Results
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4081.
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4082.
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4083.
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Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy. [electronic resource] by
- Mastaglia, F L
- Nowak, K J
- Stell, R
- Phillips, B A
- Edmondston, J E
- Dorosz, S M
- Wilton, S D
- Hallmayer, J
- Kakulas, B A
- Laing, N G
Producer: 19990902
In:
Journal of neurology, neurosurgery, and psychiatry vol. 67
Availability: No items available.
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4084.
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4085.
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4086.
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4087.
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4088.
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4089.
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4090.
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A novel GDAP1 Q218E mutation in autosomal dominant Charcot-Marie-Tooth disease. [electronic resource] by
- Chung, Ki Wha
- Kim, Seung Min
- Sunwoo, Il Nam
- Cho, Sun Young
- Hwang, Su Jin
- Kim, Joonki
- Kang, Sung Hee
- Park, Kee-Duk
- Choi, Kyoung-Gyu
- Choi, Il Saing
- Choi, Byung-Ok
Producer: 20080617
In:
Journal of human genetics vol. 53
Availability: No items available.
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4091.
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4092.
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Central nervous system involvement in n-hexane polyneuropathy demonstrated by MRI and proton MR spectroscopy. [electronic resource] by
- Hashizume, A
- Koike, H
- Kawagashira, Y
- Banno, H
- Suzuki, K
- Ito, M
- Katsuno, M
- Watanabe, H
- Tanaka, F
- Naganawa, S
- Kaneko, R
- Ishii, A
- Sobue, G
Producer: 20110930
In:
Clinical neurology and neurosurgery vol. 113
Availability: No items available.
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4093.
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4094.
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4095.
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4096.
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4097.
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4098.
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4099.
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4100.
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