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Testing an online screening tool for epilepsy surgery evaluation.
Madeira BC, Schönwald SV, Winckler PB, Martin KC, Torres CM, Bizzi JWJ, Bianchin MM. Madeira BC, et al. Among authors: winckler pb. Arq Neuropsiquiatr. 2024 Oct;82(10):1-8. doi: 10.1055/s-0044-1791659. Epub 2024 Nov 11. Arq Neuropsiquiatr. 2024. PMID: 39529325 Free article. English.
Clinicogenetic characterization and response to disease-modifying therapies in spinal muscular atrophy: real-world experience from a reference center in Southern Brazil.
de Albuquerque ALA, Chadanowicz JK, Bevilacqua IP, Staub ALP, Winckler PB, da Silva PZ, Fagondes SC, Ferrari RS, Trojahn CDO, Sacharuk VZ, Kowalski TW, Donis KC, Becker MM, Saute JAM. de Albuquerque ALA, et al. Among authors: winckler pb. J Pediatr (Rio J). 2024 Oct 16:S0021-7557(24)00126-8. doi: 10.1016/j.jped.2024.07.011. Online ahead of print. J Pediatr (Rio J). 2024. PMID: 39426797 Free article.
Clinical and molecular characterization of limb-girdle muscular dystrophy 2G/R7 in a large cohort of Brazilian patients.
Gaviraghi T, Cavalcanti EBU, Lorenzoni PJ, Cotta A, de Souza PVS, de Oliveira AD, de Moraes MT, Marques MVO, Donis KC, Winckler PB, Costa E Silva C, Pinto WBVR, Kay CSK, Ducci RD, Rodrigues PRVP, Fustes OJH, da Silva AMS, Zanoteli E, França MC Jr, Sobreira CFR, Oliveira ASB, Carvalho EHT, Scola RH, Carvalho AAS, Saute JAM. Gaviraghi T, et al. Among authors: winckler pb. Clin Genet. 2024 Nov;106(5):644-649. doi: 10.1111/cge.14589. Epub 2024 Jul 17. Clin Genet. 2024. PMID: 39015008
57 results