Panas M - Search Results

1

Mutational screening of Greek patients with axonal Charcot-Marie-Tooth disease using targeted next-generation sequencing: Clinical and molecular spectrum delineation.

Kontogeorgiou Z, Kartanou C, Rentzos M, Kokotis P, Anagnostou E, Zambelis T, Chroni E, Dinopoulos A, Panas M, Koutsis G, Karadima G. Kontogeorgiou Z, et al. Among authors: panas m. J Peripher Nerv Syst. 2023 Dec;28(4):642-650. doi: 10.1111/jns.12598. Epub 2023 Oct 5. J Peripher Nerv Syst. 2023. PMID: 37747677

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

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. J Neurol. 2004 Apr;251(4):484-5. doi: 10.1007/s00415-004-0376-5. J Neurol. 2004. PMID: 15083299 No abstract available.

9

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.

10

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: panas m. 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.

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