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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2011 | 1 |
2012 | 1 |
2013 | 1 |
2018 | 1 |
2021 | 2 |
2022 | 1 |
2023 | 1 |
2024 | 0 |
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Page 1
Abnormal gait and hypoglycorrhachia in a toddler with seizures.
Pediatr Investig. 2022 Feb 21;6(1):47-49. doi: 10.1002/ped4.12311. eCollection 2022 Mar.
Pediatr Investig. 2022.
PMID: 35382425
Free PMC article.
Miller Fisher Syndrome Triggered by Infections: A Review of the Literature and a Case Report.
Spyromitrou-Xioufi P, Ntoulios G, Ladomenou F, Niotakis G, Tritou I, Vlachaki G.
Spyromitrou-Xioufi P, et al. Among authors: niotakis g.
J Child Neurol. 2021 Aug;36(9):785-794. doi: 10.1177/0883073820988428.
J Child Neurol. 2021.
PMID: 34448412
Review.
Item in Clipboard
CSF diversion in refractory idiopathic intracranial hypertension: single-centre experience and review of efficacy.
Niotakis G, Grigoratos D, Chandler C, Morrison D, Lim M.
Niotakis G, et al.
Childs Nerv Syst. 2013 Feb;29(2):263-7. doi: 10.1007/s00381-012-1895-5. Epub 2012 Aug 24.
Childs Nerv Syst. 2013.
PMID: 22918619
Review.
Item in Clipboard
Miller Fisher Syndrome Triggered by Infections: A Review of the Literature and a Case Report.
Spyromitrou-Xioufi P, Ntoulios G, Ladomenou F, Niotakis G, Tritou I, Vlachaki G.
Spyromitrou-Xioufi P, et al. Among authors: niotakis g.
J Child Neurol. 2021 Feb 11:883073821988428. doi: 10.1177/0883073821988428. Online ahead of print.
J Child Neurol. 2021.
PMID: 33570020
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Clinical and Functional Characterization of the Recurrent TUBA1A p.(Arg2His) Mutation.
Gardner JF, Cushion TD, Niotakis G, Olson HE, Grant PE, Scott RH, Stoodley N, Cohen JS, Naidu S, Attie-Bitach T, Bonnières M, Boutaud L, Encha-Razavi F, Palmer-Smith SM, Mugalaasi H, Mullins JGL, Pilz DT, Fry AE.
Gardner JF, et al. Among authors: niotakis g.
Brain Sci. 2018 Aug 7;8(8):145. doi: 10.3390/brainsci8080145.
Brain Sci. 2018.
PMID: 30087272
Free PMC article.
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Combined exome analysis and exome depth assessment achieve a high diagnostic yield in an epilepsy case series, revealing significant genomic heterogeneity and novel mechanisms.
Veltra D, Tilemis FN, Marinakis NM, Svingou M, Mitrakos A, Kosma K, Tsoutsou I, Makrythanasis P, Theodorou V, Katsalouli M, Vorgia P, Niotakis G, Vartzelis G, Dinopoulos A, Evangeliou A, Mouskou S, Korona A, Mastroyianni S, Papavasiliou A, Tzetis M, Pons R, Traeger-Synodinos J, Sofocleous C.
Veltra D, et al. Among authors: niotakis g.
Expert Rev Mol Diagn. 2023 Jan;23(1):85-103. doi: 10.1080/14737159.2023.2173578. Epub 2023 Feb 14.
Expert Rev Mol Diagn. 2023.
PMID: 36714946
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Acute life threatening cerebellitis presenting with no apparent cerebellar signs.
Hacohen Y, Niotakis G, Aujla A, Siddiqui A, McCormick D, Bassi S, Clarke A, Lim M.
Hacohen Y, et al. Among authors: niotakis g.
Clin Neurol Neurosurg. 2011 Dec;113(10):928-30. doi: 10.1016/j.clineuro.2011.06.014. Epub 2011 Jul 27.
Clin Neurol Neurosurg. 2011.
PMID: 21798661
No abstract available.
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