Rinne JO - Search Results

1

Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.

Luoma P, Melberg A, Rinne JO, Kaukonen JA, Nupponen NN, Chalmers RM, Oldfors A, Rautakorpi I, Peltonen L, Majamaa K, Somer H, Suomalainen A. Luoma P, et al. Among authors: rinne jo. Lancet. 2004 Sep 4-10;364(9437):875-82. doi: 10.1016/S0140-6736(04)16983-3. Lancet. 2004. PMID: 15351195

2

Do carriers of POLG mutation W748S have disease manifestations?

Rantamäki M, Luoma P, Virta JJ, Rinne JO, Paetau A, Suomalainen A, Udd B. Rantamäki M, et al. Among authors: rinne jo. Clin Genet. 2007 Dec;72(6):532-7. doi: 10.1111/j.1399-0004.2007.00908.x. Epub 2007 Sep 25. Clin Genet. 2007. PMID: 17894835

3

Cerebral oxygen and glucose metabolism in patients with mitochondrial m.3243A>G mutation.

Lindroos MM, Borra RJ, Parkkola R, Virtanen SM, Lepomäki V, Bucci M, Virta JR, Rinne JO, Nuutila P, Majamaa K. Lindroos MM, et al. Among authors: rinne jo. Brain. 2009 Dec;132(Pt 12):3274-84. doi: 10.1093/brain/awp259. Brain. 2009. PMID: 19843652

4

Striatal uptake of the dopamine reuptake ligand [11C]beta-CFT is reduced in Alzheimer's disease assessed by positron emission tomography.

Rinne JO, Sahlberg N, Ruottinen H, Någren K, Lehikoinen P. Rinne JO, et al. Neurology. 1998 Jan;50(1):152-6. doi: 10.1212/wnl.50.1.152. Neurology. 1998. PMID: 9443472

5

An FDOPA PET study in patients with periodic limb movement disorder and restless legs syndrome.

Ruottinen HM, Partinen M, Hublin C, Bergman J, Haaparanta M, Solin O, Rinne JO. Ruottinen HM, et al. Among authors: rinne jo. Neurology. 2000 Jan 25;54(2):502-4. doi: 10.1212/wnl.54.2.502. Neurology. 2000. PMID: 10668725

6

Variant Alzheimer's disease with spastic paraparesis: clinical characterization.

Verkkoniemi A, Somer M, Rinne JO, Myllykangas L, Crook R, Hardy J, Viitanen M, Kalimo H, Haltia M. Verkkoniemi A, et al. Among authors: rinne jo. Neurology. 2000 Mar 14;54(5):1103-9. doi: 10.1212/wnl.54.5.1103. Neurology. 2000. PMID: 10720282

7

Risk for Parkinson's disease: twin studies for the detection of asymptomatic subjects using [18F]6-fluorodopa PET.

Laihinen A, Ruottinen H, Rinne JO, Haaparanta M, Bergman J, Solin O, Koskenvuo M, Marttila R, Rinne UK. Laihinen A, et al. Among authors: rinne jo, rinne uk. J Neurol. 2000 Apr;247 Suppl 2:II110-3. doi: 10.1007/pl00022911. J Neurol. 2000. PMID: 10991657

8

Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation.

Tuominen S, Juvonen V, Amberla K, Jolma T, Rinne JO, Tuisku S, Kurki T, Marttila R, Pöyhönen M, Savontaus ML, Viitanen M, Kalimo H. Tuominen S, et al. Among authors: rinne jo. Stroke. 2001 Aug;32(8):1767-74. doi: 10.1161/01.str.32.8.1767. Stroke. 2001. PMID: 11486103

9

A rare mitochondrial DNA haplotype observed in Koreans.

Snäll N, Savontaus ML, Kares S, Lee MS, Cho EK, Rinne JO, Huoponen K. Snäll N, et al. Among authors: rinne jo. Hum Biol. 2002 Apr;74(2):253-62. doi: 10.1353/hub.2002.0024. Hum Biol. 2002. PMID: 12030653

10

Neuropsychological functions in variant Alzheimer's disease with spastic paraparesis.

Verkkoniemi A, Ylikoski R, Rinne JO, Somer M, Hietaharju A, Erkinjuntti T, Viitanen M, Kalimo H, Haltia M. Verkkoniemi A, et al. Among authors: rinne jo. J Neurol Sci. 2004 Mar 15;218(1-2):29-37. doi: 10.1016/j.jns.2003.10.020. J Neurol Sci. 2004. PMID: 14759630

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