Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 17


Managing juvenile Huntington's disease.

Quarrell OW, Nance MA, Nopoulos P, Paulsen JS, Smith JA, Squitieri F.

Neurodegener Dis Manag. 2013 Jun 1;3(3). doi: 10.2217/nmt.13.18.


Atomistic simulations of the effects of polyglutamine chain length and solvent quality on conformational equilibria and spontaneous homodimerization.

Vitalis A, Wang X, Pappu RV.

J Mol Biol. 2008 Dec 5;384(1):279-97. doi: 10.1016/j.jmb.2008.09.026. Epub 2008 Sep 18.


Pathological cell-cell interactions are necessary for striatal pathogenesis in a conditional mouse model of Huntington's disease.

Gu X, André VM, Cepeda C, Li SH, Li XJ, Levine MS, Yang XW.

Mol Neurodegener. 2007 Apr 30;2:8.


Association of Huntington's disease and schizophrenia-like psychosis in a Huntington's disease pedigree.

Corrêa BB, Xavier M, Guimarães J.

Clin Pract Epidemiol Ment Health. 2006 Feb 15;2:1. doi: 10.1186/1745-0179-2-1.


Genetic polymorphisms adjacent to the CAG repeat influence clinical features at onset in Huntington's disease.

Vuillaume I, Vermersch P, Destée A, Petit H, Sablonnière B.

J Neurol Neurosurg Psychiatry. 1998 Jun;64(6):758-62.


The likelihood of being affected with Huntington disease by a particular age, for a specific CAG size.

Brinkman RR, Mezei MM, Theilmann J, Almqvist E, Hayden MR.

Am J Hum Genet. 1997 May;60(5):1202-10.


Huntington disease--another chapter rewritten.

Nance MA.

Am J Hum Genet. 1996 Jul;59(1):1-6. Review.


Clinical genetics in neurological disease.

MacMillan JC, Harper PS.

J Neurol Neurosurg Psychiatry. 1994 Jan;57(1):7-15. Review. No abstract available.


A specific mutation for Huntington's disease.

Harper PS.

J Med Genet. 1993 Dec;30(12):975-7. Review. No abstract available.


Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary chorea.

MacMillan JC, Morrison PJ, Nevin NC, Shaw DJ, Harper PS, Quarrell OW, Snell RG.

J Med Genet. 1993 Dec;30(12):1012-3.


Imaging the head: functional imaging.

Sawle GV.

J Neurol Neurosurg Psychiatry. 1995 Feb;58(2):132-44. Review. No abstract available.


Trinucleotide repeat length and progression of illness in Huntington's disease.

Kieburtz K, MacDonald M, Shih C, Feigin A, Steinberg K, Bordwell K, Zimmerman C, Srinidhi J, Sotack J, Gusella J, et al.

J Med Genet. 1994 Nov;31(11):872-4.


Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein gene.

Nicholl D, Windl O, de Silva R, Sawcer S, Dempster M, Ironside JW, Estibeiro JP, Yuill GM, Lathe R, Will RG.

J Neurol Neurosurg Psychiatry. 1995 Jan;58(1):65-9.


DNA analysis of Huntington's disease in southern Chinese.

Chan V, Yu YL, Chan TP, Yip B, Chang CM, Wong MT, Chan YW, Chan TK.

J Med Genet. 1995 Feb;32(2):120-4.


Molecular diagnostic analysis for Huntington's disease: a prospective evaluation.

MacMillan JC, Davies P, Harper PS.

J Neurol Neurosurg Psychiatry. 1995 Apr;58(4):496-8.


Supplemental Content

Support Center