Lane R - Search Results

1

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. Among authors: lane r. J Med Genet. 1993 Apr;30(4):318. doi: 10.1136/jmg.30.4.318. J Med Genet. 1993. PMID: 8487280 Free PMC article.

2

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: lane r. Biochem Soc Trans. 1994 May;22(2):149S. doi: 10.1042/bst022149s. Biochem Soc Trans. 1994. PMID: 7958219 No abstract available.

3

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: lane rj. 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.

4

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: lane rj. 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.

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: lane rj. Ann Neurol. 1996 Jun;39(6):810-2. doi: 10.1002/ana.410390620. Ann Neurol. 1996. PMID: 8651656

6

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

7

The relationship of spinal muscular atrophy to motor neuron disease: investigation of SMN and NAIP gene deletions in sporadic and familial ALS.

Orrell RW, Habgood JJ, de Belleroche JS, Lane RJ. Orrell RW, et al. Among authors: lane rj. J Neurol Sci. 1997 Jan;145(1):55-61. doi: 10.1016/s0022-510x(96)00240-7. J Neurol Sci. 1997. PMID: 9073029

8

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. Among authors: lane rj. 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

9

Abnormal glycine metabolism in motor neurone disease: studies on plasma and cerebrospinal fluid.

Lane RJ, Bandopadhyay R, de Belleroche J. Lane RJ, et al. J R Soc Med. 1993 Sep;86(9):501-5. J R Soc Med. 1993. PMID: 8410884 Free PMC article.

10

Oculomotor function in amyotrophic lateral sclerosis: evidence for frontal impairment.

Shaunak S, Orrell RW, O'Sullivan E, Hawken MB, Lane RJ, Henderson L, Kennard C. Shaunak S, et al. Among authors: lane rj. Ann Neurol. 1995 Jul;38(1):38-44. doi: 10.1002/ana.410380109. Ann Neurol. 1995. PMID: 7611722

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