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

Year Number of Results
2009 2
2010 4
2011 17
2012 7
2013 9
2014 17
2015 14
2016 10
2017 7
2018 3
2020 0
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76 results
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Page 1
Pediatric arterial ischemic stroke: Epidemiology, risk factors, and management.
Felling RJ, Sun LR, Maxwell EC, Goldenberg N, Bernard T. Felling RJ, et al. Blood Cells Mol Dis. 2017 Sep;67:23-33. doi: 10.1016/j.bcmd.2017.03.003. Epub 2017 Mar 7. Blood Cells Mol Dis. 2017. PMID: 28336156 Review.
GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects.
Platzer K, Yuan H, Schütz H, Winschel A, Chen W, Hu C, Kusumoto H, Heyne HO, Helbig KL, Tang S, Willing MC, Tinkle BT, Adams DJ, Depienne C, Keren B, Mignot C, Frengen E, Strømme P, Biskup S, Döcker D, Strom TM, Mefford HC, Myers CT, Muir AM, LaCroix A, Sadleir L, Scheffer IE, Brilstra E, van Haelst MM, van der Smagt JJ, Bok LA, Møller RS, Jensen UB, Millichap JJ, Berg AT, Goldberg EM, De Bie I, Fox S, Major P, Jones JR, Zackai EH, Abou Jamra R, Rolfs A, Leventer RJ, Lawson JA, Roscioli T, Jansen FE, Ranza E, Korff CM, Lehesjoki AE, Courage C, Linnankivi T, Smith DR, Stanley C, Mintz M, McKnight D, Decker A, Tan WH, Tarnopolsky MA, Brady LI, Wolff M, Dondit L, Pedro HF, Parisotto SE, Jones KL, Patel AD, Franz DN, Vanzo R, Marco E, Ranells JD, Di Donato N, Dobyns WB, Laube B, Traynelis SF, Lemke JR. Platzer K, et al. J Med Genet. 2017 Jul;54(7):460-470. doi: 10.1136/jmedgenet-2016-104509. Epub 2017 Apr 4. J Med Genet. 2017. PMID: 28377535 Free PMC article.
KCNQ2 encephalopathy: Features, mutational hot spots, and ezogabine treatment of 11 patients.
Millichap JJ, Park KL, Tsuchida T, Ben-Zeev B, Carmant L, Flamini R, Joshi N, Levisohn PM, Marsh E, Nangia S, Narayanan V, Ortiz-Gonzalez XR, Patterson MC, Pearl PL, Porter B, Ramsey K, McGinnis EL, Taglialatela M, Tracy M, Tran B, Venkatesan C, Weckhuysen S, Cooper EC. Millichap JJ, et al. Neurol Genet. 2016 Aug 22;2(5):e96. doi: 10.1212/NXG.0000000000000096. eCollection 2016 Oct. Neurol Genet. 2016. PMID: 27602407 Free PMC article.
Homozygous boricua TBCK mutation causes neurodegeneration and aberrant autophagy.
Ortiz-González XR, Tintos-Hernández JA, Keller K, Li X, Foley AR, Bharucha-Goebel DX, Kessler SK, Yum SW, Crino PB, He M, Wallace DC, Bönnemann CG. Ortiz-González XR, et al. Ann Neurol. 2018 Jan;83(1):153-165. doi: 10.1002/ana.25130. Ann Neurol. 2018. PMID: 29283439 Free PMC article.
De novo GABRG2 mutations associated with epileptic encephalopathies.
Shen D, Hernandez CC, Shen W, Hu N, Poduri A, Shiedley B, Rotenberg A, Datta AN, Leiz S, Patzer S, Boor R, Ramsey K, Goldberg E, Helbig I, Ortiz-Gonzalez XR, Lemke JR, Marsh ED, Macdonald RL. Shen D, et al. Brain. 2017 Jan;140(1):49-67. doi: 10.1093/brain/aww272. Epub 2016 Nov 17. Brain. 2017. PMID: 27864268 Free PMC article. Clinical Trial.
βIV Spectrinopathies Cause Profound Intellectual Disability, Congenital Hypotonia, and Motor Axonal Neuropathy.
Wang CC, Ortiz-González XR, Yum SW, Gill SM, White A, Kelter E, Seaver LH, Lee S, Wiley G, Gaffney PM, Wierenga KJ, Rasband MN. Wang CC, et al. Am J Hum Genet. 2018 Jun 7;102(6):1158-1168. doi: 10.1016/j.ajhg.2018.04.012. Epub 2018 May 31. Am J Hum Genet. 2018. PMID: 29861105 Free PMC article.
Pediatric cerebral venous sinus thrombosis or compression in the setting of skull fractures from blunt head trauma.
Hersh DS, Shimony N, Groves ML, Tuite GF, Jallo GI, Liu A, Garzon-Muvdi T, Huisman TAGM, Felling RJ, Kufera JA, Ahn ES. Hersh DS, et al. J Neurosurg Pediatr. 2018 Mar;21(3):258-269. doi: 10.3171/2017.9.PEDS17311. Epub 2017 Dec 15. J Neurosurg Pediatr. 2018. PMID: 29243974 Clinical Trial.
GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers.
Li D, Yuan H, Ortiz-Gonzalez XR, Marsh ED, Tian L, McCormick EM, Kosobucki GJ, Chen W, Schulien AJ, Chiavacci R, Tankovic A, Naase C, Brueckner F, von Stülpnagel-Steinbeis C, Hu C, Kusumoto H, Hedrich UB, Elsen G, Hörtnagel K, Aizenman E, Lemke JR, Hakonarson H, Traynelis SF, Falk MJ. Li D, et al. Am J Hum Genet. 2016 Oct 6;99(4):802-816. doi: 10.1016/j.ajhg.2016.07.013. Epub 2016 Sep 8. Am J Hum Genet. 2016. PMID: 27616483 Free PMC article.
The Potential for Advanced Magnetic Resonance Neuroimaging Techniques in Pediatric Stroke Research.
Domi T, Vossough A, Stence NV, Felling RJ, Leung J, Krishnan P, Watson CG, Grant PE, Kassner A. Domi T, et al. Pediatr Neurol. 2017 Apr;69:24-36. doi: 10.1016/j.pediatrneurol.2016.12.015. Epub 2017 Jan 24. Pediatr Neurol. 2017. PMID: 28237248 Review.
Targeting secondary injury in intracerebral haemorrhage--perihaematomal oedema.
Urday S, Kimberly WT, Beslow LA, Vortmeyer AO, Selim MH, Rosand J, Simard JM, Sheth KN. Urday S, et al. Nat Rev Neurol. 2015 Feb;11(2):111-22. doi: 10.1038/nrneurol.2014.264. Epub 2015 Jan 27. Nat Rev Neurol. 2015. PMID: 25623787 Review.
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