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Long-term observational study of sporadic inclusion body myositis. [electronic resource] by
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- Dubourg, Odile
- Squier, Waney
- Maisonobe, Thierry
- Stojkovic, Tanya
- Leite, Maria Isabel
- Allenbach, Yves
- Herson, Serge
- Brady, Stefen
- Eymard, Bruno
- Hilton-Jones, David
Producer: 20120118
In:
Brain : a journal of neurology vol. 134
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Widespread RNA metabolism impairment in sporadic inclusion body myositis TDP43-proteinopathy. [electronic resource] by
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- Brady, Stefen
- Simone, Roberto
- Lashley, Tammaryn
- Acevedo-Arozena, Abraham
- de Silva, Rohan
- Greensmith, Linda
- Holton, Janice
- Hanna, Michael G
- Fisher, Elizabeth M C
- Fratta, Pietro
Producer: 20141125
In:
Neurobiology of aging vol. 35
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666.
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Partial laminin alpha2 chain deficiency in a patient with myopathy resembling inclusion body myositis. [electronic resource] by
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- Vignier, N
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- Guicheney, P
- Morandi, L
Producer: 20000623
In:
Annals of neurology vol. 47
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669.
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Transgenic expression of beta-APP in fast-twitch skeletal muscle leads to calcium dyshomeostasis and IBM-like pathology. [electronic resource] by
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- Fu, Qinghao
- Kumar, Pravir
- Shtifman, Alexander
- Lopez, Jose R
- Allen, Paul D
- LaFerla, Frank
- Weinberg, David
- Magrane, Jordi
- Aprahamian, Tamar
- Walsh, Kenneth
- Rosen, Kenneth M
- Querfurth, Henry W
Producer: 20061020
In:
FASEB journal : official publication of the Federation of American Societies for Experimental Biology vol. 20
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674.
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675.
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676.
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677.
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Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia. [electronic resource] by
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- Thomasova, D
- Ramdeen, S K
- Fulchiero, E C
- Mehta, S G
- Drachman, D A
- Weihl, C C
- Jamrozik, Z
- Kwiecinski, H
- Kaminska, A
- Kimonis, V E
Producer: 20080104
In:
Clinical genetics vol. 72
Availability: No items available.
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