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

Year Number of Results
1994 2
1997 1
2000 3
2001 3
2002 5
2003 2
2004 2
2005 6
2006 3
2007 3
2008 6
2009 2
2010 4
2011 2
2012 6
2013 6
2014 9
2015 8
2016 2
2017 5
2018 2
2019 7
2020 2
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77 results
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Page 1
MOG Antibodies in Pediatric Neurology.
Huppke P. Huppke P. Neuropediatrics. 2018 Feb;49(1):1-2. doi: 10.1055/s-0037-1606545. Epub 2017 Sep 15. Neuropediatrics. 2018. PMID: 28915516 No abstract available.
Activating de novo mutations in NFE2L2 encoding NRF2 cause a multisystem disorder.
Huppke P, Weissbach S, Church JA, Schnur R, Krusen M, Dreha-Kulaczewski S, Kühn-Velten WN, Wolf A, Huppke B, Millan F, Begtrup A, Almusafri F, Thiele H, Altmüller J, Nürnberg P, Müller M, Gärtner J. Huppke P, et al. Among authors: Huppke B. Nat Commun. 2017 Oct 10;8(1):818. doi: 10.1038/s41467-017-00932-7. Nat Commun. 2017. PMID: 29018201 Free PMC article.
Tectonic gene mutations in patients with Joubert syndrome.
Huppke P, Wegener E, Böhrer-Rabel H, Bolz HJ, Zoll B, Gärtner J, Bergmann C. Huppke P, et al. Eur J Hum Genet. 2015 May;23(5):616-20. doi: 10.1038/ejhg.2014.160. Epub 2014 Aug 13. Eur J Hum Genet. 2015. PMID: 25118024 Free PMC article. Review.
Homozygous NMNAT2 mutation in sisters with polyneuropathy and erythromelalgia.
Huppke P, Wegener E, Gilley J, Angeletti C, Kurth I, Drenth JPH, Stadelmann C, Barrantes-Freer A, Brück W, Thiele H, Nürnberg P, Gärtner J, Orsomando G, Coleman MP. Huppke P, et al. Exp Neurol. 2019 Oct;320:112958. doi: 10.1016/j.expneurol.2019.112958. Epub 2019 May 24. Exp Neurol. 2019. PMID: 31132363
A synaptic protein defect associated with reflex seizure disorder.
Striano P, Huppke P. Striano P, et al. Among authors: Huppke P. Neurology. 2019 Jan 8;92(2):63-64. doi: 10.1212/WNL.0000000000006720. Epub 2018 Dec 12. Neurology. 2019. PMID: 30541867 No abstract available.
Therapy of highly active pediatric multiple sclerosis.
Huppke P, Huppke B, Ellenberger D, Rostasy K, Hummel H, Stark W, Brück W, Gärtner J. Huppke P, et al. Among authors: Huppke B. Mult Scler. 2019 Jan;25(1):72-80. doi: 10.1177/1352458517732843. Epub 2017 Sep 21. Mult Scler. 2019. PMID: 28933245
Apheresis in treatment of acute inflammatory demyelinating disorders.
Mühlhausen J, Kitze B, Huppke P, Müller GA, Koziolek MJ. Mühlhausen J, et al. Among authors: Huppke P. Atheroscler Suppl. 2015 May;18:251-6. doi: 10.1016/j.atherosclerosissup.2015.02.037. Atheroscler Suppl. 2015. PMID: 25936333 Review.
Fatigue and depression predict health-related quality of life in patients with pediatric-onset multiple sclerosis.
Storm Van's Gravesande K, Blaschek A, Calabrese P, Rostásy K, Huppke P, Kessler J J, Kalbe E, Mall V; MUSICADO Study group. Storm Van's Gravesande K, et al. Among authors: Huppke P. Mult Scler Relat Disord. 2019 Nov;36:101368. doi: 10.1016/j.msard.2019.08.010. Epub 2019 Aug 9. Mult Scler Relat Disord. 2019. PMID: 31557681
Age-Dependent Seroprevalence of JCV Antibody in Children.
Hennes EM, Kornek B, Huppke P, Reindl M, Rostasy K, Berger T. Hennes EM, et al. Among authors: Huppke P. Neuropediatrics. 2016 Apr;47(2):112-4. doi: 10.1055/s-0035-1565272. Epub 2015 Oct 19. Neuropediatrics. 2016. PMID: 26479766
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