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Page 1
A hill walker with long chains.
Breen DP, Stinton V, De Silva RN. Breen DP, et al. Among authors: stinton v. Pract Neurol. 2017 Jan;17(1):71-73. doi: 10.1136/practneurol-2016-001464. Epub 2016 Nov 3. Pract Neurol. 2017. PMID: 27811128 No abstract available.
Novel c.775_781dup,p(Thr261fs) mutation in SPG 7 gene in a patient with hereditary spastic paraparesis.
Bhattacharjee S, Stinton V, Cairns D, Murray B. Bhattacharjee S, et al. Among authors: stinton v. Neurol India. 2017 Sep-Oct;65(5):1141-1142. doi: 10.4103/neuroindia.NI_96_17. Neurol India. 2017. PMID: 28879915 Free article. No abstract available.
Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.
Sinha KK, Worth PF, Jha DK, Sinha S, Stinton VJ, Davis MB, Wood NW, Sweeney MG, Bhatia KP. Sinha KK, et al. Among authors: stinton vj. J Neurol Neurosurg Psychiatry. 2004 Mar;75(3):448-52. doi: 10.1136/jnnp.2002.004895. J Neurol Neurosurg Psychiatry. 2004. PMID: 14966163 Free PMC article.
Multiple mitochondrial DNA deletions in monozygotic twins with OPMD.
Muqit MM, Larner AJ, Sweeney MG, Sewry C, Stinton VJ, Davis MB, Healy DG, Payne SJ, Chotai K, Wood NW, Lane RJ. Muqit MM, et al. Among authors: stinton vj. J Neurol Neurosurg Psychiatry. 2008 Jan;79(1):68-71. doi: 10.1136/jnnp.2006.112250. Epub 2007 Jun 5. J Neurol Neurosurg Psychiatry. 2008. PMID: 17550990
A Yorkshire family with adult-onset cranio-cervical primary torsion dystonia.
Münchau A, Valente EM, Davis MB, Stinton V, Wood NW, Quinn NP, Bhatia KP. Münchau A, et al. Among authors: stinton v. Mov Disord. 2000 Sep;15(5):954-9. doi: 10.1002/1531-8257(200009)15:5<954::aid-mds1028>3.0.co;2-i. Mov Disord. 2000. PMID: 11009204
Distal myopathy with tubular aggregates: a new phenotype associated with multiple deletions in mitochondrial DNA?
Garrard P, Blake J, Stinton V, Hanna MG, Reilly MM, Holton JL, Landon DN, Honan WP. Garrard P, et al. Among authors: stinton v. J Neurol Neurosurg Psychiatry. 2002 Aug;73(2):207-8. doi: 10.1136/jnnp.73.2.207. J Neurol Neurosurg Psychiatry. 2002. PMID: 12122190 Free PMC article. No abstract available.
Acquired isodisomy for chromosome 13 is common in AML, and associated with FLT3-itd mutations.
Griffiths M, Mason J, Rindl M, Akiki S, McMullan D, Stinton V, Powell H, Curtis A, Bown N, Craddock C. Griffiths M, et al. Among authors: stinton v. Leukemia. 2005 Dec;19(12):2355-8. doi: 10.1038/sj.leu.2403988. Leukemia. 2005. PMID: 16239911 No abstract available.
An alternative phototherapy light combination.
Furst E, Stinton VD, Moore FA, Harris TR. Furst E, et al. Among authors: stinton vd. J Pediatr. 1978 Jul;93(1):102-5. doi: 10.1016/s0022-3476(78)80615-5. J Pediatr. 1978. PMID: 650317
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