Kalfakis N - Search Results

1

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. Neurology. 2002 Nov 12;59(9):1470-1. doi: 10.1212/01.wnl.0000032505.45389.94. Neurology. 2002. PMID: 12427913 No abstract available.

2

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: kalfakis n. J Neurol. 2000 Dec;247(12):940-2. doi: 10.1007/s004150070050. J Neurol. 2000. PMID: 11200686

3

Episodes of generalized weakness in two sibs with the C164T mutation of the connexin 32 gene.

Panas M, Kalfakis N, Karadimas C, Vassilopoulos D. Panas M, et al. Among authors: kalfakis n. Neurology. 2001 Nov 27;57(10):1906-8. doi: 10.1212/wnl.57.10.1906. Neurology. 2001. PMID: 11723288

4

Charcot-Marie-Tooth disease type 1A with central nervous system involvement in two generations.

Panas M, Karadima G, Kalfakis N, Floroskufi P, Vassilopoulos D. Panas M, et al. Among authors: kalfakis n. J Neurol. 2004 Apr;251(4):484-5. doi: 10.1007/s00415-004-0376-5. J Neurol. 2004. PMID: 15083299 No abstract available.

5

Four novel connexin 32 mutations in X-linked Charcot-Marie-Tooth disease with phenotypic variability.

Karadima G, Panas M, Floroskufi P, Kalfakis N, Vassilopoulos D. Karadima G, et al. Among authors: kalfakis n. J Neurol. 2006 Feb;253(2):263-4. doi: 10.1007/s00415-005-0955-0. Epub 2005 Aug 17. J Neurol. 2006. PMID: 16096811 No abstract available.

6

CSF biomarker profile and diagnostic value in vascular dementia.

Paraskevas GP, Kapaki E, Papageorgiou SG, Kalfakis N, Andreadou E, Zalonis I, Vassilopoulos D. Paraskevas GP, et al. Among authors: kalfakis n. Eur J Neurol. 2009 Feb;16(2):205-11. doi: 10.1111/j.1468-1331.2008.02387.x. Eur J Neurol. 2009. PMID: 19146641 Clinical Trial.

7

Distribution of muscle fibre types in human skeletal muscle fascicles: an autopsy study of three human muscles.

Manta P, Kalfakis N, Kararizou E, Vassilopoulos D, Papageorgiou K. Manta P, et al. Among authors: kalfakis n. Funct Neurol. 1995 May-Jun;10(3):137-41. Funct Neurol. 1995. PMID: 8557215 Clinical Trial.

8

Platelet monoamine oxidase activity in subjects tested for Huntington's disease gene mutation.

Markianos M, Panas M, Kalfakis N, Vassilopoulos D. Markianos M, et al. Among authors: kalfakis n. J Neural Transm (Vienna). 2004 Apr;111(4):475-83. doi: 10.1007/s00702-003-0103-x. Epub 2004 Feb 4. J Neural Transm (Vienna). 2004. PMID: 15057517

9

Pseudodominant Friedreich's ataxia with phenotypic heterogeneity.

Panas M, Kalfakis N, Vassilopoulos D. Panas M, et al. Among authors: kalfakis n. Acta Neurol Scand. 2007 May;115(5):364-6. doi: 10.1111/j.1600-0404.2007.00734.x. Acta Neurol Scand. 2007. PMID: 17489949

10

Huntington's disease in Greece: the experience of 14 years.

Panas M, Karadima G, Vassos E, Kalfakis N, Kladi A, Christodoulou K, Vassilopoulos D. Panas M, et al. Among authors: kalfakis n. Clin Genet. 2011 Dec;80(6):586-90. doi: 10.1111/j.1399-0004.2010.01603.x. Epub 2010 Dec 20. Clin Genet. 2011. PMID: 21166788

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