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

Year Number of Results
1996 2
1997 2
1998 1
2000 2
2001 5
2002 4
2003 3
2004 4
2005 3
2006 4
2007 7
2008 3
2009 4
2010 7
2011 4
2012 5
2013 8
2014 4
2015 7
2016 3
2017 6
2018 3
2019 2
2020 9
2021 8
2022 1
2024 0

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Similar articles for PMID: 12044443

98 results

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Page 1
[Creatine deficiency syndromes].
Cheillan D, Cognat S, Vandenberghe N, Des Portes V, Vianey-Saban C. Cheillan D, et al. Rev Neurol (Paris). 2005 Mar;161(3):284-9. doi: 10.1016/s0035-3787(05)85034-9. Rev Neurol (Paris). 2005. PMID: 15800449 Review. French.
Creatine deficiency syndromes.
Schulze A. Schulze A. Mol Cell Biochem. 2003 Feb;244(1-2):143-50. Mol Cell Biochem. 2003. PMID: 12701824 Review.
Inborn errors of creatine metabolism and epilepsy.
Leuzzi V, Mastrangelo M, Battini R, Cioni G. Leuzzi V, et al. Epilepsia. 2013 Feb;54(2):217-27. doi: 10.1111/epi.12020. Epub 2012 Nov 13. Epilepsia. 2013. PMID: 23157605 Free article. Review.
Disorders of creatine transport and metabolism.
Longo N, Ardon O, Vanzo R, Schwartz E, Pasquali M. Longo N, et al. Am J Med Genet C Semin Med Genet. 2011 Feb 15;157C(1):72-8. doi: 10.1002/ajmg.c.30292. Epub 2011 Feb 9. Am J Med Genet C Semin Med Genet. 2011. PMID: 21308988
Creatine biosynthesis and transport in health and disease.
Joncquel-Chevalier Curt M, Voicu PM, Fontaine M, Dessein AF, Porchet N, Mention-Mulliez K, Dobbelaere D, Soto-Ares G, Cheillan D, Vamecq J. Joncquel-Chevalier Curt M, et al. Biochimie. 2015 Dec;119:146-65. doi: 10.1016/j.biochi.2015.10.022. Epub 2015 Nov 2. Biochimie. 2015. PMID: 26542286 Review.
98 results