Karadima G - Search Results

1

Expanding the spectrum of C9ORF72-related neurodegenerative disorders in the Greek population.

Kartanou C, Kontogeorgiou Z, Rentzos M, Potagas C, Aristeidou S, Kapaki E, Paraskevas GP, Constantinides VC, Stefanis L, Papageorgiou SG, Houlden H, Panas M, Koutsis G, Karadima G. Kartanou C, et al. Among authors: karadima g. J Neurol Sci. 2022 Nov 15;442:120450. doi: 10.1016/j.jns.2022.120450. Epub 2022 Oct 5. J Neurol Sci. 2022. PMID: 36252286

2

Apolipoprotein E polymorphism in the Greek population.

Sklavounou E, Economou-Petersen E, Karadima G, Panas M, Avramopoulos D, Varsou A, Vassilopoulos D, Petersen MB. Sklavounou E, et al. Among authors: karadima g. Clin Genet. 1997 Oct;52(4):216-8. doi: 10.1111/j.1399-0004.1997.tb02550.x. Clin Genet. 1997. PMID: 9383026

3

Apolipoprotein E and presenilin-1 genotypes in Huntington's disease.

Panas M, Avramopoulos D, Karadima G, Petersen MB, Vassilopoulos D. Panas M, et al. Among authors: karadima g. J Neurol. 1999 Jul;246(7):574-7. doi: 10.1007/s004150050406. J Neurol. 1999. PMID: 10463359

4

Genotyping of presenilin-1 polymorphism in amyotrophic lateral sclerosis.

Panas M, Karadima G, Kalfakis N, Psarrou O, Floroskoufi P, Kladi A, Petersen MB, Vassilopoulos D. Panas M, et al. Among authors: karadima g. J Neurol. 2000 Dec;247(12):940-2. doi: 10.1007/s004150070050. J Neurol. 2000. PMID: 11200686

5

Friedreich's ataxia mimicking hereditary motor and sensory neuropathy.

Panas M, Kalfakis N, Karadima G, Davaki P, Vassilopoulos D. Panas M, et al. Among authors: karadima g. J Neurol. 2002 Nov;249(11):1583-6. doi: 10.1007/s00415-002-0902-2. J Neurol. 2002. PMID: 12420100

6

Hereditary neuropathy with liability to pressure palsies emerging during vincristine treatment.

Kalfakis N, Panas M, Karadima G, Floroskufi P, Kokolakis N, Vassilopoulos D. Kalfakis N, et al. Among authors: karadima g. Neurology. 2002 Nov 12;59(9):1470-1. doi: 10.1212/01.wnl.0000032505.45389.94. Neurology. 2002. PMID: 12427913 No abstract available.

7

A V38A mutation in X-linked Charcot-Marie-Tooth neuropathy with unusual clinical features.

Karadima G, Panas M, Floroskufi P, Kalfakis N, Vassilopoulos D. Karadima G, et al. J Neurol. 2004 Feb;251(2):222-3. doi: 10.1007/s00415-004-0284-8. J Neurol. 2004. PMID: 14991359 No abstract available.

8

New mutation of the MPZ gene in a family with the Dejerine-Sottas disease phenotype.

Floroskufi P, Panas M, Karadima G, Vassilopoulos D. Floroskufi P, et al. Among authors: karadima g. Muscle Nerve. 2007 May;35(5):667-9. doi: 10.1002/mus.20703. Muscle Nerve. 2007. PMID: 17143884

9

APOE epsilon4 is associated with impaired verbal learning in patients with MS.

Koutsis G, Panas M, Giogkaraki E, Potagas C, Karadima G, Sfagos C, Vassilopoulos D. Koutsis G, et al. Among authors: karadima g. Neurology. 2007 Feb 20;68(8):546-9. doi: 10.1212/01.wnl.0000254468.51973.44. Neurology. 2007. PMID: 17310023

10

APOE genotypes in Greek multiple sclerosis patients: no effect on the MS Severity Score.

Koutsis G, Panas M, Karadima G, Mandellos D, Sfagos C, Potagas C, Vassilopoulos D. Koutsis G, et al. Among authors: karadima g. J Neurol. 2007 Mar;254(3):394-5. doi: 10.1007/s00415-006-0375-9. Epub 2007 Mar 7. J Neurol. 2007. PMID: 17345041 No abstract available.

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