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

Year Number of Results
1966 1
1983 1
1988 5
1989 1
1991 1
1992 1
1993 3
1994 1
1995 1
1996 2
1999 1
2000 2
2001 1
2002 1
2003 1
2006 3
2007 1
2008 2
2009 2
2010 2
2011 2
2013 2
2014 4
2015 1
2016 2
2017 2
2018 2
2019 1
2020 2
2023 2
2024 0

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50 results

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Page 1
Schnyder corneal dystrophy.
Weiss JS. Weiss JS. Curr Opin Ophthalmol. 2009 Jul;20(4):292-8. doi: 10.1097/ICU.0b013e32832b753e. Curr Opin Ophthalmol. 2009. PMID: 19398911 Review.
RECENT FINDINGS: Retrospective case series of 115 affected individuals from 34 SCD families identified since 1989 reports the clinical findings in a large cohort and the long-term visual morbidity of SCD. The configuration of the progressive corneal clouding is predictable …
RECENT FINDINGS: Retrospective case series of 115 affected individuals from 34 SCD families identified since 1989 reports the clinical findi …
The genetic tyrosinemias.
Scott CR. Scott CR. Am J Med Genet C Semin Med Genet. 2006 May 15;142C(2):121-6. doi: 10.1002/ajmg.c.30092. Am J Med Genet C Semin Med Genet. 2006. PMID: 16602095 Review.
It clinically presents with hyperkeratotic plaques on the hands and soles of the feet and photophobia due to deposition of tyrosine crystals within the cornea. Tyrosinemia Type III is an extremely rare disorder caused by a deficiency of 4-hydroxyphenylpyruvic dioxyg …
It clinically presents with hyperkeratotic plaques on the hands and soles of the feet and photophobia due to deposition of tyrosine cryst …
Development, structure, and bioengineering of the human corneal stroma: A review of collagen-based implants.
Tidu A, Schanne-Klein MC, Borderie VM. Tidu A, et al. Exp Eye Res. 2020 Nov;200:108256. doi: 10.1016/j.exer.2020.108256. Epub 2020 Sep 21. Exp Eye Res. 2020. PMID: 32971095 Free article. Review.
Bio-engineering technologies are currently used to produce biomimetic artificial corneas that should present structural, chemical, optical, and biomechanical properties close to the native tissue. These properties are mainly supported by the corneal stroma which accounts f …
Bio-engineering technologies are currently used to produce biomimetic artificial corneas that should present structural, chemical, optical, …
Corneal Manifestation in Patients with Infantile Nephropathic Cystinosis.
Kruse F, Keidel LF, Priglinger S, Luft N, Priglinger C. Kruse F, et al. Klin Monbl Augenheilkd. 2023 Mar;240(3):260-265. doi: 10.1055/a-2020-0926. Epub 2023 Jan 25. Klin Monbl Augenheilkd. 2023. PMID: 36696914 Review. English.
This causes dysfunction of cystinosin, a protein that transports cystine out of lysosomes, causing cystine crystals to accumulate in cells in most organ systems. While renal complications predominate in the early forms of cystinosis, corneal crystal accumulat …
This causes dysfunction of cystinosin, a protein that transports cystine out of lysosomes, causing cystine crystals to accumulate in …
Beyond Joints: a Review of Ocular Abnormalities in Gout and Hyperuricemia.
Sharon Y, Schlesinger N. Sharon Y, et al. Curr Rheumatol Rep. 2016 Jun;18(6):37. doi: 10.1007/s11926-016-0586-8. Curr Rheumatol Rep. 2016. PMID: 27138165 Review.
Gout results from an elevated body uric acid pool, which leads to deposition of monosodium urate (MSU) crystals, mainly in and around the joints. The MSU crystals trigger release of proinflammatory cytokines, such as interleukin (IL)-1beta, IL-6, and tumor necrosis …
Gout results from an elevated body uric acid pool, which leads to deposition of monosodium urate (MSU) crystals, mainly in and around …
Corneal crystals in nephropathic cystinosis: natural history and treatment with cysteamine eyedrops.
Gahl WA, Kuehl EM, Iwata F, Lindblad A, Kaiser-Kupfer MI. Gahl WA, et al. Mol Genet Metab. 2000 Sep-Oct;71(1-2):100-20. doi: 10.1006/mgme.2000.3062. Mol Genet Metab. 2000. PMID: 11001803 Review.
Moreover, the extent of corneal crystal accumulation reflects the course and severity of the disease itself, and the cornea is accessible to direct examination. ...In this natural history study, infants in the first year of life had absent or minimal corne …
Moreover, the extent of corneal crystal accumulation reflects the course and severity of the disease itself, and the cornea …
Paraproteinemic crystalline keratopathy.
Ormerod LD, Collin HB, Dohlman CH, Craft JL, Desforges JF, Albert DM. Ormerod LD, et al. Ophthalmology. 1988 Feb;95(2):202-12. doi: 10.1016/s0161-6420(88)33200-8. Ophthalmology. 1988. PMID: 3140156 Review.
A case of 16 years' duration was associated with an IgG kappa monoclonal gammopathy and recurrent uveitis. The corneal changes were unusually extensive and distributed throughout all corneal layers. ...Ultrastructurally, pleomorphic deposits were found in every c …
A case of 16 years' duration was associated with an IgG kappa monoclonal gammopathy and recurrent uveitis. The corneal changes were u …
Cholesteric liquid crystals in living matter.
Mitov M. Mitov M. Soft Matter. 2017 Jun 14;13(23):4176-4209. doi: 10.1039/c7sm00384f. Soft Matter. 2017. PMID: 28589190 Review.
Liquid crystals play an important role in biology because the combination of order and mobility is a basic requirement for self-organisation and structure formation in living systems. Cholesteric liquid crystals are omnipresent in living matter under both in vivo an …
Liquid crystals play an important role in biology because the combination of order and mobility is a basic requirement for self-organ …
Protein farnesyltransferase inhibitors.
Ayral-Kaloustian S, Salaski EJ. Ayral-Kaloustian S, et al. Curr Med Chem. 2002 May;9(10):1003-32. doi: 10.2174/0929867024606687. Curr Med Chem. 2002. PMID: 12733981 Review.
FTase has been implicated as a potential target in inhibiting the prenylation of a variety of proteins, thus in controlling varied disease states (e.g. cancer, neurofibromatosis, restenosis, viral hepatitis, bone resorption, parasitic infections, corneal inflammations, and …
FTase has been implicated as a potential target in inhibiting the prenylation of a variety of proteins, thus in controlling varied disease s …
Effects of long-term cysteamine treatment in patients with cystinosis.
Ariceta G, Giordano V, Santos F. Ariceta G, et al. Pediatr Nephrol. 2019 Apr;34(4):571-578. doi: 10.1007/s00467-017-3856-4. Epub 2017 Dec 19. Pediatr Nephrol. 2019. PMID: 29260317 Free PMC article. Review.
Patients with infantile nephropathic cystinosis, the most common and most severe clinical form of cystinosis, commonly present with renal Fanconi syndrome by 6-12 months of age, and without specific treatment, almost all will develop end-stage renal disease (ESRD) by 10-12 years …
Patients with infantile nephropathic cystinosis, the most common and most severe clinical form of cystinosis, commonly present with renal Fa …
50 results