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MJFF Publications

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2261 - 2270 of 6258 Results
Title
Year
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  • Multiple system atrophy is not caused by C9orf72 hexanucleotide repeat expansions
    2014
    Summary Details
    OPEN
    Title: Multiple system atrophy is not caused by C9orf72 hexanucleotide repeat expansions
    Author(s): Sonja W. Scholz, Elisa Majounie, Tamás Révész, Janice L. Holton, Michael S. Okun, Henry Houlden, Andrew Singleton
    Journal Name: Neurobiology of Aging
    Publisher: Elsevier BV
    Vol: 36
    Issue #: 2
    Start Page: 1223.e1
    End Page: 1223.e2
    Publication Date:
    Open Access(OA) Status: OPEN
    License:
    DOI - Digital Object Identifier: 10.1016/j.neurobiolaging.2014.08.033
    Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/4315721
    Citation Count: 30
  • Mutational analysis of parkin and PINK1 in multiple system atrophy
    2010
    Summary Details
    OPEN
    Title: Mutational analysis of parkin and PINK1 in multiple system atrophy
    Author(s): Janet Brooks, Henry Houlden, Anna Melchers, Ansha J. Islam, Jinhui Ding, Abi Li, Reema Paudel, Tamás Révész, Janice L. Holton, Nicholas Wood, Andrew J. Lees, Andrew Singleton, Sonja W. Scholz
    Journal Name: Neurobiology of Aging
    Publisher: Elsevier BV
    Vol: 32
    Issue #: 3
    Start Page: 548.e5
    End Page: 548.e7
    Publication Date:
    Open Access(OA) Status: OPEN
    License:
    DOI - Digital Object Identifier: 10.1016/j.neurobiolaging.2009.11.020
    Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/3934211
    Citation Count: 21
  • Microglial responses to dopamine in a cell culture model of Parkinson's disease
    2008
    Summary Details
    OPEN
    Title: Microglial responses to dopamine in a cell culture model of Parkinson's disease
    Author(s): Diego Mastroeni, Andrew Grover, Brian Leonard, Jeffrey N. Joyce, Paul D. Coleman, Brooke Kozik, Denise L. Bellinger, Joseph Rogers
    Journal Name: Neurobiology of Aging
    Publisher: Elsevier BV
    Vol: 30
    Issue #: 11
    Start Page: 1805
    End Page: 1817
    Publication Date:
    Open Access(OA) Status: OPEN
    License:
    DOI - Digital Object Identifier: 10.1016/j.neurobiolaging.2008.01.001
    Best OA location URL:
    Citation Count: 109
  • MAPT H1 haplotype is a risk factor for essential tremor and multiple system atrophy
    2011
    Summary Details
    OPEN
    Title: MAPT H1 haplotype is a risk factor for essential tremor and multiple system atrophy
    Author(s): Carles Vilariño‐Güell, Alexandra I. Soto‐Ortolaza, Alex Rajput, Deborah C. Mash, Spyridon Papapetropoulos, Rajesh Pahwa, Kelly E. Lyons, Ryan J. Uitti, Zbigniew K. Wszołek, Dennis W. Dickson, Matthew J. Farrer, Owen A. Ross
    Journal Name: Neurology
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Vol: 76
    Issue #: 7
    Start Page: 670
    End Page: 672
    Publication Date:
    Open Access(OA) Status: OPEN
    License:
    DOI - Digital Object Identifier: 10.1212/wnl.0b013e31820c30c1
    Best OA location URL: http://n.neurology.org/content/neurology/76/7/670.full.pdf
    Citation Count: 72
  • Aberrant intracellular localization of H3k4me3 demonstrates an early epigenetic phenomenon in Alzheimer's disease
    2015
    Summary Details
    OPEN
    Title: Aberrant intracellular localization of H3k4me3 demonstrates an early epigenetic phenomenon in Alzheimer's disease
    Author(s): Diego Mastroeni, Elaine Delvaux, Jennifer Nolz, Yuyan Tan, Andrew Grover, Salvatore Oddo, Paul D. Coleman
    Journal Name: Neurobiology of Aging
    Publisher: Elsevier BV
    Vol: 36
    Issue #: 12
    Start Page: 3121
    End Page: 3129
    Publication Date:
    Open Access(OA) Status: OPEN
    License:
    DOI - Digital Object Identifier: 10.1016/j.neurobiolaging.2015.08.017
    Best OA location URL: http://doi.org/10.1016/j.neurobiolaging.2015.08.017
    Citation Count: 54
  • Quantitative EEG as a predictive biomarker for Parkinson disease dementia
    2011
    Summary Details
    OPEN
    Title: Quantitative EEG as a predictive biomarker for Parkinson disease dementia
    Author(s): Bryan T. Klassen, Joseph G. Hentz, Holly A. Shill, Erika Driver‐Dunckley, Virgilio Gerald H. Evidente, Marwan N. Sabbagh, Charles H. Adler, John N. Caviness
    Journal Name: Neurology
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Vol: 77
    Issue #: 2
    Start Page: 118
    End Page: 124
    Publication Date:
    Open Access(OA) Status: OPEN
    License:
    DOI - Digital Object Identifier: 10.1212/wnl.0b013e318224af8d
    Best OA location URL: https://n.neurology.org/content/neurology/77/2/118.full.pdf
    Citation Count: 201
  • Olfaction in Parkin heterozygotes and compound heterozygotes
    2010
    Summary Details
    OPEN
    Title: Olfaction in Parkin heterozygotes and compound heterozygotes
    Author(s): Roy N. Alcalay, Andrew Siderowf, Ruth Ottman, Elise Caccappolo, Helen Mejia‐Santana, Ming Tang, L. Rosado, Erik K. St. Louis, Dylanis Lopez Ruiz, Cheryl Waters, Stanley Fahn, L. Côté, Steven J. Frucht, B. Ford, Martha Orbe‐Reilly, B. Ross, Miguel Verbitsky, Sergey Kisselev, Cynthia L. Comella, Amy Colcher, Danna Jennings, Martha Nance, Susan Bressman, William K. Scott, Caroline M. Tanner, Stuart J. Mickel, Michael Rezak, Kevin Novak, Joseph H. Friedman, Ronald F. Pfeiffer, Laura Marsh, Bradley C. Hiner, Lorraine N. Clark, Karen Marder
    Journal Name: Neurology
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Vol: 76
    Issue #: 4
    Start Page: 319
    End Page: 326
    Publication Date:
    Open Access(OA) Status: OPEN
    License:
    DOI - Digital Object Identifier: 10.1212/wnl.0b013e31820882aa
    Best OA location URL: https://n.neurology.org/content/neurology/76/4/319.full.pdf
    Citation Count: 48
  • Olfactory dysfunction in LRRK2 G2019S mutation carriers
    2011
    Summary Details
    OPEN
    Title: Olfactory dysfunction in LRRK2 G2019S mutation carriers
    Author(s): Rachel Saunders‐Pullman, Kaili Stanley, C. Wang, Marta San Luciano, Vicki Shanker, Amelia R. Hunt, Lawrence Severt, Deborah Raymond, Laurie J. Ozelius, Richard B. Lipton, Susan Bressman
    Journal Name: Neurology
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Vol: 77
    Issue #: 4
    Start Page: 319
    End Page: 324
    Publication Date:
    Open Access(OA) Status: OPEN
    License:
    DOI - Digital Object Identifier: 10.1212/wnl.0b013e318227041c
    Best OA location URL: https://n.neurology.org/content/neurology/77/4/319.full.pdf
    Citation Count: 62
  • Mitochondrial DNA haplogroups and mutations in children with acquired central demyelination
    2011
    Summary Details
    OPEN
    Title: Mitochondrial DNA haplogroups and mutations in children with acquired central demyelination
    Author(s): S Venkateswaran, Keni Zheng, Maria Luisa Sacchetti, Donald Gagné, Douglas L. Arnold, A. Dessa Sadovnick, Stephen W. Scherer, Brenda Banwell, Amit Bar‐Or, David K. Simon
    Journal Name: Neurology
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Vol: 76
    Issue #: 9
    Start Page: 774
    End Page: 780
    Publication Date:
    Open Access(OA) Status: OPEN
    License:
    DOI - Digital Object Identifier: 10.1212/wnl.0b013e31820ee1bb
    Best OA location URL: https://n.neurology.org/content/neurology/76/9/774.full.pdf
    Citation Count: 17
  • A family with parkinsonism, essential tremor, restless legs syndrome, and depression
    2011
    Summary Details
    OPEN
    Title: A family with parkinsonism, essential tremor, restless legs syndrome, and depression
    Author(s): Andreas Puschmann, Ronald F. Pfeiffer, A. Jon Stoessl, Renju Kuriakose, Jennifer Lash, J. A. Searcy, Audrey Strongosky, Carles Vilariño‐Güell, Matthew J. Farrer, Owen A. Ross, Dennis W. Dickson, Zbigniew K. Wszołek
    Journal Name: Neurology
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Vol: 76
    Issue #: 19
    Start Page: 1623
    End Page: 1630
    Publication Date:
    Open Access(OA) Status: OPEN
    License:
    DOI - Digital Object Identifier: 10.1212/wnl.0b013e318219fb42
    Best OA location URL: https://n.neurology.org/content/neurology/76/19/1623.full.pdf
    Citation Count: 28
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