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Genetic linkage
Citations 1-10 of 81 total displayed.
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Most recent content
(24 Nov 2009):
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- ARTICLES
A novel stroke locus identified in a northern Sweden pedigree: Linkage to chromosome 9q31-33
- T. Janunger, S. Nilsson-Ardnor, P. -G. Wiklund, P. Lindgren, S. A. Escher, K. Lackovic, A. K. Nilsson, B. Stegmayr, K. Asplund, and D. Holmberg
Neurology 2009; 73: 1767-1773.
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Past content
(since Jan 2001):
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- ARTICLES
Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+
- A. Poduri, Y. Wang, D. Gordon, S. Barral-Rodriguez, C. Barker-Cummings, A. Ulgen, V. Chitsazzadeh, R. S. Hill, N. Risch, W. A. Hauser, T. A. Pedley, C. A. Walsh, and R. Ottman
Neurology 2009; 73: 1264-1272.
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- CLINICAL/SCIENTIFIC NOTES
16p11.2-RELATED PAROXYSMAL KINESIGENIC DYSKINESIA AND DOPA-RESPONSIVE PARKINSONISM IN A CHILD
- Jonathan Lipton and Michael J. Rivkin
Neurology 2009; 73: 479-480.
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- EDITORIALS
Paraoxonase genes and susceptibility to ALS
- David A. Greenberg, William C.L. Stewart, and Lewis P. Rowland
Neurology 2009; 73: 11-12.
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- ARTICLES
Abnormal striatal and thalamic dopamine neurotransmission: Genotype-related features of dystonia
- M. Carbon, M. Niethammer, S. Peng, D. Raymond, V. Dhawan, T. Chaly, Y. Ma, S. Bressman, and D. Eidelberg
Neurology 2009; 72: 2097-2103.
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- EDITORIALS
Variation on a theme: Identifying sequence variation in disease genes and defining pathogenicity
- Lorraine N. Clark
Neurology 2009; 72: 1882-1883.
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- ARTICLES
Variation in GIGYF2 is not associated with Parkinson disease
- W. C. Nichols, D. K. Kissell, N. Pankratz, M. W. Pauciulo, V. E. Elsaesser, K. A. Clark, C. A. Halter, A. Rudolph, J. Wojcieszek, R. F. Pfeiffer, T. Foroud For the Parkinson Study Group–PROGENI Investigators
Neurology 2009; 72: 1886-1892.
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- ARTICLES
Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24
- R. Schüle, M. Bonin, A. Dürr, S. Forlani, A. D. Sperfeld, S. Klimpe, J. C. Mueller, A. Seibel, B. P. van de Warrenburg, P. Bauer, and L. Schöls
Neurology 2009; 72: 1893-1898.
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- ARTICLES
Age and founder effect of SOD1 A4V mutation causing ALS
- M. Saeed, Y. Yang, H-X Deng, W-Y Hung, N. Siddique, L. Dellefave, C. Gellera, P. M. Andersen, and T. Siddique
Neurology 2009; 72: 1634-1639.
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- ARTICLES
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease
- I. Le Ber, A. Camuzat, E. Berger, D. Hannequin, A. Laquerrière, V. Golfier, D. Seilhean, G. Viennet, P. Couratier, P. Verpillat, S. Heath, W. Camu, O. Martinaud, L. Lacomblez, M. Vercelletto, F. Salachas, F. Sellal, M. Didic, C. Thomas-Anterion, M. Puel, B-F Michel, C. Besse, C. Duyckaerts, V. Meininger, D. Campion, B. Dubois, A. Brice For the French Research Network on FTD/FTD-MND
Neurology 2009; 72: 1669-1676.
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