Results
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1041.
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Hereditary motor and sensory neuropathy with proximal dominancy in the lower extremities, urinary disturbance, and paroxysmal dry cough. [electronic resource] by
- Miura, Shiroh
- Shibata, Hiroki
- Kida, Hiroshi
- Noda, Kazuhito
- Tomiyasu, Katsuro
- Yamamoto, Ken
- Iwaki, Akiko
- Ayabe, Mitsuyoshi
- Aizawa, Hisamichi
- Taniwaki, Takayuki
- Fukumaki, Yasuyuki
Producer: 20090206
In:
Journal of the neurological sciences vol. 273
Availability: No items available.
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1042.
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1043.
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1044.
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1045.
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1046.
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1047.
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Phenotypic clustering in MPZ mutations. [electronic resource] by
- Shy, Michael E
- Jáni, Agnes
- Krajewski, Karen
- Grandis, Marina
- Lewis, Richard A
- Li, Jun
- Shy, Rosemary R
- Balsamo, Janne
- Lilien, Jack
- Garbern, James Y
- Kamholz, John
Producer: 20040224
In:
Brain : a journal of neurology vol. 127
Availability: No items available.
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1048.
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1049.
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1050.
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1051.
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1052.
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1053.
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Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination. [electronic resource] by
- Warner, L E
- Hilz, M J
- Appel, S H
- Killian, J M
- Kolodry, E H
- Karpati, G
- Carpenter, S
- Watters, G V
- Wheeler, C
- Witt, D
- Bodell, A
- Nelis, E
- Van Broeckhoven, C
- Lupski, J R
Producer: 19961101
In:
Neuron vol. 17
Availability: No items available.
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1054.
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1055.
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1056.
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1057.
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1058.
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1059.
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1060.
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