Stokholm J - Search Results

1

Heterogeneity in executive impairment in patients with very mild Alzheimer's disease.

Stokholm J, Vogel A, Gade A, Waldemar G. Stokholm J, et al. Dement Geriatr Cogn Disord. 2006;22(1):54-9. doi: 10.1159/000093262. Epub 2006 May 8. Dement Geriatr Cogn Disord. 2006. PMID: 16682794 Clinical Trial.

2

Diagnostic profile of young and middle-aged memory clinic patients.

Vraamark Elberling T, Stokholm J, Høgh P, Waldemar G. Vraamark Elberling T, et al. Among authors: stokholm j. Neurology. 2002 Oct 22;59(8):1259-62. doi: 10.1212/wnl.59.8.1259. Neurology. 2002. PMID: 12391361

3

[Frontotemporal dementia--new understanding of Pick disease].

Stokholm J, Waldemar G. Stokholm J, et al. Ugeskr Laeger. 2003 Feb 3;165(6):553-6. Ugeskr Laeger. 2003. PMID: 12608020 Review. Danish.

4

Awareness of deficits in mild cognitive impairment and Alzheimer's disease: do MCI patients have impaired insight?

Vogel A, Stokholm J, Gade A, Andersen BB, Hejl AM, Waldemar G. Vogel A, et al. Among authors: stokholm j. Dement Geriatr Cogn Disord. 2004;17(3):181-7. doi: 10.1159/000076354. Epub 2004 Jan 20. Dement Geriatr Cogn Disord. 2004. PMID: 14739542

5

Semantic memory impairment in the earliest phases of Alzheimer's disease.

Vogel A, Gade A, Stokholm J, Waldemar G. Vogel A, et al. Among authors: stokholm j. Dement Geriatr Cogn Disord. 2005;19(2-3):75-81. doi: 10.1159/000082352. Epub 2004 Nov 29. Dement Geriatr Cogn Disord. 2005. PMID: 15572875

6

Years of severe and isolated amnesia can precede the development of dementia in early-onset Alzheimer's disease.

Stokholm J, Jakobsen O, Czarna JM, Mortensen HV, Waldemar G. Stokholm J, et al. Neurocase. 2005 Feb;11(1):48-55. doi: 10.1080/13554790490896965. Neurocase. 2005. PMID: 15804924

7

The executive interview as a screening test for executive dysfunction in patients with mild dementia.

Stokholm J, Vogel A, Gade A, Waldemar G. Stokholm J, et al. J Am Geriatr Soc. 2005 Sep;53(9):1577-81. doi: 10.1111/j.1532-5415.2005.53470.x. J Am Geriatr Soc. 2005. PMID: 16137290

8

Atypical early-onset Alzheimer's disease caused by the Iranian APP mutation.

Lindquist SG, Nielsen JE, Stokholm J, Schwartz M, Batbayli M, Ballegaard M, Erdal J, Krabbe K, Waldemar G. Lindquist SG, et al. Among authors: stokholm j. J Neurol Sci. 2008 May 15;268(1-2):124-30. doi: 10.1016/j.jns.2007.11.021. Epub 2008 Jan 9. J Neurol Sci. 2008. PMID: 18187157

9

Alzheimer disease-like clinical phenotype in a family with FTDP-17 caused by a MAPT R406W mutation.

Lindquist SG, Holm IE, Schwartz M, Law I, Stokholm J, Batbayli M, Waldemar G, Nielsen JE. Lindquist SG, et al. Among authors: stokholm j. Eur J Neurol. 2008 Apr;15(4):377-85. doi: 10.1111/j.1468-1331.2008.02069.x. Epub 2008 Feb 16. Eur J Neurol. 2008. PMID: 18284428

10

A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment.

Lindquist SG, Hasholt L, Bahl JM, Heegaard NH, Andersen BB, Nørremølle A, Stokholm J, Schwartz M, Batbayli M, Laursen H, Pardossi-Piquard R, Chen F, St George-Hyslop P, Waldemar G, Nielsen JE. Lindquist SG, et al. Among authors: stokholm j. Eur J Neurol. 2008 Oct;15(10):1135-9. doi: 10.1111/j.1468-1331.2008.02256.x. Epub 2008 Aug 22. Eur J Neurol. 2008. PMID: 18727676

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