Johnson N - Search Results

1

TARDBP 3'-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy.

Gitcho MA, Bigio EH, Mishra M, Johnson N, Weintraub S, Mesulam M, Rademakers R, Chakraverty S, Cruchaga C, Morris JC, Goate AM, Cairns NJ. Gitcho MA, et al. Among authors: johnson n. Acta Neuropathol. 2009 Nov;118(5):633-45. doi: 10.1007/s00401-009-0571-7. Epub 2009 Jul 18. Acta Neuropathol. 2009. PMID: 19618195 Free PMC article.

2

Apolipoprotein E genotypes in primary progressive aphasia.

Mesulam MM, Johnson N, Grujic Z, Weintraub S. Mesulam MM, et al. Among authors: johnson n. Neurology. 1997 Jul;49(1):51-5. doi: 10.1212/wnl.49.1.51. Neurology. 1997. PMID: 9222169

3

Dopamine agonists reorient visual exploration away from the neglected hemispace.

Grujic Z, Mapstone M, Gitelman DR, Johnson N, Weintraub S, Hays A, Kwasnica C, Harvey R, Mesulam MM. Grujic Z, et al. Among authors: johnson n. Neurology. 1998 Nov;51(5):1395-8. doi: 10.1212/wnl.51.5.1395. Neurology. 1998. PMID: 9818867 Clinical Trial.

4

Primary progressive aphasia: PPA and the language network.

Sonty SP, Mesulam MM, Thompson CK, Johnson NA, Weintraub S, Parrish TB, Gitelman DR. Sonty SP, et al. Ann Neurol. 2003 Jan;53(1):35-49. doi: 10.1002/ana.10390. Ann Neurol. 2003. PMID: 12509846

5

Neuronal ubiquitinated intranuclear inclusions in familial and non-familial frontotemporal dementia of the motor neuron disease type associated with amyotrophic lateral sclerosis.

Bigio EH, Johnson NA, Rademaker AW, Fung BB, Mesulam MM, Siddique N, Dellefave L, Caliendo J, Freeman S, Siddique T. Bigio EH, et al. Among authors: johnson na. J Neuropathol Exp Neurol. 2004 Aug;63(8):801-11. doi: 10.1093/jnen/63.8.801. J Neuropathol Exp Neurol. 2004. PMID: 15330335

6

The Activities of Daily Living Questionnaire: a validation study in patients with dementia.

Johnson N, Barion A, Rademaker A, Rehkemper G, Weintraub S. Johnson N, et al. Alzheimer Dis Assoc Disord. 2004 Oct-Dec;18(4):223-30. Alzheimer Dis Assoc Disord. 2004. PMID: 15592135

7

Prion protein codon 129 genotype prevalence is altered in primary progressive aphasia.

Li X, Rowland LP, Mitsumoto H, Przedborski S, Bird TD, Schellenberg GD, Peskind E, Johnson N, Siddique T, Mesulam MM, Weintraub S, Mastrianni JA. Li X, et al. Among authors: johnson n. Ann Neurol. 2005 Dec;58(6):858-64. doi: 10.1002/ana.20646. Ann Neurol. 2005. PMID: 16315279

8

Word list versus story memory in Alzheimer disease and frontotemporal dementia.

Wicklund AH, Johnson N, Rademaker A, Weitner BB, Weintraub S. Wicklund AH, et al. Among authors: johnson n. Alzheimer Dis Assoc Disord. 2006 Apr-Jun;20(2):86-92. doi: 10.1097/01.wad.0000213811.97305.49. Alzheimer Dis Assoc Disord. 2006. PMID: 16772743

9

Vasectomy in men with primary progressive aphasia.

Weintraub S, Fahey C, Johnson N, Mesulam MM, Gitelman DR, Weitner BB, Rademaker A. Weintraub S, et al. Among authors: johnson n. Cogn Behav Neurol. 2006 Dec;19(4):190-3. doi: 10.1097/01.wnn.0000213923.48632.ab. Cogn Behav Neurol. 2006. PMID: 17159614

10

Progranulin mutations in primary progressive aphasia: the PPA1 and PPA3 families.

Mesulam M, Johnson N, Krefft TA, Gass JM, Cannon AD, Adamson JL, Bigio EH, Weintraub S, Dickson DW, Hutton ML, Graff-Radford NR. Mesulam M, et al. Among authors: johnson n. Arch Neurol. 2007 Jan;64(1):43-7. doi: 10.1001/archneur.64.1.43. Arch Neurol. 2007. PMID: 17210807

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