Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene

Neurology ◽  
2005 ◽  
Vol 65 (8) ◽  
pp. 1304-1305 ◽  
Author(s):  
D. Haubenberger ◽  
R. E. Bittner ◽  
S. Rauch-Shorny ◽  
F. Zimprich ◽  
C. Mannhalter ◽  
...  
Keyword(s):  
Inclusion Body ◽  
Novel Mutation ◽  
Inclusion Body Myopathy ◽  
Paget Disease

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

O2-05-03: Inclusion body myopathy with paget disease of the bone and frontotemporal dementia: New families, a novel mutation, and a new clinical presentation

2008 ◽  
Vol 4 ◽  
pp. T141-T141 ◽  
Author(s):  
Salvatore Spina ◽  
Amber D. Van Laar ◽  
Jill R. Murrell ◽  
Gabrielle de Courten-Myers ◽  
Ronald L. Hamilton ◽  
...  
Keyword(s):  
Frontotemporal Dementia ◽  
Inclusion Body ◽  
Clinical Presentation ◽  
Novel Mutation ◽  
Inclusion Body Myopathy ◽  
Paget Disease

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 VCP Associated Inclusion Body Myopathy and Paget Disease of Bone Knock-In Mouse Model Exhibits Tissue Pathology Typical of Human Disease

PLoS ONE ◽  
2010 ◽  
Vol 5 (10) ◽  
pp. e13183 ◽  
Author(s):  
Mallikarjun Badadani ◽  
Angèle Nalbandian ◽  
Giles D. Watts ◽  
Jouni Vesa ◽  
Masashi Kitazawa ◽  
...  
Keyword(s):  
Mouse Model ◽  
Inclusion Body ◽  
Human Disease ◽  
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
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