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All Genetics
Citations 151-160 of 679 total displayed.
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Past content
(since Jan 2001):
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- CLINICAL/SCIENTIFIC NOTES
MONOZYGOTIC TWINS WITH MIRROR IMAGE CYSTS: INDICATION OF A GENETIC MECHANISM IN ARACHNOID CYSTS?
- Christian A. Helland and Knut Wester
Neurology 2007; 69: 110-111.
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- CLINICAL/SCIENTIFIC NOTES
REPORTING AND INTERPRETATION OF GENETIC VARIANTS IN CASES AND CONTROLS
- John Hardy and Andrew Singleton
Neurology 2007; 69: 111-112.
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- ARTICLES
Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3
- P. Hedera, M. A. Blair, E. Andermann, F. Andermann, D. D'Agostino, K. A. Taylor, L. Chahine, M. Pandolfo, Y. Bradford, J. L. Haines, and B. Abou-Khalil
Neurology 2007; 68: 2107-2112.
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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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