Martins VR - Search Results

1

Asymmetric cortical high signal on diffusion weighted-MRI in a case of Creutzfeldt-Jakob disease.

Nitrini R, Areza-Fegyveres R, Martins VR, Castro RM, Landemberger MC, Huang N, Bacheschi LA, Bacheschi LE, Leite CC, Buchpiguel CA, Rosemberg S. Nitrini R, et al. Among authors: martins vr. Arq Neuropsiquiatr. 2005 Jun;63(2B):519-22. doi: 10.1590/s0004-282x2005000300028. Epub 2005 Jul 25. Arq Neuropsiquiatr. 2005. PMID: 16059609 Free article.

2

Codon 129 polymorphism of prion protein gene in is not a risk factor for Alzheimer's disease.

Smid J, Landemberger MC, Bahia VS, Martins VR, Nitrini R. Smid J, et al. Among authors: martins vr. Arq Neuropsiquiatr. 2013 Jul;71(7):423-7. doi: 10.1590/0004-282X20130055. Arq Neuropsiquiatr. 2013. PMID: 23857619 Free article.

3

High phenotypic variability in Gerstmann-Sträussler-Scheinker disease.

Smid J, Studart A Neto, Landemberger MC, Machado CF, Nóbrega PR, Canedo NHS, Schultz RR, Naslavsky MS, Rosemberg S, Kok F, Chimelli L, Martins VR, Nitrini R. Smid J, et al. Among authors: martins vr. Arq Neuropsiquiatr. 2017 Jun;75(6):331-338. doi: 10.1590/0004-282X20170049. Arq Neuropsiquiatr. 2017. PMID: 28658400 Free article.

4

Second-Generation RT-QuIC Assay for the Diagnosis of Creutzfeldt-Jakob Disease Patients in Brazil.

Barbosa BJAP, Castrillo BB, Alvim RP, de Brito MH, Gomes HR, Brucki SMD, Smid J, Nitrini R, Landemberger MC, Martins VR, Silva JL, Vieira TCRG. Barbosa BJAP, et al. Among authors: martins vr. Front Bioeng Biotechnol. 2020 Aug 6;8:929. doi: 10.3389/fbioe.2020.00929. eCollection 2020. Front Bioeng Biotechnol. 2020. PMID: 32850757 Free PMC article.

5

Creutzfeldt-Jakob disease associated with a missense mutation at codon 200 of the prion protein gene in Brazil.

Smid J, Martins VR, Landemberger MC, Riva D, Anghinah R, Nitrini R. Smid J, et al. Among authors: martins vr. Dement Neuropsychol. 2007 Apr-Jun;1(2):222-224. doi: 10.1590/s1980-57642008dn10200017. Dement Neuropsychol. 2007. PMID: 29213392 Free PMC article.

6

Prion diseases are undercompulsory notification in Brazil: Surveillance of cases evaluated by biochemicaland/or genetic markers from 2005 to 2007.

Martins VR, Gomes HR, Chimelli L, Rosemberg S, Landemberger MC. Martins VR, et al. Dement Neuropsychol. 2007 Oct-Dec;1(4):347-355. doi: 10.1590/S1980-57642008DN10400004. Dement Neuropsychol. 2007. PMID: 29213410 Free PMC article.

7

High capacity and low cost detection of prion protein gene variant alleles by denaturing HPLC.

Castro RM, Landemberger MC, Walz R, Carlotti CG Jr, Huang N, Cunha DR, Moura R, Caballero OL, Sakamoto AC, Nitrini R, Brentani RR, Martins VR. Castro RM, et al. Among authors: martins vr. J Neurosci Methods. 2004 Oct 30;139(2):263-9. doi: 10.1016/j.jneumeth.2004.05.001. J Neurosci Methods. 2004. PMID: 15488240

8

Prnp gene and cerebellum volume in patients with refractory mesial temporal lobe epilepsy.

Valadão MN, Coimbra ER, Landemberger MC, Velasco TR, Terra VC, Wichert-Ana L, Alexandre V Jr, Araújo D Jr, Guarnieri R, Martins VR, Santos AC, Sakamoto AC, Walz R. Valadão MN, et al. Among authors: martins vr. Neurol Sci. 2014 Feb;35(2):239-44. doi: 10.1007/s10072-013-1494-6. Epub 2013 Oct 5. Neurol Sci. 2014. PMID: 24091711

9

Loss of STI1-mediated neuronal survival and differentiation in disease-associated mutations of prion protein.

Landemberger MC, de Oliveira GP, Machado CF, Gollob KJ, Martins VR. Landemberger MC, et al. Among authors: martins vr. J Neurochem. 2018 Jun;145(5):409-416. doi: 10.1111/jnc.14305. Epub 2018 Apr 2. J Neurochem. 2018. PMID: 29337365 Free article.

10

Disease-associated mutations in the prion protein impair laminin-induced process outgrowth and survival.

Machado CF, Beraldo FH, Santos TG, Bourgeon D, Landemberger MC, Roffé M, Martins VR. Machado CF, et al. Among authors: martins vr. J Biol Chem. 2012 Dec 21;287(52):43777-88. doi: 10.1074/jbc.M112.428235. Epub 2012 Nov 6. J Biol Chem. 2012. PMID: 23132868 Free PMC article.

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