Janssen JC - Search Results

1

Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation.

Janssen JC, Warrington EK, Morris HR, Lantos P, Brown J, Revesz T, Wood N, Khan MN, Cipolotti L, Fox NC, Rossor MN. Janssen JC, et al. Neurology. 2002 Apr 23;58(8):1161-8. doi: 10.1212/wnl.58.8.1161. Neurology. 2002. PMID: 11971081

2

Assessing the onset of structural change in familial Alzheimer's disease.

Schott JM, Fox NC, Frost C, Scahill RI, Janssen JC, Chan D, Jenkins R, Rossor MN. Schott JM, et al. Among authors: janssen jc. Ann Neurol. 2003 Feb;53(2):181-8. doi: 10.1002/ana.10424. Ann Neurol. 2003. PMID: 12557284

3

The natural history of Alzheimer disease: a longitudinal presymptomatic and symptomatic study of a familial cohort.

Godbolt AK, Cipolotti L, Watt H, Fox NC, Janssen JC, Rossor MN. Godbolt AK, et al. Among authors: janssen jc. Arch Neurol. 2004 Nov;61(11):1743-8. doi: 10.1001/archneur.61.11.1743. Arch Neurol. 2004. PMID: 15534185

4

Mutation in the tau exon 10 splice site region in familial frontotemporal dementia.

Morris HR, Perez-Tur J, Janssen JC, Brown J, Lees AJ, Wood NW, Hardy J, Hutton M, Rossor MN. Morris HR, et al. Among authors: janssen jc. Ann Neurol. 1999 Feb;45(2):270-1. Ann Neurol. 1999. PMID: 9989634 No abstract available.

5

The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases.

Morris HR, Janssen JC, Bandmann O, Daniel SE, Rossor MN, Lees AJ, Wood NW. Morris HR, et al. Among authors: janssen jc. J Neurol Neurosurg Psychiatry. 1999 May;66(5):665-7. doi: 10.1136/jnnp.66.5.665. J Neurol Neurosurg Psychiatry. 1999. PMID: 10209184 Free PMC article.

6

Thalamic degeneration with negative prion protein immunostaining.

Janssen JC, Lantos PL, Al-Sarraj S, Rossor MN. Janssen JC, et al. J Neurol. 2000 Jan;247(1):48-51. doi: 10.1007/s004150050009. J Neurol. 2000. PMID: 10701897

7

Alzheimer's disease due to an intronic presenilin-1 (PSEN1 intron 4) mutation: A clinicopathological study.

Janssen JC, Hall M, Fox NC, Harvey RJ, Beck J, Dickinson A, Campbell T, Collinge J, Lantos PL, Cipolotti L, Stevens JM, Rossor MN. Janssen JC, et al. Brain. 2000 May;123 ( Pt 5):894-907. doi: 10.1093/brain/123.5.894. Brain. 2000. PMID: 10775535

8

Autopsy-confirmed familial early-onset Alzheimer disease caused by the l153V presenilin 1 mutation.

Janssen JC, Lantos PL, Fox NC, Harvey RJ, Beck J, Dickinson A, Campbell TA, Collinge J, Hanger DP, Cipolotti L, Stevens JM, Rossor MN. Janssen JC, et al. Arch Neurol. 2001 Jun;58(6):953-8. doi: 10.1001/archneur.58.6.953. Arch Neurol. 2001. PMID: 11405810

9

The genetic and pathological classification of familial frontotemporal dementia.

Morris HR, Khan MN, Janssen JC, Brown JM, Perez-Tur J, Baker M, Ozansoy M, Hardy J, Hutton M, Wood NW, Lees AJ, Revesz T, Lantos P, Rossor MN. Morris HR, et al. Among authors: janssen jc. Arch Neurol. 2001 Nov;58(11):1813-6. doi: 10.1001/archneur.58.11.1813. Arch Neurol. 2001. PMID: 11708988

10

Sequence analysis of tau in familial and sporadic progressive supranuclear palsy.

Morris HR, Katzenschlager R, Janssen JC, Brown JM, Ozansoy M, Quinn N, Revesz T, Rossor MN, Daniel SE, Wood NW, Lees AJ. Morris HR, et al. Among authors: janssen jc. J Neurol Neurosurg Psychiatry. 2002 Mar;72(3):388-90. doi: 10.1136/jnnp.72.3.388. J Neurol Neurosurg Psychiatry. 2002. PMID: 11861703 Free PMC article.

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