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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1996 1
1999 2
2000 3
2001 1
2002 1
2003 3
2004 1
2005 2
2008 3
2009 1
2010 2
2011 2
2012 3
2014 4
2015 1
2017 3
2018 3
2019 1
2020 2
2021 4
2023 2
2024 0

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43 results

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Page 1
Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group.
Klepper J, Akman C, Armeno M, Auvin S, Cervenka M, Cross HJ, De Giorgis V, Della Marina A, Engelstad K, Heussinger N, Kossoff EH, Leen WG, Leiendecker B, Monani UR, Oguni H, Neal E, Pascual JM, Pearson TS, Pons R, Scheffer IE, Veggiotti P, Willemsen M, Zuberi SM, De Vivo DC. Klepper J, et al. Among authors: monani ur. Epilepsia Open. 2020 Aug 13;5(3):354-365. doi: 10.1002/epi4.12414. eCollection 2020 Sep. Epilepsia Open. 2020. PMID: 32913944 Free PMC article.
Therapeutic strategies for glucose transporter 1 deficiency syndrome.
Tang M, Park SH, De Vivo DC, Monani UR. Tang M, et al. Among authors: monani ur. Ann Clin Transl Neurol. 2019 Sep;6(9):1923-1932. doi: 10.1002/acn3.50881. Epub 2019 Aug 28. Ann Clin Transl Neurol. 2019. PMID: 31464092 Free PMC article. Review.
Spinal muscular atrophy: journeying from bench to bedside.
Awano T, Kim JK, Monani UR. Awano T, et al. Among authors: monani ur. Neurotherapeutics. 2014 Oct;11(4):786-95. doi: 10.1007/s13311-014-0293-y. Neurotherapeutics. 2014. PMID: 24990202 Free PMC article. Review.
Animal models of spinal muscular atrophy.
Monani UR, Coovert DD, Burghes AH. Monani UR, et al. Hum Mol Genet. 2000 Oct;9(16):2451-7. doi: 10.1093/hmg/9.16.2451. Hum Mol Genet. 2000. PMID: 11005801 Review.
43 results