Houlden H - Search Results

1

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17.

Hutton M, Lendon CL, Rizzu P, Baker M, Froelich S, Houlden H, Pickering-Brown S, Chakraverty S, Isaacs A, Grover A, Hackett J, Adamson J, Lincoln S, Dickson D, Davies P, Petersen RC, Stevens M, de Graaff E, Wauters E, van Baren J, Hillebrand M, Joosse M, Kwon JM, Nowotny P, Che LK, Norton J, Morris JC, Reed LA, Trojanowski J, Basun H, Lannfelt L, Neystat M, Fahn S, Dark F, Tannenberg T, Dodd PR, Hayward N, Kwok JB, Schofield PR, Andreadis A, Snowden J, Craufurd D, Neary D, Owen F, Oostra BA, Hardy J, Goate A, van Swieten J, Mann D, Lynch T, Heutink P. Hutton M, et al. Among authors: houlden h. Nature. 1998 Jun 18;393(6686):702-5. doi: 10.1038/31508. Nature. 1998. PMID: 9641683

2

A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid.

Mullan M, Crawford F, Axelman K, Houlden H, Lilius L, Winblad B, Lannfelt L. Mullan M, et al. Among authors: houlden h. Nat Genet. 1992 Aug;1(5):345-7. doi: 10.1038/ng0892-345. Nat Genet. 1992. PMID: 1302033

3

A locus for familial early-onset Alzheimer's disease on the long arm of chromosome 14, proximal to the alpha 1-antichymotrypsin gene.

Mullan M, Houlden H, Windelspecht M, Fidani L, Lombardi C, Diaz P, Rossor M, Crook R, Hardy J, Duff K, et al. Mullan M, et al. Among authors: houlden h. Nat Genet. 1992 Dec;2(4):340-2. doi: 10.1038/ng1292-340. Nat Genet. 1992. PMID: 1303291

4

Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein gene.

Chartier-Harlin MC, Crawford F, Houlden H, Warren A, Hughes D, Fidani L, Goate A, Rossor M, Roques P, Hardy J, et al. Chartier-Harlin MC, et al. Among authors: houlden h. Nature. 1991 Oct 31;353(6347):844-6. doi: 10.1038/353844a0. Nature. 1991. PMID: 1944558

5

Apolipoprotein E alleles but neither apolipoprotein B nor apolipoprotein AI/CIII alleles are associated with late onset, familial Alzheimer's disease.

Houlden H, Crook R, Duff K, Hutton M, Collinge J, Roques P, Rossor M, Hardy J. Houlden H, et al. Neurosci Lett. 1995 Mar 31;188(3):202-4. doi: 10.1016/0304-3940(95)11422-s. Neurosci Lett. 1995. PMID: 7609909

6

Microsatellite D21S210 (GT-12) allele frequencies in sporadic Alzheimer's disease.

Lannfelt L, Lilius L, Viitanen M, Houlden H, Rossor M, Hardy J, Winblad B, Basun H. Lannfelt L, et al. Among authors: houlden h. Acta Neurol Scand. 1995 Feb;91(2):145-8. doi: 10.1111/j.1600-0404.1995.tb00422.x. Acta Neurol Scand. 1995. PMID: 7785426

7

Exclusion mapping in familial non-specific dementia.

Brown J, Gydesen S, Sorensen SA, Brun A, Duff K, Houlden H, Fidani L, Kullkarni S, Cummings J, Goate A, et al. Brown J, et al. Among authors: houlden h. Dementia. 1993 May-Aug;4(3-4):163-6. doi: 10.1159/000107317. Dementia. 1993. PMID: 8401786

8

Absence of linkage between chromosome 21 loci and familial amyotrophic lateral sclerosis.

King A, Houlden H, Hardy J, Lane R, Chancellor A, de Belleroche J. King A, et al. Among authors: houlden h. J Med Genet. 1993 Apr;30(4):318. doi: 10.1136/jmg.30.4.318. J Med Genet. 1993. PMID: 8487280 Free PMC article.

9

Polymorphism in AACT gene may lower age of onset of Alzheimer's disease.

Talbot C, Houlden H, Craddock N, Crook R, Hutton M, Lendon C, Prihar G, Morris JC, Hardy J, Goate A. Talbot C, et al. Among authors: houlden h. Neuroreport. 1996 Jan 31;7(2):534-6. doi: 10.1097/00001756-199601310-00038. Neuroreport. 1996. PMID: 8730823 Clinical Trial.

10

Complete analysis of the presenilin 1 gene in early onset Alzheimer's disease.

Hutton M, Busfield F, Wragg M, Crook R, Perez-Tur J, Clark RF, Prihar G, Talbot C, Phillips H, Wright K, Baker M, Lendon C, Duff K, Martinez A, Houlden H, Nichols A, Karran E, Roberts G, Roques P, Rossor M, Venter JC, Adams MD, Cline RT, Phillips CA, Goate A, et al. Hutton M, et al. Among authors: houlden h. Neuroreport. 1996 Feb 29;7(3):801-5. doi: 10.1097/00001756-199602290-00029. Neuroreport. 1996. PMID: 8733749

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