All Genetics

Citations 61-70 of 676 total displayed.

Past content (since Jan 2001):

ARTICLES
Neurodegeneration associated with genetic defects in phospholipase A₂

A. Gregory, S. K. Westaway, I. E. Holm, P. T. Kotzbauer, P. Hogarth, S. Sonek, J. C. Coryell, T. M. Nguyen, N. Nardocci, G. Zorzi, D. Rodriguez, I. Desguerre, E. Bertini, A. Simonati, B. Levinson, C. Dias, C. Barbot, I. Carrilho, M. Santos, I. Malik, J. Gitschier, and S. J. Hayflick
Neurology 2008; 71: 1402-1409. [Abstract] [Full text] [PDF]  

ARTICLES
A novel PRNP-P105S mutation associated with atypical prion disease and a rare PrP^Sc conformation

E. Tunnell, R. Wollman, S. Mallik, C. J. Cortes, S. J. DeArmond, and J. A. Mastrianni
Neurology 2008; 71: 1431-1438. [Abstract] [Full text] [PDF]  

ARTICLES
Distinct genetic forms of frontotemporal dementia

H. Seelaar, W. Kamphorst, S. M. Rosso, A. Azmani, R. Masdjedi, I. de Koning, J. A. Maat-Kievit, B. Anar, L. Donker Kaat, G. J. Breedveld, D. Dooijes, J. M. Rozemuller, I. F. Bronner, P. Rizzu, and J. C. van Swieten
Neurology 2008; 71: 1220-1226. [Abstract] [Full text] [PDF]  

ARTICLES
Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration

R. Ghidoni, L. Benussi, M. Glionna, M. Franzoni, and G. Binetti
Neurology 2008; 71: 1235-1239. [Abstract] [Full text] [PDF]  

ARTICLES
Autosomal recessive myosclerosis myopathy is a collagen VI disorder

L. Merlini, E. Martoni, P. Grumati, P. Sabatelli, S. Squarzoni, A. Urciuolo, A. Ferlini, F. Gualandi, and P. Bonaldo
Neurology 2008; 71: 1245-1253. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
PROGRESSIVE ENCEPHALOMYELITIS, RIGIDITY, AND MYOCLONUS: A NOVEL GLYCINE RECEPTOR ANTIBODY

M. Hutchinson, P. Waters, J. McHugh, G. Gorman, S. O’Riordan, S. Connolly, H. Hager, P. Yu, C. -M. Becker, and A. Vincent
Neurology 2008; 71: 1291-1292. [Full text] [PDF]  

ARTICLES
Progranulin variability has no major role in Parkinson disease genetic etiology

K. Nuytemans, P. Pals, K. Sleegers, S. Engelborghs, E. Corsmit, K. Peeters, B. Pickut, M. Mattheijssens, P. Cras, P. P. De Deyn, J. Theuns, and C. Van Broeckhoven
Neurology 2008; 71: 1147-1151. [Abstract] [Full text] [PDF]  

SPECIAL ARTICLES
Invited Article: The Alzheimer disease–frontotemporal lobar degeneration spectrum

Julie van der Zee, Kristel Sleegers, and Christine Van Broeckhoven
Neurology 2008; 71: 1191-1197. [Abstract] [Full text] [PDF]  

ARTICLES
CDKL5 mutations in boys with severe encephalopathy and early-onset intractable epilepsy

M. Elia, M. Falco, R. Ferri, A. Spalletta, M. Bottitta, G. Calabrese, M. Carotenuto, S. A. Musumeci, M. Lo Giudice, and M. Fichera
Neurology 2008; 71: 997-999. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
TWO SETS OF IDENTICAL TWINS WITH CERVICAL ARTERY DISSECTION CONCORDANT FOR TEMPORAL ARTERY PATHOLOGY

W. Völker, G. Kuhlenbäumer, R. Dittrich, S. Appenzeller, S. Grewe, D. Maintz, W. Heindel, K. H. Grotemeyer, and E. B. Ringelstein
Neurology 2008; 71: 1035-1037. [Full text] [PDF]  

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