Koutsis G - Search Results

1

Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene.

Bougea A, Koros C, Stamelou M, Simitsi A, Papagiannakis N, Antonelou R, Papadimitriou D, Breza M, Tasios K, Fragkiadaki S, Geronicola Trapali X, Bourbouli M, Koutsis G, Papageorgiou SG, Kapaki E, Paraskevas GP, Stefanis L. Bougea A, et al. Among authors: koutsis g. Parkinsonism Relat Disord. 2017 Feb;35:82-87. doi: 10.1016/j.parkreldis.2016.12.002. Epub 2016 Dec 6. Parkinsonism Relat Disord. 2017. PMID: 28012952

2

Effects of an endurance training programme on the passive and noradrenaline-activated compliances of rat aorta.

Koutsis G, Kadi F, Vandewalle H, Lechat P, Hadjiisky P, Monod H. Koutsis G, et al. Eur J Appl Physiol Occup Physiol. 1995;71(2-3):173-9. doi: 10.1007/BF00854976. Eur J Appl Physiol Occup Physiol. 1995. PMID: 7588686

3

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

4

Late-onset Huntington's disease: diagnostic and prognostic considerations.

Koutsis G, Karadima G, Kladi A, Panas M. Koutsis G, et al. Parkinsonism Relat Disord. 2014 Jul;20(7):726-30. doi: 10.1016/j.parkreldis.2014.03.017. Epub 2014 Mar 27. Parkinsonism Relat Disord. 2014. PMID: 24721491

5

From mild ataxia to huntington disease phenocopy: the multiple faces of spinocerebellar ataxia 17.

Koutsis G, Panas M, Paraskevas GP, Bougea AM, Kladi A, Karadima G, Kapaki E. Koutsis G, et al. Case Rep Neurol Med. 2014;2014:643289. doi: 10.1155/2014/643289. Epub 2014 Oct 2. Case Rep Neurol Med. 2014. PMID: 25349749 Free PMC article.

6

Hereditary spastic paraplegia in Greece: characterisation of a previously unexplored population using next-generation sequencing.

Lynch DS, Koutsis G, Tucci A, Panas M, Baklou M, Breza M, Karadima G, Houlden H. Lynch DS, et al. Among authors: koutsis g. Eur J Hum Genet. 2016 Jun;24(6):857-63. doi: 10.1038/ejhg.2015.200. Epub 2015 Sep 16. Eur J Hum Genet. 2016. PMID: 26374131 Free PMC article.

7

Spinobulbar muscular atrophy (Kennedy's disease): A rare diagnosis in the Greek population.

Koutsis G, Kladi A, Breza M, Karadima G, Panas M. Koutsis G, et al. J Neurol Sci. 2015 Dec 15;359(1-2):450-1. doi: 10.1016/j.jns.2015.10.021. Epub 2015 Oct 21. J Neurol Sci. 2015. PMID: 26481168 No abstract available.

8

Neck flexion-induced finger tremor: A novel observation in Hirayama disease.

Koutsis G, Velonakis G, Breza M, Karavasilis E, Zambelis T, Panas M. Koutsis G, et al. J Neurol Sci. 2016 May 15;364:42-4. doi: 10.1016/j.jns.2016.03.012. Epub 2016 Mar 5. J Neurol Sci. 2016. PMID: 27084213 No abstract available.

9

Spastic paretic hemifacial contracture as a presenting feature of multiple sclerosis.

Koutsis G, Breza M, Evangelopoulos ME, Anagnostouli M, Andreadou E, Karagiorgis G, Kokotis P, Kilidireas C, Karandreas N. Koutsis G, et al. Mult Scler Relat Disord. 2017 Apr;13:112-115. doi: 10.1016/j.msard.2017.02.017. Epub 2017 Feb 24. Mult Scler Relat Disord. 2017. PMID: 28427691

10

Screening for the C9ORF72 repeat expansion in a greek frontotemporal dementia cohort.

Kartanou C, Karadima G, Koutsis G, Breza M, Papageorgiou SG, Paraskevas GP, Kapaki E, Panas M. Kartanou C, et al. Among authors: koutsis g. Amyotroph Lateral Scler Frontotemporal Degener. 2018 Feb;19(1-2):152-154. doi: 10.1080/21678421.2017.1400070. Epub 2017 Nov 23. Amyotroph Lateral Scler Frontotemporal Degener. 2018. PMID: 29166782

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