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Results: 1 to 20 of 356

1.

Identify the signature genes for diagnose of uveal melanoma by weight gene co-expression network analysis.

Shi K, Bing ZT, Cao GQ, Guo L, Cao YN, Jiang HO, Zhang MX.

Int J Ophthalmol. 2015 Apr 18;8(2):269-74. doi: 10.3980/j.issn.2222-3959.2015.02.10. eCollection 2015.

PMID:
25938039
2.

Osteoporosis: Clinical Evaluation.

Lewiecki EM.

In: De Groot LJ, Beck-Peccoz P, Chrousos G, Dungan K, Grossman A, Hershman JM, Koch C, McLachlan R, New M, Rebar R, Singer F, Vinik A, Weickert MO, editors. Endotext [Internet]. South Dartmouth (MA): MDText.com, Inc.; 2000-.
2015 Feb 28.

3.

Sodium fluorescein use during intraoperative cystoscopy.

Doyle PJ, Lipetskaia L, Duecy E, Buchsbaum G, Wood RW.

Obstet Gynecol. 2015 Mar;125(3):548-50. doi: 10.1097/AOG.0000000000000675.

PMID:
25730214
4.

A Novel Mgp-Cre Knock-in Mouse Reveals an Anti-calcification/anti-stiffness Candidate Gene in the Trabecular Meshwork and Scleral Peripapillary Region.

Borras T, Smith MH, Buie LK.

Invest Ophthalmol Vis Sci. 2015 Feb 24. pii: IOVS-15-16460. doi: 10.1167/iovs.15-16460. [Epub ahead of print]

PMID:
25711639
5.

Osteogenesis imperfecta Type I caused by a novel mutation in the start codon of the COL1A1 gene in a Korean family.

Cho SY, Lee JH, Ki CS, Chang MS, Jin DK, Han HS.

Ann Clin Lab Sci. 2015 Winter;45(1):100-5.

PMID:
25696019
6.

Heterozygous mutation of c.3521C>T in COL1A1 may cause mild osteogenesis imperfecta/Ehlers-Danlos syndrome in a Chinese family.

Shi X, Lu Y, Wang Y, Zhang YA, Teng Y, Han W, Han Z, Li T, Chen M, Liu J, Fang F, Dou C, Ren X, Han J.

Intractable Rare Dis Res. 2015 Feb;4(1):49-53. doi: 10.5582/irdr.2014.01039.

7.

New antiepileptic medication linked to blue discoloration of the skin and eyes.

Clark S, Antell A, Kaufman K.

Ther Adv Drug Saf. 2015 Feb;6(1):15-9. doi: 10.1177/2042098614560736. Review.

8.

Cosmetic preservatives as therapeutic corneal and scleral tissue cross-linking agents.

Babar N, Kim M, Cao K, Shimizu Y, Kim SY, Takaoka A, Trokel SL, Paik DC.

Invest Ophthalmol Vis Sci. 2015 Jan 29;56(2):1274-82. doi: 10.1167/iovs.14-16035.

PMID:
25634979
9.

Dose-dependent collagen cross-linking of rabbit scleral tissue by blue light and riboflavin treatment probed by dynamic shear rheology.

Schuldt C, Karl A, Körber N, Koch C, Liu Q, Fritsch AW, Reichenbach A, Wiedemann P, Käs JA, Francke M, Iseli HP.

Acta Ophthalmol. 2014 Dec 16. doi: 10.1111/aos.12621. [Epub ahead of print]

PMID:
25516112
10.

Osteogenesis imperfecta and primary open angle glaucoma: genotypic analysis of a new phenotypic association.

Wallace DJ, Chau FY, Santiago-Turla C, Hauser M, Challa P, Lee PP, Herndon LW, Allingham RR.

Mol Vis. 2014 Aug 29;20:1174-81. eCollection 2014.

11.

Retinal biocompatibility of brilliant blue g with deuterated water for chromovitrectomy.

Badaró E, Moraes-Filho M, Maia M, Penha FM, Novais EA, Souza-Lima RA, Hirai F, Meyer CH, Farah ME, Rodrigues EB.

J Ophthalmic Vis Res. 2014 Apr;9(2):204-9.

12.

Two years' experience with denosumab for children with osteogenesis imperfecta type VI.

Hoyer-Kuhn H, Netzer C, Koerber F, Schoenau E, Semler O.

Orphanet J Rare Dis. 2014 Sep 26;9:145. doi: 10.1186/s13023-014-0145-1.

13.

Osteogenesis imperfecta--multi-systemic and life-long disease that affects whole family.

Primorac D, Anticević D, Barisić I, Hudetz D, Ivković A.

Coll Antropol. 2014 Jun;38(2):767-72. Review.

PMID:
25145021
14.

[Osteogenesis imperfecta].

Salzmann M, Krohn C, Berger N.

Orthopade. 2014 Aug;43(8):764-71. doi: 10.1007/s00132-013-2229-3. German.

PMID:
25116245
15.

Reduction of conjunctival fibrosis after trabeculectomy using topical α-lipoic acid in rabbit eyes.

Ekinci M, Cagatay HH, Ceylan E, Keles S, Koban Y, Gokce G, Huseyinoğlu U, Ozcan E, Oba ME.

J Glaucoma. 2014 Aug;23(6):372-9. doi: 10.1097/IJG.0000000000000052.

16.

What is new in genetics and osteogenesis imperfecta classification?

Valadares ER, Carneiro TB, Santos PM, Oliveira AC, Zabel B.

J Pediatr (Rio J). 2014 Nov-Dec;90(6):536-41. doi: 10.1016/j.jped.2014.05.003. Epub 2014 Jul 18.

17.

Osteogenesis imperfecta type I: A case report.

Ren J, Xu X, Jian X, Wang J.

Exp Ther Med. 2014 Jun;7(6):1535-1538. Epub 2014 Mar 31.

18.

Enrichment of pathogenic alleles in the brittle cornea gene, ZNF469, in keratoconus.

Lechner J, Porter LF, Rice A, Vitart V, Armstrong DJ, Schorderet DF, Munier FL, Wright AF, Inglehearn CF, Black GC, Simpson DA, Manson F, Willoughby CE.

Hum Mol Genet. 2014 Oct 15;23(20):5527-35. doi: 10.1093/hmg/ddu253. Epub 2014 Jun 3.

PMID:
24895405
19.

Spectroscopic measurements in scleritis: bluish-red or deep red?

Bannister NP, Wakefield MJ, Tatham A, Bugby SL, Molyneux PM, Prydal JI.

Br J Ophthalmol. 2014 Dec;98(12):1761-4. doi: 10.1136/bjophthalmol-2013-304086. Epub 2014 May 2.

PMID:
24795332
20.

A novel mild variant of osteogenesis imperfecta type I caused by a Gly1088Glu mutation in COL1A1.

Xia XY, Li WW, Li N, Wu QY, Cui YX, Li XJ.

Mol Med Rep. 2014 Jun;9(6):2187-90. doi: 10.3892/mmr.2014.2084. Epub 2014 Mar 28.

PMID:
24682174
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