Kellar-Wood H - Search Results

1

The British Isles survey of multiple sclerosis in twins.

Mumford CJ, Wood NW, Kellar-Wood H, Thorpe JW, Miller DH, Compston DA. Mumford CJ, et al. Neurology. 1994 Jan;44(1):11-5. doi: 10.1212/wnl.44.1.11. Neurology. 1994. PMID: 8290043

2

The T-cell receptor beta locus and susceptibility to multiple sclerosis.

Wood NW, Sawcer SJ, Kellar-Wood HF, Holmans P, Clayton D, Robertson N, Compston DA. Wood NW, et al. Among authors: kellar wood hf. Neurology. 1995 Oct;45(10):1859-63. doi: 10.1212/wnl.45.10.1859. Neurology. 1995. PMID: 7477982

3

Multiple sclerosis and the HLA-D region: linkage and association studies.

Kellar-Wood HF, Wood NW, Holmans P, Clayton D, Robertson N, Compston DA. Kellar-Wood HF, et al. J Neuroimmunol. 1995 May;58(2):183-90. doi: 10.1016/0165-5728(95)00015-t. J Neuroimmunol. 1995. PMID: 7759607

4

Susceptibility to multiple sclerosis and the immunoglobulin heavy chain variable region.

Wood NW, Sawcer SJ, Kellar-Wood HF, Holmans P, Clayton D, Robertson N, Compston DA. Wood NW, et al. Among authors: kellar wood hf. J Neurol. 1995 Oct;242(10):677-82. doi: 10.1007/BF00866919. J Neurol. 1995. PMID: 8568530

5

Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation.

Harding AE, Sweeney MG, Miller DH, Mumford CJ, Kellar-Wood H, Menard D, McDonald WI, Compston DA. Harding AE, et al. Brain. 1992 Aug;115 ( Pt 4):979-89. doi: 10.1093/brain/115.4.979. Brain. 1992. PMID: 1393514

6

Sequence of the human homologue of a mitochondrially encoded murine transplantation antigen in patients with multiple sclerosis.

Chalmers RM, Robertson N, Kellar-Wood H, Compston DA, Harding AE. Chalmers RM, et al. Among authors: kellar wood h. J Neurol. 1995 May;242(5):332-4. doi: 10.1007/BF00878877. J Neurol. 1995. PMID: 7643143

7

Multiple sclerosis.

Compston A, Kellar-Wood H, Wood N. Compston A, et al. Among authors: kellar wood h. Baillieres Clin Neurol. 1994 Aug;3(2):353-71. Baillieres Clin Neurol. 1994. PMID: 7952852 Review.

8

Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis.

Kellar-Wood H, Robertson N, Govan GG, Compston DA, Harding AE. Kellar-Wood H, et al. Ann Neurol. 1994 Jul;36(1):109-12. doi: 10.1002/ana.410360121. Ann Neurol. 1994. PMID: 8024249

9

No linkage between multiple sclerosis and the T cell receptor alpha chain locus.

Eoli M, Wood NW, Kellar-Wood HF, Holmans P, Clayton D, Compston DA. Eoli M, et al. J Neurol Sci. 1994 Jun;124(1):32-7. doi: 10.1016/0022-510x(94)90007-8. J Neurol Sci. 1994. PMID: 7931419

10

MHC-encoded TAP1 and TAP2 dimorphisms in multiple sclerosis.

Kellar-Wood HF, Powis SH, Gray J, Compston DA. Kellar-Wood HF, et al. Tissue Antigens. 1994 Feb;43(2):129-32. doi: 10.1111/j.1399-0039.1994.tb02313.x. Tissue Antigens. 1994. PMID: 8016841 No abstract available.

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