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

Year Number of Results
1984 1
1985 1
1989 1
1990 3
1991 1
1993 3
1994 3
1995 3
1996 5
1997 3
1998 3
1999 5
2000 1
2001 1
2002 4
2003 5
2004 4
2005 3
2006 1
2007 3
2008 5
2009 2
2010 3
2011 4
2012 3
2013 4
2015 4
2016 2
2017 1
2018 4
2019 1
2020 4
2021 0
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87 results
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Page 1
Pyridoxine dependent epilepsy and antiquitin deficiency: clinical and molecular characteristics and recommendations for diagnosis, treatment and follow-up.
Stockler S, Plecko B, Gospe SM Jr, Coulter-Mackie M, Connolly M, van Karnebeek C, Mercimek-Mahmutoglu S, Hartmann H, Scharer G, Struijs E, Tein I, Jakobs C, Clayton P, Van Hove JL. Stockler S, et al. Among authors: tein i. Mol Genet Metab. 2011 Sep-Oct;104(1-2):48-60. doi: 10.1016/j.ymgme.2011.05.014. Epub 2011 May 24. Mol Genet Metab. 2011. PMID: 21704546 Review.
Metabolic myopathies.
Tein I. Tein I. Semin Pediatr Neurol. 1996 Jun;3(2):59-98. doi: 10.1016/s1071-9091(96)80038-6. Semin Pediatr Neurol. 1996. PMID: 8795843 Review.
Rationale for dopa-responsive CTNNB1/ß-catenin deficient dystonia.
Pipo-Deveza J, Fehlings D, Chitayat D, Yoon G, Sroka H, Tein I. Pipo-Deveza J, et al. Among authors: tein i. Mov Disord. 2018 Apr;33(4):656-657. doi: 10.1002/mds.27320. Epub 2018 Feb 13. Mov Disord. 2018. PMID: 29436745 No abstract available.
Disorders of fatty acid oxidation.
Tein I. Tein I. Handb Clin Neurol. 2013;113:1675-88. doi: 10.1016/B978-0-444-59565-2.00035-6. Handb Clin Neurol. 2013. PMID: 23622388 Review.
Neonatal metabolic myopathies.
Tein I. Tein I. Semin Perinatol. 1999 Apr;23(2):125-51. doi: 10.1016/s0146-0005(99)80046-9. Semin Perinatol. 1999. PMID: 10331465 Review.
Recurrent childhood myoglobinuria.
Tein I, DiMauro S, DeVivo DC. Tein I, et al. Adv Pediatr. 1990;37:77-117. Adv Pediatr. 1990. PMID: 2264536 Review.
87 results
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