Gibbons V - Search Results

1

Young-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family.

Kojovic M, Sheerin UM, Rubio-Agusti I, Saha A, Bras J, Gibbons V, Palmer R, Houlden H, Hardy J, Wood NW, Bhatia KP. Kojovic M, et al. Among authors: gibbons v. Mov Disord. 2012 Dec;27(14):1827-9. doi: 10.1002/mds.25199. Mov Disord. 2012. PMID: 23283657 Free article. No abstract available.

2

Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data.

Khan NL, Jain S, Lynch JM, Pavese N, Abou-Sleiman P, Holton JL, Healy DG, Gilks WP, Sweeney MG, Ganguly M, Gibbons V, Gandhi S, Vaughan J, Eunson LH, Katzenschlager R, Gayton J, Lennox G, Revesz T, Nicholl D, Bhatia KP, Quinn N, Brooks D, Lees AJ, Davis MB, Piccini P, Singleton AB, Wood NW. Khan NL, et al. Among authors: gibbons v. Brain. 2005 Dec;128(Pt 12):2786-96. doi: 10.1093/brain/awh667. Epub 2005 Nov 4. Brain. 2005. PMID: 16272164

3

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: gibbons v. 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

4

GJB1 gene mutations in suspected inflammatory demyelinating neuropathies not responding to treatment.

Michell AW, Laura M, Blake J, Lunn MP, Cox A, Gibbons VS, Davis MB, Wood NW, Manji H, Houlden H, Murray NM, Reilly MM. Michell AW, et al. Among authors: gibbons vs. J Neurol Neurosurg Psychiatry. 2009 Jun;80(6):699-700. doi: 10.1136/jnnp.2008.150557. J Neurol Neurosurg Psychiatry. 2009. PMID: 19448103 No abstract available.

5

Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations.

Polke JM, Laurá M, Pareyson D, Taroni F, Milani M, Bergamin G, Gibbons VS, Houlden H, Chamley SC, Blake J, Devile C, Sandford R, Sweeney MG, Davis MB, Reilly MM. Polke JM, et al. Among authors: gibbons vs. Neurology. 2011 Jul 12;77(2):168-73. doi: 10.1212/WNL.0b013e3182242d4d. Epub 2011 Jun 29. Neurology. 2011. PMID: 21715711 Free PMC article.

6

In vivo impact of presynaptic calcium channel dysfunction on motor axons in episodic ataxia type 2.

Tomlinson SE, Tan SV, Burke D, Labrum RW, Haworth A, Gibbons VS, Sweeney MG, Griggs RC, Kullmann DM, Bostock H, Hanna MG. Tomlinson SE, et al. Among authors: gibbons vs. Brain. 2016 Feb;139(Pt 2):380-91. doi: 10.1093/brain/awv380. Brain. 2016. PMID: 26912519 Free PMC article.

7

MFN2 mutations cause severe phenotypes in most patients with CMT2A.

Feely SM, Laura M, Siskind CE, Sottile S, Davis M, Gibbons VS, Reilly MM, Shy ME. Feely SM, et al. Among authors: gibbons vs. Neurology. 2011 May 17;76(20):1690-6. doi: 10.1212/WNL.0b013e31821a441e. Epub 2011 Apr 20. Neurology. 2011. PMID: 21508331 Free PMC article.

8

Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.

Catarino CB, Liu JY, Liagkouras I, Gibbons VS, Labrum RW, Ellis R, Woodward C, Davis MB, Smith SJ, Cross JH, Appleton RE, Yendle SC, McMahon JM, Bellows ST, Jacques TS, Zuberi SM, Koepp MJ, Martinian L, Scheffer IE, Thom M, Sisodiya SM. Catarino CB, et al. Brain. 2011 Oct;134(Pt 10):2982-3010. doi: 10.1093/brain/awr129. Epub 2011 Jun 29. Brain. 2011. PMID: 21719429 Free PMC article.

9

Localization of interictal spikes using SAM(g2) and dipole fit.

Robinson SE, Nagarajan SS, Mantle M, Gibbons V, Kirsch H. Robinson SE, et al. Among authors: gibbons v. Neurol Clin Neurophysiol. 2004 Nov 30;2004:74. Neurol Clin Neurophysiol. 2004. PMID: 16012648 Free PMC article.

10

Comparison of Hard and Soft Cervical Collars for the Management of Odontoid Peg Fractures in the Elderly.

Coleman N, Chan HH, Gibbons V, Baker JF. Coleman N, et al. Among authors: gibbons v. Geriatr Orthop Surg Rehabil. 2022 Mar 18;13:21514593211070263. doi: 10.1177/21514593211070263. eCollection 2022. Geriatr Orthop Surg Rehabil. 2022. PMID: 35320993 Free PMC article.

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