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Page 1
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.
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
Surgical outcome in mesial temporal sclerosis correlates with prion protein gene variant.
Walz R, Castro RM, Velasco TR, Alexandre V Jr, Lopes MH, Leite JP, Santos AC, Assirati JA Jr, Wichert-Ana L, Terra-Bustamante VC, Bianchin MM, Maciag PC, Ribeiro KB, Guarnieri R, Araújo D, Cabalero O, Moura R, Salim AC, Kindlmann K, Landemberger MC, Marques W Jr, Fernandes RM, Serafini LN, Machado HR, Carlotti CG Jr, Brentani RR, Sakamoto AC, Martins VR. Walz R, et al. Among authors: martins vr. Neurology. 2003 Nov 11;61(9):1204-10. doi: 10.1212/01.wnl.0000096940.92986.02. Neurology. 2003. PMID: 14610121 Clinical Trial.
Cortical malformations are associated with a rare polymorphism of cellular prion protein.
Walz R, Castro RM, Landemberger MC, Velasco TR, Terra-Bustamante VC, Bastos AC, Bianchin M, Wichert-Ana L, Araújo D, Alexandre V Jr, Santos AC, Machado HR, Carlotti CG Jr, Brentani RR, Martins VR, Sakamoto AC. Walz R, et al. Among authors: martins vr. Neurology. 2004 Aug 10;63(3):557-60. doi: 10.1212/01.wnl.0000133400.34423.ad. Neurology. 2004. PMID: 15304595
130 results