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Ataxia with oculomotor apraxia type 2: a clinical and genetic study of 19 patients. [electronic resource] by
- Tazir, M
- Ali-Pacha, L
- M'Zahem, A
- Delaunoy, J P
- Fritsch, M
- Nouioua, S
- Benhassine, T
- Assami, S
- Grid, D
- Vallat, J M
- Hamri, A
- Koenig, M
Producer: 20090504
In:
Journal of the neurological sciences vol. 278
Availability: No items available.
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Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arrays. [electronic resource] by
- H'mida-Ben Brahim, D
- M'zahem, A
- Assoum, M
- Bouhlal, Y
- Fattori, F
- Anheim, M
- Ali-Pacha, L
- Ferrat, F
- Chaouch, M
- Lagier-Tourenne, C
- Drouot, N
- Thibaut, C
- Benhassine, T
- Sifi, Y
- Stoppa-Lyonnet, D
- N'Guyen, K
- Poujet, J
- Hamri, A
- Hentati, F
- Amouri, R
- Santorelli, F M
- Tazir, M
- Koenig, M
Producer: 20110425
In:
Journal of neurology vol. 258
Availability: No items available.
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4.
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Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients. [electronic resource] by
- Anheim, M
- Monga, B
- Fleury, M
- Charles, P
- Barbot, C
- Salih, M
- Delaunoy, J P
- Fritsch, M
- Arning, L
- Synofzik, M
- Schöls, L
- Sequeiros, J
- Goizet, C
- Marelli, C
- Le Ber, I
- Koht, J
- Gazulla, J
- De Bleecker, J
- Mukhtar, M
- Drouot, N
- Ali-Pacha, L
- Benhassine, T
- Chbicheb, M
- M'Zahem, A
- Hamri, A
- Chabrol, B
- Pouget, J
- Murphy, R
- Watanabe, M
- Coutinho, P
- Tazir, M
- Durr, A
- Brice, A
- Tranchant, C
- Koenig, M
Producer: 20100203
In:
Brain : a journal of neurology vol. 132
Availability: No items available.
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