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Page 1
Neurocognitive clinical outcome assessments for inborn errors of metabolism and other rare conditions.
Shapiro E, Bernstein J, Adams HR, Barbier AJ, Buracchio T, Como P, Delaney KA, Eichler F, Goldsmith JC, Hogan M, Kovacs S, Mink JW, Odenkirchen J, Parisi MA, Skrinar A, Waisbren SE, Mulberg AE. Shapiro E, et al. Among authors: como p. Mol Genet Metab. 2016 Jun;118(2):65-9. doi: 10.1016/j.ymgme.2016.04.006. Epub 2016 Apr 14. Mol Genet Metab. 2016. PMID: 27132782 Free PMC article.
A randomized, double-blind, placebo-controlled trial of antidepressants in Parkinson disease.
Richard IH, McDermott MP, Kurlan R, Lyness JM, Como PG, Pearson N, Factor SA, Juncos J, Serrano Ramos C, Brodsky M, Manning C, Marsh L, Shulman L, Fernandez HH, Black KJ, Panisset M, Christine CW, Jiang W, Singer C, Horn S, Pfeiffer R, Rottenberg D, Slevin J, Elmer L, Press D, Hyson HC, McDonald W; SAD-PD Study Group. Richard IH, et al. Among authors: como pg. Neurology. 2012 Apr 17;78(16):1229-36. doi: 10.1212/WNL.0b013e3182516244. Epub 2012 Apr 11. Neurology. 2012. PMID: 22496199 Free PMC article. Clinical Trial.
FDA Regulation of Neurological and Physical Medicine Devices: Access to Safe and Effective Neurotechnologies for All Americans.
Anderson L, Antkowiak P, Asefa A, Ballard A, Bansal T, Bello A, Berne B, Bowsher K, Blumenkopf B, Broverman I, Bydon M, Chao K, Como P, Cork K, Costello A, De Laurentis K, DeMarco A, Dean H, Doucet J, Dworak B, Epperson L, Franca E, Ghassemian N, Ghosh C, Govindarajan A, Gupta J, Gutowski S, Herrmann R, Hoffmann M, Heetderks W, Hsu S, Kaufman D, Keegan E, Kittlesen G, Khuu K, Lee H, Lo L, Marcus I, Marjenin T, Mathews B, Misra S, Pinto V, Ramos V, Raben S, Russell A, Saha D, Seog J, Shenouda C, Smith M, Tang X, Wachrathit K, Waterhouse J, Williams D, Zheng X, Peña C. Anderson L, et al. Among authors: como p. Neuron. 2016 Dec 7;92(5):943-948. doi: 10.1016/j.neuron.2016.10.036. Neuron. 2016. PMID: 27930909 Free article.
Family-based genetic association study of DLGAP3 in Tourette Syndrome.
Crane J, Fagerness J, Osiecki L, Gunnell B, Stewart SE, Pauls DL, Scharf JM; Tourette Syndrome International Consortium for Genetics (TSAICG). Crane J, et al. Am J Med Genet B Neuropsychiatr Genet. 2011 Jan;156B(1):108-14. doi: 10.1002/ajmg.b.31134. Epub 2010 Nov 2. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21184590 Free PMC article.
Challenges assessing clinical endpoints in early Huntington disease.
Paulsen JS, Wang C, Duff K, Barker R, Nance M, Beglinger L, Moser D, Williams JK, Simpson S, Langbehn D, van Kammen DP; PREDICT-HD Investigators of the Huntington Study Group. Paulsen JS, et al. Mov Disord. 2010 Nov 15;25(15):2595-603. doi: 10.1002/mds.23337. Mov Disord. 2010. PMID: 20623772 Free PMC article.
Segregation and linkage analyses of Tourette's syndrome and related disorders.
Pauls DL, Pakstis AJ, Kurlan R, Kidd KK, Leckman JF, Cohen DJ, Kidd JR, Como P, Sparkes R. Pauls DL, et al. Among authors: como p. J Am Acad Child Adolesc Psychiatry. 1990 Mar;29(2):195-203. doi: 10.1097/00004583-199003000-00007. J Am Acad Child Adolesc Psychiatry. 1990. PMID: 2324061
81 results