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D Vassilopoulos

Showing results (51-60 of 146) with videos related to

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Headache|May 1, 1996
Migraine with aura: segregation analysis and heritability estimationN Kalfakis, M Panas, D Vassilopoulos, 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.
Neuroepidemiology|January 1, 1991
Amyotrophic lateral sclerosis in southern Greece: an epidemiologic studyN Kalfakis, D Vassilopoulos, C Voumvourakis, et al.
Functional Neurology|May 1, 1995
Distribution of muscle fibre types in human skeletal muscle fascicles: an autopsy study of three human musclesP Manta, N Kalfakis, E Kararizou, et al.
Clinical Immunology and Immunopathology|December 1, 1996
Defective CD3-mediated cell death in activated T cells from patients with systemic lupus erythematosus: role of decreased intracellular TNF-alphaB Kovacs, D Vassilopoulos, S A Vogelgesang, et al.
Human Mutation|April 29, 1999
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. OnlineC Karadimas, M Panas, P Chronopoulou, et al.
Clinical Neuropathology|March 1, 1996
Size and proportion of fiber types in human muscle fasciclesP Manta, N Kalfakis, E Kararizou, et al.
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.
Pageof 15

Showing results (51-60 of 146) with videos related to

Sort By:
Pageof 15
Headache|May 1, 1996
Migraine with aura: segregation analysis and heritability estimationN Kalfakis, M Panas, D Vassilopoulos, 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.
Neuroepidemiology|January 1, 1991
Amyotrophic lateral sclerosis in southern Greece: an epidemiologic studyN Kalfakis, D Vassilopoulos, C Voumvourakis, et al.
Functional Neurology|May 1, 1995
Distribution of muscle fibre types in human skeletal muscle fascicles: an autopsy study of three human musclesP Manta, N Kalfakis, E Kararizou, et al.
Clinical Immunology and Immunopathology|December 1, 1996
Defective CD3-mediated cell death in activated T cells from patients with systemic lupus erythematosus: role of decreased intracellular TNF-alphaB Kovacs, D Vassilopoulos, S A Vogelgesang, et al.
Human Mutation|April 29, 1999
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. OnlineC Karadimas, M Panas, P Chronopoulou, et al.
Clinical Neuropathology|March 1, 1996
Size and proportion of fiber types in human muscle fasciclesP Manta, N Kalfakis, E Kararizou, et al.
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.
Pageof 15