Familial amyloid polyneuropathy associated with the novel transthyretin variant Arg34Gly

By Levy Jaime  

Amyloid: The Journal of Protein Folding Disorders, Vol. 19, Iss. 4, 2012-12 ,pp. : 201-203

Informa Healthcare

Access to resources Recommend Favorite

Anti-Ma2/Ta antibodies in a woman with primary lateral sclerosis-like phenotype and Sjögren syndrome

By Piccolo Giovanni  

Neurological Sciences, Vol. 32, Iss. 5, 2011-10 ,pp. : 915-917

Springer Publishing Company

Access to resources Recommend Favorite

Recurrent K3E mutation in Cu/Zn superoxide dismutase gene associated with amyotrophic lateral sclerosis

By Kuźma-Kozakiewicz Magdalena   Berdyński Mariusz   Morita Mitsuya   Takahashi Yuji   Kawata Akihiro   Kaida Ken-Ichi   Kaźmierczak Beata   Łusakowska Anna   Goto Jun   Tsuji Shoji   Żekanowski Cezary   Kwieciński Hubert  

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Vol. 14, Iss. 7-8, 2013-12 ,pp. : 608-614

Informa Healthcare

Access to resources Recommend Favorite

A novel compound heterozygous ALS2 mutation in two Italian siblings with juvenile amyotrophic lateral sclerosis

By Luigetti Marco  

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Vol. 14, Iss. 5-6, 2013-09 ,pp. : 470-472

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