Kalfakis N - Search Results

1

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

2

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

3

Phenotypic discordance in a pair of monozygotic twins with Huntington's disease.

Panas M, Karadima G, Markianos M, Kalfakis N, Vassilopoulos D. Panas M, et al. Among authors: kalfakis n. Clin Genet. 2008 Sep;74(3):291-2. doi: 10.1111/j.1399-0004.2008.01036.x. Epub 2008 Jul 9. Clin Genet. 2008. PMID: 18616735 No abstract available.

4

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

5

Amyotrophic lateral sclerosis in southern Greece: an epidemiologic study.

Kalfakis N, Vassilopoulos D, Voumvourakis C, Ndjeveleka M, Papageorgiou C. Kalfakis N, et al. Neuroepidemiology. 1991;10(4):170-3. doi: 10.1159/000110266. Neuroepidemiology. 1991. PMID: 1745326

6

Migraine with aura: segregation analysis and heritability estimation.

Kalfakis N, Panas M, Vassilopoulos D, Malliara-Loulakaki S. Kalfakis N, et al. Headache. 1996 May;36(5):320-2. doi: 10.1046/j.1526-4610.1996.3605320.x. Headache. 1996. PMID: 8682675

7

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

8

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

9

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.

10

Evidence for seasonal variation in polymyositis.

Manta P, Kalfakis N, Vassilopoulos D. Manta P, et al. Among authors: kalfakis n. Neuroepidemiology. 1989;8(5):262-5. doi: 10.1159/000110192. Neuroepidemiology. 1989. PMID: 2812185

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