de Belleroche J - Search Results

1

Copper, zinc superoxide dismutase (SOD1) and its role in neuronal function and disease with particular relevance to motor neurone disease/amyotrophic lateral sclerosis.

de Belleroche J, Orrell RW, Virgo L, Habgood J, Gardiner IM, Malaspina A, Kaushik N, Mitchell J, Greenwood J. de Belleroche J, et al. Biochem Soc Trans. 1998 Aug;26(3):476-80. doi: 10.1042/bst0260476. Biochem Soc Trans. 1998. PMID: 9765899 Review. No abstract available.

2

A new familial amyotrophic lateral sclerosis locus on chromosome 16q12.1-16q12.2.

Abalkhail H, Mitchell J, Habgood J, Orrell R, de Belleroche J. Abalkhail H, et al. Among authors: de belleroche j. Am J Hum Genet. 2003 Aug;73(2):383-9. doi: 10.1086/377156. Epub 2003 Jun 26. Am J Hum Genet. 2003. PMID: 12830400 Free PMC article.

3

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. Among authors: de belleroche js. Biochem Soc Trans. 1994 May;22(2):149S. doi: 10.1042/bst022149s. Biochem Soc Trans. 1994. PMID: 7958219 No abstract available.

4

Superoxide dismutase and ALS.

Orrell RW, deBelleroche JS. Orrell RW, et al. Lancet. 1994 Dec 17;344(8938):1651-2. doi: 10.1016/s0140-6736(94)90452-9. Lancet. 1994. PMID: 7996955 No abstract available.

5

Difficulties in distinguishing sporadic from familial amyotrophic lateral sclerosis.

Orrell RW, Habgood J, Rudge P, Lane RJ, de Belleroche JS. Orrell RW, et al. Among authors: de belleroche js. Ann Neurol. 1996 Jun;39(6):810-2. doi: 10.1002/ana.410390620. Ann Neurol. 1996. PMID: 8651656

6

Familial ALS is associated with mutations in all exons of SOD1: a novel mutation in exon 3 (Gly72Ser).

Orrell RW, Marklund SL, deBelleroche JS. Orrell RW, et al. J Neurol Sci. 1997 Dec 9;153(1):46-9. doi: 10.1016/s0022-510x(97)00181-0. J Neurol Sci. 1997. PMID: 9455977

7

Clinical characteristics of SOD1 gene mutations in UK families with ALS.

Orrell RW, Habgood JJ, Malaspina A, Mitchell J, Greenwood J, Lane RJ, deBelleroche JS. Orrell RW, et al. J Neurol Sci. 1999 Oct 31;169(1-2):56-60. doi: 10.1016/s0022-510x(99)00216-6. J Neurol Sci. 1999. PMID: 10540008

8

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. 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.

9

Amyotrophic lateral sclerosis: recent advances in understanding disease mechanisms.

de Belleroche J, Orrell RW, Virgo L. de Belleroche J, et al. J Neuropathol Exp Neurol. 1996 Jul;55(7):747-57. J Neuropathol Exp Neurol. 1996. PMID: 8965091 Review. No abstract available.

10

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. Neurology. 1997 Mar;48(3):746-51. doi: 10.1212/wnl.48.3.746. Neurology. 1997. PMID: 9065559

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