|
All Genetics
Citations 581-590 of 679 total displayed.
|
Past content
(since Jan 2001):
|
- BRIEF COMMUNICATIONS
Genetic association of  2-macroglobulin polymorphisms with AD in southern Italy
- M. Zappia, R. Cittadella, I. Manna, G. Nicoletti, V. Andreoli, S. Bonavita, A. Gambardella, and A. Quattrone
Neurology 2002; 59: 756-758.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Expression of X-linked bulbospinal muscular atrophy (Kennedy disease) in two homozygous women
- Brian J. Schmidt, Cheryl R. Greenberg, Diane J. Allingham–Hawkins, and Elizabeth L. Spriggs
Neurology 2002; 59: 770-772.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
Adverse effects of phenytoin given for late-onset seizures in adults with Down syndrome
- John A. Tsiouris, Paul J. Patti, Omer Tipu, and Simhachalam Raguthu
Neurology 2002; 59: 779-780.
[Full text]
[PDF]
- 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.
[Full text]
[PDF]
- 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.
[Full text]
[PDF]
- 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.
[Abstract]
[Full text]
[PDF]
- 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.
[Abstract]
[Full text]
[PDF]
- 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.
[Abstract]
[Full text]
[PDF]
- 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.
[Abstract]
[Full text]
[PDF]
- 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.
[Full text]
[PDF]
|
|
