Related content

Valosin Containing Protein Associated Fronto-Temporal Lobar Degeneration:Clinical Presentation, Pathologic Features and Pathogenesis

By  

Current Alzheimer Research, Vol. 8, Iss. 3, 2011-05 ,pp. : 252-260

Bentham Science Publishers

Access to resources Recommend Favorite

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

Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases

By Clemen Christoph S.  

Brain, Vol. 133, Iss. 10, 2010-10 ,pp. : 2920-2941

Oxford University Press

Access to resources Recommend Favorite

A novel homozygous missense mutation in the GNE gene of a patient with quadriceps-sparing hereditary inclusion body myopathy associated with muscle inflammation

By Krause S.   Schlotter-Weigel B.   Walter M.C.   Najmabadi H.   Wiendl H.   Muller-Hocker J.   Muller-Felber W.   Pongratz D.   Lochmuller H.  

Neuromuscular Disorders, Vol. 13, Iss. 10, 2003-12 ,pp. : 830-834

Elsevier

Access to resources Recommend Favorite

Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes

By Watts G.D.J.   Thorne M.   Kovach M.J.   Pestronk A.   Kimonis V.E.  

Neuromuscular Disorders, Vol. 13, Iss. 7, 2003-09 ,pp. : 559-567

Elsevier

Access to resources Recommend Favorite