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Neurology
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All Clinical Neurology

Citations 61-70 of 226 total displayed.

Past content (since Mar 2001):

EDITORIALS
Antibody–phenotype correlation in stiff-person syndrome
Amelia Evoli
Neurology 2008; 71: 1938-1939. [Full text] [PDF]  

ARTICLES
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa
P. Richard, K. Gaudon, H. Haddad, A. Ben Ammar, E. Genin, S. Bauché, M. Paturneau-Jouas, J. S. Müller, H. Lochmüller, D. Grid, A. Hamri, S. Nouioua, M. Tazir, M. Mayer, C. Desnuelle, A. Barois, B. Chabrol, J. Pouget, J. Koenig, N. Gouider-Khouja, F. Hentati, B. Eymard, and D. Hantaï
Neurology 2008; 71: 1967-1972. [Abstract] [Full text] [PDF]  

ARTICLES
Medial temporal lobe atrophy on MRI scans and the diagnosis of Alzheimer disease
R. Duara, D. A. Loewenstein, E. Potter, J. Appel, M. T. Greig, R. Urs, Q. Shen, A. Raj, B. Small, W. Barker, E. Schofield, Y. Wu, and H. Potter
Neurology 2008; 71: 1986-1992. [Abstract] [Full text] [PDF]  

ARTICLES
New morphologic and genetic findings in cap disease associated with β-tropomyosin (TPM2) mutations
M. Ohlsson, S. Quijano-Roy, N. Darin, G. Brochier, E. Lacène, D. Avila-Smirnow, M. Fardeau, A. Oldfors, and H. Tajsharghi
Neurology 2008; 71: 1896-1901. [Abstract] [Full text] [PDF]  

ARTICLES
Orthostatic headache without CSF leak
Andrea N. Leep Hunderfund and Bahram Mokri
Neurology 2008; 71: 1902-1906. [Abstract] [Full text] [PDF]  

ARTICLES
Diffusion tensor imaging of the pyramidal tracts in infants with motor dysfunction
N. A. Ludeman, J. I. Berman, Y. W. Wu, R. J. Jeremy, J. Kornak, A. I. Bartha, A. J. Barkovich, D. M. Ferriero, R. G. Henry, and O. A. Glenn
Neurology 2008; 71: 1676-1682. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
LONG-TERM EFFECT OF RITUXIMAB IN ANTI-MAG POLYNEUROPATHY
L. Benedetti, C. Briani, D. Franciotta, M. Carpo, L. Padua, G. Zara, R. Zambello, M. P. Sormani, G. L. Mancardi, E. Nobile-Orazio, and A. Schenone
Neurology 2008; 71: 1742-1744. [Full text] [PDF]  

EDITORIALS
Sporadically occurring neurologic disease: HSP genes and apparently sporadic spastic paraplegia
John K. Fink
Neurology 2008; 71: 1468-1469. [Full text] [PDF]  

ARTICLES
Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes
F. Brugman, H. Scheffer, J.H.J. Wokke, W. M. Nillesen, M. de Visser, E. Aronica, J. H. Veldink, and L. H. van den Berg
Neurology 2008; 71: 1500-1505. [Abstract] [Full text] [PDF]  

ARTICLES
Weight loss in Huntington disease increases with higher CAG repeat number
N. A. Aziz, J.M.M. van der Burg, G. B. Landwehrmeyer, P. Brundin, T. Stijnen, EHDI Study Group, and R. A.C. Roos
Neurology 2008; 71: 1506-1513. [Abstract] [Full text] [PDF]  

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