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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2005 | 2 |
2006 | 1 |
2007 | 1 |
2010 | 1 |
2024 | 0 |
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4 results
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Page 1
Lack of an association between candidate gene loci and idiopathic generalized epilepsy in Kuwaiti Arab children.
J Biomed Sci. 2005 Oct;12(5):815-8. doi: 10.1007/s11373-005-9009-y. Epub 2005 Nov 9.
J Biomed Sci. 2005.
PMID: 16205844
Hemojuvelin (HJV)-associated hemochromatosis: analysis of HJV and HFE mutations and iron overload in three families.
Wallace DF, Dixon JL, Ramm GA, Anderson GJ, Powell LW, Subramaniam N.
Wallace DF, et al.
Haematologica. 2005 Feb;90(2):254-5.
Haematologica. 2005.
PMID: 15710580
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Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations.
Scheffer IE, Harkin LA, Grinton BE, Dibbens LM, Turner SJ, Zielinski MA, Xu R, Jackson G, Adams J, Connellan M, Petrou S, Wellard RM, Briellmann RS, Wallace RH, Mulley JC, Berkovic SF.
Scheffer IE, et al.
Brain. 2007 Jan;130(Pt 1):100-9. doi: 10.1093/brain/awl272. Epub 2006 Oct 4.
Brain. 2007.
PMID: 17020904
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Augmented currents of an HCN2 variant in patients with febrile seizure syndromes.
Dibbens LM, Reid CA, Hodgson B, Thomas EA, Phillips AM, Gazina E, Cromer BA, Clarke AL, Baram TZ, Scheffer IE, Berkovic SF, Petrou S.
Dibbens LM, et al.
Ann Neurol. 2010 Apr;67(4):542-6. doi: 10.1002/ana.21909.
Ann Neurol. 2010.
PMID: 20437590
Free PMC article.
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