Kjer B - Search Results

1

Genotype-phenotype associations in Danish patients with ocular and oculocutaneous albinism.

Kessel L, Kjer B, Lei U, Duno M, Grønskov K. Kessel L, et al. Among authors: kjer b. Ophthalmic Genet. 2021 Jun;42(3):230-238. doi: 10.1080/13816810.2021.1881979. Epub 2021 Feb 22. Ophthalmic Genet. 2021. PMID: 33612058

2

Trabeculotomy in juvenile primary open-angle glaucoma.

Kjer B, Kessing SV. Kjer B, et al. Ophthalmic Surg. 1993 Oct;24(10):663-8. Ophthalmic Surg. 1993. PMID: 8259243

3

Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.

Eiberg H, Hansen L, Kjer B, Hansen T, Pedersen O, Bille M, Rosenberg T, Tranebjaerg L. Eiberg H, et al. Among authors: kjer b. J Med Genet. 2006 May;43(5):435-40. doi: 10.1136/jmg.2005.034892. J Med Genet. 2006. PMID: 16648378 Free PMC article.

4

Refinement of the dominant optic atrophy locus (OPA1) to a 1.4-cM interval on chromosome 3q28-3q29, within a 3-Mb YAC contig.

Jonasdottir A, Eiberg H, Kjer B, Kjer P, Rosenberg T. Jonasdottir A, et al. Among authors: kjer b. Hum Genet. 1997 Jan;99(1):115-20. doi: 10.1007/s004390050323. Hum Genet. 1997. PMID: 9003507

5

Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I. Linkage analysis.

Eiberg H, Kjer B, Kjer P, Rosenberg T. Eiberg H, et al. Among authors: kjer b, kjer p. Hum Mol Genet. 1994 Jun;3(6):977-80. doi: 10.1093/hmg/3.6.977. Hum Mol Genet. 1994. PMID: 7951248

6

Surveillance for retinopathy of prematurity in a Danish country. Epidemiological experience over 20 years.

Fledelius HC, Kjer B. Fledelius HC, et al. Among authors: kjer b. Acta Ophthalmol Scand. 2004 Feb;82(1):38-41. doi: 10.1046/j.1600-0420.2003.00199.x. Acta Ophthalmol Scand. 2004. PMID: 14982044 Free article.

7

Dominant optic atrophy mapped to chromosome 3q region. II. Clinical and epidemiological aspects.

Kjer B, Eiberg H, Kjer P, Rosenberg T. Kjer B, et al. Among authors: kjer p. Acta Ophthalmol Scand. 1996 Feb;74(1):3-7. doi: 10.1111/j.1600-0420.1996.tb00672.x. Acta Ophthalmol Scand. 1996. PMID: 8689476

8

A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect.

Thiselton DL, Alexander C, Morris A, Brooks S, Rosenberg T, Eiberg H, Kjer B, Kjer P, Bhattacharya SS, Votruba M. Thiselton DL, et al. Among authors: kjer b. Hum Genet. 2001 Nov;109(5):498-502. doi: 10.1007/s004390100600. Epub 2001 Oct 3. Hum Genet. 2001. PMID: 11735024

9

Retinopathy of prematurity in a Copenhagen high-risk sample 1997-98. The allover surveillance for ROP appears more and more complete.

Fledelius HC, Kjer B, Rosenberg T. Fledelius HC, et al. Among authors: kjer b. Acta Ophthalmol Scand. 2000 Jun;78(3):362-5. doi: 10.1034/j.1600-0420.2000.078003362.x. Acta Ophthalmol Scand. 2000. PMID: 10893074 Free article.

10

Metastatic bacterial endophthalmitis. A report of four cases all leading to blindness.

Piczenik Y, Kjer B, Fledelius HC. Piczenik Y, et al. Among authors: kjer b. Acta Ophthalmol Scand. 1997 Aug;75(4):466-9. doi: 10.1111/j.1600-0420.1997.tb00416.x. Acta Ophthalmol Scand. 1997. PMID: 9374263 Free article.

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