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All Genetics
Citations 151-160 of 676 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Limb-girdle muscular dystrophy in the Netherlands: Gene defect identified in half the families
- A. J. van der Kooi, W. S. Frankhuizen, P. G. Barth, C. J. Howeler, G. W. Padberg, F. Spaans, A. R. Wintzen, J.H.J. Wokke, G. -J.B. van Ommen, M. de Visser, E. Bakker, and H. B. Ginjaar
Neurology 2007; 68: 2125-2128.
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- ARTICLES
Multitissular involvement in a family with LMNA and EMD mutations: Role of digenic mechanism?
- R. Ben Yaou, A. Toutain, T. Arimura, L. Demay, C. Massart, C. Peccate, A. Muchir, S. Llense, N. Deburgrave, F. Leturcq, K. E. Litim, N. Rahmoun-Chiali, P. Richard, D. Babuty, D. Récan-Budiartha, and G. Bonne
Neurology 2007; 68: 1883-1894.
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- ARTICLES
A controlled study of reverse transcriptase in serum and CSF of HIV-negative patients with ALS
- D.J.L. MacGowan, S. N. Scelsa, T. E. Imperato, K.-N Liu, P. Baron, and B. Polsky
Neurology 2007; 68: 1944-1946.
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- ARTICLES
Genotype–phenotype correlation of paroxysmal nonkinesigenic dyskinesia
- M. K. Bruno, H.-Y Lee, G.W.J. Auburger, A. Friedman, J. E. Nielsen, A. E. Lang, E. Bertini, P. Van Bogaert, Y. Averyanov, M. Hallett, K. Gwinn-Hardy, B. Sorenson, M. Pandolfo, H. Kwiecinski, S. Servidei, Y.-H Fu, and L. Ptácek
Neurology 2007; 68: 1782-1789.
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- ARTICLES
Temozolomide for low-grade gliomas: Predictive impact of 1p/19q loss on response and outcome
- G. Kaloshi, A. Benouaich-Amiel, F. Diakite, S. Taillibert, J. Lejeune, F. Laigle-Donadey, M.-A Renard, W. Iraqi, A. Idbaih, S. Paris, L. Capelle, H. Duffau, P. Cornu, J.-M Simon, K. Mokhtari, M. Polivka, A. Omuro, A. Carpentier, M. Sanson, J.-Y Delattre, and K. Hoang-Xuan
Neurology 2007; 68: 1831-1836.
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- ARTICLES
A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21
- G. Stevanin, C. Paternotte, P. Coutinho, S. Klebe, N. Elleuch, J. L. Loureiro, E. Denis, V. T. Cruz, A. Dürr, J.-F Prud’homme, J. Weissenbach, A. Brice, and J. Hazan
Neurology 2007; 68: 1837-1840.
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- CLINICAL/SCIENTIFIC NOTES
ATYPICAL CLINICAL COURSE OF FXTAS: RAPIDLY PROGRESSIVE DEMENTIA AS THE MAJOR SYMPTOM
- M.R.R. Gonçalves, L. P. Capelli, R. Nitrini, E. R. Barbosa, C. S. Porto, L. T. Lucato, and A. M. Vianna-Morgante
Neurology 2007; 68: 1864-1866.
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- ARTICLES
Phenotype of Charcot–Marie–Tooth disease Type 2
- H.M.E. Bienfait, F. Baas, J. H.T.M. Koelman, R. J. de Haan, B. G.M. van Engelen, A. A.W.M. Gabreëls-Festen, B. W. Ongerboer de Visser, F. Meggouh, M. A.J. Weterman, P. De Jonghe, V. Timmerman, and M. de Visser
Neurology 2007; 68: 1658-1667.
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- EDITORIALS
Clinical heterogeneity of ATP13A2 linked disease (Kufor-Rakeb) justifies a PARK designation
- Andrew J. Lees and Andrew B. Singleton
Neurology 2007; 68: 1553-1554.
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- ARTICLES
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease
- A. Di Fonzo, H. F. Chien, M. Socal, S. Giraudo, C. Tassorelli, G. Iliceto, G. Fabbrini, R. Marconi, E. Fincati, G. Abbruzzese, P. Marini, F. Squitieri, M. W. Horstink, P. Montagna, A. Dalla Libera, F. Stocchi, S. Goldwurm, J. J. Ferreira, G. Meco, E. Martignoni, L. Lopiano, L. B. Jardim, B. A. Oostra, E. R. Barbosa, The Italian Parkinson Genetics Network, and V. Bonifati
Neurology 2007; 68: 1557-1562.
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