Panas M - Search Results

1

Hereditary spastic paraplegia in Greece: characterisation of a previously unexplored population using next-generation sequencing.

Lynch DS, Koutsis G, Tucci A, Panas M, Baklou M, Breza M, Karadima G, Houlden H. Lynch DS, et al. Among authors: panas m. Eur J Hum Genet. 2016 Jun;24(6):857-63. doi: 10.1038/ejhg.2015.200. Epub 2015 Sep 16. Eur J Hum Genet. 2016. PMID: 26374131 Free PMC article.

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

8

Acute painful sensory neuropathy with subclinical autonomic dysfunction as a presenting feature of Hodgkin's disease.

Koutsis G, Spengos K, Panas M, Dimitrakopoulos A, Sfagos C, Vassilopoulos D. Koutsis G, et al. Among authors: panas m. Eur Neurol. 2005;53(3):157-9. doi: 10.1159/000086125. Epub 2004 May 28. Eur Neurol. 2005. PMID: 15942238 No abstract available.

9

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: panas m. Muscle Nerve. 2007 May;35(5):667-9. doi: 10.1002/mus.20703. Muscle Nerve. 2007. PMID: 17143884

10

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: panas m. Neurology. 2007 Feb 20;68(8):546-9. doi: 10.1212/01.wnl.0000254468.51973.44. Neurology. 2007. PMID: 17310023

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