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129 results
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Clinical features and genotype of adenine phosphoribosyltransferase deficiency in iceland.
Edvardsson V, Palsson R, Olafsson I, Hjaltadottir G, Laxdal T. Edvardsson V, et al. Among authors: olafsson i. Am J Kidney Dis. 2001 Sep;38(3):473-80. doi: 10.1053/ajkd.2001.26826. Am J Kidney Dis. 2001. PMID: 11532677
Association of BsmI vitamin-D receptor gene polymorphism with combined bone mass in spine and proximal femur in Icelandic women.
Sigurdsson G, Magnusdottir DN, Kristinsson JO, Kristjansson K, Olafsson I. Sigurdsson G, et al. Among authors: olafsson i. J Intern Med. 1997 Jun;241(6):501-5. doi: 10.1111/j.1365-2796.1997.tb00008.x. J Intern Med. 1997. PMID: 10497626
[A mutation detection in a transcription factor for adipocyte development in children with severe obesity.].
Agústsson TT, Hákonarson H, Olafsson I, Hjaltadóttir G, Thornórsson AV. Agústsson TT, et al. Among authors: olafsson i. Laeknabladid. 2001 Feb;87(2):119-24. Laeknabladid. 2001. PMID: 16940676 Icelandic.
[Hereditary hearing impairment. Mutation analysis of connexin 26 and POU3F4 genes in Icelanders with nonsyndromic hearing impairment.].
Olafsson I, Hjaltadóttir G, Cook E, Thornórisson HM, Eiríksdóttir G, Petersen H. Olafsson I, et al. Laeknabladid. 2000 Dec;86(12):833-9. Laeknabladid. 2000. PMID: 17018967 Icelandic.
A population-based study on epidemiology of intensive care unit treated traumatic brain injury in Iceland.
Jonsdottir GM, Lund SH, Snorradottir B, Karason S, Olafsson IH, Reynisson K, Mogensen B, Sigvaldason K. Jonsdottir GM, et al. Among authors: olafsson ih. Acta Anaesthesiol Scand. 2017 Apr;61(4):408-417. doi: 10.1111/aas.12869. Epub 2017 Feb 13. Acta Anaesthesiol Scand. 2017. PMID: 28194757
Serum 25-hydroxyvitamin D levels and bone mineral density in 16-20 years-old girls: lack of association.
Kristinsson JO, Valdimarsson O, Sigurdsson G, Franzson L, Olafsson I, Steingrimsdottir L. Kristinsson JO, et al. Among authors: olafsson i. J Intern Med. 1998 May;243(5):381-8. doi: 10.1046/j.1365-2796.1998.00302.x. J Intern Med. 1998. PMID: 9651561
[Complete androgen insensitivity in an Icelandic family caused by mutation in the steroid binding region of the androgen receptor.].
Olafsson I, Kristjánsson K, Hjaltadóttir G, Schwartz M, Thornórsson AV. Olafsson I, et al. Laeknabladid. 2000 Mar;86(3):163-6. Laeknabladid. 2000. PMID: 17018919 Icelandic.
[Factor VQ50f) and prothrombin 20210 A mutations in an Icelandic apparently healthy population and patients suffering from venous thrombosis.].
Olafsson I, Hjaltadottir S, Onundarson PT, Thorarinsdottir R, Haraldsdottir V. Olafsson I, et al. Laeknabladid. 1997 Jul;83(7):486-91. Laeknabladid. 1997. PMID: 19679906 Icelandic.
[Distribution of alpha1-antitrypsin phenotypes in Icelanders.].
Olafsson I, Hjaltadottir S. Olafsson I, et al. Laeknabladid. 1996 Apr;82(4):293-6. Laeknabladid. 1996. PMID: 20065412 Icelandic.
Secondary insults following traumatic brain injury enhance complement activation in the human brain and release of the tissue damage marker S100B.
Bellander BM, Olafsson IH, Ghatan PH, Bro Skejo HP, Hansson LO, Wanecek M, Svensson MA. Bellander BM, et al. Acta Neurochir (Wien). 2011 Jan;153(1):90-100. doi: 10.1007/s00701-010-0737-z. Epub 2010 Aug 6. Acta Neurochir (Wien). 2011. PMID: 20686797 Free PMC article.
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