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PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.
Gardiner AR, Bhatia KP, Stamelou M, Dale RC, Kurian MA, Schneider SA, Wali GM, Counihan T, Schapira AH, Spacey SD, Valente EM, Silveira-Moriyama L, Teive HA, Raskin S, Sander JW, Lees A, Warner T, Kullmann DM, Wood NW, Hanna M, Houlden H. Gardiner AR, et al. Among authors: warner t. Neurology. 2012 Nov 20;79(21):2115-21. doi: 10.1212/WNL.0b013e3182752c5a. Epub 2012 Oct 17. Neurology. 2012. PMID: 23077024 Free PMC article.
Complex I function in familial and sporadic dystonia.
Schapira AH, Warner T, Gash MT, Cleeter MW, Marinho CF, Cooper JM. Schapira AH, et al. Among authors: warner t. Ann Neurol. 1997 Apr;41(4):556-9. doi: 10.1002/ana.410410421. Ann Neurol. 1997. PMID: 9124815
Genetic counselling in mitochondrial diseases.
Warner TT, Schapira AH. Warner TT, et al. Curr Opin Neurol. 1997 Oct;10(5):408-12. doi: 10.1097/00019052-199710000-00009. Curr Opin Neurol. 1997. PMID: 9330887 Review.
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: warner tt. Brain. 1998 Dec;121 ( Pt 12):2335-9. doi: 10.1093/brain/121.12.2335. Brain. 1998. PMID: 9874484
A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family members.
Mead SH, Proukakis C, Wood N, Crosby AH, Plant GT, Warner TT. Mead SH, et al. Among authors: warner tt. J Neurol Neurosurg Psychiatry. 2001 Dec;71(6):788-91. doi: 10.1136/jnnp.71.6.788. J Neurol Neurosurg Psychiatry. 2001. PMID: 11723204 Free PMC article.
1,068 results