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2601.
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2602.
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2603.
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A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6. [electronic resource] by
- Takahashi, Hiroki
- Ishikawa, Kinya
- Tsutsumi, Takeshi
- Fujigasaki, Hiroto
- Kawata, Akihiro
- Okiyama, Ryoichi
- Fujita, Tsuneo
- Yoshizawa, Kazuo
- Yamaguchi, Shigeki
- Tomiyasu, Hitoshi
- Yoshii, Fumihito
- Mitani, Kazuko
- Shimizu, Natsue
- Yamazaki, Mineo
- Miyamoto, Tomoyuki
- Orimo, Tomoyuki
- Shoji, Shin'ichi
- Kitamura, Ken
- Mizusawa, Hidehiro
Producer: 20041021
In:
Journal of human genetics vol. 49
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2604.
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2605.
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2606.
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2607.
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2608.
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2609.
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Spinocerebellar ataxias type 8, 12, and 17 and dentatorubro-pallidoluysian atrophy in Czech ataxic patients. [electronic resource] by
- Musova, Zuzana
- Sedlacek, Zdenek
- Mazanec, Radim
- Klempir, Jiri
- Roth, Jan
- Plevova, Pavlina
- Vyhnalek, Martin
- Kopeckova, Marta
- Apltova, Ludmila
- Krepelova, Anna
- Zumrova, Alena
Producer: 20130905
In:
Cerebellum (London, England) vol. 12
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2610.
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2611.
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2612.
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2613.
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Biological and clinical manifestations of juvenile Huntington's disease: a retrospective analysis. [electronic resource] by
- Fusilli, Caterina
- Migliore, Simone
- Mazza, Tommaso
- Consoli, Federica
- De Luca, Alessandro
- Barbagallo, Gaetano
- Ciammola, Andrea
- Gatto, Emilia Mabel
- Cesarini, Martin
- Etcheverry, Jose Luis
- Parisi, Virginia
- Al-Oraimi, Musallam
- Al-Harrasi, Salma
- Al-Salmi, Qasem
- Marano, Massimo
- Vonsattel, Jean-Paul Gerard
- Sabatini, Umberto
- Landwehrmeyer, Georg Bernhard
- Squitieri, Ferdinando
Producer: 20190606
In:
The Lancet. Neurology vol. 17
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2614.
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2615.
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Differential pattern in tissue-specific somatic mosaicism of expanded CAG trinucleotide repeats in dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and X-linked recessive spinal and bulbar muscular atrophy. [electronic resource] by
- Tanaka, F
- Sobue, G
- Doyu, M
- Ito, Y
- Yamamoto, M
- Shimada, N
- Yamamoto, K
- Riku, S
- Hshizume, Y
- Mitsuma, T
Producer: 19961104
In:
Journal of the neurological sciences vol. 135
Availability: No items available.
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2616.
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Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice. [electronic resource] by
- Mangiarini, L
- Sathasivam, K
- Seller, M
- Cozens, B
- Harper, A
- Hetherington, C
- Lawton, M
- Trottier, Y
- Lehrach, H
- Davies, S W
- Bates, G P
Producer: 19961216
In:
Cell vol. 87
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2617.
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2618.
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2619.
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2620.
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