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D Vassilopoulos

Showing results (131-140 of 146) with videos related to

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Acta Neurologica Scandinavica|November 8, 2007
Circulating interleukin-15 and RANTES chemokine in Parkinson's diseaseM Rentzos, C Nikolaou, E Andreadou, et al.
Acta Neurologica Scandinavica|November 4, 2008
Circulating interleukin-10 and interleukin-12 in Parkinson's diseaseM Rentzos, C Nikolaou, E Andreadou, et al.
Psychiatric Genetics|March 4, 2000
Association between the dopamine D3 receptor gene locus (DRD3) and unipolar affective disorderD G Dikeos, G N Papadimitriou, D Avramopoulos, et al.
Clinical and Experimental Rheumatology|July 17, 2009
The epidemiology of primary systemic vasculitides involving small vessels in Crete (southern Greece): a comparison of older versus younger adult patientsS H Panagiotakis, G S Perysinakis, H Kritikos, et al.
European Neurology|June 10, 2010
The onset of multiple sclerosis in Greece: a single-center study of 1,034 consecutive patientsG Koutsis, M E Evangelopoulos, E Andreadou, et al.
Clinical and Experimental Rheumatology|November 27, 2008
Evidence-based recommendations for the management of ankylosing spondylitis: results of the Hellenic working group of the 3E Initiative in RheumatologyA Raptopoulou, P Sidiropoulos, P Siakka, et al.
Clinical and Experimental Rheumatology|January 27, 2004
Study of host and virological factors of patients with chronic HCV infection and associated laboratory or clinical autoimmune manifestationsD Vassilopoulos, Z M Younossi, E Hadziyannis, et al.
American Journal of Medical Genetics|May 2, 1997
Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: case report and review of the literature on partial trisomy 17qterC Sarri, J Gyftodimou, D Avramopoulos, et al.
Journal of Neurology|March 1, 1996
Hereditary neuropathy with liability to pressure palsies: the same molecular defect can result in diverse clinical presentationE Andreadou, C Yapijakis, G P Paraskevas, et al.
Blood|October 27, 1998
Apolipoprotein E epsilon4 allele as a genetic risk factor for left ventricular failure in homozygous beta-thalassemiaE Economou-Petersen, A Aessopos, A Kladi, et al.
Pageof 15

Showing results (131-140 of 146) with videos related to

Sort By:
Pageof 15
Acta Neurologica Scandinavica|November 8, 2007
Circulating interleukin-15 and RANTES chemokine in Parkinson's diseaseM Rentzos, C Nikolaou, E Andreadou, et al.
Acta Neurologica Scandinavica|November 4, 2008
Circulating interleukin-10 and interleukin-12 in Parkinson's diseaseM Rentzos, C Nikolaou, E Andreadou, et al.
Psychiatric Genetics|March 4, 2000
Association between the dopamine D3 receptor gene locus (DRD3) and unipolar affective disorderD G Dikeos, G N Papadimitriou, D Avramopoulos, et al.
Clinical and Experimental Rheumatology|July 17, 2009
The epidemiology of primary systemic vasculitides involving small vessels in Crete (southern Greece): a comparison of older versus younger adult patientsS H Panagiotakis, G S Perysinakis, H Kritikos, et al.
European Neurology|June 10, 2010
The onset of multiple sclerosis in Greece: a single-center study of 1,034 consecutive patientsG Koutsis, M E Evangelopoulos, E Andreadou, et al.
Clinical and Experimental Rheumatology|November 27, 2008
Evidence-based recommendations for the management of ankylosing spondylitis: results of the Hellenic working group of the 3E Initiative in RheumatologyA Raptopoulou, P Sidiropoulos, P Siakka, et al.
Clinical and Experimental Rheumatology|January 27, 2004
Study of host and virological factors of patients with chronic HCV infection and associated laboratory or clinical autoimmune manifestationsD Vassilopoulos, Z M Younossi, E Hadziyannis, et al.
American Journal of Medical Genetics|May 2, 1997
Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: case report and review of the literature on partial trisomy 17qterC Sarri, J Gyftodimou, D Avramopoulos, et al.
Journal of Neurology|March 1, 1996
Hereditary neuropathy with liability to pressure palsies: the same molecular defect can result in diverse clinical presentationE Andreadou, C Yapijakis, G P Paraskevas, et al.
Blood|October 27, 1998
Apolipoprotein E epsilon4 allele as a genetic risk factor for left ventricular failure in homozygous beta-thalassemiaE Economou-Petersen, A Aessopos, A Kladi, et al.
Pageof 15