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Primary torsion dystonia: the search for genes is not over.
Jarman PR, del Grosso N, Valente EM, Leube B, Cassetta E, Bentivoglio AR, Waddy HM, Uitti RJ, Maraganore DM, Albanese A, Frontali M, Auburger G, Bressman SB, Wood NW, Nygaard TG. Jarman PR, et al. J Neurol Neurosurg Psychiatry. 1999 Sep;67(3):395-7. doi: 10.1136/jnnp.67.3.395. J Neurol Neurosurg Psychiatry. 1999. PMID: 10449567 Free PMC article.
Genetics of movement disorders and ataxia.
Jarman PR, Wood NW. Jarman PR, et al. J Neurol Neurosurg Psychiatry. 2002 Dec;73 Suppl 2(Suppl 2):II22-6. doi: 10.1136/jnnp.73.suppl_2.ii22. J Neurol Neurosurg Psychiatry. 2002. PMID: 12536155 Free PMC article. Review. No abstract available.
The role of DYT1 in primary torsion dystonia in Europe.
Valente EM, Warner TT, Jarman PR, Mathen D, Fletcher NA, Marsden CD, Bhatia KP, Wood NW. Valente EM, et al. Among authors: jarman pr. Brain. 1998 Dec;121 ( Pt 12):2335-9. doi: 10.1093/brain/121.12.2335. Brain. 1998. PMID: 9874484
Parkinson's disease genetics comes of age.
Jarman P, Wood N. Jarman P, et al. BMJ. 1999 Jun 19;318(7199):1641-2. doi: 10.1136/bmj.318.7199.1641. BMJ. 1999. PMID: 10373154 Free PMC article. No abstract available.
The glucocerobrosidase E326K variant predisposes to Parkinson's disease, but does not cause Gaucher's disease.
Duran R, Mencacci NE, Angeli AV, Shoai M, Deas E, Houlden H, Mehta A, Hughes D, Cox TM, Deegan P, Schapira AH, Lees AJ, Limousin P, Jarman PR, Bhatia KP, Wood NW, Hardy J, Foltynie T. Duran R, et al. Among authors: jarman pr. Mov Disord. 2013 Feb;28(2):232-236. doi: 10.1002/mds.25248. Epub 2012 Dec 5. Mov Disord. 2013. PMID: 23225227 Free PMC article.
31 results