Gränse L - Search Results

1

A novel phenotype associated with the R162W variant in the KCNJ13 gene.

Schroeder M, Peter VG, Gränse L, Andréasson S, Rivolta C, Kjellström U. Schroeder M, et al. Among authors: granse l. Ophthalmic Genet. 2022 Aug;43(4):500-507. doi: 10.1080/13816810.2022.2068041. Epub 2022 Apr 27. Ophthalmic Genet. 2022. PMID: 35477418

2

Electrophysiological findings in two young patients with Bothnia dystrophy and a mutation in the RLBP1 gene.

Gränse L, Abrahamson M, Ponjavic V, Andréasson S. Gränse L, et al. Ophthalmic Genet. 2001 Jun;22(2):97-105. doi: 10.1076/opge.22.2.97.2231. Ophthalmic Genet. 2001. PMID: 11449319

3

Retinal dysfunction and anterior segment deposits in a patient treated with rifabutin.

Ponjavic V, Gränse L, Bengtsson Stigmar E, Andréasson S. Ponjavic V, et al. Among authors: granse l. Acta Ophthalmol Scand. 2002 Oct;80(5):553-6. doi: 10.1034/j.1600-0420.2002.800519.x. Acta Ophthalmol Scand. 2002. PMID: 12390172 Free article.

4

Electrophysiology and ocular blood flow in a family with dominant optic nerve atrophy and a mutation in the OPA1 gene.

Gränse L, Bergstrand I, Thiselton D, Ponjavic V, Heijl A, Votruba M, Andréasson S. Gränse L, et al. Ophthalmic Genet. 2003 Dec;24(4):233-45. doi: 10.1076/opge.24.4.233.17230. Ophthalmic Genet. 2003. PMID: 14566653

5

Reduced full-field electroretinogram (ERG) in a patient treated with methotrexate.

Ponjavic V, Gränse L, Stigmar EB, Andréasson S. Ponjavic V, et al. Among authors: granse l. Acta Ophthalmol Scand. 2004 Feb;82(1):96-9. doi: 10.1046/j.1600-0420.2003.00181.x. Acta Ophthalmol Scand. 2004. PMID: 14982050 Free article.

6

Alterations in electroretinograms and retinal morphology in rabbits treated with vigabatrin.

Ponjavic V, Gränse L, Kjellström S, Andréasson S, Bruun A. Ponjavic V, et al. Among authors: granse l. Doc Ophthalmol. 2004 Mar;108(2):125-33. doi: 10.1023/b:doop.0000036780.96560.74. Doc Ophthalmol. 2004. PMID: 15455795

7

Full-field ERG, multifocal ERG and multifocal VEP in patients with retinitis pigmentosa and residual central visual fields.

Gränse L, Ponjavic V, Andréasson S. Gränse L, et al. Acta Ophthalmol Scand. 2004 Dec;82(6):701-6. doi: 10.1111/j.1600-0420.2004.00362.x. Acta Ophthalmol Scand. 2004. PMID: 15606467 Free article.

8

Macular dysfunction and morphology in spinocerebellar ataxia type 7 (SCA 7).

Hugosson T, Gränse L, Ponjavic V, Andréasson S. Hugosson T, et al. Among authors: granse l. Ophthalmic Genet. 2009 Mar;30(1):1-6. doi: 10.1080/13816810802454081. Ophthalmic Genet. 2009. PMID: 19172503

9

Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa.

Friedman JS, Ray JW, Waseem N, Johnson K, Brooks MJ, Hugosson T, Breuer D, Branham KE, Krauth DS, Bowne SJ, Sullivan LS, Ponjavic V, Gränse L, Khanna R, Trager EH, Gieser LM, Hughbanks-Wheaton D, Cojocaru RI, Ghiasvand NM, Chakarova CF, Abrahamson M, Göring HH, Webster AR, Birch DG, Abecasis GR, Fann Y, Bhattacharya SS, Daiger SP, Heckenlively JR, Andréasson S, Swaroop A. Friedman JS, et al. Among authors: granse l. Am J Hum Genet. 2009 Jun;84(6):792-800. doi: 10.1016/j.ajhg.2009.05.007. Am J Hum Genet. 2009. PMID: 19520207 Free PMC article.

10

Multifocal Visual Evoked Potentials (mfVEP) in Diabetic Patients with and without Polyneuropathy.

Lövestam-Adrian M, Gränse L, Andersson G, Andreasson S. Lövestam-Adrian M, et al. Among authors: granse l. Open Ophthalmol J. 2012;6:98-103. doi: 10.2174/1874364101206010098. Epub 2012 Nov 16. Open Ophthalmol J. 2012. PMID: 23198007 Free PMC article.

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