Koutsis G - Search Results

1

Expanding the Spectrum of AP5Z1-Related Hereditary Spastic Paraplegia (HSP-SPG48): A Multicenter Study on a Rare Disease.

Breza M, Hirst J, Chelban V, Banneau G, Tissier L, Kol B, Bourinaris T, Said SA, Péréon Y, Heinzmann A, Debs R, Juntas-Morales R, Martinez VG, Camdessanche JP, Scherer-Gagou C, Zola JM, Athanasiou-Fragkouli A, Efthymiou S, Vavougios G, Velonakis G, Stamelou M, Tzartos J, Potagas C, Zambelis T, Mariotti C, Blackstone C, Vandrovcova J, Mavridis T, Kartanou C, Stefanis L, Wood N, Karadima G, LeGuern E, Koutsis G, Houlden H, Stevanin G. Breza M, et al. Among authors: koutsis g. Mov Disord. 2021 Apr;36(4):1034-1038. doi: 10.1002/mds.28487. Epub 2021 Feb 5. Mov Disord. 2021. PMID: 33543803 No abstract available.

2

Intramedullary spinal cord metastases in a patient with small-cell lung cancer.

Koutsis G, Spengos K, Potagas C, Dimitrakopoulos A, Sfagos K, Zakopoulos N. Koutsis G, et al. Eur J Intern Med. 2006 Aug;17(5):372-4. doi: 10.1016/j.ejim.2005.12.014. Eur J Intern Med. 2006. PMID: 16864018

3

Occipital neuralgia as an isolated symptom of C2 myelitis.

Nikakis P, Koutsis G, Potagas C, Mandellos D, Sfagos C. Nikakis P, et al. Among authors: koutsis g. Headache. 2006 Sep;46(8):1304-6. doi: 10.1111/j.1526-4610.2006.00543_2.x. Headache. 2006. PMID: 16942479

4

Cognitive impairment in different MS subtypes and clinically isolated syndromes.

Potagas C, Giogkaraki E, Koutsis G, Mandellos D, Tsirempolou E, Sfagos C, Vassilopoulos D. Potagas C, et al. Among authors: koutsis g. J Neurol Sci. 2008 Apr 15;267(1-2):100-6. doi: 10.1016/j.jns.2007.10.002. Epub 2007 Nov 13. J Neurol Sci. 2008. PMID: 17997417

5

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.

6

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.

7

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

8

The challenge of juvenile Huntington disease: to test or not to test.

Koutsis G, Karadima G, Kladi A, Panas M. Koutsis G, et al. Neurology. 2013 Mar 12;80(11):990-6. doi: 10.1212/WNL.0b013e31828727fa. Epub 2013 Feb 6. Neurology. 2013. PMID: 23390178

9

Friedreich's ataxia and other hereditary ataxias in Greece: an 18-year perspective.

Koutsis G, Kladi A, Karadima G, Houlden H, Wood NW, Christodoulou K, Panas M. Koutsis G, et al. J Neurol Sci. 2014 Jan 15;336(1-2):87-92. doi: 10.1016/j.jns.2013.10.012. Epub 2013 Oct 16. J Neurol Sci. 2014. PMID: 24209901

10

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

11

Four novel connexin 32 mutations in X-linked Charcot-Marie-Tooth disease. Phenotypic variability and central nervous system involvement.

Karadima G, Koutsis G, Raftopoulou M, Floroskufi P, Karletidi KM, Panas M. Karadima G, et al. Among authors: koutsis g. J Neurol Sci. 2014 Jun 15;341(1-2):158-61. doi: 10.1016/j.jns.2014.04.007. Epub 2014 Apr 13. J Neurol Sci. 2014. PMID: 24768312

12

C9ORF72 hexanucleotide repeat expansions are a frequent cause of Huntington disease phenocopies in the Greek population.

Koutsis G, Karadima G, Kartanou C, Kladi A, Panas M. Koutsis G, et al. Neurobiol Aging. 2015 Jan;36(1):547.e13-6. doi: 10.1016/j.neurobiolaging.2014.08.020. Epub 2014 Aug 27. Neurobiol Aging. 2015. PMID: 25248608

13

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.

14

Symptomatic striopallidodentate calcinosis (Fahr's syndrome) in a thalassemic patient with hypoparathyroidism.

Koutsis G, Karadima G, Panas M. Koutsis G, et al. Ann Hematol. 2015 May;94(5):897-9. doi: 10.1007/s00277-014-2251-5. Epub 2014 Nov 8. Ann Hematol. 2015. PMID: 25377047 No abstract available.

15

Relapsing remitting multiple sclerosis in x-linked charcot-marie-tooth disease with central nervous system involvement.

Koutsis G, Karadima G, Floroskoufi P, Raftopoulou M, Panas M. Koutsis G, et al. Case Rep Neurol Med. 2015;2015:841897. doi: 10.1155/2015/841897. Epub 2015 Mar 25. Case Rep Neurol Med. 2015. PMID: 25883816 Free PMC article.

16

Charcot-Marie-Tooth disease type 2C and scapuloperoneal muscular atrophy overlap syndrome in a patient with the R232C TRPV4 mutation.

Koutsis G, Lynch D, Manole A, Karadima G, Reilly MM, Houlden H, Panas M. Koutsis G, et al. J Neurol. 2015 Aug;262(8):1972-5. doi: 10.1007/s00415-015-7800-x. Epub 2015 Jun 6. J Neurol. 2015. PMID: 26048687 No abstract available.

17

A novel ABCD1 mutation detected by next generation sequencing in presumed hereditary spastic paraplegia: A 30-year diagnostic delay caused by misleading biochemical findings.

Koutsis G, Lynch DS, Tucci A, Houlden H, Karadima G, Panas M. Koutsis G, et al. J Neurol Sci. 2015 Aug 15;355(1-2):199-201. doi: 10.1016/j.jns.2015.05.031. Epub 2015 May 29. J Neurol Sci. 2015. PMID: 26049658

18

Mutational analysis of Greek patients with suspected hereditary neuropathy with liability to pressure palsies (HNPP): a 15-year experience.

Karadima G, Koutsis G, Raftopoulou M, Karletidi KM, Zambelis T, Karandreas N, Panas M. Karadima G, et al. Among authors: koutsis g. J Peripher Nerv Syst. 2015 Jun;20(2):79-85. doi: 10.1111/jns.12125. J Peripher Nerv Syst. 2015. PMID: 26110377

19

Erratum to: Charcot-Marie-Tooth disease type 2C and scapuloperoneal muscular atrophy overlap syndrome in a patient with the R232C TRPV4 mutation.

Koutsis G, Lynch D, Manole A, Karadima G, Reilly MM, Houlden H, Panas M. Koutsis G, et al. J Neurol. 2015 Aug;262(8):1976. doi: 10.1007/s00415-015-7846-9. J Neurol. 2015. PMID: 26162716 No abstract available.

20

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.

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