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Lack of aggregation of ischemic stroke subtypes within affected sibling pairs.
Neurology. 2007 Feb 6;68(6):427-31. doi: 10.1212/01.wnl.0000252955.17126.6a.
Neurology. 2007.
PMID: 17283317
A novel stroke locus identified in a northern Sweden pedigree: linkage to chromosome 9q31-33.
Janunger T, Nilsson-Ardnor S, Wiklund PG, Lindgren P, Escher SA, Lackovic K, Nilsson AK, Stegmayr B, Asplund K, Holmberg D.
Janunger T, et al. Among authors: nilsson ardnor s.
Neurology. 2009 Nov 24;73(21):1767-73. doi: 10.1212/WNL.0b013e3181c34b1d.
Neurology. 2009.
PMID: 19933978
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Linkage of ischemic stroke to the PDE4D region on 5q in a Swedish population.
Nilsson-Ardnor S, Wiklund PG, Lindgren P, Nilsson AK, Janunger T, Escher SA, Hallbeck B, Stegmayr B, Asplund K, Holmberg D.
Nilsson-Ardnor S, et al.
Stroke. 2005 Aug;36(8):1666-71. doi: 10.1161/01.STR.0000174188.04716.8d. Epub 2005 Jul 14.
Stroke. 2005.
PMID: 16020760
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Genome-wide linkage scan of common stroke in families from northern Sweden.
Nilsson-Ardnor S, Janunger T, Wiklund PG, Lackovic K, Nilsson AK, Lindgren P, Escher SA, Stegmayr B, Asplund K, Holmberg D.
Nilsson-Ardnor S, et al.
Stroke. 2007 Jan;38(1):34-40. doi: 10.1161/01.STR.0000251643.37454.16. Epub 2006 Nov 22.
Stroke. 2007.
PMID: 17122438
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The CTLA4 region as a general autoimmunity factor: an extended pedigree provides evidence for synergy with the HLA locus in the etiology of type 1 diabetes mellitus, Hashimoto's thyroiditis and Graves' disease.
Einarsdottir E, Söderström I, Löfgren-Burström A, Haraldsson S, Nilsson-Ardnor S, Penha-Goncalves C, Lind L, Holmgren G, Holmberg M, Asplund K, Holmberg D.
Einarsdottir E, et al. Among authors: nilsson ardnor s.
Eur J Hum Genet. 2003 Jan;11(1):81-4. doi: 10.1038/sj.ejhg.5200903.
Eur J Hum Genet. 2003.
PMID: 12529710
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Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis.
Göransdotter Ericson K, Fadeel B, Nilsson-Ardnor S, Söderhäll C, Samuelsson A, Janka G, Schneider M, Gürgey A, Yalman N, Révész T, Egeler R, Jahnukainen K, Storm-Mathiesen I, Haraldsson A, Poole J, de Saint Basile G, Nordenskjöld M, Henter J.
Göransdotter Ericson K, et al. Among authors: nilsson ardnor s.
Am J Hum Genet. 2001 Mar;68(3):590-7. doi: 10.1086/318796. Epub 2001 Feb 6.
Am J Hum Genet. 2001.
PMID: 11179007
Free PMC article.
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[Familial hemophagocytic lymphohistiocytosis: diagnosis, treatment and pathophysiological mechanisms].
Henter JI, Samuelsson A, Ericson K, Nilsson-Ardnor S, Elinder G, Fadeel B.
Henter JI, et al. Among authors: nilsson ardnor s.
Lakartidningen. 2000 Mar 22;97(12):1405-8.
Lakartidningen. 2000.
PMID: 10765622
Review.
Swedish.
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Autopsy findings in 27 children with haemophagocytic lymphohistiocytosis.
Ost A, Nilsson-Ardnor S, Henter JI.
Ost A, et al. Among authors: nilsson ardnor s.
Histopathology. 1998 Apr;32(4):310-6. doi: 10.1046/j.1365-2559.1998.00377.x.
Histopathology. 1998.
PMID: 9602326
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