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G Karadima

Explore the profile of G Karadima including associated specialties, affiliations and a list of published articles. Areas
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Articles 33
Citations 238
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Recent Articles
1.
Katsimpouris D, Kartanou C, Breza M, Panas M, Koutsis G, Karadima G
J Neurol Sci . 2019 May; 402:131-132. PMID: 31132534
No abstract available.
2.
Varvaressos S, Breza M, Marousi S, Printzou M, Georgoulis A, Papageorgiou E, et al.
Eur J Neurol . 2019 May; 26(7):e73-e74. PMID: 31059159
No abstract available.
3.
Anagnostou E, Zachou A, Breza M, Kladi A, Karadima G, Koutsis G
Neurosci Lett . 2019 Apr; 705:94-98. PMID: 31026532
Spinal and bulbar muscular atrophy (Kennedy's disease) has been associated with balance dysfunction and falls. However, postural control has not been studied quantitatively. Here, we quantified upright stance and aimed...
4.
Karadima G, Koutsis G, Karletidi K, Panas M
Clin Genet . 2014 Mar; 86(6):603. PMID: 24635740
No abstract available.
5.
Koutsis G, Pandraud A, Karadima G, Panas M, Reilly M, Floroskufi P, et al.
Clin Genet . 2012 Jul; 83(4):388-91. PMID: 22765307
No abstract available.
6.
Koutsis G, Karadima G, Pandraud A, Sweeney M, Paudel R, Houlden H, et al.
J Neurol . 2012 Feb; 259(9):1874-8. PMID: 22297462
Huntington’s disease (HD) is an autosomal dominant disorder characterized by a triad of chorea, psychiatric disturbance and cognitive decline. Around 1% of patients with HD-like symptoms lack the causative HD...
7.
Karadima G, Floroskufi P, Koutsis G, Vassilopoulos D, Panas M
Clin Genet . 2012 Jan; 80(5):497-9. PMID: 22243284
No abstract available.
8.
Panas M, Karadima G, Vassos E, Kalfakis N, Kladi A, Christodoulou K, et al.
Clin Genet . 2010 Dec; 80(6):586-90. PMID: 21166788
A large scale genetic and epidemiological study of Huntington's disease (HD) was carried out in Greece from January 1995 to December 2008. Diagnostic testing was carried out in 461 symptomatic...
9.
Koutsis G, Panas M, Giogkaraki E, Karadima G, Sfagos C, Vassilopoulos D
Mult Scler . 2008 Sep; 15(2):174-9. PMID: 18805838
Background: Elevated ApoA1 levels have been associated with decreased dementia risk. The A-allele of the APOA1 -75G/A promoter polymorphism has been associated with elevated ApoA1 levels. Objective: We sought to...
10.
Zambelis T, Panas M, Kokotis P, Karadima G, Kararizou E, Karandreas N
Acta Neurol Belg . 2008 Sep; 108(2):44-7. PMID: 18795595
Unlabelled: The aim of the present study was to investigate the subclinical involvement of the central nervous system (CNS) in an X-linked Charcot-Marie-Toth (CMTX) family. Material And Methods: Seven subjects,...