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All Genetics
Citations 141-150 of 676 total displayed.
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Past content
(since Jan 2001):
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- EDITORIALS
Nav1.7, its mutations, and the syndromes that they cause
- Stephen G. Waxman
Neurology 2007; 69: 505-507.
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- ARTICLES
Paroxysmal extreme pain disorder (previously familial rectal pain syndrome)
- C. R. Fertleman, C. D. Ferrie, J. Aicardi, N.A.F. Bednarek, O. Eeg-Olofsson, F. V. Elmslie, D. A. Griesemer, F. Goutières, M. Kirkpatrick, I. N.O. Malmros, M. Pollitzer, M. Rossiter, E. Roulet-Perez, R. Schubert, V. V. Smith, H. Testard, V. Wong, and J. B.P. Stephenson
Neurology 2007; 69: 586-595.
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- ARTICLES
A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation
- T. Warnecke, T. Duning, A. Schwan, H. Lohmann, J. T. Epplen, and P. Young
Neurology 2007; 69: 368-375.
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- EDITORIALS
Dissecting the complexity of frontotemporal dementia: Genotypes, phenotypes, and phenocopies
- Christine Klein and Vincenzo Bonifati
Neurology 2007; 69: 129-130.
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- ARTICLES
Heterogeneity within a large kindred with frontotemporal dementia: A novel progranulin mutation
- A. C. Bruni, P. Momeni, L. Bernardi, C. Tomaino, F. Frangipane, J. Elder, T. Kawarai, C. Sato, S. Pradella, Y. Wakutani, M. Anfossi, M. Gallo, S. Geracitano, A. Costanzo, N. Smirne, S.A.M. Curcio, M. Mirabelli, G. Puccio, R. Colao, R. G. Maletta, A. Kertesz, P. St. George-Hyslop, J. Hardy, and E. Rogaeva
Neurology 2007; 69: 140-147.
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- ARTICLES
A timing-of-birth effect on multiple sclerosis clinical phenotype
- A. D. Sadovnick, P. Duquette, B. Herrera, I.M.L. Yee, and G. C. Ebers
Neurology 2007; 69: 60-62.
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- ARTICLES
Clinical and neuropathologic study of a French family with a mutation in the neuroserpin gene
- I. Gourfinkel-An, C. Duyckaerts, A. Camuzat, C. Meyrignac, P. Sonderegger, M. Baulac, and A. Brice
Neurology 2007; 69: 79-83.
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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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