Koutsis G - Search Results

1

Assessment of Parkinson's disease risk loci in Greece.

Kara E, Xiromerisiou G, Spanaki C, Bozi M, Koutsis G, Panas M, Dardiotis E, Ralli S, Bras J, Letson C, Edsall C, Pliner H, Arepalli S, Kalinderi K, Fidani L, Bostantjopoulou S, Keller MF, Wood NW, Hardy J, Houlden H, Stefanis L, Plaitakis A, Hernandez D, Hadjigeorgiou GM, Nalls MA, Singleton AB. Kara E, et al. Among authors: koutsis g. Neurobiol Aging. 2014 Feb;35(2):442.e9-442.e16. doi: 10.1016/j.neurobiolaging.2013.07.011. Epub 2013 Sep 27. Neurobiol Aging. 2014. PMID: 24080174 Free PMC article.

2

Transthyretin Amyloidosis Cardiomyopathy in Greece: Clinical Insights from the National Referral Center.

Bampatsias D, Theodorakakou F, Briasoulis A, Georgiopoulos G, Dimoula A, Papantoniou V, Papantoniou I, Skiadaresi C, Valsamaki P, Repasos E, Petropoulos I, Delialis D, Papathoma A, Koutsis G, Tselegkidi ME, Stamatelopoulos K, Kastritis E. Bampatsias D, et al. Among authors: koutsis g. Hellenic J Cardiol. 2023 Oct 5:S1109-9666(23)00190-2. doi: 10.1016/j.hjc.2023.09.019. Online ahead of print. Hellenic J Cardiol. 2023. PMID: 37805173 Free article.

3

Transthyretin (Pro24Ser) variant amyloidosis: A case report of the first patient in Greece.

Panagiotopoulos I, Papatheodorou E, Anastasakis A, Kastritis E, Gourzi P, Kontogeorgiou Z, Koutsis G, Karadima G, Koutelou M. Panagiotopoulos I, et al. Among authors: koutsis g. Hell J Nucl Med. 2023 May-Aug;26(2):145-149. doi: 10.1967/s002449912585. Hell J Nucl Med. 2023. PMID: 37610765 Free article.

4

Acute painful sensory neuropathy with subclinical autonomic dysfunction as a presenting feature of Hodgkin's disease.

Koutsis G, Spengos K, Panas M, Dimitrakopoulos A, Sfagos C, Vassilopoulos D. Koutsis G, et al. Eur Neurol. 2005;53(3):157-9. doi: 10.1159/000086125. Epub 2004 May 28. Eur Neurol. 2005. PMID: 15942238 No abstract available.

5

The rs10492972 KIF1B polymorphism and disease progression in Greek patients with multiple sclerosis.

Koutsis G, Karadima G, Floroskufi P, Sfagos C, Vassilopoulos D, Panas M. Koutsis G, et al. J Neurol. 2011 Sep;258(9):1726-8. doi: 10.1007/s00415-011-6004-2. Epub 2011 Mar 22. J Neurol. 2011. PMID: 21424745 No abstract available.

6

Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot-Marie-Tooth disease.

Koutsis G, Pandraud A, Polke JM, Wood NW, Panas M, Karadima G, Houlden H. Koutsis G, et al. Brain. 2012 Aug;135(Pt 8):e217, 1-6; author reply e218, 1-2. doi: 10.1093/brain/aws034. Epub 2012 Mar 1. Brain. 2012. PMID: 22382358 Free PMC article. No abstract available.

7

High frequency of the expanded C9ORF72 hexanucleotide repeat in familial and sporadic Greek ALS patients.

Mok KY, Koutsis G, Schottlaender LV, Polke J, Panas M, Houlden H. Mok KY, et al. Among authors: koutsis g. Neurobiol Aging. 2012 Aug;33(8):1851.e1-5. doi: 10.1016/j.neurobiolaging.2012.02.021. Epub 2012 Mar 22. Neurobiol Aging. 2012. PMID: 22445326 Free PMC article.

8

Analysis of spinocerebellar ataxias due to expanded triplet repeats in Greek patients with cerebellar ataxia.

Koutsis G, Pemble S, Sweeney MG, Paudel R, Wood NW, Panas M, Kladi A, Houlden H. Koutsis G, et al. J Neurol Sci. 2012 Jul 15;318(1-2):178-80. doi: 10.1016/j.jns.2012.03.019. Epub 2012 Apr 18. J Neurol Sci. 2012. PMID: 22520093 Free article.

9

Age at onset in Huntington's disease: replication study on the association of HAP1.

Karadima G, Dimovasili C, Koutsis G, Vassilopoulos D, Panas M. Karadima G, et al. Among authors: koutsis g. Parkinsonism Relat Disord. 2012 Nov;18(9):1027-8. doi: 10.1016/j.parkreldis.2012.05.020. Epub 2012 Jun 12. Parkinsonism Relat Disord. 2012. PMID: 22698993

10

The frequency of spinocerebellar ataxia type 23 in a UK population.

Fawcett K, Mehrabian M, Liu YT, Hamed S, Elahi E, Revesz T, Koutsis G, Herscheson J, Schottlaender L, Wardle M, Morrison PJ, Morris HR, Giunti P, Wood N, Houlden H. Fawcett K, et al. Among authors: koutsis g. J Neurol. 2013 Mar;260(3):856-9. doi: 10.1007/s00415-012-6721-1. Epub 2012 Oct 30. J Neurol. 2013. PMID: 23108490

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