Myhr KM - Search Results

1

Lack of association with the CD28/CTLA4/ICOS gene region among Norwegian multiple sclerosis patients.

Lorentzen AR, Celius EG, Ekstrøm PO, Wiencke K, Lie BA, Myhr KM, Ling V, Thorsby E, Vartdal F, Spurkland A, Harbo HF. Lorentzen AR, et al. Among authors: myhr km. J Neuroimmunol. 2005 Sep;166(1-2):197-201. doi: 10.1016/j.jneuroim.2005.06.002. J Neuroimmunol. 2005. PMID: 16005527

2

Interferon-alpha2a reduces MRI disease activity in relapsing-remitting multiple sclerosis. Norwegian Study Group on Interferon-alpha in Multiple Sclerosis.

Myhr KM, Riise T, Green Lilleås FE, Beiske TG, Celius EG, Edland A, Jensen D, Larsen JP, Nilsen R, Nortvedt MW, Smievoll AI, Vedeler C, Nyland HI. Myhr KM, et al. Neurology. 1999 Mar 23;52(5):1049-56. doi: 10.1212/wnl.52.5.1049. Neurology. 1999. PMID: 10102427 Clinical Trial.

3

IgG allotypes and subclasses in Norwegian patients with multiple sclerosis.

Raknes G, Fernandes Filho JA, Pandey JP, Myhr KM, Ulvestad E, Nyland H, Vedeler CA. Raknes G, et al. Among authors: myhr km. J Neurol Sci. 2000 Apr 15;175(2):111-5. doi: 10.1016/s0022-510x(00)00292-6. J Neurol Sci. 2000. PMID: 10831771

4

Fc receptors for immunoglobulin G--a role in the pathogenesis of Guillain-Barré syndrome and multiple sclerosis.

Vedeler CA, Myhr KM, Nyland H. Vedeler CA, et al. Among authors: myhr km. J Neuroimmunol. 2001 Aug 30;118(2):187-93. doi: 10.1016/s0165-5728(01)00344-7. J Neuroimmunol. 2001. PMID: 11498253 Review.

5

No linkage or association of the nitric oxide synthase genes to multiple sclerosis.

Modin H, Dai Y, Masterman T, Svejgaard A, Sørensen PS, Oturai A, Ryder LP, Spurkland A, Vartdal F, Laaksonen M, Sandberg-Wollheim M, Myhr KM, Nyland H, Hillert J. Modin H, et al. Among authors: myhr km. J Neuroimmunol. 2001 Sep 3;119(1):95-100. doi: 10.1016/s0165-5728(01)00366-6. J Neuroimmunol. 2001. PMID: 11525805

6

The T cell regulator gene SH2D2A contributes to the genetic susceptibility of multiple sclerosis.

Dai KZ, Harbo HF, Celius EG, Oturai A, Sørensen PS, Ryder LP, Datta P, Svejgaard A, Hillert J, Fredrikson S, Sandberg-Wollheim M, Laaksonen M, Myhr KM, Nyland H, Vartdal F, Spurkland A. Dai KZ, et al. Among authors: myhr km. Genes Immun. 2001 Aug;2(5):263-8. doi: 10.1038/sj.gene.6363774. Genes Immun. 2001. PMID: 11528519

7

Linkage analysis suggests a region of importance for multiple sclerosis in 3p14-13.

Dai Y, Xu C, Holmberg M, Oturai A, Fredrikson S, Sandberg-Wollheim M, Laaksonen M, Spurkland A, Myhr KM, Ryder LP, Sorensen PS, Svejgaard A, Hillert J. Dai Y, et al. Among authors: myhr km. Genes Immun. 2001 Dec;2(8):451-4. doi: 10.1038/sj.gene.6363805. Genes Immun. 2001. PMID: 11781712

8

A genome-wide screen for linkage in Nordic sib-pairs with multiple sclerosis.

Akesson E, Oturai A, Berg J, Fredrikson S, Andersen O, Harbo HF, Laaksonen M, Myhr KM, Nyland HI, Ryder LP, Sandberg-Wollheim M, Sorensen PS, Spurkland A, Svejgaard A, Holmans P, Compston A, Hillert J, Sawcer S. Akesson E, et al. Among authors: myhr km. Genes Immun. 2002 Aug;3(5):279-85. doi: 10.1038/sj.gene.6363866. Genes Immun. 2002. PMID: 12140746

9

[New diagnostic criteria in multiple sclerosis].

Midgard R, Beiske AG, Celius EG, Jensen D, Hovdal H, Mellgren SI, Myhr KM. Midgard R, et al. Among authors: myhr km. Tidsskr Nor Laegeforen. 2003 May 15;123(10):1345-8. Tidsskr Nor Laegeforen. 2003. PMID: 12806674 Review. Norwegian. No abstract available.

10

Two genome-wide linkage disequilibrium screens in Scandinavian multiple sclerosis patients.

Harbo HF, Datta P, Oturai A, Ryder LP, Sawcer S, Setakis E, Akesson E, Celius EG, Modin H, Sandberg-Wollheim M, Myhr KM, Andersen O, Hillert J, Sorensen PS, Svejgaard A, Compston A, Vartdal F, Spurkland A. Harbo HF, et al. Among authors: myhr km. J Neuroimmunol. 2003 Oct;143(1-2):101-6. doi: 10.1016/j.jneuroim.2003.08.021. J Neuroimmunol. 2003. PMID: 14575924

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