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Neurology
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Gene expression studies

Citations 1-10 of 25 total displayed.

Most recent content (18 Nov 2008):

EDITORIALS
Hereditary motor neuropathy and heat shock proteins: A shocking transformation
Clifton Gooch and Michael Shy
Neurology 2008; 71: 1656-1657. [Full text] [PDF]  

Past content (since Oct 2002):

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
VERTEBRAL OSTEOMYELITIS COMPLICATING PNEUMOCOCCAL MENINGITIS
M. C. Brouwer, J. de Gans, S.G.B. Heckenberg, H. Kuiper, H. B.M. van Lieshout, and D. van de Beek
Neurology 2008; 71: 612-613. [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

EDITORIALS
Association, expression, pathobiology: Is too much tau in PD a blueprint for genetic association?
Andrew Singleton and Huw Morris
Neurology 2008; 71: 11-12. [Full text] [PDF]  

ARTICLES
Haplotypes and gene expression implicate the MAPT region for Parkinson disease: The GenePD Study
J. E. Tobin, J. C. Latourelle, M. F. Lew, C. Klein, O. Suchowersky, H. A. Shill, L. I. Golbe, M. H. Mark, J. H. Growdon, G. F. Wooten, B. A. Racette, J. S. Perlmutter, R. Watts, M. Guttman, K. B. Baker, S. Goldwurm, G. Pezzoli, C. Singer, M. H. Saint-Hilaire, A. E. Hendricks, S. Williamson, M. W. Nagle, J. B. Wilk, T. Massood, J. M. Laramie, A. L. DeStefano, I. Litvan, G. Nicholson, A. Corbett, S. Isaacson, D. J. Burn, P. F. Chinnery, P. P. Pramstaller, S. Sherman, J. Al-hinti, E. Drasby, M. Nance, A. T. Moller, K. Ostergaard, R. Roxburgh, B. Snow, J. T. Slevin, F. Cambi, J. F. Gusella, and R. H. Myers
Neurology 2008; 71: 28-34. [Abstract] [Full text] [PDF]  

ARTICLES
Paraoxonase 1 (PON1) organophosphate hydrolysis is not reduced in ALS
A. -M. Wills, J. E. Landers, H. Zhang, R. J. Richter, A. J. Caraganis, M. E. Cudkowicz, C. E. Furlong, and R. H. Brown, Jr
Neurology 2008; 70: 929-934. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
CLINICOPATHOLOGIC STUDY OF A SNCA GENE DUPLICATION PATIENT WITH PARKINSON DISEASE AND DEMENTIA
T. Obi, K. Nishioka, O. A. Ross, T. Terada, K. Yamazaki, A. Sugiura, M. Takanashi, K. Mizoguchi, H. Mori, Y. Mizuno, and N. Hattori
Neurology 2008; 70: 238-241. [Full text] [PDF]  

VIEWS & REVIEWS
Parkinson disease, 10 years after its genetic revolution: Multiple clues to a complex disorder
Christine Klein and Michael G. Schlossmacher
Neurology 2007; 69: 2093-2104. [Abstract] [Full text] [PDF]  

ARTICLES
GNE protein expression and subcellular distribution are unaltered in HIBM
S. Krause, A. Aleo, S. Hinderlich, L. Merlini, I. Tournev, M. C. Walter, Z. Argov, S. Mitrani-Rosenbaum, and H. Lochmüller
Neurology 2007; 69: 655-659. [Abstract] [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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