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Page 1
Clinical profiles associated with LRRK2 and GBA mutations in Brazilians with Parkinson's disease.
da Silva CP, de M Abreu G, Cabello Acero PH, Campos M Júnior, Pereira JS, de A Ramos SR, Nascimento CM, Voigt DD, Rosso AL, Araujo Leite MA, Vasconcellos LFR, Nicaretta DH, Della Coletta MV, da Silva DJ, Gonçalves AP, Dos Santos JM, Calassara V, Valença DCT, de M Martins CJ, Santos-Rebouças CB, Pimentel MMG. da Silva CP, et al. Among authors: rosso al. J Neurol Sci. 2017 Oct 15;381:160-164. doi: 10.1016/j.jns.2017.08.3249. Epub 2017 Aug 24. J Neurol Sci. 2017. PMID: 28991672
Parkinson disease: α-synuclein mutational screening and new clinical insight into the p.E46K mutation.
Pimentel MM, Rodrigues FC, Leite MA, Campos Júnior M, Rosso AL, Nicaretta DH, Pereira JS, Silva DJ, Della Coletta MV, Vasconcellos LF, Abreu GM, Dos Santos JM, Santos-Rebouças CB. Pimentel MM, et al. Among authors: rosso al. Parkinsonism Relat Disord. 2015 Jun;21(6):586-9. doi: 10.1016/j.parkreldis.2015.03.011. Epub 2015 Mar 14. Parkinsonism Relat Disord. 2015. PMID: 25817515
Autosomal dominant Parkinson's disease: Incidence of mutations in LRRK2, SNCA, VPS35 and GBA genes in Brazil.
Abreu GM, Valença DC, Campos M Júnior, da Silva CP, Pereira JS, Araujo Leite MA, Rosso AL, Nicaretta DH, Vasconcellos LF, da Silva DJ, Della Coletta MV, Dos Santos JM, Gonçalves AP, Santos-Rebouças CB, Pimentel MM. Abreu GM, et al. Among authors: rosso al. Neurosci Lett. 2016 Dec 2;635:67-70. doi: 10.1016/j.neulet.2016.10.040. Epub 2016 Oct 21. Neurosci Lett. 2016. PMID: 27777137
CHCHD2 mutational screening in Brazilian patients with familial Parkinson's disease.
Voigt DD, Nascimento CM, de Souza RB, Cabello Acero PH, Campos Júnior M, da Silva CP, Pereira JS, Rosso AL, Araujo Leite MA, Vasconcellos LFR, Della Coletta MV, da Silva DJ, Nicaretta DH, Gonçalves AP, Dos Santos JM, Calassara V, Santos-Rebouças CB, Pimentel MMG. Voigt DD, et al. Among authors: rosso al. Neurobiol Aging. 2019 Feb;74:236.e7-236.e8. doi: 10.1016/j.neurobiolaging.2018.09.026. Epub 2018 Sep 27. Neurobiol Aging. 2019. PMID: 30342766
Dysphagia and sialorrhea: the relationship to Parkinson's disease.
Nicaretta DH, Rosso AL, Mattos JP, Maliska C, Costa MM. Nicaretta DH, et al. Among authors: rosso al. Arq Gastroenterol. 2013 Jan-Mar;50(1):42-9. doi: 10.1590/s0004-28032013000100009. Arq Gastroenterol. 2013. PMID: 23657306 Free article.
Guidelines for Parkinson's disease treatment: consensus from the Movement Disorders Scientific Department of the Brazilian Academy of Neurology - motor symptoms.
Saba RA, Maia DP, Cardoso FEC, Borges V, F Andrade LA, Ferraz HB, Barbosa ER, Rieder CRM, da Silva DJ, Chien HF, Capato T, Rosso AL, Souza Lima CF, Bezerra JMF, Nicaretta D, Povoas Barsottini OG, Godeiro-Júnior C, Broseghini Barcelos L, Cury RG, Spitz M, Azevedo Silva SMC, Della Colletta MV. Saba RA, et al. Among authors: rosso al. Arq Neuropsiquiatr. 2022 Mar;80(3):316-329. doi: 10.1590/0004-282X-ANP-2021-0219. Arq Neuropsiquiatr. 2022. PMID: 35319667 Free PMC article.
Paroxysmal dystonia and neuromyelitis optica.
Schmidt FR, Costa FH, Silva FM, Maultasch H, Rosso AL, Nicaretta DH, Mattos JP, Novis SA, Alves-Leon SV. Schmidt FR, et al. Among authors: rosso al. Arq Neuropsiquiatr. 2012 Apr;70(4):271-2. doi: 10.1590/s0004-282x2012005000011. Epub 2012 Feb 24. Arq Neuropsiquiatr. 2012. PMID: 22358312 Free article.
Dystonia induced by peripheral trauma: organic or psychogenic?
Nicaretta DH, Rosso AL, Mattos JP, Brandão L, Pimentel ML, Novis SA. Nicaretta DH, et al. Among authors: rosso al. Arq Neuropsiquiatr. 2011 Jun;69(3):565-6. doi: 10.1590/s0004-282x2011000400030. Arq Neuropsiquiatr. 2011. PMID: 21755143 Free article. No abstract available.
Cortical myoclonus masquerading as spinal myoclonus.
Rosso AL, de Mattos JP, Nicaretta DH, Cruz MW, Filho IF, Novis S. Rosso AL, et al. Mov Disord. 2008 Nov 15;23(15):2263-4. doi: 10.1002/mds.22165. Mov Disord. 2008. PMID: 18942089 No abstract available.
155 results