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All Genetics
Citations 581-590 of 676 total displayed.
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Past content
(since Jan 2001):
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- CLINICAL/SCIENTIFIC NOTES
Evidence of somatic mosaicism in Sturge–Weber syndrome
- A. H.M. Mahbubul Huq, Diane C. Chugani, Bharati Hukku, and Fatema Jahan Serajee
Neurology 2002; 59: 780-782.
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- CLINICAL/SCIENTIFIC NOTES
Copper genes are not implicated in the pathogenesis of focal dystonia
- O. Bandmann, F. Asmus, D. Sibbing, M. Grundmann, S. G. Schwab, J. Müller, D. B. Wildenauer, W. Poewe, T. Gasser, and W. H. Oertel
Neurology 2002; 59: 782-783.
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- ARTICLES
Evidence for additional genetic risk indicators of relapse-onset MS within the HLA region
- B. A. de Jong, T. W.J. Huizinga, E. Zanelli, M. J. Giphart, E. L.E.M. Bollen, B. M.J. Uitdehaag, C. H. Polman, and R. G.J. Westendorp
Neurology 2002; 59: 549-555.
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- ARTICLES
Clinical and genetic heterogeneity in benign hereditary chorea
- G. J. Breedveld, A. K. Percy, M. E. MacDonald, B. B.A. de Vries, C. Yapijakis, L. S. Dure, E. F. Ippel, L. A. Sandkuijl, P. Heutink, and W. F.M. Arts
Neurology 2002; 59: 579-584.
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- ARTICLES
Narrowing in on the causative defect of an intriguing X-linked myopathy with excessive autophagy
- B. A. Minassian, R. Aiyar, S. Alic, B. Banwell, M. Villanova, M. Fardeau, J. W. Mandell, V. C. Juel, M. Rafii, M. Auranen, and H. Kalimo
Neurology 2002; 59: 596-601.
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- BRIEF COMMUNICATIONS
Mutations of the slow muscle  -tropomyosin gene, TPM3, are a rare cause of nemaline myopathy
- D. Wattanasirichaigoon, K. J. Swoboda, F. Takada, H.-Q. Tong, V. Lip, S. T. Iannaccone, C. Wallgren-Pettersson, N. G. Laing, and A. H. Beggs
Neurology 2002; 59: 613-617.
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- CLINICAL/SCIENTIFIC NOTES
Abnormal cortical development shown by 3D MRI in Prader–Willi syndrome
- Akira Yoshii, Kalpathy S. Krishnamoorthy, and P. Ellen Grant
Neurology 2002; 59: 644.
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- EDITORIALS
Genes, brainstem development, and eye movements
- Elizabeth C. Engle and R. John Leigh
Neurology 2002; 59: 304-305.
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- VIEWS & REVIEWS
The neurogenetics of mucolipidosis type IV
- G. Altarescu, M. Sun, D. F. Moore, J. A. Smith, E. A. Wiggs, B. I. Solomon, N. J. Patronas, K. P. Frei, S. Gupta, C. R. Kaneski, O. W. Quarrell, S. A. Slaugenhaupt, E. Goldin, and R. Schiffmann
Neurology 2002; 59: 306-313.
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- ARTICLES
X-linked myoclonic epilepsy with spasticity and intellectual disability: Mutation in the homeobox gene ARX
- I. E. Scheffer, R. H. Wallace, F. L. Phillips, P. Hewson, K. Reardon, G. Parasivam, P. Stromme, S. F. Berkovic, J. Gecz, and J. C. Mulley
Neurology 2002; 59: 348-356.
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