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Plasma cells in muscle in inclusion body myositis and polymyositis. [electronic resource] by
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- Bradshaw, E M
- Pinkus, J L
- Pinkus, G S
- Burleson, T
- Due, B
- Bregoli, L
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- O'Connor, K C
- Amato, A A
Producer: 20060323
In:
Neurology vol. 65
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No mutations in hnRNPA1 and hnRNPA2B1 in Dutch patients with amyotrophic lateral sclerosis, frontotemporal dementia, and inclusion body myopathy. [electronic resource] by
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- Visser, Anne E
- Overste, Daniel J
- Kim, Hong J
- Palud, A
- Wong, Tsz H
- van Swieten, John C
- Scheltens, Philip
- Voermans, Nicol C
- Baas, Frank
- de Jong, J M B V
- van der Kooi, Anneke J
- de Visser, Marianne
- Veldink, Jan H
- Taylor, J Paul
- Van Es, Michael A
- van den Berg, Leonard H
Producer: 20141208
In:
Neurobiology of aging vol. 35
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Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia. [electronic resource] by
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- Khare, M
- Ramani, R
- Watts, G D J
- Simon, M
- Osann, K E
- Donkervoort, S
- Dec, E
- Nalbandian, A
- Platt, J
- Pasquali, M
- Wang, A
- Mozaffar, T
- Smith, C D
- Kimonis, V E
Producer: 20130923
In:
Clinical genetics vol. 83
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956.
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The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy. [electronic resource] by
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- Avidan, N
- Potikha, T
- Hochner, H
- Chen, M
- Olender, T
- Barash, M
- Shemesh, M
- Sadeh, M
- Grabov-Nardini, G
- Shmilevich, I
- Friedmann, A
- Karpati, G
- Bradley, W G
- Baumbach, L
- Lancet, D
- Asher, E B
- Beckmann, J S
- Argov, Z
- Mitrani-Rosenbaum, S
Producer: 20010927
In:
Nature genetics vol. 29
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