Nilsson S - Search Results

1

PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian families.

Bjursell C, Erlandson A, Nordling M, Nilsson S, Wahlström J, Stibler H, Kristiansson B, Martinsson T. Bjursell C, et al. Among authors: nilsson s. Hum Mutat. 2000 Nov;16(5):395-400. doi: 10.1002/1098-1004(200011)16:5<395::AID-HUMU3>3.0.CO;2-T. Hum Mutat. 2000. PMID: 11058896

2

Incidence of CSF abnormalities in siblings of multiple sclerosis patients and unrelated controls.

Haghighi S, Andersen O, Rosengren L, Bergström T, Wahlström J, Nilsson S. Haghighi S, et al. Among authors: nilsson s. J Neurol. 2000 Aug;247(8):616-22. doi: 10.1007/s004150070130. J Neurol. 2000. PMID: 11041329

3

The CTLA4/CD28 gene region on chromosome 2q33 confers susceptibility to celiac disease in a way possibly distinct from that of type 1 diabetes and other chronic inflammatory disorders.

Naluai AT, Nilsson S, Samuelsson L, Gudjónsdóttir AH, Ascher H, Ek J, Hallberg B, Kristiansson B, Martinsson T, Nerman O, Sollid LM, Wahlström J. Naluai AT, et al. Among authors: nilsson s. Tissue Antigens. 2000 Oct;56(4):350-5. doi: 10.1034/j.1399-0039.2000.560407.x. Tissue Antigens. 2000. PMID: 11098935

4

Stronger association with HLA-Cw6 than with corneodesmosin (S-gene) polymorphisms in Swedish psoriasis patients.

Enerbäck C, Nilsson S, Enlund F, Inerot A, Samuelsson L, Wahlström J, Swanbeck G, Martinsson T. Enerbäck C, et al. Among authors: nilsson s. Arch Dermatol Res. 2000 Nov;292(11):525-30. doi: 10.1007/s004030000175. Arch Dermatol Res. 2000. PMID: 11194889

5

Genome-wide linkage analysis of Scandinavian affected sib-pairs supports presence of susceptibility loci for celiac disease on chromosomes 5 and 11.

Naluai AT, Nilsson S, Gudjónsdóttir AH, Louka AS, Ascher H, Ek J, Hallberg B, Samuelsson L, Kristiansson B, Martinsson T, Nerman O, Sollid LM, Wahlström J. Naluai AT, et al. Among authors: nilsson s. Eur J Hum Genet. 2001 Dec;9(12):938-44. doi: 10.1038/sj.ejhg.5200752. Eur J Hum Genet. 2001. PMID: 11840196

6

The risk of celiac disease in 107 families with at least two affected siblings.

Gudjónsdóttir AH, Nilsson S, Ek J, Kristiansson B, Ascher H. Gudjónsdóttir AH, et al. Among authors: nilsson s. J Pediatr Gastroenterol Nutr. 2004 Mar;38(3):338-42. doi: 10.1097/00005176-200403000-00020. J Pediatr Gastroenterol Nutr. 2004. PMID: 15076637

7

Mutations in the N-terminal domain of DFF45 in a primary germ cell tumor and in neuroblastoma tumors.

Abel F, Sjöberg RM, Krona C, Nilsson S, Martinsson T. Abel F, et al. Among authors: nilsson s. Int J Oncol. 2004 Nov;25(5):1297-302. Int J Oncol. 2004. PMID: 15492818

8

Analysis of 6 genetic loci for disease susceptibility in psoriatic arthritis.

Alenius GM, Friberg C, Nilsson S, Wahlström J, Dahlqvist SR, Samuelsson L. Alenius GM, et al. Among authors: nilsson s. J Rheumatol. 2004 Nov;31(11):2230-5. J Rheumatol. 2004. PMID: 15517637

9

Imbalance of the mitochondrial pro- and anti-apoptotic mediators in neuroblastoma tumours with unfavourable biology.

Abel F, Sjöberg RM, Nilsson S, Kogner P, Martinsson T. Abel F, et al. Among authors: nilsson s. Eur J Cancer. 2005 Mar;41(4):635-46. doi: 10.1016/j.ejca.2004.12.021. Eur J Cancer. 2005. PMID: 15737569

10

Analysis of chromosome 5q31-32 and psoriasis: confirmation of a susceptibility locus but no association with SNPs within SLC22A4 and SLC22A5.

Friberg C, Björck K, Nilsson S, Inerot A, Wahlström J, Samuelsson L. Friberg C, et al. Among authors: nilsson s. J Invest Dermatol. 2006 May;126(5):998-1002. doi: 10.1038/sj.jid.5700194. J Invest Dermatol. 2006. PMID: 16484987 Free article.

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