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Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy.
Chalmers RM, Davis MB, Sweeney MG, Wood NW, Harding AE. Chalmers RM, et al. Among authors: davis mb. Am J Hum Genet. 1996 Jul;59(1):103-8. Am J Hum Genet. 1996. PMID: 8659512 Free PMC article.
Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia.
Hersheson J, Mencacci NE, Davis M, MacDonald N, Trabzuni D, Ryten M, Pittman A, Paudel R, Kara E, Fawcett K, Plagnol V, Bhatia KP, Medlar AJ, Stanescu HC, Hardy J, Kleta R, Wood NW, Houlden H. Hersheson J, et al. Among authors: davis m. Ann Neurol. 2013 Apr;73(4):546-53. doi: 10.1002/ana.23832. Epub 2013 Feb 19. Ann Neurol. 2013. PMID: 23424103 Free PMC article.
Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing.
Labrum RW, Rajakulendran S, Graves TD, Eunson LH, Bevan R, Sweeney MG, Hammans SR, Tubridy N, Britton T, Carr LJ, Ostergaard JR, Kennedy CR, Al-Memar A, Kullmann DM, Schorge S, Temple K, Davis MB, Hanna MG. Labrum RW, et al. Among authors: davis mb. J Med Genet. 2009 Nov;46(11):786-91. doi: 10.1136/jmg.2009.067967. Epub 2009 Jul 7. J Med Genet. 2009. PMID: 19586927
Genetics of Parkinsonism: a review.
Vaughan JR, Davis MB, Wood NW. Vaughan JR, et al. Among authors: davis mb. Ann Hum Genet. 2001 Mar;65(Pt 2):111-26. doi: 10.1017/S0003480001008557. Ann Hum Genet. 2001. PMID: 11427172 Review.
Genetic linkage analysis of a large family with photoparoxysmal response.
Lo C, Shorvon S, Davis M, Houlden H, Gibbons V, Wood N. Lo C, et al. Among authors: davis m. Epilepsy Res. 2012 Mar;99(1-2):38-45. doi: 10.1016/j.eplepsyres.2011.10.013. Epub 2011 Nov 8. Epilepsy Res. 2012. PMID: 22071551
Somatic and germline mosaicism in sporadic early-onset Alzheimer's disease.
Beck JA, Poulter M, Campbell TA, Uphill JB, Adamson G, Geddes JF, Revesz T, Davis MB, Wood NW, Collinge J, Tabrizi SJ. Beck JA, et al. Among authors: davis mb. Hum Mol Genet. 2004 Jun 15;13(12):1219-24. doi: 10.1093/hmg/ddh134. Epub 2004 Apr 28. Hum Mol Genet. 2004. PMID: 15115757
Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene.
Spacey SD, Valente EM, Wali GM, Warner TT, Jarman PR, Schapira AH, Dixon PH, Davis MB, Bhatia KP, Wood NW. Spacey SD, et al. Among authors: davis mb. Mov Disord. 2002 Jul;17(4):717-25. doi: 10.1002/mds.10126. Mov Disord. 2002. PMID: 12210861
Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene.
Lee MJ, Stephenson DA, Groves MJ, Sweeney MG, Davis MB, An SF, Houlden H, Salih MA, Timmerman V, de Jonghe P, Auer-Grumbach M, Di Maria E, Scaravilli F, Wood NW, Reilly MM. Lee MJ, et al. Among authors: davis mb. Hum Mol Genet. 2003 Aug 1;12(15):1917-25. doi: 10.1093/hmg/ddg198. Hum Mol Genet. 2003. PMID: 12874111
Partial epilepsy with pericentral spikes: a new familial epilepsy syndrome with evidence for linkage to chromosome 4p15.
Kinton L, Johnson MR, Smith SJ, Farrell F, Stevens J, Rance JB, Claudino AM, Duncan JS, Davis MB, Wood NW, Sander JW. Kinton L, et al. Among authors: davis mb. Ann Neurol. 2002 Jun;51(6):740-9. doi: 10.1002/ana.10221. Ann Neurol. 2002. PMID: 12112080
Coexistent hereditary and inflammatory neuropathy.
Ginsberg L, Malik O, Kenton AR, Sharp D, Muddle JR, Davis MB, Winer JB, Orrell RW, King RH. Ginsberg L, et al. Among authors: davis mb. Brain. 2004 Jan;127(Pt 1):193-202. doi: 10.1093/brain/awh017. Epub 2003 Nov 7. Brain. 2004. PMID: 14607795
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