Grøndahl J - Search Results

1

Autosomal dominant pericentral retinal dystrophy caused by a novel missense mutation in the TOPORS gene.

Selmer KK, Grøndahl J, Riise R, Brandal K, Braaten O, Bragadottir R, Undlien DE. Selmer KK, et al. Among authors: grondahl j. Acta Ophthalmol. 2010 May;88(3):323-8. doi: 10.1111/j.1755-3768.2008.01465.x. Epub 2009 Jan 30. Acta Ophthalmol. 2010. PMID: 19183411 Free article.

2

Autosomal dominant retinitis pigmentosa in Norway: a 20-year clinical follow-up study with molecular genetic analysis. Two novel rhodopsin mutations: 1003delG and I179F.

Grøndahl J, Riise R, Heiberg A, Leren T, Christoffersen T, Bragadottir R. Grøndahl J, et al. Acta Ophthalmol Scand. 2007 May;85(3):287-97. doi: 10.1111/j.1600-0420.2006.00820.x. Acta Ophthalmol Scand. 2007. PMID: 17488458 Free article.

3

Pericentral retinal dystrophy.

Grøndahl J. Grøndahl J. Acta Ophthalmol (Copenh). 1987 Jun;65(3):344-51. doi: 10.1111/j.1755-3768.1987.tb08517.x. Acta Ophthalmol (Copenh). 1987. PMID: 3618160

4

Autosomal recessive inheritance in 'senile' retinitis pigmentosa.

Grøndahl J. Grøndahl J. Acta Ophthalmol (Copenh). 1987 Apr;65(2):231-6. Acta Ophthalmol (Copenh). 1987. PMID: 3604615

5

Estimation of prognosis and prevalence of retinitis pigmentosa and Usher syndrome in Norway.

Grøndahl J. Grøndahl J. Clin Genet. 1987 Apr;31(4):255-64. doi: 10.1111/j.1399-0004.1987.tb02804.x. Clin Genet. 1987. PMID: 3594933

6

Tapeto-retinal degeneration in four Norwegian counties, I. Diagnostic evaluation of 89 probands.

Grøndahl J. Grøndahl J. Clin Genet. 1986 Jan;29(1):1-16. doi: 10.1111/j.1399-0004.1986.tb00767.x. Clin Genet. 1986. PMID: 3948427

7

Tapeto-retinal degeneration in four Norwegian counties, II. Diagnostic evaluation of 407 relatives and genetic evaluation of 87 families.

Grøndahl J. Grøndahl J. Clin Genet. 1986 Jan;29(1):17-41. Clin Genet. 1986. PMID: 3948428

8

[Presently there is no effective treatment for retinitis pigmentosa].

Grøndahl J. Grøndahl J. Tidsskr Nor Laegeforen. 1994 May 20;114(13):1510-1. Tidsskr Nor Laegeforen. 1994. PMID: 8079241 Norwegian. No abstract available.

9

HEREDOPATHIA ATACTICA POLYNEURITIFORMIS (REFSUM'S DISEASE).

NORDHAGEN E, GRONDAHL J. NORDHAGEN E, et al. Among authors: grondahl j. Acta Ophthalmol (Copenh). 1964;42:629-33. doi: 10.1111/j.1755-3768.1964.tb00912.x. Acta Ophthalmol (Copenh). 1964. PMID: 14186618 No abstract available.

10

Usher syndrome in four Norwegian counties.

Grøndahl J, Mjøen S. Grøndahl J, et al. Clin Genet. 1986 Jul;30(1):14-28. doi: 10.1111/j.1399-0004.1986.tb00564.x. Clin Genet. 1986. PMID: 3757293

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