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All Genetics
Citations 81-90 of 676 total displayed.
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Past content
(since Jan 2001):
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- NEUROIMAGES
Susceptibility-weighted imaging in familial cerebral cavernous malformations
- Alex D. Cooper, Norbert G. Campeau, and Irene Meissner
Neurology 2008; 71: 382.
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- ARTICLES
Progranulin genetic variability contributes to amyotrophic lateral sclerosis
- K. Sleegers, N. Brouwers, S. Maurer-Stroh, M. A. van Es, P. Van Damme, P.W.J. van Vught, J. van der Zee, S. Serneels, T. De Pooter, M. Van den Broeck, M. Cruts, J. Schymkowitz, P. De Jonghe, F. Rousseau, L. H. van den Berg, W. Robberecht, and C. Van Broeckhoven
Neurology 2008; 71: 253-259.
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- ARTICLES
KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes
- B. A. Neubauer, S. Waldegger, J. Heinzinger, A. Hahn, G. Kurlemann, B. Fiedler, F. Eberhard, H. Muhle, U. Stephani, S. Garkisch, O. Eeg-Olofsson, U. Müller, and T. Sander
Neurology 2008; 71: 177-183.
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- EDITORIALS
Detecting Alzheimer disease before it happens: The key to prevention?
- Joseph Quinn and Marwan N. Sabbagh
Neurology 2008; 71: 78-79.
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- ARTICLES
Biochemical markers in persons with preclinical familial Alzheimer disease
- J. M. Ringman, S. G. Younkin, D. Pratico, W. Seltzer, G. M. Cole, D. H. Geschwind, Y. Rodriguez-Agudelo, B. Schaffer, J. Fein, S. Sokolow, E. R. Rosario, K. H. Gylys, A. Varpetian, L. D. Medina, and J. L. Cummings
Neurology 2008; 71: 85-92.
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- ARTICLES
Reduced brain choline in homocystinuria due to remethylation defects
- F. -G. Debray, Y. Boulanger, A. Khiat, J. -C. Decarie, J. Orquin, M. -S. Roy, A. Lortie, F. Ramos, N. M. Verhoeven, E. Struys, H. J. Blom, C. Jakobs, E. Levy, G. A. Mitchell, and M. Lambert
Neurology 2008; 71: 44-49.
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- ARTICLES
Sensitivity and specificity of decreased CSF asialotransferrin for eIF2B-related disorder
- A. Vanderver, Y. Hathout, J. Maletkovic, E. S. Gordon, M. Mintz, M. Timmons, E. P. Hoffman, L. Horzinski, F. Niel, A. Fogli, O. Boespflug-Tanguy, and R. Schiffmann
Neurology 2008; 70: 2226-2232.
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- ARTICLES
Neurologic consequences of autoimmune polyglandular syndrome type 1
- Joseph R. Berger, Allison Weaver, John Greenlee, and George E. Wahlen
Neurology 2008; 70: 2248-2251.
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- CLINICAL/SCIENTIFIC NOTES
NEUROSCHISTOSOMIASIS PRESENTING AS BRAINSTEM ENCEPHALITIS
- Michael J. Devine, Philip A. Wilkinson, J. F. Doherty, and Paul R. Jarman
Neurology 2008; 70: 2262-2264.
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- ARTICLES
Lamotrigine in pregnancy: Clearance, therapeutic drug monitoring, and seizure frequency
- P. B. Pennell, L. Peng, D. J. Newport, J. C. Ritchie, A. Koganti, D. K. Holley, M. Newman, and Z. N. Stowe
Neurology 2008; 70: 2130-2136.
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