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Neurology
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Genetic linkage

Citations 61-70 of 81 total displayed.

Past content (since Jan 2001):

BRIEF COMMUNICATIONS
SPG3A: An additional family carrying a new atlastin mutation
A. Tessa, C. Casali, M. Damiano, C. Bruno, D. Fortini, C. Patrono, F. Cricchi, M. Valoppi, G. Nappi, G.A. Amabile, E. Bertini, and F.M. Santorelli
Neurology 2002; 59: 2002-2005. [Abstract] [Full text] [PDF]  

ARTICLES
Kleine-Levin syndrome: An autoimmune hypothesis based on clinical and genetic analyses
Y. Dauvilliers, G. Mayer, M. Lecendreux, E. Neidhart, R. Peraita-Adrados, K. Sonka, M. Billiard, and M. Tafti
Neurology 2002; 59: 1739-1745. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Clinical and genetic studies of families with the tau N279K mutation (FTDP-17)
Y. Tsuboi, M. Baker, M. L. Hutton, R. J. Uitti, O. Rascol, M.-B. Delisle, X. Soulages, J. R. Murrell, B. Ghetti, M. Yasuda, O. Komure, S. Kuno, K. Arima, N. Sunohara, T. Kobayashi, Y. Mizuno, and Z. K. Wszolek
Neurology 2002; 59: 1791-1793. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1
A. Carlsson, L. Forsgren, P.-O. Nylander, U. Hellman, K. Forsman-Semb, G. Holmgren, D. Holmberg, and M. Holmberg
Neurology 2002; 59: 1804-1807. [Abstract] [Full text] [PDF]  

ARTICLES
Chromosome 3 linked frontotemporal dementia (FTD-3)
S. Gydesen, J.M. Brown, A. Brun, L. Chakrabarti, A. Gade, P. Johannsen, M. Rossor, T. Thusgaard, A. Grove, D. Yancopoulou, M.G. Spillantini, E.M.C. Fisher, J. Collinge, and S.A. Sorensen
Neurology 2002; 59: 1585-1594. [Abstract] [Full text] [PDF]  

ARTICLES
Clinical and genetic study of a large Italian family linked to SPG12 locus
A. Orlacchio, T. Kawarai, E. Rogaeva, Y.Q. Song, A.D. Paterson, G. Bernardi, and P.H. St. George-Hyslop
Neurology 2002; 59: 1395-1401. [Abstract] [Full text] [PDF]  

ARTICLES
A novel locus for inherited myoclonus-dystonia on 18p11
D. A. Grimes, F. Han, A. E. Lang, P. St. George-Hyssop, L. Racacho, and D. E. Bulman
Neurology 2002; 59: 1183-1186. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Autosomal dominant GTP-CH deficiency presenting as a dopa-responsive myoclonus-dystonia syndrome
V. Leuzzi, Ca. Carducci, Cl. Carducci, F. Cardona, C. Artiola, and I. Antonozzi
Neurology 2002; 59: 1241-1243. [Abstract] [Full text] [PDF]  

ARTICLES
Evidence for additional genetic risk indicators of relapse-onset MS within the HLA region
B. A. de Jong, T. W.J. Huizinga, E. Zanelli, M. J. Giphart, E. L.E.M. Bollen, B. M.J. Uitdehaag, C. H. Polman, and R. G.J. Westendorp
Neurology 2002; 59: 549-555. [Abstract] [Full text] [PDF]  

EDITORIALS
Psychotic genes or forgetful ones?
Simon Lovestone and John Hardy
Neurology 2002; 59: 11-12. [Full text] [PDF]  

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* Related collections:
 Genetics
 All Genetics
 Neurofibromatosis
 Other neurocutaneous disorders
 Genetic linkage
 Association studies in genetics
 Gene expression studies
 Gene therapy
 Mitochondrial disorders
 Ion channel gene defects
 Spinocerebellar ataxia
 Trinucleotide repeat diseases
 Chromosomes


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