Murrell JR - Search Results

1

[Neurodegenerative disease associated with a mutation of codon 279 (N279K) in exon 10 of Tau protein].

Delisle MB, Uro-Coste E, Murrell JR, Rascol O, Ghetti B. Delisle MB, et al. Among authors: murrell jr. Bull Acad Natl Med. 2000;184(4):799-809; discussion 809-11. Bull Acad Natl Med. 2000. PMID: 10989564 Review. French.

2

Spectrum of amyloid beta-protein immunoreactivity in hereditary Alzheimer disease with a guanine to thymine missense change at position 1924 of the APP gene.

Ghetti B, Murrell J, Benson MD, Farlow MR. Ghetti B, et al. Brain Res. 1992 Jan 31;571(1):133-9. doi: 10.1016/0006-8993(92)90519-f. Brain Res. 1992. PMID: 1611485

3

A mutation in the amyloid precursor protein associated with hereditary Alzheimer's disease.

Murrell J, Farlow M, Ghetti B, Benson MD. Murrell J, et al. Science. 1991 Oct 4;254(5028):97-9. doi: 10.1126/science.1925564. Science. 1991. PMID: 1925564

4

RFLP analysis for APP 717 mutations associated with Alzheimer's disease.

Zeldenrust SR, Murrell J, Farlow M, Ghetti B, Roses AD, Benson MD. Zeldenrust SR, et al. J Med Genet. 1993 Jun;30(6):476-8. doi: 10.1136/jmg.30.6.476. J Med Genet. 1993. PMID: 7686976 Free PMC article.

5

Clinical characteristics in a kindred with early-onset Alzheimer's disease and their linkage to a G-->T change at position 2149 of the amyloid precursor protein gene.

Farlow M, Murrell J, Ghetti B, Unverzagt F, Zeldenrust S, Benson M. Farlow M, et al. Neurology. 1994 Jan;44(1):105-11. doi: 10.1212/wnl.44.1.105. Neurology. 1994. PMID: 8290042

6

Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments.

Spillantini MG, Goedert M, Crowther RA, Murrell JR, Farlow MR, Ghetti B. Spillantini MG, et al. Among authors: murrell jr. Proc Natl Acad Sci U S A. 1997 Apr 15;94(8):4113-8. doi: 10.1073/pnas.94.8.4113. Proc Natl Acad Sci U S A. 1997. PMID: 9108114 Free PMC article.

7

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17.

Murrell JR, Koller D, Foroud T, Goedert M, Spillantini MG, Edenberg HJ, Farlow MR, Ghetti B. Murrell JR, et al. Am J Hum Genet. 1997 Nov;61(5):1131-8. doi: 10.1086/301594. Am J Hum Genet. 1997. PMID: 9345089 Free PMC article.

8

Mutation in the tau gene in familial multiple system tauopathy with presenile dementia.

Spillantini MG, Murrell JR, Goedert M, Farlow MR, Klug A, Ghetti B. Spillantini MG, et al. Among authors: murrell jr. Proc Natl Acad Sci U S A. 1998 Jun 23;95(13):7737-41. doi: 10.1073/pnas.95.13.7737. Proc Natl Acad Sci U S A. 1998. PMID: 9636220 Free PMC article.

9

Tau pathology in a family with dementia and a P301L mutation in tau.

Mirra SS, Murrell JR, Gearing M, Spillantini MG, Goedert M, Crowther RA, Levey AI, Jones R, Green J, Shoffner JM, Wainer BH, Schmidt ML, Trojanowski JQ, Ghetti B. Mirra SS, et al. Among authors: murrell jr. J Neuropathol Exp Neurol. 1999 Apr;58(4):335-45. doi: 10.1097/00005072-199904000-00004. J Neuropathol Exp Neurol. 1999. PMID: 10218629

10

Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau.

Bugiani O, Murrell JR, Giaccone G, Hasegawa M, Ghigo G, Tabaton M, Morbin M, Primavera A, Carella F, Solaro C, Grisoli M, Savoiardo M, Spillantini MG, Tagliavini F, Goedert M, Ghetti B. Bugiani O, et al. Among authors: murrell jr. J Neuropathol Exp Neurol. 1999 Jun;58(6):667-77. doi: 10.1097/00005072-199906000-00011. J Neuropathol Exp Neurol. 1999. PMID: 10374757

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