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1
Challenges in the diagnosis of Parkinson's disease
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Artigo
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Challenges in the diagnosis of Parkinson's disease

Tolosa, Eduardo ; Garrido, Alicia ; Scholz, Sonja W ; Poewe, Werner

Lancet neurology, 2021-05, Vol.20 (5), p.385-397 [Periódico revisado por pares]

England: Elsevier Ltd

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2
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study
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Artigo
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Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

Laaksovirta, Hannu, MD ; Peuralinna, Terhi, MSc ; Schymick, Jennifer C, PhD ; Scholz, Sonja W, MD ; Lai, Shaoi-Lin, MD ; Myllykangas, Liisa, MD ; Sulkava, Raimo, MD ; Jansson, Lilja ; Hernandez, Dena G, MSc ; Gibbs, J Raphael, BS ; Nalls, Michael A, PhD ; Heckerman, David, MD ; Tienari, Pentti J, MD ; Traynor, Bryan J, Dr

Lancet neurology, 2010-10, Vol.9 (10), p.978-985 [Periódico revisado por pares]

England: Elsevier Ltd

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3
Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease
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Artigo
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Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease

Blauwendraat, Cornelis ; Reed, Xylena ; Kia, Demis A ; Gan-Or, Ziv ; Lesage, Suzanne ; Pihlstrøm, Lasse ; Guerreiro, Rita ; Gibbs, J. Raphael ; Sabir, Marya ; Ahmed, Sarah ; Ding, Jinhui ; Alcalay, Roy N ; Hassin-Baer, Sharon ; Pittman, Alan M ; Brooks, Janet ; Edsall, Connor ; Hernandez, Dena G ; Chung, Sun Ju ; Goldwurm, Stefano ; Toft, Mathias ; Schulte, Claudia ; Bras, Jose ; Wood, Nicholas W ; Brice, Alexis ; Morris, Huw R ; Scholz, Sonja W ; Nalls, Mike A ; Singleton, Andrew B ; Cookson, Mark R

JAMA neurology, 2018-11, Vol.75 (11), p.1416-1422 [Periódico revisado por pares]

United States: American Medical Association

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4
Genetics Underlying Atypical Parkinsonism and Related Neurodegenerative Disorders
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Artigo
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Genetics Underlying Atypical Parkinsonism and Related Neurodegenerative Disorders

Scholz, Sonja W ; Bras, Jose

International journal of molecular sciences, 2015-10, Vol.16 (10), p.24629-24655 [Periódico revisado por pares]

Switzerland: MDPI AG

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5
Mutational analysis of known ALS genes in an Italian population-based cohort
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Artigo
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Mutational analysis of known ALS genes in an Italian population-based cohort

Grassano, Maurizio ; Calvo, Andrea ; Moglia, Cristina ; Brunetti, Maura ; Barberis, Marco ; Sbaiz, Luca ; Canosa, Antonio ; Manera, Umberto ; Vasta, Rosario ; Corrado, Lucia ; DʼAlfonso, Sandra ; Mazzini, Letizia ; Scholz, Sonja W ; Dalgard, Clifton ; Ding, Jinhui ; Gibbs, Raphael J ; Chia, Ruth ; Traynor, Bryan J ; Chiò, Adriano

Neurology, 2021-01, Vol.96 (4), p.e600-e609 [Periódico revisado por pares]

United States: American Academy of Neurology

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6
A Double‐Blind, Randomized, Placebo‐Controlled Trial of Ursodeoxycholic Acid (UDCA) in Parkinson's Disease
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Artigo
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A Double‐Blind, Randomized, Placebo‐Controlled Trial of Ursodeoxycholic Acid (UDCA) in Parkinson's Disease

Payne, Thomas ; Appleby, Matthew ; Buckley, Ellen ; Gelder, Linda M.A. ; Mullish, Benjamin H. ; Sassani, Matilde ; Dunning, Mark J. ; Hernandez, Dena ; Scholz, Sonja W. ; McNeill, Alisdair ; Libri, Vincenzo ; Moll, Sarah ; Marchesi, Julian R. ; Taylor, Rosie ; Su, Li ; Mazzà, Claudia ; Jenkins, Thomas M. ; Foltynie, Thomas ; Bandmann, Oliver

Movement disorders, 2023-08, Vol.38 (8), p.1493-1502 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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7
Factors impacting quality of life in multiple system atrophy
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Artigo
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Factors impacting quality of life in multiple system atrophy

Ali, Nabila ; Nesspor, Vanessa ; Bang, Jee ; Scholz, Sonja W ; Pantelyat, Alexander

Frontiers in neurology, 2023-03, Vol.14, p.1111605-1111605 [Periódico revisado por pares]

Switzerland: Frontiers Media S.A

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8
Valosin-containing protein (VCP) mutations in sporadic amyotrophic lateral sclerosis
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Artigo
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Valosin-containing protein (VCP) mutations in sporadic amyotrophic lateral sclerosis

Abramzon, Yevgeniya ; Johnson, Janel O ; Scholz, Sonja W ; Taylor, J.P ; Brunetti, Maura ; Calvo, Andrea ; Mandrioli, Jessica ; Benatar, Michael ; Mora, Gabriele ; Restagno, Gabriella ; Chiò, Adriano ; Traynor, Bryan J

Neurobiology of aging, 2012-09, Vol.33 (9), p.2231.e1-2231.e6 [Periódico revisado por pares]

United States: Elsevier Inc

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9
Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodies
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Artigo
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Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodies

Geiger, Joshua T ; Ding, Jinhui ; Crain, Barbara ; Pletnikova, Olga ; Letson, Christopher ; Dawson, Ted M ; Rosenthal, Liana S ; Pantelyat, Alexander ; Gibbs, J. Raphael ; Albert, Marilyn S ; Hernandez, Dena G ; Hillis, Argye E ; Stone, David J ; Singleton, Andrew B ; Hardy, John A ; Troncoso, Juan C ; Scholz, Sonja W

Neurobiology of disease, 2016-10, Vol.94, p.55-62 [Periódico revisado por pares]

United States: Elsevier Inc

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10
Genetic analysis of neurodegenerative diseases in a pathology cohort
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Artigo
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Genetic analysis of neurodegenerative diseases in a pathology cohort

Blauwendraat, Cornelis ; Pletnikova, Olga ; Geiger, Joshua T. ; Murphy, Natalie A. ; Abramzon, Yevgeniya ; Rudow, Gay ; Mamais, Adamantios ; Sabir, Marya S. ; Crain, Barbara ; Ahmed, Sarah ; Rosenthal, Liana S. ; Bakker, Catherine C. ; Faghri, Faraz ; Chia, Ruth ; Ding, Jinhui ; Dawson, Ted M. ; Pantelyat, Alexander ; Albert, Marilyn S. ; Nalls, Mike A. ; Resnick, Susan M. ; Ferrucci, Luigi ; Cookson, Mark R. ; Hillis, Argye E. ; Troncoso, Juan C. ; Scholz, Sonja W.

Neurobiology of aging, 2019-04, Vol.76, p.214.e1-214.e9 [Periódico revisado por pares]

United States: Elsevier Inc

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