Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 341

1.

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.

PMID:
25145021
[PubMed - in process]
2.

[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
[PubMed - in process]
3.

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.

PMID:
25055213
[PubMed - in process]
4.

What is new in genetics and osteogenesis imperfecta classification?

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

J Pediatr (Rio J). 2014 Jul 18. pii: S0021-7557(14)00101-6. doi: 10.1016/j.jped.2014.05.003. [Epub ahead of print]

PMID:
25046257
[PubMed - as supplied by publisher]
Free Article
5.

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.

PMID:
24926339
[PubMed]
Free PMC Article
6.

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 Jun 3. pii: ddu253. [Epub ahead of print]

PMID:
24895405
[PubMed - as supplied by publisher]
7.

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 May 2. doi: 10.1136/bjophthalmol-2013-304086. [Epub ahead of print]

PMID:
24795332
[PubMed - as supplied by publisher]
8.

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
[PubMed - in process]
9.

Sickle cell disease with osteogenesis imperfecta.

Patil PL, Rao BV.

J Assoc Physicians India. 2013 Jun;61(6):415-7.

PMID:
24640211
[PubMed - indexed for MEDLINE]
10.

Malignant Uveal Schwannoma With Peripheral Nerve Extension in a 12-Week-Old Color-Dilute Labrador Retriever.

Duke FD, Teixeira LB, Galle LE, Green N, Dubielzig RR.

Vet Pathol. 2014 Feb 10. [Epub ahead of print]

PMID:
24513800
[PubMed - as supplied by publisher]
11.

A brown-eyed woman with blue discoloration of the sclera. Minocycline-induced hyperpigmentation.

Bosma JW, Veenstra J.

Neth J Med. 2014 Jan;72(1):33, 37. No abstract available.

PMID:
24457438
[PubMed - in process]
Free Article
12.

Alkaptonuric ochronosis: a clinical study from Ardabil, Iran.

Azami A, Maleki N, Tavosi Z.

Int J Rheum Dis. 2014 Mar;17(3):327-32. doi: 10.1111/1756-185X.12287. Epub 2014 Jan 22.

PMID:
24447956
[PubMed - in process]
13.

Congenital Keratoglobus with Multiple Cardiac Anomalies: A Case Presentation and Literature Review.

Ozer PA, Yalniz-Akkaya Z.

Semin Ophthalmol. 2014 Jan 10. [Epub ahead of print]

PMID:
24409942
[PubMed - as supplied by publisher]
14.

Four patients with Sillence type I osteogenesis imperfecta and mild bone fragility, complicated by left ventricular cardiac valvular disease and cardiac tissue fragility caused by type I collagen mutations.

Vandersteen AM, Lund AM, Ferguson DJ, Sawle P, Pollitt RC, Holder SE, Wakeling E, Moat N, Pope FM.

Am J Med Genet A. 2014 Feb;164A(2):386-91. doi: 10.1002/ajmg.a.36285. Epub 2013 Dec 5.

PMID:
24311407
[PubMed - indexed for MEDLINE]
15.

Three cases of alkaptonuria in one family in Mazandaran Province, Iran.

Yousefghahari B, Ahmadi A, Guran A.

Caspian J Intern Med. 2013 Spring;4(2):677-80.

PMID:
24009959
[PubMed]
Free PMC Article
16.

Osteogenesis imperfecta.

Ben Amor M, Rauch F, Monti E, Antoniazzi F.

Pediatr Endocrinol Rev. 2013 Jun;10 Suppl 2:397-405. Review.

PMID:
23858623
[PubMed - indexed for MEDLINE]
17.

Osteogenesis imperfecta Type VI with severe bony deformities caused by novel compound heterozygous mutations in SERPINF1.

Cho SY, Ki CS, Sohn YB, Kim SJ, Maeng SH, Jin DK.

J Korean Med Sci. 2013 Jul;28(7):1107-10. doi: 10.3346/jkms.2013.28.7.1107. Epub 2013 Jul 3.

PMID:
23853499
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

The effect of scleral spur identification methods on structural measurements by anterior segment optical coherence tomography.

Seager FE, Wang J, Arora KS, Quigley HA.

J Glaucoma. 2014 Jan;23(1):e29-38. doi: 10.1097/IJG.0b013e31829e55ae.

PMID:
23807354
[PubMed - indexed for MEDLINE]
19.

Osteogenesis imperfecta type V: clinical and radiographic manifestations in mutation confirmed patients.

Kim OH, Jin DK, Kosaki K, Kim JW, Cho SY, Yoo WJ, Choi IH, Nishimura G, Ikegawa S, Cho TJ.

Am J Med Genet A. 2013 Aug;161A(8):1972-9. doi: 10.1002/ajmg.a.36024. Epub 2013 Jun 26.

PMID:
23804581
[PubMed - indexed for MEDLINE]
20.

Unilateral open-angle glaucoma associated with the ipsilateral nevus of ota.

Magarasevic L, Abazi Z.

Case Rep Ophthalmol Med. 2013;2013:924937. doi: 10.1155/2013/924937. Epub 2013 Apr 9.

PMID:
23781367
[PubMed]
Free PMC Article

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk