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Genetic linkage
Citations 71-80 of 81 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Linkage analysis of Alzheimer disease with psychosis
- S. A. Bacanu, B. Devlin, K. V. Chowdari, S. T. DeKosky, V. L. Nimgaonkar, and R. A. Sweet
Neurology 2002; 59: 118-120.
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- BRIEF COMMUNICATIONS
Neuropathology of a case of dopa-responsive dystonia associated with a new genetic locus, DYT14
- H. Grötzsch, G.-P. Pizzolato, J. Ghika, D. Schorderet, F.J. Vingerhoets, T. Landis, and P.R. Burkhard
Neurology 2002; 58: 1839-1842.
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- BRIEF COMMUNICATIONS
Generalized epilepsy with febrile seizures plus: Mutation of the sodium channel subunit SCN1B
- R. H. Wallace, I. E. Scheffer, G. Parasivam, S. Barnett, G. B. Wallace, G. R. Sutherland, S. F. Berkovic, and J. C. Mulley
Neurology 2002; 58: 1426-1429.
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- CLINICAL/SCIENTIFIC NOTES
Association of the 5-HT6 receptor gene polymorphism C267T with Parkinson’s disease
- D. Messina, G. Annesi, P. Serra, G. Nicoletti, A. Pasqua, F. Annesi, C. Tomaino, I.C. Cirò–Candiano, S. Carrideo, M. Caracciolo, P. Spadafora, M. Zappia, G. Savettieri, and A. Quattrone
Neurology 2002; 58: 828-829.
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- ARTICLES
Novel mutations in collagen VI genes: Expansion of the Bethlem myopathy phenotype
- P. C. Scacheri, E. M. Gillanders, S. H. Subramony, V. Vedanarayanan, C. A. Crowe, N. Thakore, M. Bingler, and E. P. Hoffman
Neurology 2002; 58: 593-602.
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- ARTICLES
Epidemiologic study of 203 sibling pairs with Parkinson’s disease: The GenePD study
- N. E. Maher, L. I. Golbe, A. M. Lazzarini, M. H. Mark, L. J. Currie, G. F. Wooten, M. Saint-Hilaire, J. B. Wilk, J. Volcjak, J. E. Maher, R. G. Feldman, M. Guttman, M. Lew, S. Schuman, O. Suchowersky, A. L. Lafontaine, N. Labelle, P. Vieregge, P. P. Pramstaller, C. Klein, J. Hubble, C. Reider, J. Growdon, R. Watts, E. Montgomery, K. Baker, C. Singer, M. Stacy, and R.H. Myers
Neurology 2002; 58: 79-84.
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- BRIEF COMMUNICATIONS
A novel presenilin 2 gene mutation (D439A) in a patient with early-onset Alzheimer’s disease
- A. Lleó, R. Blesa, J. Gendre, M. Castellví, P. Pastor, R. Queralt, and R. Oliva
Neurology 2001; 57: 1926-1928.
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- ARTICLES
Linkage of HLA to myasthenia gravis and genetic heterogeneity depending on anti-titin antibodies
- M. Giraud, G. Beaurain, A. M. Yamamoto, B. Eymard, C. Tranchant, P. Gajdos, and H.-J. Garchon
Neurology 2001; 57: 1555-1560.
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- ARTICLES
Genome-wide linkage disequilibrium mapping of late-onset Alzheimer’s disease in Finland
- M. Hiltunen, A. Mannermaa, D. Thompson, D. Easton, M. Pirskanen, S. Helisalmi, A. M. Koivisto, M. Lehtovirta, M. Ryynänen, and H. Soininen
Neurology 2001; 57: 1663-1668.
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- ARTICLES
Fatal infantile leukodystrophy: A severe variant of CACH/VWM syndrome, allelic to chromosome 3q27
- P. Francalanci, E. Eymard–Pierre, C. Dionisi–Vici, R. Boldrini, F. Piemonte, R. Virgili, G. Fariello, C. Bosman, F.M. Santorelli, O. Boespflug–Tanguy, and E. Bertini
Neurology 2001; 57: 265-270.
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