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Neurology
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Leukodystrophies

Citations 21-30 of 51 total displayed.

Past content (since Jan 2001):

EDITORIALS
Alexander disease: Not just a leukodystrophy anymore
A. James Barkovich and Albee Messing
Neurology 2006; 66: 468-469. [Full text] [PDF]  

ARTICLES
Alexander disease: Ventricular garlands and abnormalities of the medulla and spinal cord
M. S. van der Knaap, V. Ramesh, R. Schiffmann, S. Blaser, M. Kyllerman, A. Gholkar, D. W. Ellison, J. P. van der Voorn, S.J.M. van Dooren, C. Jakobs, F. Barkhof, and G. S. Salomons
Neurology 2006; 66: 494-498. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Methionine metabolism and phenotypic variability in X-linked adrenoleukodystrophy
M. Linnebank, S. Kemp, R.J.A. Wanders, W. J. Kleijer, M. L.T. van der Sterre, J. Gärtner, K. Fliessbach, A. Semmler, P. Sokolowski, W. Köhler, U. Schlegel, S. Schmidt, T. Klockgether, and U. Wüllner
Neurology 2006; 66: 442-443. [Abstract] [Full text] [PDF]  

ARTICLES
Etiology of aseptic meningitis and encephalitis in an adult population
L. Kupila, T. Vuorinen, R. Vainionpää, V. Hukkanen, R. J. Marttila, and P. Kotilainen
Neurology 2006; 66: 75-80. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Mutations in the glucocerebrosidase gene and Parkinson disease: Phenotype–genotype correlation
Judith Aharon-Peretz, Samih Badarny, Hanna Rosenbaum, and Ruth Gershoni-Baruch
Neurology 2005; 65: 1460-1461. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Late-onset neurologic disease in glutaryl-CoA dehydrogenase deficiency
S. Külkens, I. Harting, S. Sauer, J. Zschocke, G. F. Hoffmann, S. Gruber, O. A. Bodamer, and S. Kölker
Neurology 2005; 64: 2142-2144. [Abstract] [Full text] [PDF]  

ARTICLES
Cognitive function predicts first-time stroke and heart disease
Jacob S. Elkins, David S. Knopman, Kristine Yaffe, and S. Claiborne Johnston
Neurology 2005; 64: 1750-1755. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
A CLN5 mutation causing an atypical neuronal ceroid lipofuscinosis of juvenile onset
N. Pineda-Trujillo, W. Cornejo, J. Carrizosa, R. B. Wheeler, S. Múnera, A. Valencia, J. Agudelo-Arango, A. Cogollo, G. Anderson, G. Bedoya, S. E. Mole, and A. Ruíz-Linares
Neurology 2005; 64: 740-742. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Autoimmunity to glutamic acid decarboxylase in the neurodegenerative disorder Batten disease
D. Ramirez-Montealegre, S. Chattopadhyay, T. M. Curran, C. Wasserfall, L. Pritchard, D. Schatz, J. Petitto, D. Hopkins, J. -X. She, P. G. Rothberg, M. Atkinson, and D. A. Pearce
Neurology 2005; 64: 743-745. [Abstract] [Full text] [PDF]  

ARTICLES
Assessment of adrenoleukodystrophy lesions by high field MRS in non-sedated pediatric patients
G. Öz, I. Tkác, L. R. Charnas, I. Y. Choi, K. J. Bjoraker, E. G. Shapiro, and R. Gruetter
Neurology 2005; 64: 434-441. [Abstract] [Full text] [PDF]  

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* Related collections:
 Medical/Systemic disease
 All Medical/Systemic disease
 Electrolyte
 Endocrine
 Gastrointestinal
 Hematologic
 Nutritional
 Hypoglycemia
 Metabolic disease (inherited)
 Amino acid
 Leukodystrophies
 Lipidoses
 Organic acid
 Peroxisomes
 Glycogenoses


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