Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Antônio R. Coimbra-Neto"'
Autor:
André M. S. Silva, Antônio R. Coimbra-Neto, Paulo Victor S. Souza, Pablo B. Winckler, Marcus V. M. Gonçalves, Eduardo B. U. Cavalcanti, Alzira A. D. S. Carvalho, Cláudia F. D. R. Sobreira, Clara G. Camelo, Rodrigo D. H. Mendonça, Eduardo D. P. Estephan, Umbertina C. Reed, Marcela C. Machado-Costa, Mario E. T. Dourado-Junior, Vanessa C. Pereira, Marcelo M. Cruzeiro, Paulo V. P. Helito, Laís U. Aivazoglou, Leonardo V. D. Camargo, Hudson H. Gomes, Amaro J. S. D. Camargo, Wladimir B. V. D. R. Pinto, Bruno M. L. Badia, Luiz H. Libardi, Mario T. Yanagiura, Acary S. B. Oliveira, Anamarli Nucci, Jonas A. M. Saute, Marcondes C. França-Junior, Edmar Zanoteli
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 7, Pp 1225-1238 (2019)
Abstract Objective ANO5‐related myopathy is an important cause of limb‐girdle muscular dystrophy (LGMD) and hyperCKemia. The main descriptions have emerged from European cohorts, and the burden of the disease worldwide is unclear. We provide a de
Externí odkaz:
https://doaj.org/article/9569ce804f2d459a98f49ce1fbcc02cb
Autor:
Cristina Saade Jaques, Orlando Graziani Povoas Barsottini, Anamarli Nucci, Antônio R. Coimbra-Neto, Francisco Cardoso, Sarah Camargos, José Luiz Pedroso, Marcondes C. França, Alberto R. M. Martinez, Marianna Pinheiro Moraes de Moraes, Eduardo Antonio Roquim Silva
Publikováno v:
Journal of neurology, neurosurgery, and psychiatry. 91(4)
Sjogren’s syndrome is a chronic autoimmune disorder characterised by lymphocytic infiltration of exocrine glands that causes dysfunction in salivary and lacrimal glands.1 Clinical features include dry eyes, dry mouth, fatigue, muscle pain and swell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67fc8a26f982f7e27960fbd1ff241f86
https://pubmed.ncbi.nlm.nih.gov/32015088
https://pubmed.ncbi.nlm.nih.gov/32015088
Autor:
Laís Uyeda Aivazoglou, Edmar Zanoteli, Bruno de Mattos Lombardi Badia, Antônio R. Coimbra-Neto, André Macedo Serafim da Silva, Paulo Victor Sgobbi de Souza, Acary Souza Bulle Oliveira, Pablo Brea Winckler, Vanessa C. Pereira, Umbertina Conti Reed, Wladimir Bocca Vieira de Rezende Pinto, Luiz H. Libardi, Paulo Victor Partezani Helito, Marcus Goncalves, Mario Emílio Teixeira Dourado-Júnior, Anamarli Nucci, Amaro J. S. D. Camargo, Marcondes Cavalcante França-Junior, Marcelo Maroco Cruzeiro, Leonardo Valente de Camargo, Marcela C. Machado-Costa, Mario Teruo Yanagiura, Eduardo de Paula Estephan, Jonas Alex Morales Saute, Hudson H. Gomes, Rodrigo de Holanda Mendonça, Eduardo B. U. Cavalcanti, Cláudia Ferreira da Rosa Sobreira, Clara Gontijo Camelo, Alzira Alves de Siqueira Carvalho
Publikováno v:
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Annals of Clinical and Translational Neurology, Vol 6, Iss 7, Pp 1225-1238 (2019)
Annals of Clinical and Translational Neurology
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Annals of Clinical and Translational Neurology, Vol 6, Iss 7, Pp 1225-1238 (2019)
Annals of Clinical and Translational Neurology
Made available in DSpace on 2019-10-06T16:41:11Z (GMT). No. of bitstreams: 0 Previous issue date: 2019-07-01 Objective: ANO5-related myopathy is an important cause of limb-girdle muscular dystrophy (LGMD) and hyperCKemia. The main descriptions have e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfc057378c2ac77b1d37b57ad2e72ad3
Autor:
Antônio R. Coimbra-Neto, Alzira Alves de Siqueira Carvalho, Jonas Alex Morales Saute, Marcia Lorena Fagundes Chaves, Regina Célia Beltrão Duarte, Cynthia Costa e Silva, Rodrigo de Holanda Mendonça, Ana Cotta, Pablo Brea Winckler, Umbertina Conti Reed, Eduardo B. U. Cavalcanti, Carlo Domenico Marrone, Renata Barreto Tenório, Marcondes C. França, Julia Filardi Paim, Marcela C. Machado-Costa, Antonette Souto El Husny, Marcus Goncalves, Marjory Irineu Bená, Isabel Cristina Neves de Souza, Cleonísio L. Rodrigues, Raimunda Helena Ferreira Feio, Daniel Fernando Arias Betancur, Cláudia Ferreira da Rosa Sobreira, André Macedo Serafim da Silva, Edmar Zanoteli, Elmano Carvalho, Camila de Aquino Cruz
Publikováno v:
Clinical geneticsREFERENCES. 96(4)
Limb-girdle muscular dystrophies (LGMD) are a group of genetically heterogeneous disorders characterized by predominantly proximal muscle weakness. We aimed to characterize epidemiological, clinical and molecular data of patients with autosomal reces
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d027c1177723db4a681d245623327edd
https://pubmed.ncbi.nlm.nih.gov/31268554
https://pubmed.ncbi.nlm.nih.gov/31268554