Rosenberg T - Search Results

1

Novel rhodopsin mutation (M216R) in a Danish family with autosomal dominant retinitis pigmentosa.

Haim M, Grundmann K, Gal A, Rosenberg T. Haim M, et al. Among authors: rosenberg t. Ophthalmic Genet. 1996 Dec;17(4):193-7. doi: 10.3109/13816819609057893. Ophthalmic Genet. 1996. PMID: 9010870

2

A population survey of retinitis pigmentosa and allied disorders in Denmark. Completeness of registration and quality of data.

Haim M, Holm NV, Rosenberg T. Haim M, et al. Among authors: rosenberg t. Acta Ophthalmol (Copenh). 1992 Apr;70(2):165-77. doi: 10.1111/j.1755-3768.1992.tb04120.x. Acta Ophthalmol (Copenh). 1992. PMID: 1609564

3

Prevalence of retinitis pigmentosa and allied disorders in Denmark. I Main results.

Haim M, Holm NV, Rosenberg T. Haim M, et al. Among authors: rosenberg t. Acta Ophthalmol (Copenh). 1992 Apr;70(2):178-86. doi: 10.1111/j.1755-3768.1992.tb04121.x. Acta Ophthalmol (Copenh). 1992. PMID: 1609565

4

Retinitis pigmentosa and allied disorders in Denmark. IV. Ophthalmic features in systemic and non-systemic cases.

Haim M, Rosenberg T. Haim M, et al. Among authors: rosenberg t. Acta Ophthalmol (Copenh). 1993 Oct;71(5):597-605. doi: 10.1111/j.1755-3768.1993.tb04648.x. Acta Ophthalmol (Copenh). 1993. PMID: 8109205

5

Autosomal dominant stationary night-blindness. A large family rediscovered.

Rosenberg T, Haim M, Piczenik Y, Simonsen SE. Rosenberg T, et al. Acta Ophthalmol (Copenh). 1991 Dec;69(6):694-702. doi: 10.1111/j.1755-3768.1991.tb02046.x. Acta Ophthalmol (Copenh). 1991. PMID: 1789082

6

Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindness.

Gal A, Orth U, Baehr W, Schwinger E, Rosenberg T. Gal A, et al. Among authors: rosenberg t. Nat Genet. 1994 May;7(1):64-8. doi: 10.1038/ng0594-64. Nat Genet. 1994. PMID: 8075643

7

A ninth locus (RP18) for autosomal dominant retinitis pigmentosa maps in the pericentromeric region of chromosome 1.

Xu SY, Schwartz M, Rosenberg T, Gal A. Xu SY, et al. Among authors: rosenberg t. Hum Mol Genet. 1996 Aug;5(8):1193-7. doi: 10.1093/hmg/5.8.1193. Hum Mol Genet. 1996. PMID: 8842740

8

The prevalence of Usher syndrome and other retinal dystrophy-hearing impairment associations.

Rosenberg T, Haim M, Hauch AM, Parving A. Rosenberg T, et al. Clin Genet. 1997 May;51(5):314-21. doi: 10.1111/j.1399-0004.1997.tb02480.x. Clin Genet. 1997. PMID: 9212179

9

Refined genetic mapping of autosomal dominant retinitis pigmentosa locus RP18 reduces the critical region to 2 cM between D1S442 and D1S2858 on chromosome 1q.

Xu SY, Rosenberg T, Gal A. Xu SY, et al. Among authors: rosenberg t. Hum Genet. 1998 Apr;102(4):493-4. doi: 10.1007/s004390050728. Hum Genet. 1998. PMID: 9600251

10

Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa.

Chakarova CF, Hims MM, Bolz H, Abu-Safieh L, Patel RJ, Papaioannou MG, Inglehearn CF, Keen TJ, Willis C, Moore AT, Rosenberg T, Webster AR, Bird AC, Gal A, Hunt D, Vithana EN, Bhattacharya SS. Chakarova CF, et al. Among authors: rosenberg t. Hum Mol Genet. 2002 Jan 1;11(1):87-92. doi: 10.1093/hmg/11.1.87. Hum Mol Genet. 2002. PMID: 11773002

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

470 results

Search Page