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All Genetics
Citations 531-540 of 676 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Benign adult familial myoclonic epilepsy: Genetic heterogeneity and allelism with ADCME
- F.A. de Falco, P. Striano, A. de Falco, S. Striano, R. Santangelo, A. Perretti, P. Balbi, M. Cecconi, and F. Zara
Neurology 2003; 60: 1381-1385.
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- CLINICAL/SCIENTIFIC NOTES
Camptocormia, axial dystonia, and parkinsonism: Phenotypic heterogeneity of a parkin mutation
- R. Inzelberg, N. Hattori, P. Nisipeanu, S. Abo Mouch, S.C. Blumen, R.L. Carasso, and Y. Mizuno
Neurology 2003; 60: 1393-1394.
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- ARTICLES
Molecular genetic investigations in the CCM1 gene in sporadic cerebral cavernomas
- P. Reich, J. Winkler, A. Straube, H.J. Steiger, and A. Peraud
Neurology 2003; 60: 1135-1138.
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- CLINICAL/SCIENTIFIC NOTES
Early Huntington disease prenatal diagnosis by maternal semiquantitative fluorescent-PCR
- M.C. González-González, M.J. Trujillo, M. Rodríguez de alba, and C. Ramos
Neurology 2003; 60: 1214-a-1215-a.
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- BRIEF COMMUNICATIONS
Hemorrhagic stroke associated with the Iowa amyloid precursor protein mutation
- S. M. Greenberg, Y. Shin, T. J. Grabowski, G. E. Cooper, G. W. Rebeck, S. Iglesias, F. Chapon, E. Tournier–Lasserve, and J.-C. Baron
Neurology 2003; 60: 1020-1022.
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- BRIEF COMMUNICATIONS
Periventricular heterotopia associated with chromosome 5p anomalies
- V.L. Sheen, J.W. Wheless, A. Bodell, E. Braverman, P.D. Cotter, K.A. Rauen, O. Glenn, K. Weisiger, S. Packman, C.A. Walsh, and E.H. Sherr
Neurology 2003; 60: 1033-1036.
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- ARTICLES
Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease
- T. Foroud, S.K. Uniacke, L. Liu, N. Pankratz, A. Rudolph, C. Halter, C. Shults, K. Marder, P.M. Conneally, W.C. Nichols, and the Parkinson Study Group
Neurology 2003; 60: 796-801.
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- BRIEF COMMUNICATIONS
Possible association of the tau H1/H1 genotype with primary progressive aphasia
- M.-J. Sobrido, A. Abu–Khalil, S. Weintraub, N. Johnson, B. Quinn, J. L. Cummings, M.-M. Mesulam, and D. H. Geschwind
Neurology 2003; 60: 862-864.
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- BRIEF COMMUNICATIONS
Phenotypic variability of aprataxin gene mutations
- C. Tranchant, M. Fleury, M. C. Moreira, M. Koenig, and J. M. Warter
Neurology 2003; 60: 868-870.
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- ARTICLES
Myotonic dystrophy type 2: Molecular, diagnostic and clinical spectrum
- J. W. Day, K. Ricker, J. F. Jacobsen, L. J. Rasmussen, K. A. Dick, W. Kress, C. Schneider, M. C. Koch, G. J. Beilman, A. R. Harrison, J. C. Dalton, and L. P.W. Ranum
Neurology 2003; 60: 657-664.
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