A novel mutation in the VCP gene (G157R) in a german family with inclusion-body myopathy with paget disease of bone and frontotemporal dementia

2009 ◽  
Vol 39 (3) ◽  
pp. 389-391 ◽  
Author(s):  
Atbin Djamshidian ◽  
Jochen Schaefer ◽  
Dietrich Haubenberger ◽  
Elisabeth Stogmann ◽  
Friedrich Zimprich ◽  
...  
Keyword(s):  
Frontotemporal Dementia ◽  
Inclusion Body ◽  
Novel Mutation ◽  
Inclusion Body Myopathy ◽  
Paget Disease Of Bone ◽  
Paget Disease ◽  
German Family

Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia

2007 ◽  
Vol 72 (5) ◽  
pp. 420-426 ◽  
Author(s):  
GDJ Watts ◽  
D Thomasova ◽  
SK Ramdeen ◽  
EC Fulchiero ◽  
SG Mehta ◽  
...  
Keyword(s):  
Frontotemporal Dementia ◽  
Inclusion Body ◽  
Inclusion Body Myopathy ◽  
Paget Disease Of Bone ◽  
Paget Disease

scholarly journals Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

2004 ◽  
Vol 36 (4) ◽  
pp. 377-381 ◽  
Author(s):  
Giles D J Watts ◽  
Jill Wymer ◽  
Margaret J Kovach ◽  
Sarju G Mehta ◽  
Steven Mumm ◽  
...  
Keyword(s):  
Frontotemporal Dementia ◽  
Inclusion Body ◽  
Inclusion Body Myopathy ◽  
Paget Disease Of Bone ◽  
Paget Disease

Inclusion Body Myopathy with Paget Disease of Bone and/or Frontotemporal Dementia

Neurogenetics ◽  
2014 ◽  
pp. 133-138
Author(s):  
Kishore R. Kumar ◽  
Carolyn M. Sue ◽  
Alexander Münchau ◽  
Christine Klein
Keyword(s):  
Frontotemporal Dementia ◽  
Inclusion Body ◽  
Inclusion Body Myopathy ◽  
Paget Disease Of Bone ◽  
Paget Disease

scholarly journals Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia

2012 ◽  
Vol 83 (5) ◽  
pp. 422-431 ◽  
Author(s):  
SG Mehta ◽  
M Khare ◽  
R Ramani ◽  
GDJ Watts ◽  
M Simon ◽  
...  
Keyword(s):  
Frontotemporal Dementia ◽  
Inclusion Body ◽  
Inclusion Body Myopathy ◽  
Paget Disease Of Bone ◽  
Paget Disease
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