Kivelä TT - Search Results

1

Population-based analysis of BAP1 germline variations in patients with uveal melanoma.

Repo P, Järvinen RS, Jäntti JE, Markkinen S, Täll M, Raivio V, Turunen JA, Kivelä TT. Repo P, et al. Among authors: kivela tt. Hum Mol Genet. 2019 Jul 15;28(14):2415-2426. doi: 10.1093/hmg/ddz076. Hum Mol Genet. 2019. PMID: 31058963

2

Very long-term prognosis of patients with malignant uveal melanoma.

Kujala E, Mäkitie T, Kivelä T. Kujala E, et al. Invest Ophthalmol Vis Sci. 2003 Nov;44(11):4651-9. doi: 10.1167/iovs.03-0538. Invest Ophthalmol Vis Sci. 2003. PMID: 14578381

3

Association of LOXL1 gene with Finnish exfoliation syndrome patients.

Lemmelä S, Forsman E, Onkamo P, Nurmi H, Laivuori H, Kivelä T, Puska P, Heger M, Eriksson A, Forsius H, Järvelä I. Lemmelä S, et al. J Hum Genet. 2009 May;54(5):289-97. doi: 10.1038/jhg.2009.28. Epub 2009 Apr 3. J Hum Genet. 2009. PMID: 19343041

4

Diagnosis of uveal melanoma.

Kivelä T. Kivelä T. Dev Ophthalmol. 2012;49:1-15. doi: 10.1159/000330613. Epub 2011 Oct 21. Dev Ophthalmol. 2012. PMID: 22042009 Review.

5

Mutations in CTC1, encoding the CTS telomere maintenance complex component 1, cause cerebroretinal microangiopathy with calcifications and cysts.

Polvi A, Linnankivi T, Kivelä T, Herva R, Keating JP, Mäkitie O, Pareyson D, Vainionpää L, Lahtinen J, Hovatta I, Pihko H, Lehesjoki AE. Polvi A, et al. Am J Hum Genet. 2012 Mar 9;90(3):540-9. doi: 10.1016/j.ajhg.2012.02.002. Epub 2012 Mar 1. Am J Hum Genet. 2012. PMID: 22387016 Free PMC article.

6

Uveal melanoma among Finnish children and young adults.

Al-Jamal RT, Kivelä T. Al-Jamal RT, et al. J AAPOS. 2014 Feb;18(1):61-6. doi: 10.1016/j.jaapos.2013.11.006. J AAPOS. 2014. PMID: 24568985

7

Improving risk estimates of metastasis from uveal melanoma through mutation profiling.

Kivelä T, Jager MJ. Kivelä T, et al. Invest Ophthalmol Vis Sci. 2014 Aug 20;55(8):5168. doi: 10.1167/iovs.14-15285. Invest Ophthalmol Vis Sci. 2014. PMID: 25143043 No abstract available.

8

Long-term Risk of Melanoma-Related Mortality After Uveal Melanoma.

Kivelä T, Kujala E. Kivelä T, et al. JAMA Ophthalmol. 2016 Feb;134(2):238-9. doi: 10.1001/jamaophthalmol.2015.5233. JAMA Ophthalmol. 2016. PMID: 26720623 No abstract available.

9

A novel transthyretin Lys70Glu (p.Lys90Glu) mutation presenting with vitreous amyloidosis and carpal tunnel syndrome.

Raivio VE, Jonasson J, Myllykangas L, Ala-Mello S, Kankuri-Tammilehto M, Kiuru-Enari S, Westermark P, Tanskanen M, Kivelä T. Raivio VE, et al. Amyloid. 2016;23(1):46-50. doi: 10.3109/13506129.2015.1126574. Epub 2016 Feb 1. Amyloid. 2016. PMID: 26828956

10

BAP1 Germline Mutations in Finnish Patients with Uveal Melanoma.

Turunen JA, Markkinen S, Wilska R, Saarinen S, Raivio V, Täll M, Lehesjoki AE, Kivelä TT. Turunen JA, et al. Among authors: kivela tt. Ophthalmology. 2016 May;123(5):1112-7. doi: 10.1016/j.ophtha.2016.01.008. Epub 2016 Feb 12. Ophthalmology. 2016. PMID: 26876698

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