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Low, Phillip A, Prof, Reich, Stephen G, Prof, Jankovic, Joseph, Prof, Shults, Clifford W, Prof, Stern, Matthew B, Prof, Novak, Peter, MD, Tanner, Caroline M, Prof, Gilman, Sid, Prof, Marshall, Frederick J, MD, Wooten, Frederick, Prof, Racette, Brad, Prof, Chelimsky, Thomas, Prof, Singer, Wolfgang, MD, Sletten, David M, MBA, Sandroni, Paola, Prof, Mandrekar, Jay, Prof
Published in Lancet neurology (01.07.2015)
Published in Lancet neurology (01.07.2015)
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Classification and natural history of the neuronal ceroid lipofuscinoses
Mink, Jonathan W, Augustine, Erika F, Adams, Heather R, Marshall, Frederick J, Kwon, Jennifer M
Published in Journal of child neurology (01.09.2013)
Published in Journal of child neurology (01.09.2013)
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The CLN3 disease staging system: A new tool for clinical research in Batten disease
Masten, Margaux C, Williams, Justin D, Vermilion, Jennifer, Adams, Heather R, Vierhile, Amy, Collins, Alyssa, Marshall, Frederick J, Augustine, Erika F, Mink, Jonathan W
Published in Neurology (09.06.2020)
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Thalamic DBS with a constant-current device in essential tremor: A controlled clinical trial
Wharen, Robert E., MD, Okun, Michael S., MD, Guthrie, Barton L., MD, Uitti, Ryan J., MD, Larson, Paul, MD, Foote, Kelly, MD, Walker, Harrison, MD, Marshall, Frederick J., MD, Schwalb, Jason, MD, Ford, Blair, MD, Jankovic, Joseph, MD, Simpson, Richard, MD, PhD, Dashtipour, Khashayar, MD, Phibbs, Fenna, MD, Neimat, Joseph S., MD, Stewart, R. Malcolm, MD, Peichel, DeLea, BS, Pahwa, Rajesh, MD, Ostrem, Jill L., MD
Published in Parkinsonism & related disorders (01.07.2017)
Published in Parkinsonism & related disorders (01.07.2017)
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Benefits and risks of unilateral and bilateral ventral intermediate nucleus deep brain stimulation for axial essential tremor symptoms
Mitchell, Kyle T., Larson, Paul, Starr, Philip A., Okun, Michael S., Wharen, Robert E., Uitti, Ryan J., Guthrie, Barton L., Peichel, DeLea, Pahwa, Rajesh, Walker, Harrison C., Foote, Kelly, Marshall, Frederick J., Jankovic, Joseph, Simpson, Richard, Phibbs, Fenna, Neimat, Joseph S., Stewart, R. Malcolm, Dashtipour, Khashayar, Ostrem, Jill L.
Published in Parkinsonism & related disorders (01.03.2019)
Published in Parkinsonism & related disorders (01.03.2019)
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Multivariate Analyses of Peripheral Blood Leukocyte Transcripts Distinguish Alzheimer’s, Parkinson’s, Control and Those at Risk for Developing Alzheimer’s
Delvaux, E, Mastroeni, D, Nolz, J, Chow, N, Sabbagh, M, Caselli, R.J, Reiman, E.M, Marshall, F.J, Coleman, P.D
Published in Neurobiology of aging (01.10.2017)
Published in Neurobiology of aging (01.10.2017)
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A novel, hybrid, single- and multi-site clinical trial design for CLN3 disease, an ultra-rare lysosomal storage disorder
Adams, Heather R, Defendorf, Sara, Vierhile, Amy, Mink, Jonathan W, Marshall, Frederick J, Augustine, Erika F
Published in Clinical trials (London, England) (01.10.2019)
Published in Clinical trials (London, England) (01.10.2019)
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Females experience a more severe disease course in batten disease
Cialone, Jennifer, Adams, Heather, Augustine, Erika F., Marshall, Frederick J., Kwon, Jennifer M., Newhouse, Nicole, Vierhile, Amy, Levy, Erika, Dure, Leon S., Rose, Katherine R., Ramirez-Montealegre, Denia, de Blieck, Elisabeth A., Mink, Jonathan W.
Published in Journal of inherited metabolic disease (01.05.2012)
Published in Journal of inherited metabolic disease (01.05.2012)
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Short-Term Administration of Mycophenolate Is Well-Tolerated in CLN3 Disease (Juvenile Neuronal Ceroid Lipofuscinosis)
Augustine, Erika F., Beck, Christopher A., Adams, Heather R., Defendorf, Sara, Vierhile, Amy, Timm, Derek, Weimer, Jill M., Mink, Jonathan W., Marshall, Frederick J.
Published in JIMD Reports, Volume 43 (2019)
Published in JIMD Reports, Volume 43 (2019)
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Book Chapter
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A U.S. survey of patients with Parkinson's disease: Satisfaction with medical care and support groups
Dorsey, E. Ray, Voss, Tiffini S., Shprecher, David R., Deuel, Lisa M., Beck, Christopher A., Gardiner, Irenita F., Coles, Margaret A., Burns, Richard S., Marshall, Frederick J., Biglan, Kevin M.
Published in Movement disorders (15.10.2010)
Published in Movement disorders (15.10.2010)
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Safety and Tolerability of SRX246, a Vasopressin 1a Antagonist, in Irritable Huntington's Disease Patients-A Randomized Phase 2 Clinical Trial
Brownstein, Michael J, Simon, Neal G, Long, Jeffrey D, Yankey, Jon, Maibach, Hilda T, Cudkowicz, Merit, Coffey, Christopher, Conwit, Robin A, Lungu, Codrin, Anderson, Karen E, Hersch, Steven M, Ecklund, Dixie J, Damiano, Eve M, Itzkowitz, Debra E, Lu, Shifang, Chase, Marianne K, Shefner, Jeremy M, McGarry, Andrew, Thornell, Brenda, Gladden, Catherine, Costigan, Michele, O'Suilleabhain, Padraig, Marshall, Frederick J, Chesire, Amy M, Deritis, Paul, Adams, Jamie L, Hedera, Peter, Lowen, Kelly, Rosas, H Diana, Hiller, Amie L, Quinn, Joseph, Keith, Kellie, Duker, Andrew P, Gruenwald, Christina, Molloy, Angela, Jacob, Cara, Factor, Stewart, Sperin, Elaine, Bega, Danny, Brown, Zsazsa R, Seeberger, Lauren C, Sung, Victor W, Benge, Melanie, Kostyk, Sandra K, Daley, Allison M, Perlman, Susan, Suski, Valerie, Conlon, Patricia, Barrett, Matthew J, Lowenhaupt, Stephanie, Quigg, Mark, Perlmutter, Joel S, Wright, Brenton A, Most, Elaine, Schwartz, Guy J, Lamb, Jessica, Chuang, Rosalind S, Singer, Carlos, Marder, Karen, Moran, Joyce A, Singleton, John R, Zorn, Meghan, Wall, Paola V, Dubinsky, Richard M, Gray, Carolyn, Drazinic, Carolyn
Published in Journal of clinical medicine (16.11.2020)
Published in Journal of clinical medicine (16.11.2020)
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Potential outcome measures and trial design issues for multiple system atrophy
May, Susanne, Gilman, Sid, Sowell, B. Brooke, Thomas, Ronald G., Stern, Matthew B., Colcher, Amy, Tanner, Caroline M., Huang, Neng, Novak, Peter, Reich, Stephen G., Jankovic, Joseph, Ondo, William G., Low, Phillip A., Sandroni, Paola, Lipp, Axel, Marshall, Frederick J., Wooten, Frederick, Shults, Clifford W.
Published in Movement disorders (01.12.2007)
Published in Movement disorders (01.12.2007)
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Experience, knowledge, and opinions about childhood genetic testing in Batten disease
Adams, Heather R., Rose, Katherine, Augustine, Erika F., Kwon, Jennifer M., deBlieck, Elisabeth A., Marshall, Frederick J., Vierhile, Amy, Mink, Jonathan W., Nance, Martha A.
Published in Molecular genetics and metabolism (01.02.2014)
Published in Molecular genetics and metabolism (01.02.2014)
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Methodology of clinical research in rare diseases: Development of a research program in juvenile neuronal ceroid lipofuscinosis (JNCL) via creation of a patient registry and collaboration with patient advocates
de Blieck, Elisabeth A, Augustine, Erika F, Marshall, Frederick J, Adams, Heather, Cialone, Jennifer, Dure, Leon, Kwon, Jennifer M, Newhouse, Nicole, Rose, Katherine, Rothberg, Paul G, Vierhile, Amy, Mink, Jonathan W
Published in Contemporary clinical trials (01.07.2013)
Published in Contemporary clinical trials (01.07.2013)
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Genotype does not predict severity of behavioural phenotype in juvenile neuronal ceroid lipofuscinosis (Batten disease)
ADAMS, HEATHER R, BECK, CHRISTOPHER A, LEVY, ERIKA, JORDAN, RACHEL, KWON, JENNIFER M, MARSHALL, FREDERICK J, VIERHILE, AMY, AUGUSTINE, ERIKA F, DE BLIECK, ELISABETH A, PEARCE, DAVID A, MINK, JONATHAN W
Published in Developmental medicine and child neurology (01.07.2010)
Published in Developmental medicine and child neurology (01.07.2010)
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Journal Article
Parent-reported benefits of flupirtine in juvenile neuronal ceroid lipofuscinosis (Batten disease; CLN3) are not supported by quantitative data
Cialone, Jennifer, Augustine, Erika F., Newhouse, Nicole, Adams, Heather, Vierhile, Amy, Marshall, Frederick J., de Blieck, Elisabeth A., Kwon, Jennifer, Rothberg, Paul G., Mink, Jonathan W.
Published in Journal of inherited metabolic disease (01.10.2011)
Published in Journal of inherited metabolic disease (01.10.2011)
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Erratum to: Females experience a more severe disease course in batten disease
Cialone, Jennifer, Adams, Heather, Augustine, Erika F., Marshall, Frederick J., Kwon, Jennifer M., Newhouse, Nicole, Vierhile, Amy, Levy, Erika, Dure, Leon S., Rose, Katherine R., Ramirez-Montealegre, Denia, de Blieck, Elisabeth A., Mink, Jonathan W.
Published in Journal of inherited metabolic disease (01.05.2012)
Published in Journal of inherited metabolic disease (01.05.2012)
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G2019S mutation in the leucine-rich repeat kinase 2 gene is not associated with multiple system atrophy
Ozelius, Laurie J., Foroud, Tatiana, May, Susanne, Senthil, Geetha, Sandroni, Paola, Low, Phillip A., Reich, Stephen, Colcher, Amy, Stern, Matthew B., Ondo, William G., Jankovic, Joseph, Huang, Neng, Tanner, Caroline M., Novak, Peter, Gilman, Sid, Marshall, Frederick J., Wooten, G. Frederick, Chelimsky, Thomas C., Shults, Clifford W.
Published in Movement disorders (15.03.2007)
Published in Movement disorders (15.03.2007)
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