Kalfakis N - Search Results

1

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. Among authors: kalfakis n. J Neurol. 2004 Feb;251(2):222-3. doi: 10.1007/s00415-004-0284-8. J Neurol. 2004. PMID: 14991359 No abstract available.

2

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: kalfakis n. J Neurol. 2002 Nov;249(11):1583-6. doi: 10.1007/s00415-002-0902-2. J Neurol. 2002. PMID: 12420100

3

Symptomatic focal mononeuropathies in diabetic patients: increased or not?

Stamboulis E, Vassilopoulos D, Kalfakis N. Stamboulis E, et al. Among authors: kalfakis n. J Neurol. 2005 Apr;252(4):448-52. doi: 10.1007/s00415-005-0672-8. Epub 2005 Feb 23. J Neurol. 2005. PMID: 15726259

4

Co-segregation of Huntington disease and hereditary spastic paraplegia in 4 generations.

Panas M, Karadima G, Kalfakis N, Vassilopoulos D. Panas M, et al. Among authors: kalfakis n. Neurologist. 2011 Jul;17(4):211-2. doi: 10.1097/NRL.0b013e3182173567. Neurologist. 2011. PMID: 21712667

5

Low plasma total cholesterol in patients with Huntington's disease and first-degree relatives.

Markianos M, Panas M, Kalfakis N, Vassilopoulos D. Markianos M, et al. Among authors: kalfakis n. Mol Genet Metab. 2008 Mar;93(3):341-6. doi: 10.1016/j.ymgme.2007.10.002. Epub 2007 Nov 19. Mol Genet Metab. 2008. PMID: 18006350

6

Association of genetically proven Huntington's disease and sporadic amyotrophic lateral sclerosis in a 72-year-old woman.

Papageorgiou SG, Antelli A, Bonakis A, Vassos E, Zalonis I, Kalfakis N, Panas M. Papageorgiou SG, et al. Among authors: kalfakis n. J Neurol. 2006 Dec;253(12):1649-50. doi: 10.1007/s00415-006-0267-z. J Neurol. 2006. PMID: 17219039 No abstract available.

7

Diagnostic value of CSF biomarker profile in frontotemporal lobar degeneration.

Kapaki E, Paraskevas GP, Papageorgiou SG, Bonakis A, Kalfakis N, Zalonis I, Vassilopoulos D. Kapaki E, et al. Among authors: kalfakis n. Alzheimer Dis Assoc Disord. 2008 Jan-Mar;22(1):47-53. doi: 10.1097/WAD.0b013e3181610fea. Alzheimer Dis Assoc Disord. 2008. PMID: 18317246

8

Asymptomatic elevation of serum creatine kinase leading to the diagnosis of 4q35 facioscapulohumeral muscular dystrophy.

Zouvelou V, Manta P, Kalfakis N, Evdokimidis I, Vassilopoulos D. Zouvelou V, et al. Among authors: kalfakis n. J Clin Neurosci. 2009 Sep;16(9):1218-9. doi: 10.1016/j.jocn.2008.12.004. Epub 2009 Jun 6. J Clin Neurosci. 2009. PMID: 19502063

9

Hereditary neuropathy unmasked by levofloxacin.

Panas M, Karadima G, Kalfakis N, Vassilopoulos D. Panas M, et al. Among authors: kalfakis n. Ann Pharmacother. 2011 Oct;45(10):1312-3. doi: 10.1345/aph.1P786. Epub 2011 Aug 31. Ann Pharmacother. 2011. PMID: 21881033 No abstract available.

10

Psychosis as presenting symptom in adult-onset Hallervorden-Spatz syndrome.

Panas M, Spengos K, Koutsis G, Tsivgoulis G, Sfagos K, Kalfakis N, Vassilopoulos D. Panas M, et al. Among authors: kalfakis n. Acta Neuropsychiatr. 2007 Apr;19(2):122-4. doi: 10.1111/j.1601-5215.2006.00163.x. Acta Neuropsychiatr. 2007. PMID: 26952824

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