scholarly journals Global Gene Profiling of VCP-associated Inclusion Body Myopathy

2012 ◽  
Vol 5 (3) ◽  
pp. 226-234 ◽  
Author(s):  
Angèle Nalbandian ◽  
Svetlana Ghimbovschi ◽  
Shlomit Radom-Aizik ◽  
Eric Dec ◽  
Jouni Vesa ◽  
...  
Keyword(s):  
Inclusion Body ◽  
Gene Profiling ◽  
Inclusion Body Myopathy

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

scholarly journals Isolated inclusion body myopathy caused by a multisystem proteinopathy–linkedhnRNPA1mutation

2015 ◽  
Vol 1 (3) ◽  
pp. e23 ◽  
Author(s):  
Rumiko Izumi ◽  
Hitoshi Warita ◽  
Tetsuya Niihori ◽  
Toshiaki Takahashi ◽  
Maki Tateyama ◽  
...  
Keyword(s):  
Inclusion Body ◽  
Inclusion Body Myopathy

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

2007 ◽  
Vol 114 (1) ◽  
pp. 55-61 ◽  
Author(s):  
Jake B. Guinto ◽  
Gillian P. Ritson ◽  
J. Paul Taylor ◽  
Mark S. Forman
Keyword(s):  
Frontotemporal Dementia ◽  
Inclusion Body ◽  
Inclusion Body Myopathy

scholarly journals Hereditary Inclusion Body Myopathy Maps to Chromosome 9p1-q1

1996 ◽  
Vol 5 (1) ◽  
pp. 159-163 ◽  
Author(s):  
S. Mitrani-Rosenbaum ◽  
Z. Argov ◽  
A. Blumenfeld ◽  
C. E. Seidman ◽  
J. G. Seidman
Keyword(s):  
Inclusion Body ◽  
Inclusion Body Myopathy ◽  
Hereditary Inclusion Body Myopathy

Mo1591 Inclusion Body Myopathy: Recognition of a New Entity in the Pathophysiology of Diabetic Gastroparesis

2016 ◽  
Vol 150 (4) ◽  
pp. S722
Author(s):  
Sharareh Moraveji ◽  
Mohammad Bashashati ◽  
Lyan Gondin ◽  
Irene Sarosiek ◽  
Brian R. Davis ◽  
...  
Keyword(s):  
Inclusion Body ◽  
Diabetic Gastroparesis ◽  
Inclusion Body Myopathy
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