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Results: 1-14 |
Results: 14
An open letter to the Committee on the Nobel Prize in Medicine
Authors: Abbruzzese, G Agid, Y Albanese, A Alf, C Allen, R Amar, K de Andrade, LA Ang, LC Angelini, C Archer, RL Arunodaya, GR Baltzan, M Baral, K Barnett, H Bergamasco, B Berger, M Bernard, J Bharucha, NE Bhatia, K Blary, N Black, S Bodis-Wollner, I Boyson, SJ Bral-Kulaksizoglu, I Brooks, DJ Brown, JD Burke, RE Calne, DOC Calne, SM Cardoso, F Cardozo-Pelaez, F Chang, YJ Chen, CC Chen, RS Chen, R Chowdhury, A Christie, S Chu, CC Chu, NS Clarida, L Collette, EM Comella, C Conneally, PM Crossman, AR Csanda, E Dalmau, J Dalvi, A De Feijter, A Deecke, L Desai, H De Ybenes, J Dihenia, B Direnfeld, L Dodel, R Donat, J Doudet, D Duane, DD Duff, J Duvoisin, R Eggert, K Elble, RJ Elmer, LW Emre, M Fariello, R Fernendy, HH Findley, LJ Fink, S Freissmuth, M Friedman, JH de la Fuente-Fernandez, R Furtado, S Furukawa, Y Galvez-Jimenez, N Gauthier, S Gawel, MJ Gilman, S Gladstone, RM Goetz, CG Gomori, A Gopinathan, G Gordin, A Gorell, JM Greenamyre, JT Grimes, DA Gurvit, H Guttman, M Guzman, DA Hachinski, V Hanagasi, H Hardy, J Harik, SJ Hassan, MN Hattori, N Hauser, RA Hayashi, H Heller, GL Hobson, D Hochschorner, G Hortnagel, H Horowski, R Howse, DC Huang, CC Huk, II Hurtig, H Hutton, JT Jaffe, ME Jankovic, J Jardine, M Jog, M Johnson, B Kagamihara, Y Karagoz, N Kasper, S Kato, S Kebabian, JW Kertsz, A Khadilkar, SV Kirk, A Kish, S Kitaguchi, T Kofman, OS Koide, R Komori, T Kostyuk, PG Kumar, R Kuo, HC Kurlan, R Kurland, L Kurtuncu, M Lalkaka, JA Lambert, M Landau, W Lang, AE Lassmann, H Lee, CS Lees, AJ Lieberman, A Litvan, I Loeb, C Logan, WJ Lozano, AM Lu, CS Lucy, D Lynch, T Manyam, BV Maraganore, D Marshall, FT Martin, WRW Martin, WE Mathias, C Matsubera, S Mendis, T Menkes, JH Metz, LN Miyazaki, Y Mizuno, Y Mohr, E Moodley, LG Moore, R Morris, JL Muthane, U Nagaraja, D Nair, CPV Narabayashi, H Nomura, Y Norris, JW Obeso, JA O'Brien, C Oertel, W Ohtake, T Okiyama, R Ozdemir, C Pal, PK Panisset, M Paty, DW Paulson, GW Perlmutter, J Pfeiffer, RF Pifl, C Pincus, JH Poewe, W Quinn, N Rajput, AH Rajput, A Ransmayr, G Rascol, O Robinson, R Rocca, WA Roos, RAC Rosenfeld, MR Russell, D Ruth, TJ Ryu, SJ Sachdev, H Safoschnik, G Sahin, H Sanchez-Ramos, J Satishchandra, P Schapira, A",Scheltens,"Schmidley, JW Schnaberth, G Schneider, E Schneider, JS Schutz, W Seeberger, LC Segawa, M Sethi, KD Shah, A Shannon, K Shelton, P Shihabuddin, B Shimizu, T Shinotoh, H Siddique, T Siderowf, A Sieghart, W Simard, A Simmonds, DC Singhal, BS Sluga, E Snow, BJ Soukop, W Sperk, G Spieker, S Steele, JC Stewart, S Stoessl, AJ Subramony, SH Sundaram, M Sung, CY Surya, N Sweet, RD Tabbal, SD Takahashi, H Taniguchi, M Tarsy, D Teravainen, H Tetrud, JW Tolosa, E Tourtellotte, WW Troupin, AS Tsui, JKC Tuite, P Uc, EY Ueki, Y Uitti, R Uyu, C van Hilten, JJ Veerendrakumar, M Veloso, F Viallet, F Voll, C Vrooman, M Wang, X Ward, I Ward, A Waters, C Weng, YH Wenning, GK Williams, BJ Wilson, TW Wolters, EC Wooten, FG Wszolek, Z Yahr, MD Yanagisawa, N Yokochi, F Young, RR Yu, CM Zifko, U
Citation: G. Abbruzzese et al., An open letter to the Committee on the Nobel Prize in Medicine, PARKINS R D, 7(2), 2001, pp. 149-155
The gene encoding alsin, a protein with three guanine-nucleoticle exchangefactor domains, is mutated in a form of recessive amyotrophic lateral sclerosis (vol 29, pg 160, 2001)
Authors: Yang, Y Hentati, A Deng, HX Dabbagh, O Sasaki, T Hirano, M Hung, WY Ouahchi, K Yan, J Azim, AC Cole, N Gascon, G Yagmour, A Ben-Hamida, M Pericak-Vance, M Hentati, F Siddique, T
Citation: Y. Yang et al., The gene encoding alsin, a protein with three guanine-nucleoticle exchangefactor domains, is mutated in a form of recessive amyotrophic lateral sclerosis (vol 29, pg 160, 2001), NAT GENET, 29(3), 2001, pp. 352-352
The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis
Authors: Yang, Y Hentati, A Deng, HX Dabbagh, O Sasaki, T Hirano, M Hung, WY Ouahchi, K Yan, JH Azim, AC Cole, N Gascon, G Yagmour, A Ben-Hamida, M Pericak-Vance, M Hentati, F Siddique, T
Citation: Y. Yang et al., The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis, NAT GENET, 29(2), 2001, pp. 160-165
Current status of SOD1 mutations in familial amyotrophic lateral sclerosis
Authors: Gaudette, M Hirano, M Siddique, T
Citation: M. Gaudette et al., Current status of SOD1 mutations in familial amyotrophic lateral sclerosis, AMYOTROPH L, 1(2), 2000, pp. 83-89
Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22
Authors: Hosler, BA Siddique, T Sapp, PC Sailor, W Huang, MC Hossain, A Daube, JR Nance, M Fan, CH Kaplan, J Hung, WY McKenna-Yasek, D Haines, JL Pericak-Vance, MA Horvitz, HR Brown, RH
Citation: Ba. Hosler et al., Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22, J AM MED A, 284(13), 2000, pp. 1664-1669
Novel mutations in spastin gene and absence of correlation with age at onset of symptoms
Authors: Hentati, A Deng, HX Zhai, H Chen, W Yang, Y Hung, WY Azim, AC Bohlega, S Tandan, R Warner, C Laing, NG Cambi, F Mitsumoto, H Roos, RP Boustany, RM Ben Hamida, M Hentati, F Siddique, T
Citation: A. Hentati et al., Novel mutations in spastin gene and absence of correlation with age at onset of symptoms, NEUROLOGY, 55(9), 2000, pp. 1388-1390
Increased reactive oxygen species in familial amyotrophic lateral sclerosis with mutations in SOD1
Authors: Ahmed, MS Hung, WY Zu, JS Hockberger, P Siddique, T
Citation: Ms. Ahmed et al., Increased reactive oxygen species in familial amyotrophic lateral sclerosis with mutations in SOD1, J NEUR SCI, 176(2), 2000, pp. 88-94
Multiple transcripts of the human Cu,Zn superoxide dismutase gene
Authors: Hirano, M Hung, WY Cole, N Azim, AC Deng, HX Siddique, T
Citation: M. Hirano et al., Multiple transcripts of the human Cu,Zn superoxide dismutase gene, BIOC BIOP R, 276(1), 2000, pp. 52-56
Transgenic mouse models and human neurodegenerative disorders
Authors: Deng, HX Siddique, T
Citation: Hx. Deng et T. Siddique, Transgenic mouse models and human neurodegenerative disorders, ARCH NEUROL, 57(12), 2000, pp. 1695-1702
Genetic disorders of motor neurons
Authors: Cole, N Siddique, T
Citation: N. Cole et T. Siddique, Genetic disorders of motor neurons, SEM NEUROL, 19(4), 1999, pp. 407-418
Neurodegenerative diseases of Guam: Analysis of TAU
Authors: Perez-Tur, J Buee, L Morris, HR Waring, SC Onstead, L Wavrant-De Vrieze, F Crook, R Buee-Scherrer, V Hof, PR Petersen, RC McGeer, PL Delacourte, A Hutton, M Siddique, T Ahlskog, JE Hardy, J Steele, JC
Citation: J. Perez-tur et al., Neurodegenerative diseases of Guam: Analysis of TAU, NEUROLOGY, 53(2), 1999, pp. 411-413
A controlled trial of recombinant methionyl human BDNF in ALS
Authors: Kasarskis, EJ Shefner, JM Miller, R Smith, RA Licht, J Mitsumoto, H Hopkins, LC Rosenfeld, J Pascuzzi, R Cornblath, DR Armon, C Strong, MJ Kula, R Windebank, A Bosch, EP Smith, BE Cashman, N Sivak, M Sergay, S Siddique, T Sufit, RL Johnston, W Brooke, MB Graves, MC Olney, RK Roos, RP Neville, H Ringel, SP Ross, M Bradley, WG Sharma, KR Parry, G Mandler, R Giuliani, M Thornton, CA Jackson, C Bryan, W Bromberg, M Tandan, R Fries, T Phillips, L Brooks, BR Fenichel, G Pestronk, A Bear, M Beatey, R Fuller, C Hill, R Malta, E Nakanishi, A Patel, A Thurmond, B Cedarbaum, JM Stambler, N
Citation: Ej. Kasarskis et al., A controlled trial of recombinant methionyl human BDNF in ALS, NEUROLOGY, 52(7), 1999, pp. 1427-1433
Macrostatin, a novel macromolecular inhibitor of topoisomerases produced by Streptomyces avermitilis No. C-127
Authors: Suzuki, K Sekimoto, J Siddique, T Kamiya, A Uyeda, M
Citation: K. Suzuki et al., Macrostatin, a novel macromolecular inhibitor of topoisomerases produced by Streptomyces avermitilis No. C-127, J ENZ INHIB, 14(1), 1998, pp. 69-83
Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factor
Authors: Al-Chalabi, A Andersen, PM Chioza, B Shaw, C Sham, PC Robberecht, W Matthijs, G Camu, V Marklund, SL Forsgren, L Rouleau, G Laing, NG Hurse, PV Siddique, T Leigh, PN Powell, JF
Citation: A. Al-chalabi et al., Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factor, HUM MOL GEN, 7(13), 1998, pp. 2045-2050
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