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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2008 | 1 |
2009 | 1 |
2010 | 2 |
2011 | 1 |
2024 | 0 |
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5 results
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Page 1
Glut1 deficiency syndrome and erythrocyte glucose uptake assay.
Ann Neurol. 2011 Dec;70(6):996-1005. doi: 10.1002/ana.22640.
Ann Neurol. 2011.
PMID: 22190371
Murine Glut-1 transporter haploinsufficiency: postnatal deceleration of brain weight and reactive astrocytosis.
Ullner PM, Di Nardo A, Goldman JE, Schobel S, Yang H, Engelstad K, Wang D, Sahin M, De Vivo DC.
Ullner PM, et al.
Neurobiol Dis. 2009 Oct;36(1):60-9. doi: 10.1016/j.nbd.2009.06.014. Epub 2009 Jul 8.
Neurobiol Dis. 2009.
PMID: 19591936
Free PMC article.
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The molecular basis of pyruvate carboxylase deficiency: mosaicism correlates with prolonged survival.
Wang D, Yang H, De Braganca KC, Lu J, Yu Shih L, Briones P, Lang T, De Vivo DC.
Wang D, et al.
Mol Genet Metab. 2008 Sep-Oct;95(1-2):31-8. doi: 10.1016/j.ymgme.2008.06.006. Epub 2008 Aug 3.
Mol Genet Metab. 2008.
PMID: 18676167
Free PMC article.
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Glut1 deficiency: inheritance pattern determined by haploinsufficiency.
Rotstein M, Engelstad K, Yang H, Wang D, Levy B, Chung WK, De Vivo DC.
Rotstein M, et al.
Ann Neurol. 2010 Dec;68(6):955-8. doi: 10.1002/ana.22088.
Ann Neurol. 2010.
PMID: 20687207
Free PMC article.
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Uncovering microdeletions in patients with severe Glut-1 deficiency syndrome using SNP oligonucleotide microarray analysis.
Levy B, Wang D, Ullner PM, Engelstad K, Yang H, Nahum O, Chung WK, De Vivo DC.
Levy B, et al.
Mol Genet Metab. 2010 Jun;100(2):129-35. doi: 10.1016/j.ymgme.2010.03.007. Epub 2010 Mar 17.
Mol Genet Metab. 2010.
PMID: 20382060
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