Causative genes for familial amyotrophic lateral sclerosis
Hadano, S.
Seikagaku. Journal of Japanese Biochemical Society 74(6): 483-489
2002
ISSN/ISBN: 0037-1017 PMID: 12138710 Document Number: 551364
Document emailed within 1 workday
Related Documents
Bai, K.I.; Sastry, V.N.; Rao, G.K. 1978: Juvenile familial amyotrophic lateral sclerosis Indian Pediatrics 15(12): 1047-1048Saillant, A.; Fauchier, C.; Labarthe, J.C.; Despert, F.; Combe, P. 1981: Juvenile and familial amyotrophic lateral sclerosis. 2 case reports Archives Francaises de Pediatrie 38(4): 247-251
Constantinidis, J. 1987: A familial syndrome: a combination of Pick's disease and amyotrophic lateral sclerosis L'Encephale 13(5): 285-293
Koide, T.; Igarashi, S.; Kikugawa, K.; Nakano, R.; Inuzuka, T.; Tsuji, S.; Yamada, M.; Takahashi, H. 1999: Familial amyotrophic lateral sclerosis associated with mutant Cu/Zn superoxide dismutase as a conformational disease Rinsho Shinkeigaku 39(12): 1283-1284
Spooren, W.P.; Hengerer, B. 2000: DNA laddering and caspase 3-like activity in the spinal cord of a mouse model of familial amyotrophic lateral sclerosis Cellular and Molecular Biology 46(1): 63-69
Mochizuki, Y.; Mizutani, T.; Nakano, R.; Fukushima, T.; Honma, T.; Nemoto, N.; Takei, K. 2003: Clinical features and neuropathological findings of familial amyotrophic lateral sclerosis with an H43R mutation in Cu/Zn superoxide dismutase Rinsho Shinkeigaku 43(8): 491-495
Hamasaki, H.; Takeuchi, Y.; Masui, Y.; Ohta, Y.; Abe, K.; Yoshino, H.; Yanai, H. 2015: Development of diabetes in a familial amyotrophic lateral sclerosis patient carrying the I113T SOD1 mutation. Case Report Neuro Endocrinology Letters 36(5): 414-416
Yang, Y.; Fan, D. 2014: To screen for SQSTM1/p62 gene in Chinese patients with familial amyotrophic lateral sclerosis carrying superoxide dismutase 1 mutation Zhonghua Nei Ke Za Zhi 53(12): 957-960
Tsuchiya, K.; Matsunaga, T.; Aoki, M.; Haga, C.; Ooe, K.; Abe, K.; Ikeda, K.; Nakano, I. 2001: Familial amyotrophic lateral sclerosis with posterior column degeneration and basophilic inclusion bodies: a clinical, genetic and pathological study Clinical Neuropathology 20(2): 53-59
Yoshida, M.; Okuda, S.; Murakami, N.; Hashizume, Y.; Sobue, G. 1995: Two siblings of familial amyotrophic lateral sclerosis with multisystemic degeneration characterized by mild involvement of the middle root zone of the posterior column, Clarke's nuclei and spinocerebellar tract Rinsho Shinkeigaku 35(6): 589-599
Alonso, K.; Medenica, R. 1995: Immunomodulation in the treatment of multiple sclerosis and amyotrophic lateral sclerosis: a model for autoimmune disorders Journal of the National Medical Association 87(8): 561-568
Gallagher, J.P. 1986: Is it amyotrophic lateral sclerosis or something else? Journal of the South Carolina Medical Association 82(1): 19-22
Zavalishin, I.A.; Zakharova, M.N. 1999: Amyotrophic lateral sclerosis Zhurnal Nevrologii i Psikhiatrii Imeni S.S. Korsakova 99(4): 60-64
1995: Riluzole for amyotrophic lateral sclerosis Medical Letter on Drugs and Therapeutics 37(963): 113-114
Bali, T.; Miller, T.M. 2013: Management of amyotrophic lateral sclerosis Missouri medicine 110(5): 417-421
Vemireddi, N.K.; Crevoiserat, C.A. 1978: Amyotrophic lateral sclerosis in cancer Journal of the Mississippi State Medical Association 19(11): 201-204
Kuźma-Kozakiewicz, M.; Kwieciński, H. 2009: The genetics of amyotrophic lateral sclerosis Neurologia i Neurochirurgia Polska 43(6): 538-549
Bouche, P.; Castaigne, P.; Meininger, V. 1989: Management of amyotrophic lateral sclerosis Revue Neurologique (Paris) 145(1): 49-54
Barkhatova, V.P.; Zavalishin, I.A.; Kostiuk, A.V.; Demina, E.G.; Moskvitina, T.A. 1996: Neurotransmitter changes in amyotrophic lateral sclerosis Zhurnal Nevrologii i Psikhiatrii Imeni S.S. Korsakova 96(4): 78-85
Lupo, V.R.; Rusterholz, J.H.; Reichert, J.A.; Hanson, A.S. 1993: Amyotrophic lateral sclerosis in pregnancy Obstetrics and Gynecology 82(4 Pt 2(Suppl): 682-685