Carbon M - Search Results

1

The visual perception of natural motion: abnormal task-related neural activity in DYT1 dystonia.

Sako W, Fujita K, Vo A, Rucker JC, Rizzo JR, Niethammer M, Carbon M, Bressman SB, Uluğ AM, Eidelberg D. Sako W, et al. Among authors: carbon m. Brain. 2015 Dec;138(Pt 12):3598-609. doi: 10.1093/brain/awv282. Epub 2015 Sep 29. Brain. 2015. PMID: 26419798 Free PMC article.

2

Regional metabolism in primary torsion dystonia: effects of penetrance and genotype.

Carbon M, Su S, Dhawan V, Raymond D, Bressman S, Eidelberg D. Carbon M, et al. Neurology. 2004 Apr 27;62(8):1384-90. doi: 10.1212/01.wnl.0000120541.97467.fe. Neurology. 2004. PMID: 15111678

3

Decreased striatal D2 receptor binding in non-manifesting carriers of the DYT1 dystonia mutation.

Asanuma K, Ma Y, Okulski J, Dhawan V, Chaly T, Carbon M, Bressman SB, Eidelberg D. Asanuma K, et al. Among authors: carbon m. Neurology. 2005 Jan 25;64(2):347-9. doi: 10.1212/01.WNL.0000149764.34953.BF. Neurology. 2005. PMID: 15668438

4

Abnormal structure-function relationships in hereditary dystonia.

Carbon M, Eidelberg D. Carbon M, et al. Neuroscience. 2009 Nov 24;164(1):220-9. doi: 10.1016/j.neuroscience.2008.12.041. Epub 2009 Jan 1. Neuroscience. 2009. PMID: 19162138 Free PMC article. Review.

5

Abnormal striatal and thalamic dopamine neurotransmission: Genotype-related features of dystonia.

Carbon M, Niethammer M, Peng S, Raymond D, Dhawan V, Chaly T, Ma Y, Bressman S, Eidelberg D. Carbon M, et al. Neurology. 2009 Jun 16;72(24):2097-103. doi: 10.1212/WNL.0b013e3181aa538f. Neurology. 2009. PMID: 19528516 Free PMC article.

6

Functional imaging in hereditary dystonia.

Carbon M, Argyelan M, Eidelberg D. Carbon M, et al. Eur J Neurol. 2010 Jul;17 Suppl 1(0 1):58-64. doi: 10.1111/j.1468-1331.2010.03054.x. Eur J Neurol. 2010. PMID: 20590810 Free PMC article.

7

Impaired sequence learning in carriers of the DYT1 dystonia mutation.

Ghilardi MF, Carbon M, Silvestri G, Dhawan V, Tagliati M, Bressman S, Ghez C, Eidelberg D. Ghilardi MF, et al. Among authors: carbon m. Ann Neurol. 2003 Jul;54(1):102-9. doi: 10.1002/ana.10610. Ann Neurol. 2003. PMID: 12838525

8

Microstructural white matter changes in carriers of the DYT1 gene mutation.

Carbon M, Kingsley PB, Su S, Smith GS, Spetsieris P, Bressman S, Eidelberg D. Carbon M, et al. Ann Neurol. 2004 Aug;56(2):283-6. doi: 10.1002/ana.20177. Ann Neurol. 2004. PMID: 15293281

9

Increased cerebellar activation during sequence learning in DYT1 carriers: an equiperformance study.

Carbon M, Ghilardi MF, Argyelan M, Dhawan V, Bressman SB, Eidelberg D. Carbon M, et al. Brain. 2008 Jan;131(Pt 1):146-54. doi: 10.1093/brain/awm243. Epub 2007 Oct 18. Brain. 2008. PMID: 17947338 Free PMC article.

10

Microstructural white matter changes in primary torsion dystonia.

Carbon M, Kingsley PB, Tang C, Bressman S, Eidelberg D. Carbon M, et al. Mov Disord. 2008 Jan 30;23(2):234-9. doi: 10.1002/mds.21806. Mov Disord. 2008. PMID: 17999428 Free PMC article.

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