Related content

Autosomal dominant juvenile amyotrophic lateral sclerosis

By Rabin Bruce A.   Griffin John W.   Crain Barbara J.   Scavina Mena   Chance Philip F.  

Brain, Vol. 122, Iss. 8, 1999-08 ,pp. : 1539-1550

Oxford University Press

Access to resources Recommend Favorite

New mutation in the SOD1 (copper/zinc superoxide dismutase-1) gene in a Chinese amyotrophic lateral sclerosis (ALS) patient

By Cui Fang   Cai Wanshi   Wang Zhanjun   Ren Yuting   Li Mao   Sun Zhongsheng   Huang Xusheng  

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Vol. 14, Iss. 7-8, 2013-12 ,pp. : 635-637

Informa Healthcare

Access to resources Recommend Favorite

An amyotrophic lateral sclerosis-like syndrome revealing an amyloid polyneuropathy associated with a novel transthyretin mutation

By Lozeron Pierre   Lacroix Catherine   Theaudin Marie   Richer Anne   Gugenheim Michel   Adams David   Misrahi Micheline  

Amyloid: The Journal of Protein Folding Disorders, Vol. 20, Iss. 3, 2013-09 ,pp. : 188-192

Informa Healthcare

Access to resources Recommend Favorite

Familial amyotrophic lateral sclerosis with bulbar onset and a novel Asp101Tyr Cu/Zn superoxide dismutase gene mutation

By Tan Chun-Feng   Piao Yue-Shan   Hayashi Shintaro   Obata Hiroaki   Umeda Yoshitaka   Sato Masahisa   Fukushima Takao   Nakano Ryoichi   Tsuji Shoji   Takahashi Hitoshi  

Acta Neuropathologica, Vol. 108, Iss. 4, 2004-10 ,pp. : 332-336

Springer Publishing Company

Access to resources Recommend Favorite

Detection of a novel frameshift mutation and regions with homozygosis within ARHGEF28 gene in familial amyotrophic lateral sclerosis

By Droppelmann Cristian A.   Wang Jian   Campos-Melo Danae   Keller Brian   Volkening Kathryn   Hegele Robert A.   Strong Michael J.  

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Vol. 14, Iss. 5-6, 2013-09 ,pp. : 444-451

Informa Healthcare

Access to resources Recommend Favorite