S Nilsson-Ardnor
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Explore the profile of S Nilsson-Ardnor including associated specialties, affiliations and a list of published articles.
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5
Citations
103
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Recent Articles
1.
Janunger T, Nilsson-Ardnor S, Wiklund P, Lindgren P, Escher S, Lackovic K, et al.
Neurology
. 2009 Nov;
73(21):1767-73.
PMID: 19933978
Objectives: The population of northern Sweden is characterized by reduced genetic diversity and a high incidence of stroke. We sought to reduce genetic variation further, using genealogic analysis in a...
2.
Wiklund P, Brown W, Brott T, Stegmayr B, Brown Jr R, Nilsson-Ardnor S, et al.
Neurology
. 2007 Feb;
68(6):427-31.
PMID: 17283317
Objective: To establish whether subtypes of ischemic stroke aggregate within ischemic stroke-affected sibling pairs more than expected by chance alone. Methods: This retrospective family study was based on a pooled...
3.
Goransdotter Ericson K, Fadeel B, Nilsson-Ardnor S, Soderhall C, Samuelsson A, Janka G, et al.
Am J Hum Genet
. 2001 Feb;
68(3):590-7.
PMID: 11179007
Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive disease of early childhood characterized by nonmalignant accumulation and multivisceral infiltration of activated T lymphocytes and histiocytes (macrophages). Cytotoxic T and natural...
4.
Henter J, Samuelsson A, Ericson K, Nilsson-Ardnor S, Elinder G, Fadeel B
Lakartidningen
. 2000 Apr;
97(12):1405-8.
PMID: 10765622
Familial hemophagocytic lymphohistiocytosis (FHL) is an invariably fatal disease typically seen in infancy and early childhood, with a median survival without therapy of two months. It is characterized by prolonged...
5.
Ost A, Nilsson-Ardnor S, Henter J
Histopathology
. 1998 May;
32(4):310-6.
PMID: 9602326
Aims: Primary haemophagocytic lymphohistiocytosis (HLH) is a fatal childhood disorder. The diagnosis is difficult to establish, clinically as well as histopathologically, and it is markedly underdiagnosed. Because of these difficulties,...