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Results: 1-16 |
Results: 16
Association between-G308A tumor necrosis factor alpha gene polymorphism and schizophrenia
Authors: Boin, F Zanardini, R Pioli, R Altamura, CA Maes, M Gennarelli, M
Citation: F. Boin et al., Association between-G308A tumor necrosis factor alpha gene polymorphism and schizophrenia, MOL PSYCHI, 6(1), 2001, pp. 79-82
Human Y-chromosome variation in the Western Mediterranean area: Implications for the peopling of the region
Authors: Scozzari, R Cruciani, F Pangrazio, A Santolamazza, P Vona, G Moral, P Latini, V Varesi, L Memmi, MM Romano, V De Leo, G Gennarelli, M Jaruzelska, J Villems, R Parik, J Macaulay, V Torroni, A
Citation: R. Scozzari et al., Human Y-chromosome variation in the Western Mediterranean area: Implications for the peopling of the region, HUMAN IMMUN, 62(9), 2001, pp. 871-884
Serine/threonine kinases as molecular targets of antidepressants: implications for pharmacological treatment and pathophysiology of affective disorders
Authors: Popoli, M Mori, S Brunello, N Perez, J Gennarelli, M Racagni, G
Citation: M. Popoli et al., Serine/threonine kinases as molecular targets of antidepressants: implications for pharmacological treatment and pathophysiology of affective disorders, PHARM THERA, 89(2), 2001, pp. 149-170
Decreased hippocampal BDNF expression after acute systemic injection of quinpirole
Authors: Fumagalli, F Santero, R Gennarelli, M Racagni, G Riva, MA
Citation: F. Fumagalli et al., Decreased hippocampal BDNF expression after acute systemic injection of quinpirole, NEUROPHARM, 40(7), 2001, pp. 954-957
Stimulatory role of dopamine on fibroblast growth factor-2 expression in rat striatum
Authors: Roceri, M Molteni, R Fumagalli, F Racagni, G Gennarelli, M Corsini, GU Maggio, R Riva, MA
Citation: M. Roceri et al., Stimulatory role of dopamine on fibroblast growth factor-2 expression in rat striatum, J NEUROCHEM, 76(4), 2001, pp. 990-997
Epidemiology of myotonic dystrophy in Italy: re-apprisal after genetic diagnosis
Authors: Siciliano, G Manca, ML Gennarelli, M Angelini, C Rocchi, A Iudice, A Miorin, M Mostacciuolo, ML
Citation: G. Siciliano et al., Epidemiology of myotonic dystrophy in Italy: re-apprisal after genetic diagnosis, CLIN GENET, 59(5), 2001, pp. 344-349
Long-term treatment with S-adenosylmethionine induces changes in presynaptic CaM kinase II and synapsin I
Authors: Consogno, E Tiraboschi, E Iuliano, E Gennarelli, M Racagni, G Popoli, M
Citation: E. Consogno et al., Long-term treatment with S-adenosylmethionine induces changes in presynaptic CaM kinase II and synapsin I, BIOL PSYCHI, 50(5), 2001, pp. 337-344
Modulation of glutamate receptors in response to the novel antipsychotic olanzapine in rats
Authors: Tascedda, F Blom, JMC Brunello, N Zolin, K Gennarelli, M Colzi, A Bravi, D Carra, S Racagni, G Riva, MA
Citation: F. Tascedda et al., Modulation of glutamate receptors in response to the novel antipsychotic olanzapine in rats, BIOL PSYCHI, 50(2), 2001, pp. 117-122
Natural history of cardiac involvement in myotonic dystrophy: Correlation with CTG repeats
Authors: Antonini, G Giubilei, F Mammarella, A Amicucci, P Fiorelli, M Gragnani, F Morino, S Ceschin, V Fragola, PV Gennarelli, M
Citation: G. Antonini et al., Natural history of cardiac involvement in myotonic dystrophy: Correlation with CTG repeats, NEUROLOGY, 55(8), 2000, pp. 1207-1209
New nomenclature and DNA testing guidelines for myotonic dystrophy type 1(DM1)
Authors: Gonzalez, I Ohsawa, N Singer, RH Devillers, M Ashizawa, T Balasubramanyam, A Cooper, TA Khajavi, M Lia-Baldini, AS Miller, G Philips, AV Timchenko, LT Waring, J Yamagata, H Barbet, JP Klesert, TR Tapscott, SJ Roses, AD Wagner, M Baiget, M Martorell, L Browne, GB Eymard, B Gourdon, G Junien, C Seznec, H Carey, N Gosling, M Maire, P Gennarelli, M Sato, S Ansved, T Kvist, U Eriksson, M Furling, D Chen, EJ Housman, DE Luciano, B Siciliano, M Spring, N Shimizu, M Eddy, E Morris, GE Krahe, R Furuya, H Adelman, J Pribnow, D Furutama, D Mathieu, J Hilton-Jones, D Kinoshita, M Abbruzzese, C Sinden, RR Wells, RD Pearson, CE Kobayashi, T Johansson, A Salvatori, S Perryman, B Swanson, MS Gould, FK Harris, SE Johnson, K Mitchell, AM Monckton, DG Winchester, CL Antonini, G Day, JW Liquori, C Ranum, LPW Westerlaken, J Wieringa, B Griffith, JD Michalowski, S Moore, H Hamshere, M Korade, Z Thornton, CA Jaeger, H Lehmann, F Moorman, JR Mounsey, JP Mahadevan, MS
Citation: I. Gonzalez et al., New nomenclature and DNA testing guidelines for myotonic dystrophy type 1(DM1), NEUROLOGY, 54(6), 2000, pp. 1218-1221
Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma
Authors: Amicucci, P Gennarelli, M Novelli, G Dallapiccola, B
Citation: P. Amicucci et al., Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma, CLIN CHEM, 46(2), 2000, pp. 301-302
Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expression
Authors: Korade-Mirnics, Z Tarleton, J Servidei, S Casey, RR Gennarelli, M Pegoraro, E Angelini, C Hoffman, EP
Citation: Z. Korade-mirnics et al., Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expression, HUM MOL GEN, 8(6), 1999, pp. 1017-1023
Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patients
Authors: Gennarelli, M Pavoni, M Amicucci, P Angelini, C Menegazzo, E Zelano, G Novelli, G Dallapiccola, B
Citation: M. Gennarelli et al., Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patients, NEUROMUSC D, 9(4), 1999, pp. 215-219
CTG repeats distribution and Alu insertion polymorphism at myotonic dystrophy (DM) gene in Amhara and Oromo populations of Ethiopia
Authors: Gennarelli, M Pavoni, M Cruciani, F De Stefano, G Dallapiccola, B Novelli, G
Citation: M. Gennarelli et al., CTG repeats distribution and Alu insertion polymorphism at myotonic dystrophy (DM) gene in Amhara and Oromo populations of Ethiopia, HUM GENET, 105(1-2), 1999, pp. 165-167
A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13
Authors: Servidei, S Capon, F Spinazzola, A Mirabella, M Semprini, S de Rosa, G Gennarelli, M Sangiuolo, F Ricci, E Mohrenweiser, HW Dallapiccola, B Tonali, P Novelli, G
Citation: S. Servidei et al., A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13, NEUROLOGY, 53(4), 1999, pp. 830-837
Cognitive impairment and (CTG)n expansion in myotonic dystrophy patients
Authors: Perini, GI Menegazzo, E Ermani, M Zara, M Gemma, A Ferruzza, E Gennarelli, M Angelini, C
Citation: Gi. Perini et al., Cognitive impairment and (CTG)n expansion in myotonic dystrophy patients, BIOL PSYCHI, 46(3), 1999, pp. 425-431
Risultati: 1-16 |