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Results: 1-12 |
Results: 12
Hepatitis B e antigen-negative chronic hepatitis B
Authors: Hadziyannis, SJ Vassilopoulos, D
Citation: Sj. Hadziyannis et D. Vassilopoulos, Hepatitis B e antigen-negative chronic hepatitis B, HEPATOLOGY, 34(4), 2001, pp. 617-624
Immunopathogenesis of hepatitis B e antigen negative chronic hepatitis B infection
Authors: Hadziyannis, SJ Vassilopoulos, D
Citation: Sj. Hadziyannis et D. Vassilopoulos, Immunopathogenesis of hepatitis B e antigen negative chronic hepatitis B infection, ANTIVIR RES, 52(2), 2001, pp. 91-98
Episodes of generalized weakness in two sibs with the C164T mutation of the connexin 32 gene
Authors: Panas, M Kalfakis, N Karadimas, C Vassilopoulos, D
Citation: M. Panas et al., Episodes of generalized weakness in two sibs with the C164T mutation of the connexin 32 gene, NEUROLOGY, 57(10), 2001, pp. 1906-1908
Watermelon stomach and familial mediterranean fever
Authors: Michopoulos, S Tsibouris, P Sotiropoulou, M Petraki, K Vassilopoulos, D Kralios, N
Citation: S. Michopoulos et al., Watermelon stomach and familial mediterranean fever, AM J GASTRO, 96(8), 2001, pp. 2512-2513
Complex management issues: management of HCV in the atypical patient
Authors: Hadziyannis, SJ Vassilopoulos, D
Citation: Sj. Hadziyannis et D. Vassilopoulos, Complex management issues: management of HCV in the atypical patient, BEST PR RES, 14(2), 2000, pp. 277-291
Genotyping of presenilin-1 polymorphism in amyotrophic lateral sclerosis
Authors: Panas, M Karadima, G Kalfakis, N Psarrou, O Floroskoufi, P Kladi, A Petersen, MB Vassilopoulos, D
Citation: M. Panas et al., Genotyping of presenilin-1 polymorphism in amyotrophic lateral sclerosis, J NEUROL, 247(12), 2000, pp. 940-942
Association between presenilin-1 polymorphism and maternal meiosis II errors in Down syndrome
Authors: Petersen, MB Karadima, G Samaritaki, M Avramopoulos, D Vassilopoulos, D Mikkelsen, M
Citation: Mb. Petersen et al., Association between presenilin-1 polymorphism and maternal meiosis II errors in Down syndrome, AM J MED G, 93(5), 2000, pp. 366-372
Clinical utility of testing for antineutrophil cytoplasmic antibodies
Authors: Vassilopoulos, D Hoffman, GS
Citation: D. Vassilopoulos et Gs. Hoffman, Clinical utility of testing for antineutrophil cytoplasmic antibodies, CL DIAG LAB, 6(5), 1999, pp. 645-651
Selected drug complications and treatment conflicts in the presence of coexistent diseases
Authors: Vassilopoulos, D Camisa, C Strauss, RM
Citation: D. Vassilopoulos et al., Selected drug complications and treatment conflicts in the presence of coexistent diseases, RHEUM DIS C, 25(3), 1999, pp. 745
Apolipoprotein E and presenilin-1 genotypes in Huntington's disease
Authors: Panas, M Avramopoulos, D Karadima, G Petersen, MB Vassilopoulos, D
Citation: M. Panas et al., Apolipoprotein E and presenilin-1 genotypes in Huntington's disease, J NEUROL, 246(7), 1999, pp. 574-577
Angelman syndrome with uniparental disomy due to paternal meiosis II nondisjunction
Authors: Gyftodimou, J Karadima, G Pandelia, E Vassilopoulos, D Petersen, MB
Citation: J. Gyftodimou et al., Angelman syndrome with uniparental disomy due to paternal meiosis II nondisjunction, CLIN GENET, 55(6), 1999, pp. 483-486
Central nervous system involvement in four patients with Charcot-Marie-Tooth disease with connexin 32 extracellular mutations
Authors: Panas, M Karadimas, C Avramopoulos, D Vassilopoulos, D
Citation: M. Panas et al., Central nervous system involvement in four patients with Charcot-Marie-Tooth disease with connexin 32 extracellular mutations, J NE NE PSY, 65(6), 1998, pp. 947-948
Risultati: 1-12 |