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

Year Number of Results
2008 1
2009 1
2010 2
2011 1
2012 2
2013 2
2014 1
2016 1
2017 1
2018 1
2020 1
2021 1
2024 0

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12 results

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Page 1
Beyond Typical Ataxia Telangiectasia: How to Identify the Ataxia Telangiectasia-Like Disorders.
Raslan IR, de Assis Pereira Matos PCA, Boaratti Ciarlariello V, Daghastanli KH, Rosa ABR, Arita JH, Aranda CS, Barsottini OGP, Pedroso JL. Raslan IR, et al. Among authors: arita jh. Mov Disord Clin Pract. 2020 Nov 19;8(1):118-125. doi: 10.1002/mdc3.13110. eCollection 2021 Jan. Mov Disord Clin Pract. 2020. PMID: 33426167 Free PMC article. Review.
Mongolian spots are not always a benign sign.
Hackbart BA, Arita JH, Pinho RS, Masruha MR, Vilanova LC. Hackbart BA, et al. Among authors: arita jh. J Pediatr. 2013 May;162(5):1070. doi: 10.1016/j.jpeds.2012.12.044. Epub 2013 Jan 30. J Pediatr. 2013. PMID: 23374678 No abstract available.
ACTH-induced dyskinesia in a child with West syndrome (infantile spasms).
Arita JH, Vale TC, Pedroso JL, Faria EC, Arita FN, Masruha MR, Barsottini OG. Arita JH, et al. Parkinsonism Relat Disord. 2016 Mar;24:145-6. doi: 10.1016/j.parkreldis.2016.01.004. Epub 2016 Jan 9. Parkinsonism Relat Disord. 2016. PMID: 26810914 No abstract available.
LMNB1 mutation causes cerebellar involvement and a genome instability defect.
Pedroso JL, Munford V, Bastos AU, Castro LP, Marussi VHR, Silva GS, Arita JH, Menck CFM, Barsottini OG. Pedroso JL, et al. Among authors: arita jh. J Neurol Sci. 2017 Aug 15;379:249-252. doi: 10.1016/j.jns.2017.06.027. Epub 2017 Jun 16. J Neurol Sci. 2017. PMID: 28716252 No abstract available.
Cystic leukoencephalopathy without megalencephaly.
Faria EC, Arita JH, Peruchi MM, Lin J, Masruha MR, Vilanova LC. Faria EC, et al. Among authors: arita jh. Arq Neuropsiquiatr. 2008 Jun;66(2A):261-3. doi: 10.1590/s0004-282x2008000200027. Arq Neuropsiquiatr. 2008. PMID: 18545798 Free article. No abstract available.
Metabolic studies of a patient harbouring a novel S487L mutation in the catalytic subunit of AMPK.
Arita JH, Barros MH, Ravagnani FG, Ziosi M, Sanches LR, Picosse FR, Lopes TO, de Carvalho Aguiar P, Macabelli CH, Chiaratti MR, Pedroso JL, Quinzii CM, Barsottini OGP, Ferreiro-Barros CC. Arita JH, et al. Biochim Biophys Acta Mol Basis Dis. 2018 May;1864(5 Pt A):1896-1903. doi: 10.1016/j.bbadis.2018.03.011. Epub 2018 Mar 8. Biochim Biophys Acta Mol Basis Dis. 2018. PMID: 29526819 Free article.
Inherited manganism: the "cock-walk" gait and typical neuroimaging features.
Avelino MA, Fusão EF, Pedroso JL, Arita JH, Ribeiro RT, Pinho RS, Tuschl K, Barsottini OG, Masruha MR. Avelino MA, et al. Among authors: arita jh. J Neurol Sci. 2014 Jun 15;341(1-2):150-2. doi: 10.1016/j.jns.2014.03.057. Epub 2014 Apr 4. J Neurol Sci. 2014. PMID: 24746291
Adolescents with chronic migraine commonly exhibit depressive symptoms.
Arita JH, Lin J, Pinho RS, Minett TS, de Souza Vitalle MS, Fisberg M, Peres MF, Vilanova LC, Masruha MR. Arita JH, et al. Acta Neurol Belg. 2013 Mar;113(1):61-5. doi: 10.1007/s13760-012-0135-9. Epub 2012 Oct 2. Acta Neurol Belg. 2013. PMID: 23055110
12 results