Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Eduardo de Paula Estephan"'
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 81, Iss 12, Pp 1040-1052 (2023)
The nerve terminal and muscle membrane compose the neuromuscular junction. After opening the voltage-gated calcium channels, action potentials from the motor axons provoke a cascade for the acetylcholine release from synaptic vesicles to the synaptic
Externí odkaz:
https://doaj.org/article/9bd63dc4fee44b34a922eb000c300e56
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 80, Iss 5 suppl 1, Pp 257-265 (2022)
ABSTRACT Background: Myasthenia gravis is largely a treatable disease, but it can result in significant morbidity and even mortality, which can usually be avoided, or at least mitigated, with timely diagnosis and appropriate treatment of the disease.
Externí odkaz:
https://doaj.org/article/ed12bf3b5799478ba4736dd7f2e7f485
Autor:
Cristiane Araujo Martins Moreno, Clara Gontijo Camelo, Pedro Henrique Marte de Arruda Sampaio, Alulin Tácio Quadros Santos Monteiro Fonseca, Eduardo de Paula Estephan, André Macedo Serafim Silva, Renann Nunes Pirola, Luiz Henrique Libardi Silva, Karlla Danielle Ferreira Lima, Marco Antônio Veloso de Albuquerque, Antonio Edvan Camelo Filho, Marcos Vinícius Oliveira Marques, Mario Teruo Yanagiura, Wagner Cid Palmeira Cavalcante, Ciro Matsui Junior, Lucas Michielon de Augusto Isihi, Rodrigo Holanda Mendonça, Ana Flávia Pincerno Pouza, Mary Souza de Carvalho, Umbertina Conti Reed, Edmar Zanoteli
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 80, Iss 6, Pp 563-569 (2022)
ABSTRACT Background The COVID-19 pandemic has brought substantial challenges for current practices in treating hereditary neuromuscular disorders (hNMDs). However, this infection has not been the only concern for these patients. Social distancing has
Externí odkaz:
https://doaj.org/article/f3e2a97787fe4753822c0bf4d96d6fc2
Autor:
Ronnyson Susano Grativvol, André Macedo Serafim da Silva, Bruno Fukelmann Guedes, Eduardo de Paula Estephan, Rodrigo de Holanda Mendonça, Antônio Alberto Zambon, Carlos Otto Heise, Edmar Zanoteli
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 75, Iss 3, Pp 197-198
Externí odkaz:
https://doaj.org/article/c47d7e86c044431686e5e3deae0dbdc2
Autor:
Eduardo de Paula Estephan, Cristiane Araújo Martins Moreno, André Macedo Serafim da Silva, Rodrigo de Holanda Mendonça, Osório Abath Neto, Patrícia Yoshi Nishimura, Layla Testa Galindo, Edmar Zanoteli
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 75, Iss 1, Pp 72-73
Externí odkaz:
https://doaj.org/article/d330d78480504cefb41f643e27348e76
Publikováno v:
Arquivos de Neuro-Psiquiatria, Volume: 80, Issue: 5 Supplement 1, Pages: 257-265, Published: 12 AUG 2022
Arquivos de Neuro-Psiquiatria v.80 n.5 suppl.1 2022
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria v.80 n.5 suppl.1 2022
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Background: Myasthenia gravis is largely a treatable disease, but it can result in significant morbidity and even mortality, which can usually be avoided, or at least mitigated, with timely diagnosis and appropriate treatment of the disease. Objectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6917ebbfbfb533e563f65ed2f6350913
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2022000700257&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2022000700257&lng=en&tlng=en
Autor:
André Macedo Serafim Silva, Patricia Rodrigo, Cristiane Araújo Martins Moreno, Rodrigo de Holanda Mendonça, Eduardo de Paula Estephan, Clara Gontijo Camelo, Eliene Dutra Campos, Alexandre Torchio Dias, Amom Mendes Nascimento, Leslie Domenici Kulikowski, Acary Souza Bulle Oliveira, Umbertina Conti Reed, Lev G Goldfarb, Montse Olivé, Edmar Zanoteli
Publikováno v:
Journal of neuropathology and experimental neurology. 81(9)
Desmin (DES) is the main intermediate muscle filament that connects myofibrils individually and with the nucleus, sarcolemma, and organelles. Pathogenic variants of DES cause desminopathy, a disorder affecting the heart and skeletal muscles. We aimed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc0df23e71533709a7d78919418cd592
https://pubmed.ncbi.nlm.nih.gov/35898174
https://pubmed.ncbi.nlm.nih.gov/35898174
Autor:
Cristiane de Araújo Martins Moreno, Maria Sheila Guimarães Rocha, Samila Marissa Pinheiro Gomes, Eduardo de Paula Estephan, Sheila Aparecida Coelho Siqueira, Pedro Henrique Martins Arruda Sampaio, Daniel Thomas Pereira Lopes, Fernando Pereira Frassetto
Publikováno v:
The Thoracic and Cardiovascular Surgeon Reports
The Thoracic & Cardiovascular Surgeon Reports, Vol 09, Iss 01, Pp e33-e36 (2020)
The Thoracic & Cardiovascular Surgeon Reports, Vol 09, Iss 01, Pp e33-e36 (2020)
Myasthenia gravis and thymoma are often presented in association with ∼10% of myasthenic cases having concomitant thymoma. Thymic carcinoma is one of the rarest/aggressive human epithelial tumors and has no correlation with myasthenia gravis hither
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b51293335bbec2fdd7a895e7fab0f6c0
https://doi.org/10.1055/s-0040-1714075
https://doi.org/10.1055/s-0040-1714075
Autor:
Sandra Donkervoort, Cristiane de Araújo Martins Moreno, Eduardo de Paula Estephan, Umbertina Conti Reed, Osorio Abath Neto, Alan Fappi, Edmar Zanoteli, Matthew B. Harms, Soledad Monges, Carsten G. Bönnemann, Fabiana Lubieniecki
Publikováno v:
Neuromuscular Disorders. 30:54-58
Congenital fiber type disproportion (CFTD) is a rare congenital myopathy subtype defined by slow type 1 hypotrophy in the absence of any other major structural findings such as rods, central nuclei or cores. Dominant missense changes in slow alpha-tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::425f71235822ce57f8af7484dea04aa0
https://doi.org/10.1016/j.nmd.2019.11.001
https://doi.org/10.1016/j.nmd.2019.11.001
Autor:
Paulo Victor Partezani Helito, A A Zambon, Umbertina Conti Reed, Hanns Lochmüller, Rachel Thompson, Cristiane de Araújo Martins Moreno, Maria da Penha Morita, Danny Jomaa, Carlos Otto Heise, André Macedo Serafim da Silva, Eduardo de Paula Estephan, João Aris Kouyoumdjian, K. Polavarapu, Edmar Zanoteli, Ana Töpf
Publikováno v:
European journal of neurologyREFERENCES. 29(3)
Objectives To present phenotype features of a large cohort of congenital myasthenic syndromes (CMS) and correlate them with their molecular diagnosis. Methods Suspected CMS patients were divided into three groups: group A (limb, bulbar or axial weakn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f6a13906fee9c38da5ad0adc91e9ff6
https://pubmed.ncbi.nlm.nih.gov/34749429
https://pubmed.ncbi.nlm.nih.gov/34749429