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4741.
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4742.
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4745.
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4746.
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4747.
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4748.
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4749.
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Clinicopathological and genetic study of early-onset demyelinating neuropathy. [electronic resource] by
- Parman, Yesim
- Battaloglu, Esra
- Baris, Ibrahim
- Bilir, Birdal
- Poyraz, Mürüvvet
- Bissar-Tadmouri, Nisrine
- Williams, Anna
- Ammar, Nadia
- Nelis, Eva
- Timmerman, Vincent
- De Jonghe, Peter
- Najafov, Ayaz
- Necefov, Ayaz
- Deymeer, Feza
- Serdaroglu, Piraye
- Brophy, Peter J
- Said, G
Producer: 20050118
In:
Brain : a journal of neurology vol. 127
Availability: No items available.
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4750.
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4751.
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Effect of an R69C mutation in the myelin protein zero gene on myelination and ion channel subtypes. [electronic resource] by
- Bai, Yunhong
- Ianokova, Emilia
- Pu, Qin
- Ghandour, Khaled
- Levinson, Rock
- Martin, Jean-Jacques
- Ceuterick-de Groote, Chantal
- Mazanec, Radim
- Seeman, Pavel
- Shy, Michael E
- Li, Jun
Producer: 20070123
In:
Archives of neurology vol. 63
Availability: No items available.
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4752.
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A compound heterozygous mutation in HADHB gene causes an axonal Charcot-Marie-tooth disease. [electronic resource] by
- Hong, Young Bin
- Lee, Ja Hyun
- Park, Jin-Mo
- Choi, Yu-Ri
- Hyun, Young Se
- Yoon, Bo Ram
- Yoo, Jeong Hyun
- Koo, Heasoo
- Jung, Sung-Chul
- Chung, Ki Wha
- Choi, Byung-Ok
Producer: 20140408
In:
BMC medical genetics vol. 14
Availability: No items available.
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4753.
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4754.
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4755.
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4756.
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4757.
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Late onset Friedreich's disease: clinical features and mapping of mutation to the FRDA locus. [electronic resource] by
- De Michele, G
- Filla, A
- Cavalcanti, F
- Di Maio, L
- Pianese, L
- Castaldo, I
- Calabrese, O
- Monticelli, A
- Varrone, S
- Campanella, G
Producer: 19940909
In:
Journal of neurology, neurosurgery, and psychiatry vol. 57
Availability: No items available.
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4758.
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4759.
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4760.
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