Results
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981.
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982.
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983.
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984.
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985.
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Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His. [electronic resource] by
- van der Zee, J
- Pirici, D
- Van Langenhove, T
- Engelborghs, S
- Vandenberghe, R
- Hoffmann, M
- Pusswald, G
- Van den Broeck, M
- Peeters, K
- Mattheijssens, M
- Martin, J-J
- De Deyn, P P
- Cruts, M
- Haubenberger, D
- Kumar-Singh, S
- Zimprich, A
- Van Broeckhoven, C
Producer: 20090914
In:
Neurology vol. 73
Availability: No items available.
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986.
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Global gene profiling of VCP-associated inclusion body myopathy. [electronic resource] by
- Nalbandian, Angèle
- Ghimbovschi, Svetlana
- Radom-Aizik, Shlomit
- Dec, Eric
- Vesa, Jouni
- Martin, Barbara
- Knoblach, Susan
- Smith, Charles
- Hoffman, Eric
- Kimonis, Virginia E
Producer: 20121004
In:
Clinical and translational science vol. 5
Availability: No items available.
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987.
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988.
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989.
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990.
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991.
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992.
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993.
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Polymorphism in the TOMM40 gene modifies the risk of developing sporadic inclusion body myositis and the age of onset of symptoms. [electronic resource] by
- Mastaglia, F L
- Rojana-udomsart, A
- James, I
- Needham, M
- Day, T J
- Kiers, L
- Corbett, J A
- Saunders, A M
- Lutz, M W
- Roses, A D
Producer: 20140724
In:
Neuromuscular disorders : NMD vol. 23
Availability: No items available.
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994.
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995.
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996.
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A high incidence of disease flares in an open pilot study of infliximab in patients with refractory inflammatory myopathies. [electronic resource] by
- Dastmalchi, M
- Grundtman, C
- Alexanderson, H
- Mavragani, C P
- Einarsdottir, H
- Helmers, S Barbasso
- Elvin, K
- Crow, M K
- Nennesmo, I
- Lundberg, I E
Producer: 20081215
In:
Annals of the rheumatic diseases vol. 67
Availability: No items available.
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997.
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998.
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Characterization of the Asian myopathy patients with VCP mutations. [electronic resource] by
- Shi, Z
- Hayashi, Y K
- Mitsuhashi, S
- Goto, K
- Kaneda, D
- Choi, Y-C
- Toyoda, C
- Hieda, S
- Kamiyama, T
- Sato, H
- Wada, M
- Noguchi, S
- Nonaka, I
- Nishino, I
Producer: 20120607
In:
European journal of neurology vol. 19
Availability: No items available.
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999.
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Sporadic inclusion body myositis: HLA-DRB1 allele interactions influence disease risk and clinical phenotype. [electronic resource] by
- Mastaglia, Frank L
- Needham, Merrilee
- Scott, Adrian
- James, Ian
- Zilko, Paul
- Day, Timothy
- Kiers, Lynette
- Corbett, Alastair
- Witt, Campbell S
- Allcock, Richard
- Laing, Nigel
- Garlepp, Michael
- Christiansen, Frank T
Producer: 20100105
In:
Neuromuscular disorders : NMD vol. 19
Availability: No items available.
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1000.
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The homozygote VCP(R¹⁵⁵H/R¹⁵⁵H) mouse model exhibits accelerated human VCP-associated disease pathology. [electronic resource] by
- Nalbandian, Angèle
- Llewellyn, Katrina J
- Kitazawa, Masashi
- Yin, Hong Z
- Badadani, Mallikarjun
- Khanlou, Negar
- Edwards, Robert
- Nguyen, Christopher
- Mukherjee, Jogeshwar
- Mozaffar, Tahseen
- Watts, Giles
- Weiss, John
- Kimonis, Virginia E
Producer: 20130221
In:
PloS one vol. 7
Availability: No items available.
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