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G Karadima

Showing results (1-10 of 33) with videos related to

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Clinical Genetics|January 17, 2012
Mutational analysis of PMP22, GJB1 and MPZ in Greek Charcot-Marie-Tooth type 1 neuropathy patientsG Karadima, P Floroskufi, G Koutsis, et al.
Journal of Neurology|August 13, 2005
Four novel connexin 32 mutations in X-linked Charcot-Marie-Tooth disease with phenotypic variabilityG Karadima, M Panas, P Floroskufi, et al.
Journal of Neurology|April 15, 2004
Charcot-Marie-Tooth disease type 1A with central nervous system involvement in two generationsM Panas, G Karadima, N Kalfakis, et al.
Clinical Genetics|July 12, 2008
Phenotypic discordance in a pair of monozygotic twins with Huntington's diseaseM Panas, G Karadima, M Markianos, et al.
Clinical Genetics|August 18, 1999
Angelman syndrome with uniparental disomy due to paternal meiosis II nondisjunctionJ Gyftodimou, G Karadima, E Pandelia, et al.
Journal of Neurology|August 27, 1999
Apolipoprotein E and presenilin-1 genotypes in Huntington's diseaseM Panas, D Avramopoulos, G Karadima, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|September 23, 2008
An APOA1 promoter polymorphism is associated with cognitive performance in patients with multiple sclerosisG Koutsis, M Panas, E Giogkaraki, et al.
Neuroscience Letters|April 27, 2019
Disentangling balance impairments in spinal and bulbar muscular atrophyE Anagnostou, A Zachou, M Breza, et al.
Acta Neurologica Belgica|September 18, 2008
Central motor and sensory pathway involvement in an X-linked Charcot-Marie-Tooth familyT Zambelis, M Panas, P Kokotis, et al.
Neurology|November 13, 2002
Hereditary neuropathy with liability to pressure palsies emerging during vincristine treatmentN Kalfakis, M Panas, G Karadima, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Clinical Genetics|January 17, 2012
Mutational analysis of PMP22, GJB1 and MPZ in Greek Charcot-Marie-Tooth type 1 neuropathy patientsG Karadima, P Floroskufi, G Koutsis, et al.
Journal of Neurology|August 13, 2005
Four novel connexin 32 mutations in X-linked Charcot-Marie-Tooth disease with phenotypic variabilityG Karadima, M Panas, P Floroskufi, et al.
Journal of Neurology|April 15, 2004
Charcot-Marie-Tooth disease type 1A with central nervous system involvement in two generationsM Panas, G Karadima, N Kalfakis, et al.
Clinical Genetics|July 12, 2008
Phenotypic discordance in a pair of monozygotic twins with Huntington's diseaseM Panas, G Karadima, M Markianos, et al.
Clinical Genetics|August 18, 1999
Angelman syndrome with uniparental disomy due to paternal meiosis II nondisjunctionJ Gyftodimou, G Karadima, E Pandelia, et al.
Journal of Neurology|August 27, 1999
Apolipoprotein E and presenilin-1 genotypes in Huntington's diseaseM Panas, D Avramopoulos, G Karadima, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|September 23, 2008
An APOA1 promoter polymorphism is associated with cognitive performance in patients with multiple sclerosisG Koutsis, M Panas, E Giogkaraki, et al.
Neuroscience Letters|April 27, 2019
Disentangling balance impairments in spinal and bulbar muscular atrophyE Anagnostou, A Zachou, M Breza, et al.
Acta Neurologica Belgica|September 18, 2008
Central motor and sensory pathway involvement in an X-linked Charcot-Marie-Tooth familyT Zambelis, M Panas, P Kokotis, et al.
Neurology|November 13, 2002
Hereditary neuropathy with liability to pressure palsies emerging during vincristine treatmentN Kalfakis, M Panas, G Karadima, et al.
Pageof 4