Camargos S - Search Results

1

DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA.

Camargos S, Scholz S, Simón-Sánchez J, Paisán-Ruiz C, Lewis P, Hernandez D, Ding J, Gibbs JR, Cookson MR, Bras J, Guerreiro R, Oliveira CR, Lees A, Hardy J, Cardoso F, Singleton AB. Camargos S, et al. Lancet Neurol. 2008 Mar;7(3):207-15. doi: 10.1016/S1474-4422(08)70022-X. Epub 2008 Feb 1. Lancet Neurol. 2008. PMID: 18243799

2

Juvenile parkinsonism: a heterogeneous entity.

Cardoso F, Camargos S. Cardoso F, et al. Among authors: camargos s. Eur J Neurol. 2000 Sep;7(5):467-71. doi: 10.1046/j.1468-1331.2000.t01-1-00100.x. Eur J Neurol. 2000. PMID: 11054129

3

Parkinsonism associated with basal ganglia cryptococcal abscesses in an immunocompetent patient.

Camargos ST, Teixeira AL Jr, Cardoso F. Camargos ST, et al. Mov Disord. 2006 May;21(5):714-5. doi: 10.1002/mds.20789. Mov Disord. 2006. PMID: 16437588

4

A Brazilian family with Brown-Vialetto-van Laere syndrome with autosomal recessive inheritance.

Malheiros JA, Camargos ST, Oliveira JT, Cardoso FE. Malheiros JA, et al. Arq Neuropsiquiatr. 2007 Mar;65(1):32-5. doi: 10.1590/s0004-282x2007000100008. Arq Neuropsiquiatr. 2007. PMID: 17420823 Free article. Review.

5

Novel GCH1 mutation in a Brazilian family with dopa-responsive dystonia.

Camargos ST, Cardoso F, Momeni P, Gianetti JG, Lees A, Hardy J, Singleton A. Camargos ST, et al. Mov Disord. 2008 Jan 30;23(2):299-302. doi: 10.1002/mds.21842. Mov Disord. 2008. PMID: 18044725

6

Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations.

Camargos ST, Dornas LO, Momeni P, Lees A, Hardy J, Singleton A, Cardoso F. Camargos ST, et al. Mov Disord. 2009 Apr 15;24(5):662-6. doi: 10.1002/mds.22365. Mov Disord. 2009. PMID: 19205068 Free PMC article.

7

Ziprasidone-related oculogyric crisis in an adult.

Viana Bde M, Prais HA, Camargos ST, Cardoso FE. Viana Bde M, et al. Clin Neurol Neurosurg. 2009 Dec;111(10):883-5. doi: 10.1016/j.clineuro.2009.07.015. Epub 2009 Aug 29. Clin Neurol Neurosurg. 2009. PMID: 19717224

8

Low prevalence of PANK2 mutations in Brazilian patients with early onset generalised dystonia and basal ganglia abnormalities on MRI.

Camargos ST, Gurgel-Giannetti J, Lees A, Hardy J, Singleton A, Cardoso F. Camargos ST, et al. J Neurol Neurosurg Psychiatry. 2011 Sep;82(9):1059-60. doi: 10.1136/jnnp.2009.200808. Epub 2010 Jun 15. J Neurol Neurosurg Psychiatry. 2011. PMID: 20551478 Free PMC article. No abstract available.

9

POLG1 Arg953Cys mutation: expanded phenotype and recessive inheritance in a Brazilian family.

Gurgel-Giannetti J, Camargos ST, Cardoso F, Hirano M, DiMauro S. Gurgel-Giannetti J, et al. Among authors: camargos st. Muscle Nerve. 2012 Mar;45(3):453-4. doi: 10.1002/mus.22330. Muscle Nerve. 2012. PMID: 22334187 Free PMC article. No abstract available.

10

DYT16: the original cases.

Camargos S, Lees AJ, Singleton A, Cardoso F. Camargos S, et al. J Neurol Neurosurg Psychiatry. 2012 Oct;83(10):1012-4. doi: 10.1136/jnnp-2012-302841. Epub 2012 Jul 28. J Neurol Neurosurg Psychiatry. 2012. PMID: 22842711 Free PMC article.

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