King A - Search Results

1

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.

Nicolas A, Kenna KP, Renton AE, Ticozzi N, Faghri F, Chia R, Dominov JA, Kenna BJ, Nalls MA, Keagle P, Rivera AM, van Rheenen W, Murphy NA, van Vugt JJFA, Geiger JT, Van der Spek RA, Pliner HA, Shankaracharya, Smith BN, Marangi G, Topp SD, Abramzon Y, Gkazi AS, Eicher JD, Kenna A; ITALSGEN Consortium; Mora G, Calvo A, Mazzini L, Riva N, Mandrioli J, Caponnetto C, Battistini S, Volanti P, La Bella V, Conforti FL, Borghero G, Messina S, Simone IL, Trojsi F, Salvi F, Logullo FO, D'Alfonso S, Corrado L, Capasso M, Ferrucci L; Genomic Translation for ALS Care (GTAC) Consortium; Moreno CAM, Kamalakaran S, Goldstein DB; ALS Sequencing Consortium; Gitler AD, Harris T, Myers RM; NYGC ALS Consortium; Phatnani H, Musunuri RL, Evani US, Abhyankar A, Zody MC; Answer ALS Foundation; Kaye J, Finkbeiner S, Wyman SK, LeNail A, Lima L, Fraenkel E, Svendsen CN, Thompson LM, Van Eyk JE, Berry JD, Miller TM, Kolb SJ, Cudkowicz M, Baxi E; Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium; Benatar M, Taylor JP, Rampersaud E, Wu G, Wuu J; SLAGEN Consortium; Lauria G, Verde F, Fogh I, Tiloca C, Comi GP, Sorarù G, Cereda C; French ALS Consortium; Corcia P, Laaks… See abstract for full author list ➔ Nicolas A, et al. Among authors: king a. Neuron. 2018 Mar 21;97(6):1267-1288. doi: 10.1016/j.neuron.2018.02.027. Neuron. 2018. PMID: 29566793 Free PMC article.

2

Familial amyotrophic lateral sclerosis with a point mutation of SOD-1: intrafamilial heterogeneity of disease duration associated with neurofibrillary tangles.

Orrell RW, King AW, Hilton DA, Campbell MJ, Lane RJ, de Belleroche JS. Orrell RW, et al. Among authors: king aw. J Neurol Neurosurg Psychiatry. 1995 Sep;59(3):266-70. doi: 10.1136/jnnp.59.3.266. J Neurol Neurosurg Psychiatry. 1995. PMID: 7673954 Free PMC article.

3

Parental influence on inheritance of familial amyotrophic lateral sclerosis.

Orrell RW, King AW, deBelleroche JS. Orrell RW, et al. Among authors: king aw. Lancet. 1995 Feb 11;345(8946):391-2. doi: 10.1016/s0140-6736(95)90381-x. Lancet. 1995. PMID: 7845144 No abstract available.

4

More than one locus for familial amyotrophic lateral sclerosis: absence of linkage to the SMA locus.

King AW, Orrell RW, Lane R, de Belleroche JS. King AW, et al. Biochem Soc Trans. 1994 May;22(2):149S. doi: 10.1042/bst022149s. Biochem Soc Trans. 1994. PMID: 7958219 No abstract available.

5

Absence of linkage between chromosome 21 loci and familial amyotrophic lateral sclerosis.

King A, Houlden H, Hardy J, Lane R, Chancellor A, de Belleroche J. King A, et al. J Med Genet. 1993 Apr;30(4):318. doi: 10.1136/jmg.30.4.318. J Med Genet. 1993. PMID: 8487280 Free PMC article.

6

Investigation of a null mutation of the CNTF gene in familial amyotrophic lateral sclerosis.

Orrell RW, King AW, Lane RJ, de Belleroche JS. Orrell RW, et al. Among authors: king aw. J Neurol Sci. 1995 Oct;132(2):126-8. doi: 10.1016/0022-510x(95)00129-p. J Neurol Sci. 1995. PMID: 8543936 Clinical Trial.

7

Familial amyotrophic lateral sclerosis/motor neurone disease (FALS): a review of current developments.

de Belleroche J, Orrell R, King A. de Belleroche J, et al. Among authors: king a. J Med Genet. 1995 Nov;32(11):841-7. doi: 10.1136/jmg.32.11.841. J Med Genet. 1995. PMID: 8592323 Free PMC article. Review. No abstract available.

8

Clinical and functional investigation of 10 missense mutations and a novel frameshift insertion mutation of the gene for copper-zinc superoxide dismutase in UK families with amyotrophic lateral sclerosis.

Orrell RW, Habgood JJ, Gardiner I, King AW, Bowe FA, Hallewell RA, Marklund SL, Greenwood J, Lane RJ, deBelleroche J. Orrell RW, et al. Among authors: king aw. Neurology. 1997 Mar;48(3):746-51. doi: 10.1212/wnl.48.3.746. Neurology. 1997. PMID: 9065559

9

A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series.

Beck J, Rohrer JD, Campbell T, Isaacs A, Morrison KE, Goodall EF, Warrington EK, Stevens J, Revesz T, Holton J, Al-Sarraj S, King A, Scahill R, Warren JD, Fox NC, Rossor MN, Collinge J, Mead S. Beck J, et al. Among authors: king a. Brain. 2008 Mar;131(Pt 3):706-20. doi: 10.1093/brain/awm320. Epub 2008 Jan 29. Brain. 2008. PMID: 18234697 Free PMC article.

10

Frontotemporal lobar degeneration with ubiquitinated tau-negative inclusions and additional alpha-synuclein pathology but also unusual cerebellar ubiquitinated p62-positive, TDP-43-negative inclusions.

King A, Al-Sarraj S, Shaw C. King A, et al. Neuropathology. 2009 Aug;29(4):466-71. doi: 10.1111/j.1440-1789.2008.00966.x. Epub 2008 Aug 18. Neuropathology. 2009. PMID: 18715271

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