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Refinado por: Nome da Publicação: Neurology remover assunto: Medical Sciences remover
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β-Synuclein gene alterations in dementia with Lewy bodies
β-Synuclein gene alterations in dementia with Lewy bodies
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β-Synuclein gene alterations in dementia with Lewy bodies

OHTAKE, H ; LIMPRASERT, P ; TROJANOWSKI, J. Q ; ISHIKAWA, A ; IDEZUKA, J ; MURATA, M ; TODA, T ; BIRD, T. D ; LEVERENZ, J. B ; TSUJI, S ; LA SPADA, A. R ; FAN, Y ; ONODERA, O ; KAKITA, A ; TAKAHASHI, H ; BONNER, L. T ; TSUANG, D. W ; MURRAY, I. V. J ; LEE, V. M.-Y

Neurology, 2004-09, Vol.63 (5), p.805-811 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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2
The clinical and genetic spectrum of spinocerebellar ataxia 14
The clinical and genetic spectrum of spinocerebellar ataxia 14
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The clinical and genetic spectrum of spinocerebellar ataxia 14

CHEN, D.-H ; CIMINO, P. J ; WOLFF, J ; MORGAN, C ; LAU, D ; FERNANDEZ, M ; SASAKI, H ; RASKIND, W. H ; BIRD, T. D ; RANUM, L. P. W ; ZOGHBI, H. Y ; YABE, I ; SCHUT, L ; MARGOLIS, R. L ; LIPE, H. P ; FELEKE, A ; MATSUSHITA, M

Neurology, 2005-04, Vol.64 (7), p.1258-1260 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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3
Symptom onset in autosomal dominant Alzheimer disease: A systematic review and meta-analysis
Symptom onset in autosomal dominant Alzheimer disease: A systematic review and meta-analysis
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Symptom onset in autosomal dominant Alzheimer disease: A systematic review and meta-analysis

Ryman, Davis C ; Acosta-Baena, Natalia ; Aisen, Paul S ; Bird, Thomas ; Danek, Adrian ; Fox, Nick C ; Goate, Alison ; Frommelt, Peter ; Ghetti, Bernardino ; Langbaum, Jessica B.S ; Lopera, Francisco ; Martins, Ralph ; Masters, Colin L ; Mayeux, Richard P ; McDade, Eric ; Moreno, Sonia ; Reiman, Eric M ; Ringman, John M ; Salloway, Steve ; Schofield, Peter R ; Sperling, Reisa ; Tariot, Pierre N ; Xiong, Chengjie ; Morris, John C ; Bateman, Randall J

Neurology, 2014-07, Vol.83 (3), p.253-260 [Periódico revisado por pares]

Hagerstown, MD: American Academy of Neurology

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4
Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memory
Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memory
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Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memory

BARRAL, S ; BIRD, T ; WILSON, R. S ; FOROUD, T ; OTT, J ; MAYEUX, R ; GOATE, A ; FARLOW, M. R ; DIAZ-ARRASTIA, R ; BENNETT, D. A ; GRAFF-RADFORD, N ; BOEVE, B. F ; SWEET, R. A ; STERN, Y

Neurology, 2012-05, Vol.78 (19), p.1464-1471 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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5
SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy
SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy
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SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy

HANNIBAL, M. C ; RUZZO, E. K ; BEDFORD, H. M ; WORRALL, B. B ; LOVITT, S ; APPEL, S. H ; ANDERMANN, E ; BIRD, T. D ; CHANCE, P. F ; MILLER, L. R ; BETZ, B ; BUCHAN, J. G ; KNUTZEN, D. M ; BARNETT, K ; LANDSVERK, M. L ; BRICE, A ; LEGUERN, E

Neurology, 2009-05, Vol.72 (20), p.1755-1759 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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6
DNMT1 mutation hot spot causes varied phenotypes of HSAN1 with dementia and hearing loss
DNMT1 mutation hot spot causes varied phenotypes of HSAN1 with dementia and hearing loss
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DNMT1 mutation hot spot causes varied phenotypes of HSAN1 with dementia and hearing loss

KLEIN, Christopher J ; BIRD, Tom ; ERTEKIN-TANER, Nilufer ; LINCOLN, Sarah ; HJORTH, Robert ; YANHONG WU ; KWOK, John ; MER, Georges ; DYCK, Peter J ; NICHOLSON, Garth A

Neurology, 2013-02, Vol.80 (9), p.824-828 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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7
C9ORF72 repeat expansions in cases with previously identified pathogenic mutations
C9ORF72 repeat expansions in cases with previously identified pathogenic mutations
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C9ORF72 repeat expansions in cases with previously identified pathogenic mutations

van Blitterswijk, Marka ; Baker, Matthew C ; DeJesus-Hernandez, Mariely ; Ghidoni, Roberta ; Benussi, Luisa ; Finger, Elizabeth ; Hsiung, Ging-Yuek R ; Kelley, Brendan J ; Murray, Melissa E ; Rutherford, Nicola J ; Brown, Patricia E ; Ravenscroft, Thomas ; Mullen, Bianca ; Ash, Peter E.A ; Bieniek, Kevin F ; Hatanpaa, Kimmo J ; Karydas, Anna ; Wood, Elisabeth McCarty ; Coppola, Giovanni ; Bigio, Eileen H ; Lippa, Carol ; Strong, Michael J ; Beach, Thomas G ; Knopman, David S ; Huey, Edward D ; Mesulam, Marsel ; Bird, Thomas ; White, Charles L ; Kertesz, Andrew ; Geschwind, Dan H ; Van Deerlin, Vivianna M ; Petersen, Ronald C ; Binetti, Giuliano ; Miller, Bruce L ; Petrucelli, Leonard ; Wszolek, Zbigniew K ; Boylan, Kevin B ; Graff-Radford, Neill R ; Mackenzie, Ian R ; Boeve, Bradley F ; Dickson, Dennis W ; Rademakers, Rosa

Neurology, 2013-10, Vol.81 (15), p.1332-1341 [Periódico revisado por pares]

Hagerstown, MD: American Academy of Neurology

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8
Evidence for the GluR6 gene associated with younger onset age of Huntington's disease
Evidence for the GluR6 gene associated with younger onset age of Huntington's disease
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Evidence for the GluR6 gene associated with younger onset age of Huntington's disease

MACDONALD, M. E ; VONSATTEL, J. P ; SHRINIDHI, J ; COUROPMITREE, N. N ; CUPPLES, L. A ; BIRD, E. D ; GUSELLA, J. F ; MYERS, R. H

Neurology, 1999-10, Vol.53 (6), p.1330-1332 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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9
Copolymer 1 reduces relapse rate and improves disability in relapsing-remitting multiple sclerosis : results of a phase III multicenter, double-blind, placebo-controlled trial
Copolymer 1 reduces relapse rate and improves disability in relapsing-remitting multiple sclerosis : results of a phase III multicenter, double-blind, placebo-controlled trial
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Copolymer 1 reduces relapse rate and improves disability in relapsing-remitting multiple sclerosis : results of a phase III multicenter, double-blind, placebo-controlled trial

JOHNSON, K. P ; BROOKS, B. R ; VOLLMER, T ; WEINER, L. P ; WOLINSKY, J. S ; COHEN, J. A ; FORD, C. C ; GOLDSTEIN, J ; LISAK, R. P ; MYERS, L. W ; PANITCH, H. S ; ROSE, J. W ; SCHIFFER, R. B

Neurology, 1995-07, Vol.45 (7), p.1268-1276 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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10
KYNURENINE PATHWAY ABNORMALITIES IN PARKINSONS-DISEASE
KYNURENINE PATHWAY ABNORMALITIES IN PARKINSONS-DISEASE
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KYNURENINE PATHWAY ABNORMALITIES IN PARKINSONS-DISEASE

OGAWA, T ; MATSON, WR ; BEAL, MF ; MYERS, RH ; BIRD, ED ; MILBURY, P ; SASO, S

Neurology, 1992-09, Vol.42 (9), p.1702-1706 [Periódico revisado por pares]

PHILADELPHIA: Lippincott Williams & Wilkins

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