Panas M - Search Results

1

HINT1-related neuropathy in Greek patients with Charcot-Marie-Tooth disease.

Kontogeorgiou Z, Voudommatis C, Kartanou C, Pandis D, Breza M, Zambelis T, Stefanis L, Panas M, Koutsis G, Karadima G. Kontogeorgiou Z, et al. Among authors: panas m. J Peripher Nerv Syst. 2021 Dec;26(4):444-448. doi: 10.1111/jns.12473. Epub 2021 Oct 29. J Peripher Nerv Syst. 2021. PMID: 34694653

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

Three novel mutations in the gap junction beta 1 (GJB1) gene coding region identified in Charcot-Marie-Tooth patients of Greek origin: T55I, R164Q, V120E. Mutation in brief no 236. Online.

Karadimas C, Panas M, Chronopoulou P, Avramopoulos D, Vassilopoulos D. Karadimas C, et al. Among authors: panas m. Hum Mutat. 1999;13(4):339. doi: 10.1002/(SICI)1098-1004(1999)13:4<339::AID-HUMU18>3.0.CO;2-S. Hum Mutat. 1999. PMID: 10220155

4

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

5

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

6

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

7

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.

8

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.

9

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.

10

[Superficial siderosis of the CNS. Case report and literature review].

Spengos K, Koutsis G, Tsivgoulis G, Panas M, Vemmos K, Vassilopoulos D. Spengos K, et al. Among authors: panas m. Nervenarzt. 2004 May;75(5):492-5. doi: 10.1007/s00115-003-1600-8. Nervenarzt. 2004. PMID: 15252890 Review. German.

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