Houlden H - Search Results

1

Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia.

Hersheson J, Mencacci NE, Davis M, MacDonald N, Trabzuni D, Ryten M, Pittman A, Paudel R, Kara E, Fawcett K, Plagnol V, Bhatia KP, Medlar AJ, Stanescu HC, Hardy J, Kleta R, Wood NW, Houlden H. Hersheson J, et al. Among authors: houlden h. Ann Neurol. 2013 Apr;73(4):546-53. doi: 10.1002/ana.23832. Epub 2013 Feb 19. Ann Neurol. 2013. PMID: 23424103 Free PMC article.

2

Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21-22.

Baker M, Kwok JB, Kucera S, Crook R, Farrer M, Houlden H, Isaacs A, Lincoln S, Onstead L, Hardy J, Wittenberg L, Dodd P, Webb S, Hayward N, Tannenberg T, Andreadis A, Hallupp M, Schofield P, Dark F, Hutton M. Baker M, et al. Among authors: houlden h. Ann Neurol. 1997 Nov;42(5):794-8. doi: 10.1002/ana.410420516. Ann Neurol. 1997. PMID: 9392579

3

Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia.

Worth PF, Houlden H, Giunti P, Davis MB, Wood NW. Worth PF, et al. Among authors: houlden h. Nat Genet. 2000 Mar;24(3):214-5. doi: 10.1038/73411. Nat Genet. 2000. PMID: 10700168 No abstract available.

4

Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-beta concentrations.

Houlden H, Baker M, McGowan E, Lewis P, Hutton M, Crook R, Wood NW, Kumar-Singh S, Geddes J, Swash M, Scaravilli F, Holton JL, Lashley T, Tomita T, Hashimoto T, Verkkoniemi A, Kalimo H, Somer M, Paetau A, Martin JJ, Van Broeckhoven C, Golde T, Hardy J, Haltia M, Revesz T. Houlden H, et al. Ann Neurol. 2000 Nov;48(5):806-8. Ann Neurol. 2000. PMID: 11079548

5

Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14.

McEntagart M, Norton N, Williams H, Teare MD, Dunstan M, Baker P, Houlden H, Reilly M, Wood N, Harper PS, Futreal PA, Williams N, Rahman N. McEntagart M, et al. Among authors: houlden h. Am J Hum Genet. 2001 May;68(5):1270-6. doi: 10.1086/320122. Epub 2001 Apr 4. Am J Hum Genet. 2001. PMID: 11294660 Free PMC article.

6

A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V.

Houlden H, King RH, Hashemi-Nejad A, Wood NW, Mathias CJ, Reilly M, Thomas PK. Houlden H, et al. Ann Neurol. 2001 Apr;49(4):521-5. Ann Neurol. 2001. PMID: 11310631

7

Mutations in the 5' region of the myotubularin-related protein 2 (MTMR2) gene in autosomal recessive hereditary neuropathy with focally folded myelin.

Houlden H, King RH, Wood NW, Thomas PK, Reilly MM. Houlden H, et al. Brain. 2001 May;124(Pt 5):907-15. doi: 10.1093/brain/124.5.907. Brain. 2001. PMID: 11335693

8

Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype.

Houlden H, Baker M, Morris HR, MacDonald N, Pickering-Brown S, Adamson J, Lees AJ, Rossor MN, Quinn NP, Kertesz A, Khan MN, Hardy J, Lantos PL, St George-Hyslop P, Munoz DG, Mann D, Lang AE, Bergeron C, Bigio EH, Litvan I, Bhatia KP, Dickson D, Wood NW, Hutton M. Houlden H, et al. Neurology. 2001 Jun 26;56(12):1702-6. doi: 10.1212/wnl.56.12.1702. Neurology. 2001. PMID: 11425937

9

A novel presenilin mutation (M233V) causing very early onset Alzheimer's disease with Lewy bodies.

Houlden H, Crook R, Dolan RJ, McLaughlin J, Revesz T, Hardy J. Houlden H, et al. Neurosci Lett. 2001 Nov 2;313(1-2):93-5. doi: 10.1016/s0304-3940(01)02254-6. Neurosci Lett. 2001. PMID: 11684347

10

Analysis of tau haplotypes in Pick's disease.

Morris HR, Baker M, Yasojima K, Houlden H, Khan MN, Wood NW, Hardy J, Grossman M, Trojanowski J, Revesz T, Bigio EH, Bergeron C, Janssen JC, McGeer PL, Rossor MN, Lees AJ, Lantos PL, Hutton M. Morris HR, et al. Among authors: houlden h. Neurology. 2002 Aug 13;59(3):443-5. doi: 10.1212/wnl.59.3.443. Neurology. 2002. PMID: 12177383

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