Brain,volume 129,issue 9  (09-2013)

Period of time: 2013年9期

Publisher: Oxford University Press

Founded in: 1878

Total resources: 168

ISSN: 1460-2156

Subject: R74 Neurology and Psychiatry

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Brain,volume 129,issue 9

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Editorial

By Compston Alastair in (2006)

Brain,volume 129,issue 9 , Vol. 129, Iss. 9, 2006-09 , pp. 2231-2232

Oxford University Press

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Classification of sporadic Creutzfeldt–Jakob disease revisited

By Cali Ignazio,Castellani Rudolph,Yuan Jue,Al-Shekhlee Amer,Cohen Mark L.,Xiao Xiangzhu,Moleres Francisco J.,Parchi Piero,Zou Wen-Quan,Gambetti Pierluigi in (2006)

Brain,volume 129,issue 9 , Vol. 129, Iss. 9, 2006-09 , pp. 2266-2277

Oxford University Press

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Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt–Jakob disease

By Collins S. J.,Sanchez-Juan P.,Klug G. M.,van Duijn C.,Poleggi A.,Pocchiari M.,Almonti S.,Cuadrado-Corrales N.,de Pedro-Cuesta J.,Budka H.,Gelpi E.,Glatzel M.,Tolnay M.,Hewer E.,Zerr I.,Heinemann U.,Kretszchmar H. A.,Jansen G. H.,Olsen E.,Mitrova E.,Alpérovitch A.,Brandel J.-P.,Mackenzie J.,Murray K.,Will R. G. in (2006)

Brain,volume 129,issue 9 , Vol. 129, Iss. 9, 2006-09 , pp. 2278-2287

Oxford University Press

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Clinical findings and diagnostic tests in the MV2 subtype of sporadic CJD

By Krasnianski Anna,Schulz-Schaeffer Walter J.,Kallenberg Kai,Meissner Bettina,Collie Donald A.,Roeber Sigrun,Bartl Mario,Heinemann Uta,Varges Daniela,Kretzschmar Hans A.,Zerr Inga in (2006)

Brain,volume 129,issue 9 , Vol. 129, Iss. 9, 2006-09 , pp. 2288-2296

Oxford University Press

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Inherited prion disease with six octapeptide repeat insertional mutation—molecular analysis of phenotypic heterogeneity

By Mead Simon,Poulter Mark,Beck Jon,Webb Thomas E. F.,Campbell Tracy A.,Linehan Jacqueline M.,Desbruslais Melanie,Joiner Susan,Wadsworth Jonathan D. F.,King Andrew,Lantos Peter,Collinge John in (2006)

Brain,volume 129,issue 9 , Vol. 129, Iss. 9, 2006-09 , pp. 2297-2317

Oxford University Press

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Genomewide scans in North American families reveal genetic linkage of essential tremor to a region on chromosome 6p23

By Shatunov Alexey,Sambuughin Nyamkhishig,Jankovic Joseph,Elble Rodger,Lee Hee Suk,Singleton Andrew B.,Dagvadorj Ayush,Ji Jay,Zhang Yiping,Kimonis Virginia E.,Hardy John,Hallett Mark,Goldfarb Lev G. in (2006)

Brain,volume 129,issue 9 , Vol. 129, Iss. 9, 2006-09 , pp. 2318-2331

Oxford University Press

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A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33–34

By Thiffault I.,Rioux M. F.,Tetreault M.,Jarry J.,Loiselle L.,Poirier J.,Gros-Louis F.,Mathieu J.,Vanasse M.,Rouleau G. A.,Bouchard J. P.,Lesage J.,Brais B. in (2006)

Brain,volume 129,issue 9 , Vol. 129, Iss. 9, 2006-09 , pp. 2332-2340

Oxford University Press

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