COMPULSORY NOTIFICATION OF PRION DISEASES IN BRAZIL: WHAT HAS CHANGED SINCE 2005?

Autor: José Eriton Gomes da Cunha, João Ricardo M. Oliveira

Publikováno v: Dementia & Neuropsychologia, Vol 2, Iss 2, Pp 155-156

Externí odkaz: https://doaj.org/article/690130afb8d34e2cbcc13d8433a48337

Seeding variability of different alpha synuclein strains in synucleinopathies

Autor: Susana Margarida da Silva Correia, Inga Zerr, Tiago F. Outeiro, Maria Cramm, Marella de Angelis, Niccolò Candelise, Alberto Rábano, Valentina González Alvarez, Tobias Thom, Cristiano D’Andrea, Matthias Schmitz, Saima Zafar, José Eriton Gomes da Cunha, Wiebke Möbius, Martina Banchelli, Anna Villar-Piqué, Franc Llorens, Paolo Matteini

Publikováno v: Annals of neurology 85(5), 691-703 (2019). doi:10.1002/ana.25446
Annals of neurology 85 (2019): 691–703. doi:10.1002/ana.25446
info:cnr-pdr/source/autori:Candelise N.; Schmitz M.; Llorens F.; Villar-Pique A.; Cramm M.; Thom T.; da Silva Correia S.M.; da Cunha J.E.G.; Mobius W.; Outeiro T.F.; Alvarez V.G.; Banchelli M.; D'Andrea C.; de Angelis M.; Zafar S.; Rabano A.; Matteini P.; Zerr I./titolo:Seeding variability of different alpha synuclein strains in synucleinopathies/doi:10.1002%2Fana.25446/rivista:Annals of neurology/anno:2019/pagina_da:691/pagina_a:703/intervallo_pagine:691–703/volume:85

Objectives Currently, the exact reasons why different α-synucleinopathies exhibit variable pathologies and phenotypes are still unknown. A potential explanation may be the existence of distinctive α-synuclein conformers or strains. Here, we intend

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bda085287116104b7a3b02940a507e74
https://doi.org/10.1002/ana.25446

Exaggerated blood pressure response during exercise treadmill testing: functional and hemodynamic features, and risk factors

Autor: Sandro G de Lima, Maria de Fátima Pessoa Militão de Albuquerque, João Ricardo Mendes de Oliveira, Danyllo Oliveira, José Eriton Gomes da Cunha, Manuela Barbosa Rodrigues de Souza, Odwaldo Barbosae e Silva, Constância Flávia Junqueira Ayres, R. R. Lemos

Publikováno v: Hypertension Research. 35:733-738

The factors which contribute to an exaggerated blood pressure response (EBPR) during the exercise treadmill test (ETT) are not wholly understood. The association between the insertion/deletion polymorphisms of the angiotensin-converting enzyme (ACE)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57a29a749c60b5ebc6c458d96dfcb4eb
https://doi.org/10.1038/hr.2012.14

Epidemiological genetics and meta-analysis of a polymorphism at codon 129 of the PRNP gene in Alzheimer's disease in Brazil

Autor: José Eriton Gomes da Cunha, Lylyan Fragoso Pimentel, Renato Lírio Morelato, João Ricardo Mendes de Oliveira, Flavia de Paula

Publikováno v: Neurological research. 36(9)

The polymorphism at codon 129 of the prion protein gene (PRNP) is a major risk factor for Creutzfeldt–Jakob disease (CJD). Several authors reported neuropathological and clinical overlapping between CJD and Alzheimer’s disease (AD), with a few as

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::489d352efca767d56a86ebcc86cc7032
https://pubmed.ncbi.nlm.nih.gov/24620982

Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice

Autor: María García-Murias, Maarja Mäe, Katja Zschiedrich, Michael Preuss, Andrés Ordóñez-Ugalde, Elisabeth J. Rushing, I. Navas, Aloysius Domingo, Valerija Dobricic, Ana Westenberger, Milena Jankovic, Janis M. Miyasaki, Didier Hannequin, Christer Betsholtz, Isabelle Le Ber, Carmen Dering, Kioomars Saliminejad, Irina Abakumova, Mayana Zatz, Giovanni Coppola, Elisabeth Raschperger, Elizabeth Spiteri, María Jesús Sobrido, Martin Paucar, Gilles Defer, Per Svenningsson, Moritz C. Wurnig, Vladimir S. Kostic, Renee L. Sears, J.M. Prieto, Hamid Reza Khorram Khorshid, Angel Carracedo, Gaël Nicolas, Michael Hugelshofer, José Eriton Gomes da Cunha, Igor Petrović, Adriano Aguzzi, Katja Lohmann, Regina Reimann, R. R. Lemos, Annika Keller, Christine Klein, Ivana Novakovic, Andres Kaech, Dominique Campion, Jörg Klepper, Andreas Boss, João Ricardo Mendes de Oliveira, Daniel H. Geschwind

Publikováno v: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Nature Genetics

Calcifications in the basal ganglia are a common incidental finding and are sometimes inherited as an autosomal dominant trait (idiopathic basal ganglia calcification (IBGC)). Recently, mutations in the PDGFRB gene coding for the platelet-derived gro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79f908008d37c6556a52dc2d996dacbc
https://pubmed.ncbi.nlm.nih.gov/24390807