Aarskog NK - Search Results

1

Totland C, Aarskog NK, Eichler TW, Haugen M, Nøstbakken JK, Monstad SE, Salvesen HB, Mørk S, Haukanes BI, Vedeler CA. Totland C, et al. Among authors: aarskog nk. Cancer Immunol Immunother. 2011 Feb;60(2):283-9. doi: 10.1007/s00262-010-0943-9. Epub 2010 Nov 16. Cancer Immunol Immunother. 2011. PMID: 21080165 Free PMC article.

2

Antibodies against interferon-beta in multiple sclerosis.

Aarskog NK, Marøy T, Myhr KM, Vedeler CA. Aarskog NK, et al. J Neuroimmunol. 2009 Jul 25;212(1-2):148-50. doi: 10.1016/j.jneuroim.2009.04.012. Epub 2009 May 20. J Neuroimmunol. 2009. PMID: 19467718

3

[Molecular genetic diagnosis of Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies].

Aarskog NK, Vedeler CA. Aarskog NK, et al. Tidsskr Nor Laegeforen. 2002 Feb 10;122(4):382-5. Tidsskr Nor Laegeforen. 2002. PMID: 11915667 Free article. Norwegian.

4

Real-time quantitative polymerase chain reaction. A new method that detects both the peripheral myelin protein 22 duplication in Charcot-Marie-Tooth type 1A disease and the peripheral myelin protein 22 deletion in hereditary neuropathy with liability to pressure palsies.

Aarskog NK, Vedeler CA. Aarskog NK, et al. Hum Genet. 2000 Nov;107(5):494-8. doi: 10.1007/s004390000399. Hum Genet. 2000. PMID: 11140948

5

Recombination breakpoints in the Charcot-Marie-Tooth 1A repeat sequence in Norwegian families.

Aarskog NK, Vedeler CA. Aarskog NK, et al. Acta Neurol Scand. 2001 Aug;104(2):97-100. doi: 10.1034/j.1600-0404.2001.104002097.x. Acta Neurol Scand. 2001. PMID: 11493226

6

Molecular genetic analysis of Charcot-Marie-Tooth 1A duplication in Norwegian patients by quantitative photostimulated luminescence imaging.

Aarskog NK, Aadland S, Gjerde IO, Vedeler CA. Aarskog NK, et al. J Neurol Sci. 2001 Jul 15;188(1-2):21-6. doi: 10.1016/s0022-510x(01)00544-5. J Neurol Sci. 2001. PMID: 11489280

7

[Hereditary neuropathy with pressure palsies].

Gjerde IO, Aarskog N, Vedeler C. Gjerde IO, et al. Tidsskr Nor Laegeforen. 2001 Feb 10;121(4):426-8. Tidsskr Nor Laegeforen. 2001. PMID: 11255855 Free article. Norwegian.

8

[Congenital fructose intolerance. New molecular aspects].

Larsen K, Adnanes O, Aarskog NK, Runde I, Ogreid D. Larsen K, et al. Among authors: aarskog nk. Tidsskr Nor Laegeforen. 1994 Nov 20;114(28):3312-4. Tidsskr Nor Laegeforen. 1994. PMID: 7809888 Norwegian.

9

Homologous unequal cross-over involving a 2.8 kb direct repeat as a mechanism for the generation of allelic variants of human cytochrome P450 CYP2D6 gene.

Steen VM, Molven A, Aarskog NK, Gulbrandsen AK. Steen VM, et al. Among authors: aarskog nk. Hum Mol Genet. 1995 Dec;4(12):2251-7. doi: 10.1093/hmg/4.12.2251. Hum Mol Genet. 1995. PMID: 8634695

10

Aldolase B A149P mutation and hereditary fructose intolerance are not associated with sudden infant death syndrome.

Aarskog NK, Ogreid D. Aarskog NK, et al. Acta Paediatr. 1995 Aug;84(8):947-8. doi: 10.1111/j.1651-2227.1995.tb13801.x. Acta Paediatr. 1995. PMID: 7488826 No abstract available.

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