Como P - Search Results

1

Patient selection and assessment recommendations for deep brain stimulation in Tourette syndrome.

Mink JW, Walkup J, Frey KA, Como P, Cath D, Delong MR, Erenberg G, Jankovic J, Juncos J, Leckman JF, Swerdlow N, Visser-Vandewalle V, Vitek JL; Tourette Syndrome Association, Inc. Mink JW, et al. Among authors: como p. Mov Disord. 2006 Nov;21(11):1831-8. doi: 10.1002/mds.21039. Mov Disord. 2006. PMID: 16991144 Free article.

2

The course of depressive symptoms in early Parkinson's disease.

Ravina B, Elm J, Camicioli R, Como PG, Marsh L, Jankovic J, Weintraub D. Ravina B, et al. Mov Disord. 2009 Jul 15;24(9):1306-11. doi: 10.1002/mds.22572. Mov Disord. 2009. PMID: 19412939 Free PMC article.

3

A controlled trial of deprenyl in children with Tourette's syndrome and attention deficit hyperactivity disorder.

Feigin A, Kurlan R, McDermott MP, Beach J, Dimitsopulos T, Brower CA, Chapieski L, Trinidad K, Como P, Jankovic J. Feigin A, et al. Among authors: como p. Neurology. 1996 Apr;46(4):965-8. doi: 10.1212/wnl.46.4.965. Neurology. 1996. PMID: 8780073 Clinical Trial.

4

Motor abnormalities in premanifest persons with Huntington's disease: the PREDICT-HD study.

Biglan KM, Ross CA, Langbehn DR, Aylward EH, Stout JC, Queller S, Carlozzi NE, Duff K, Beglinger LJ, Paulsen JS; PREDICT-HD Investigators of the Huntington Study Group. Biglan KM, et al. Mov Disord. 2009 Sep 15;24(12):1763-72. doi: 10.1002/mds.22601. Mov Disord. 2009. PMID: 19562761 Free PMC article.

5

Obsessive-compulsive disorder in Tourette's syndrome.

Como PG, LaMarsh J, O'Brien KA. Como PG, et al. Adv Neurol. 2005;96:249-61. Adv Neurol. 2005. PMID: 16383224 Review.

6

Neuropsychological function in Tourette syndrome.

Como PG. Como PG. Adv Neurol. 2001;85:103-11. Adv Neurol. 2001. PMID: 11530420 Review.

7

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.

8

Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample.

Scharf JM, Moorjani P, Fagerness J, Platko JV, Illmann C, Galloway B, Jenike E, Stewart SE, Pauls DL; Tourette Syndrome International Consortium for Genetics. Scharf JM, et al. Neurology. 2008 Apr 15;70(16 Pt 2):1495-6. doi: 10.1212/01.wnl.0000296833.25484.bb. Neurology. 2008. PMID: 18413575 Free PMC article. No abstract available.

9

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.

10

The impact of depressive symptoms in early Parkinson disease.

Ravina B, Camicioli R, Como PG, Marsh L, Jankovic J, Weintraub D, Elm J. Ravina B, et al. Among authors: como pg. Neurology. 2007 Jul 24;69(4):342-7. doi: 10.1212/01.wnl.0000268695.63392.10. Epub 2007 Jun 20. Neurology. 2007. PMID: 17581943 Free PMC article.

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