Houlden H - Search Results

1

Recent advances in bulbar syndromes: genetic causes and disease mechanisms.

Manole A, Fratta P, Houlden H. Manole A, et al. Among authors: houlden h. Curr Opin Neurol. 2014 Oct;27(5):506-14. doi: 10.1097/WCO.0000000000000133. Curr Opin Neurol. 2014. PMID: 25159929 Review.

2

Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2.

Houlden H, Laura M, Wavrant-De Vrièze F, Blake J, Wood N, Reilly MM. Houlden H, et al. Neurology. 2008 Nov 18;71(21):1660-8. doi: 10.1212/01.wnl.0000319696.14225.67. Epub 2008 Oct 1. Neurology. 2008. PMID: 18832141

3

Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease.

Neumann J, Bras J, Deas E, O'Sullivan SS, Parkkinen L, Lachmann RH, Li A, Holton J, Guerreiro R, Paudel R, Segarane B, Singleton A, Lees A, Hardy J, Houlden H, Revesz T, Wood NW. Neumann J, et al. Among authors: houlden h. Brain. 2009 Jul;132(Pt 7):1783-94. doi: 10.1093/brain/awp044. Epub 2009 Mar 13. Brain. 2009. PMID: 19286695 Free PMC article.

4

The small, spastic, and furrowed tongue of Allgrove syndrome.

Houlden H. Houlden H. Neurology. 2009 Apr 14;72(15):1366. doi: 10.1212/WNL.0b013e3181a0fe97. Neurology. 2009. PMID: 19365062 Free PMC article. No abstract available.

5

Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in c20orf54.

Green P, Wiseman M, Crow YJ, Houlden H, Riphagen S, Lin JP, Raymond FL, Childs AM, Sheridan E, Edwards S, Josifova DJ. Green P, et al. Among authors: houlden h. Am J Hum Genet. 2010 Mar 12;86(3):485-9. doi: 10.1016/j.ajhg.2010.02.006. Epub 2010 Mar 4. Am J Hum Genet. 2010. PMID: 20206331 Free PMC article.

6

Genetic screening of Greek patients with Huntington’s disease phenocopies identifies an SCA8 expansion.

Koutsis G, Karadima G, Pandraud A, Sweeney MG, Paudel R, Houlden H, Wood NW, Panas M. Koutsis G, et al. Among authors: houlden h. J Neurol. 2012 Sep;259(9):1874-8. doi: 10.1007/s00415-012-6430-9. J Neurol. 2012. PMID: 22297462

7

Recent advances in the genetics of cerebellar ataxias.

Sailer A, Houlden H. Sailer A, et al. Among authors: houlden h. Curr Neurol Neurosci Rep. 2012 Jun;12(3):227-36. doi: 10.1007/s11910-012-0267-6. Curr Neurol Neurosci Rep. 2012. PMID: 22527681 Review.

8

Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testing.

Murphy SM, Laura M, Fawcett K, Pandraud A, Liu YT, Davidson GL, Rossor AM, Polke JM, Castleman V, Manji H, Lunn MP, Bull K, Ramdharry G, Davis M, Blake JC, Houlden H, Reilly MM. Murphy SM, et al. Among authors: houlden h. J Neurol Neurosurg Psychiatry. 2012 Jul;83(7):706-10. doi: 10.1136/jnnp-2012-302451. Epub 2012 May 10. J Neurol Neurosurg Psychiatry. 2012. PMID: 22577229 Free PMC article.

9

Genetic dysfunction of MT-ATP6 causes axonal Charcot-Marie-Tooth disease.

Pitceathly RD, Murphy SM, Cottenie E, Chalasani A, Sweeney MG, Woodward C, Mudanohwo EE, Hargreaves I, Heales S, Land J, Holton JL, Houlden H, Blake J, Champion M, Flinter F, Robb SA, Page R, Rose M, Palace J, Crowe C, Longman C, Lunn MP, Rahman S, Reilly MM, Hanna MG. Pitceathly RD, et al. Among authors: houlden h. Neurology. 2012 Sep 11;79(11):1145-54. doi: 10.1212/WNL.0b013e3182698d8d. Epub 2012 Aug 29. Neurology. 2012. PMID: 22933740 Free PMC article.

10

A novel α-synuclein missense mutation in Parkinson disease.

Proukakis C, Dudzik CG, Brier T, MacKay DS, Cooper JM, Millhauser GL, Houlden H, Schapira AH. Proukakis C, et al. Among authors: houlden h. Neurology. 2013 Mar 12;80(11):1062-4. doi: 10.1212/WNL.0b013e31828727ba. Epub 2013 Feb 20. Neurology. 2013. PMID: 23427326 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

883 results

Search Page