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A genome-wide association study in multiple system atrophy
A genome-wide association study in multiple system atrophy
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A genome-wide association study in multiple system atrophy

Sailer, Anna ; Scholz, Sonja W ; Nalls, Michael A ; Schulte, Claudia ; Federoff, Monica ; Price, T Ryan ; Lees, Andrew ; Ross, Owen A ; Dickson, Dennis W ; Mok, Kin ; Mencacci, Niccolo E ; Schottlaender, Lucia ; Chelban, Viorica ; Ling, Helen ; OʼSullivan, Sean S ; Wood, Nicholas W ; Traynor, Bryan J ; Ferrucci, Luigi ; Federoff, Howard J ; Mhyre, Timothy R ; Morris, Huw R ; Deuschl, Günther ; Quinn, Niall ; Widner, Hakan ; Albanese, Alberto ; Infante, Jon ; Bhatia, Kailash P ; Poewe, Werner ; Oertel, Wolfgang ; Höglinger, Günter U ; Wüllner, Ullrich ; Goldwurm, Stefano ; Pellecchia, Maria Teresa ; Ferreira, Joaquim ; Tolosa, Eduardo ; Bloem, Bastiaan R ; Rascol, Olivier ; Meissner, Wassilios G ; Hardy, John A ; Revesz, Tamas ; Holton, Janice L ; Gasser, Thomas ; Wenning, Gregor K ; Singleton, Andrew B ; Houlden, Henry

Neurology, 2016-10, Vol.87 (15), p.1591-1598 [Periódico revisado por pares]

United States: American Academy of Neurology

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2
Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease
Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease
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Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease

Hudson, Gavin ; Nalls, Mike ; Evans, Jonathan R ; Breen, David P ; Winder-Rhodes, Sophie ; Morrison, Karen E ; Morris, Huw R ; Williams-Gray, Caroline H ; Barker, Roger A ; Singleton, Andrew B ; Hardy, John ; Wood, Nicholas E ; Burn, David J ; Chinnery, Patrick F

Neurology, 2013-05, Vol.80 (22), p.2042-2048 [Periódico revisado por pares]

Hagerstown, MD: American Academy of Neurology

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3
Characterizing dementia with Lewy bodies by means of diffusion tensor imaging
Characterizing dementia with Lewy bodies by means of diffusion tensor imaging
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Characterizing dementia with Lewy bodies by means of diffusion tensor imaging

WATSON, Rosie ; BLAMIRE, Andrew M ; COLLOBY, Sean J ; WOOD, Josh S ; BARBER, Robert ; JIABAO HE ; O'BRIEN, John T

Neurology, 2012-08, Vol.79 (9), p.906-914 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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4
White matter correlates of cognitive dysfunction after mild traumatic brain injury
White matter correlates of cognitive dysfunction after mild traumatic brain injury
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White matter correlates of cognitive dysfunction after mild traumatic brain injury

Croall, Iain D ; Cowie, Christopher J.A ; He, Jiabao ; Peel, Anna ; Wood, Joshua ; Aribisala, Benjamin S ; Mitchell, Patrick ; Mendelow, A David ; Smith, Fiona E ; Millar, David ; Kelly, Tom ; Blamire, Andrew M

Neurology, 2014-08, Vol.83 (6), p.494-501 [Periódico revisado por pares]

Hagerstown, MD: American Academy of Neurology

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5
Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseases
Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseases
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Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseases

SAILER, Anna ; SCHOLZ, Sonja W ; HARDY, John ; FEDEROFF, Howard J ; TRAYNOR, Bryan J ; SINGLETON, Andrew B ; HOULDEN, Henry ; RAPHAEL GIBBS, J ; TUCCI, Arianna ; JOHNSON, Janel O ; WOOD, Nicholas W ; PLAGNOL, Vincent ; HUMMERICH, Holger ; JINHUI DING ; HERNANDEZ, Dena

Neurology, 2012-07, Vol.79 (2), p.127-131 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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6
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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7
Treatment of ADHD in children with tics: A randomized controlled trial
Treatment of ADHD in children with tics: A randomized controlled trial
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Treatment of ADHD in children with tics: A randomized controlled trial

Tourette's Syndrome Study Group ; The Tourette’s Syndrome Study Group

Neurology, 2002-02, Vol.58 (4), p.527-536 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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8
A genome-wide association study in multiple system atrophy
A genome-wide association study in multiple system atrophy
Material Type:
Artigo 		Adicionar ao Meu Espaço

A genome-wide association study in multiple system atrophy

Sailer, Anna ; Scholz, Sonja W ; Nalls, Michael A ; Schulte, Claudia ; Federoff, Monica ; Price, T Ryan ; Lees, Andrew ; Ross, Owen A ; Dickson, Dennis W ; Mok, Kin ; Mencacci, Niccolo E ; Schottlaender, Lucia ; Chelban, Viorica ; Ling, Helen ; O'Sullivan, Sean S ; Wood, Nicholas W ; Traynor, Bryan J ; Ferrucci, Luigi ; Federoff, Howard J ; Mhyre, Timothy R ; Morris, Huw R ; Deuschl, Günther ; Quinn, Niall ; Widner, Hakan ; Albanese, Alberto ; Infante, Jon ; Bhatia, Kailash P ; Poewe, Werner ; Oertel, Wolfgang ; Höglinger, Günter U ; Wüllner, Ullrich ; Goldwurm, Stefano ; Pellecchia, Maria Teresa ; Ferreira, Joaquim ; Tolosa, Eduardo ; Bloem, Bastiaan R ; Rascol, Olivier ; Meissner, Wassilios G ; Hardy, John A ; Revesz, Tamas ; Holton, Janice L ; Gasser, Thomas ; Wenning, Gregor K ; Singleton, Andrew B ; Houlden, Henry ; Calandra-Buonaura, Giovanna ; Capellari, Sabina ; Cortelli, Pietro

Neurology, 2016-10, Vol.87 (15), p.1591-1598

eScholarship, University of California

Sem texto completo

Citações Citado por
9
C9ORF72 repeat expansions in cases with previously identified pathogenic mutations
C9ORF72 repeat expansions in cases with previously identified pathogenic mutations
Material Type:
Artigo 		Adicionar ao Meu Espaço

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 EA ; 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

eScholarship, University of California

Sem texto completo

Citações Citado por

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