Valosin-Containing Protein Gene Mutations: Cellular Phenotypes Relevant to Neurodegeneration

By Poksay Karen   Madden David   Peter Anna   Niazi Kayvan   Banwait Surita   Crippen Danielle   Bredesen Dale   Rao Rammohan  

Journal of Molecular Neuroscience, Vol. 44, Iss. 2, 2011-06 ,pp. : 91-102

Humana Press, Inc

Access to resources Recommend Favorite

Valosin-containing protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy

By Guinto Jake   Ritson Gillian   Taylor J.   Forman Mark  

Acta Neuropathologica, Vol. 114, Iss. 1, 2007-07 ,pp. : 55-61

Springer Publishing Company

Access to resources Recommend Favorite

A novel mutation in the SPG3A gene (atlastin) in hereditary spastic paraplegia

By Matsui M.   Kawarai T.   Hase Y.   Tomimoto H.   Iseki K.   Rogaeva E.   Orlacchio A.   Bernardi G.   George-Hyslop P.   Takahashi R.   Matsui M.  

Journal of Neurology, Vol. 254, Iss. 7, 2007-07 ,pp. : 972-974

Springer Publishing Company

Access to resources Recommend Favorite

Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations

By Orthmann-Murphy Jennifer L.   Salsano Ettore   Abrams Charles K.   Bizzi Alberto   Uziel Graziella   Freidin Mona M.   Lamantea Eleonora   Zeviani Massimo   Scherer Steven S.   Pareyson Davide  

Brain, Vol. 132, Iss. 2, 2009-02 ,pp. : 426-438

Oxford University Press

Access to resources Recommend Favorite

Gait analysis of sporadic and hereditary spastic paraplegia

By Klebe S.   Stolze H.   Kopper F.   Lorenz D.   Wenzelburger R.   Volkmann J.   Porschke H.   Deuschl G.  

Journal of Neurology, Vol. 251, Iss. 5, 2004-05 ,pp. : 571-578

Springer Publishing Company

Access to resources Recommend Favorite