Martins VR - Search Results

1

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.

2

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.

3

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.

4

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.

5

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.

6

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.

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

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.

9

Complex movement disorders in fatal familial insomnia: a clinical and genetic discussion.

Pedroso JL, Pinto WB, Souza PV, Ricarte IF, Landemberger MC, Martins VR, Prado LB, Prado GF, Barsottini OG. Pedroso JL, et al. Among authors: martins vr. Neurology. 2013 Sep 17;81(12):1098-9. doi: 10.1212/WNL.0b013e3182a4a41d. Epub 2013 Aug 14. Neurology. 2013. PMID: 23946305 No abstract available.

10

Cognitive performance of patients with mesial temporal lobe epilepsy is not associated with human prion protein gene variant allele at codons 129 and 171.

Coimbra ER, Rezek K, Escorsi-Rosset S, Landemberger MC, Castro RM, Valadão MN, Guarnieri R, Velasco TR, Terra-Bustamante VC, Bianchin MM, Wichert-Ana L, Alexandre V Jr, Brentani RR, Martins VR, Sakamoto AC, Walz R. Coimbra ER, et al. Among authors: martins vr. Epilepsy Behav. 2006 May;8(3):635-42. doi: 10.1016/j.yebeh.2006.02.007. Epub 2006 Apr 3. Epilepsy Behav. 2006. PMID: 16580884

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