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Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa.
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.
Phenotype associated with mutation in the recently identified autosomal dominant retinitis pigmentosa KLHL7 gene.
Hugosson T, Friedman JS, Ponjavic V, Abrahamson M, Swaroop A, Andréasson S.
Hugosson T, et al.
Arch Ophthalmol. 2010 Jun;128(6):772-8. doi: 10.1001/archophthalmol.2010.98.
Arch Ophthalmol. 2010.
PMID: 20547956
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Macular dysfunction and morphology in spinocerebellar ataxia type 7 (SCA 7).
Hugosson T, Gränse L, Ponjavic V, Andréasson S.
Hugosson T, et al.
Ophthalmic Genet. 2009 Mar;30(1):1-6. doi: 10.1080/13816810802454081.
Ophthalmic Genet. 2009.
PMID: 19172503
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Aryl Hydrocarbon Receptor-Interacting Protein-Like 1 in Cancer-Associated Retinopathy.
Dalin F, Adamus G, Yang S, Landgren E, Palle J, Hallgren Å, Frost BM, Hugosson T, Landegren N, Eriksson D, Andréasson S, Tabbara KF, Kämpe O, Alimohammadi M.
Dalin F, et al. Among authors: hugosson t.
Ophthalmology. 2016 Jun;123(6):1401-4. doi: 10.1016/j.ophtha.2015.12.031. Epub 2016 Feb 4.
Ophthalmology. 2016.
PMID: 26854037
No abstract available.
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Upregulated Retinal Neurofilament Expression in Experimental Optic Neuritis.
Weissert R, Hugosson T, Petzold A.
Weissert R, et al. Among authors: hugosson t.
Neuroophthalmology. 2022 Jan 26;46(4):215-219. doi: 10.1080/01658107.2022.2025852. eCollection 2022.
Neuroophthalmology. 2022.
PMID: 35859627
Free PMC article.
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Corticotropin-induced reduction of plasma lipoprotein(a) concentrations in healthy individuals and hemodialysis patients: relation to apolipoprotein(a) size polymorphism.
Arnadottir M, Berg AL, Kronenberg F, Lingenhel A, Hugosson T, Hegbrant J, Nilsson-Ehle P.
Arnadottir M, et al. Among authors: hugosson t.
Metabolism. 1999 Mar;48(3):342-6. doi: 10.1016/s0026-0495(99)90083-5.
Metabolism. 1999.
PMID: 10094111
Clinical Trial.
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