doi. 10.1007/s00335-010-9275-5
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- Publication type:
- Article
Genetic and phenotypic analysis of Tcm, a mutation affecting early eye development.
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- Mammalian Genome, 2005, v. 16, n. 5, p. 332, doi. 10.1007/s00335-004-2444-7
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- Publication type:
- Article
Comparison of Nd:YAG laser (532 nm green) vs diode laser (810 nm) photocoagulation in the treatment of retinopathy of prematurity: an evaluation in terms of complications.
- Published in:
- 2020
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- Publication type:
- journal article
Risk factors for cataracts in systemic lupus erythematosus (SLE).
- Published in:
- Rheumatology International, 2015, v. 35, n. 4, p. 701, doi. 10.1007/s00296-014-3129-5
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- Publication type:
- Article
Vitamin E and risk of age-related cataract: a meta-analysis.
- Published in:
- Public Health Nutrition, 2015, v. 18, n. 15, p. 2804, doi. 10.1017/S1368980014003115
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- Publication type:
- Article
SkQ1 as a Tool for Controlling Accelerated Senescence Program: Experiments with OXYS Rats.
- Published in:
- Biochemistry (00062979), 2022, v. 87, n. 12/13, p. 1552, doi. 10.1134/S0006297922120124
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- Publication type:
- Article
Protein Aggregation and Cataract: Role of Age-Related Modifications and Mutations in α-Crystallins.
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- Biochemistry (00062979), 2022, v. 87, n. 3, p. 225, doi. 10.1134/S000629792203004X
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- Publication type:
- Article
Effect of Sorbitol on Alpha-Crystallin Structure and Function.
- Published in:
- Biochemistry (00062979), 2022, v. 87, n. 2, p. 131, doi. 10.1134/S0006297922020055
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- Publication type:
- Article
Crystallins as Important Pathogenic Targets for Accumulation of Structural Damages Resulting in Protein Aggregation and Cataract Development: Introduction to This Special Issue of Biochemistry (Moscow).
- Published in:
- Biochemistry (00062979), 2022, v. 87, n. 2, p. 87, doi. 10.1134/S0006297922020018
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- Publication type:
- Article
Artificial intelligence to detect referable diabetic retinopathy in a Chinese population in Hong Kong.
- Published in:
- Hong Kong Journal of Ophthalmology, 2023, v. 27, n. 1, p. 12, doi. 10.12809/hkjo-v27n1-355
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- Publication type:
- Article
Long-Lasting Thrombocytopenia and Senile Cataract.
- Published in:
- 2020
- Publication type:
- Case Study
Management of Bilateral Congenital and Juvenile Cataracts in a Low-Income Country: Patient Identification, Treatment Outcomes, and Follow Up.
- Published in:
- Children, 2024, v. 11, n. 9, p. 1064, doi. 10.3390/children11091064
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- Publication type:
- Article
Initial Effect of Recombinant Human Growth Hormone Treatment in a Patient with Löwe Syndrome.
- Published in:
- Children, 2023, v. 10, n. 7, p. 1166, doi. 10.3390/children10071166
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- Publication type:
- Article
Microcephaly, Short Stature, Intellectual Disability, Speech Absence and Cataract Are Associated with Novel Bi-Allelic Missense Variant in RTTN Gene: A Seckel Syndrome Case Report.
- Published in:
- Children, 2023, v. 10, n. 6, p. 1027, doi. 10.3390/children10061027
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- Publication type:
- Article
The Ophthalmic Manifestations of Down Syndrome.
- Published in:
- Children, 2023, v. 10, n. 2, p. 341, doi. 10.3390/children10020341
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- Publication type:
- Article
Molecular Genetic Analysis of Ukrainian Families with Congenital Cataracts.
- Published in:
- Children, 2023, v. 10, n. 1, p. 51, doi. 10.3390/children10010051
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- Publication type:
- Article
Screening, Diagnosis, and Treatment of Pediatric Ocular Diseases.
- Published in:
- Children, 2022, v. 9, n. 12, p. 1939, doi. 10.3390/children9121939
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- Publication type:
- Article
Successful renal transplantation following hemodialysis as bridging therapy in a patient with Fechtner syndrome: a case report and literature review.
- Published in:
- Renal Replacement Therapy, 2023, v. 9, n. 1, p. 1, doi. 10.1186/s41100-023-00507-x
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- Publication type:
- Article
The Effect of Pupil Dilation on Ocular Biometry Measurements in the Senile Cataractous Eyes.
- Published in:
- Online Turkish Journal of Health Sciences (OTJHS) / Online Türk Sağlık Bilimleri Dergisi, 2023, v. 8, n. 1, p. 74, doi. 10.26453/otjhs.1161706
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- Article
Human disease: an eye on RNA.
- Published in:
- 2011
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- Publication type:
- journal article
Prevalence, diagnoses and rehabilitation services related to severe dual sensory loss (DSL) in older persons: a cross-sectional study based on medical records.
- Published in:
- International Journal of Audiology, 2020, v. 59, n. 12, p. 921, doi. 10.1080/14992027.2020.1783003
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- Publication type:
- Article
Challenges in horizontal integration of eye care services into the pre-existing rural primary care structure: an operations research perspective from Nigeria.
- Published in:
- Family Medicine & Primary Care Review, 2017, v. 19, n. 4, p. 366, doi. 10.5114/fmpcr.2017.70811
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- Publication type:
- Article
Cataract progression after primary pars plana vitrectomy for uncomplicated rhegmatogenous retinal detachments in young adults.
- Published in:
- International Journal of Retina & Vitreous, 2024, v. 10, n. 1, p. 1, doi. 10.1186/s40942-024-00538-4
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- Publication type:
- Article
SUN'S UP! COVER UP!
- Published in:
- Journal of Family & Consumer Sciences, 1999, v. 91, n. 1, p. 92
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- Publication type:
- Article
Coculture with intraocular lens material-activated macrophages induces an inflammatory phenotype in lens epithelial cells.
- Published in:
- Journal of Biomaterials Applications, 2015, v. 29, n. 8, p. 1119, doi. 10.1177/0885328214552711
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- Publication type:
- Article
Fast in situ enzymatic gelation of PPO-PEO block copolymer for injectable intraocular lens in vivo.
- Published in:
- Journal of Biomaterials Applications, 2014, v. 28, n. 8, p. 1247, doi. 10.1177/0885328213505247
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- Publication type:
- Article
Ophthalmological involvement in wild‐type transthyretin amyloidosis: A multimodal imaging study.
- Published in:
- Journal of the Peripheral Nervous System, 2023, v. 28, n. 4, p. 586, doi. 10.1111/jns.12589
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- Publication type:
- Article
Genotype‐phenotype correlation in a novel ABHD12 mutation underlying PHARC syndrome.
- Published in:
- Journal of the Peripheral Nervous System, 2020, v. 25, n. 2, p. 112, doi. 10.1111/jns.12367
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- Publication type:
- Article
A complex homozygous mutation in ABHD12 responsible for PHARC syndrome discovered with NGS and review of the literature.
- Published in:
- Journal of the Peripheral Nervous System, 2017, v. 22, n. 2, p. 77, doi. 10.1111/jns.12216
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- Publication type:
- Article
Anterior subcapsular cataract formation with pupil sphincter tear after using massage device over the globe.
- Published in:
- 2022
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- Publication type:
- Letter to the Editor
Traumatic optic neuropathy secondary to acupuncture treatment for glaucoma: A case report.
- Published in:
- Journal of Acute Disease, 2018, v. 7, n. 3, p. 134, doi. 10.4103/2221-6189.236829
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- Publication type:
- Article
Acute lens-induced glaucomas: A review.
- Published in:
- Journal of Acute Disease, 2017, v. 6, n. 2, p. 47, doi. 10.12980/jad.6.2017JADWEB-2016-0065
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- Publication type:
- Article
Hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) and methyl-β-cyclodextrin (MβCD) down regulate caveolin expression in human lens epithelial cells (HLECs).
- Published in:
- Molecular Biology, 2007, v. 41, n. 6, p. 906, doi. 10.1134/S0026893307060064
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- Publication type:
- Article
A case of congenital cataracts with hypotrichosis caused by compound heterozygous variants in the LSS gene.
- Published in:
- 2024
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- Publication type:
- Case Study
Mutational spectrum in a Chinese cohort with congenital cataracts.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 9, p. 1, doi. 10.1002/mgg3.2196
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- Publication type:
- Article
Targeted gene sequencing of FYCO1 identified a novel mutation in a Pakistani family for autosomal recessive congenital cataract.
- Published in:
- Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 8, p. 1, doi. 10.1002/mgg3.1985
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- Publication type:
- Article
Congenital cataract: An ocular manifestation of classical homocystinuria.
- Published in:
- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 9, p. 1, doi. 10.1002/mgg3.1742
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- Publication type:
- Article