Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Oliveira,Acary S.B."'
Autor:
Lemos, Nucelio, Fernandes, Gustavo L., Ribeiro, Augusta M., Maia-Lemos, Priscila S., Contiero, Wellington, Croos-Bezerra, Victor, Tomlison, George, Faber, Jean, Oliveira, Acary S.B., Girão, Manoel J.B.C.
Publikováno v:
In Neuromodulation: Technology at the Neural Interface January 2023 26(1):233-245
Autor:
Marin, Luis Fabiano, Carvalho, Luciane B.C., Prado, Lucila B.F., Oliveira, Acary S.B., Prado, Gilmar F.
Publikováno v:
In Sleep Medicine September 2017 37:147-150
Autor:
de Boer, Eva M.J., Barritt, Andrew W., Elamin, Marwa, Anderson, Stuart J., Broad, Rebecca, Nisbet, Angus, Goedee, H. Stephan, Vázquez Costa, Juan F., Prudlo, Johannes, Vedeler, Christian A., Fernandez, Julio Pardo, Panades, Mónica Povedano, Albertí Aguilo, Maria A., Bella, Eleonora Dalla, Lauria, Giuseppe, Pinto, Wladimir B.V.R., de Souza, Paulo V.S., Oliveira, Acary S.B., Toro, Camilo, van Iersel, Joost, Parson, Malu, Harschnitz, Oliver, van den Berg, Leonard H., Veldink, Jan H., Al-Chalabi, Ammar, Leigh, Peter N., van Es, Michael A.
Publikováno v:
Neurology: Clinical Practice
article-version (Version of Record) 3
Dipòsit Digital de la UB
Universidad de Barcelona
article-version (Version of Record) 3
Dipòsit Digital de la UB
Universidad de Barcelona
Purpose of review: To improve our clinical understanding of facial onset sensory and motor neuronopathy (FOSMN). Recent findings: We identified 29 new cases and 71 literature cases, resulting in a cohort of 100 patients with FOSMN. During follow-up,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ede3bd6b7b021581a47550c1f8c1847c
http://europepmc.org/articles/PMC8032419
http://europepmc.org/articles/PMC8032419
Dominant or recessive mutations in the RYR1 gene causing central core myopathy in Brazilian patients
Autor:
Galleni Leão, Leonardo, Santos Souza, Lucas, Nogueira, Letícia, Pavanello, Rita de Cássia Mingroni, Gurgel-Giannetti, Juliana, Reed, Umbertina C, Oliveira, Acary S.B., Cuperman, Thais, Cotta, Ana, FPaim, Julia, Zatz, Mayana, Vainzof, Mariz
Publikováno v:
Acta Myologica
Central Core Disease (CCD) is an inherited neuromuscular disorder characterized by the presence of cores in muscle biopsy. CCD is caused by mutations in the RYR1 gene. This gene encodes the ryanodine receptor 1, which is an intracellular calcium rele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::334c963301da1616cfbe5f23c8d1d73c
http://europepmc.org/articles/PMC7783440
http://europepmc.org/articles/PMC7783440
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 59, Iss 3B, Pp 681-685 (2001)
Myasthenia gravis (MG) in childhood is rare comprising 10 to 20 % of all myasthenic patients. We studied 18 patients with MG whose first symptoms started from 1 to 12 years of age, followed at the Department of Neurology of the UNIFESP-EPM, from Janu
Externí odkaz:
https://doaj.org/article/0416c8d94fa14ccfa65895c72ea13a6d
Autor:
da Costa, Carina K., Kiyomoto, Beatriz H., Schmidt, Beny, Oliveira, Acary S.B., Gabbai, Alberto A., Tengan, Célia H.
Publikováno v:
In Journal of the Neurological Sciences 2007 263(1):139-144
Autor:
Zanoteli, Edmar, Yamashita, Helio K., Suzuki, Hideo, Oliveira, Acary S.B., Gabbai, Alberto A.
Publikováno v:
In Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endodontology August 2002 94(2):262-271
Autor:
Tengan, Célia H *, Ferreiro-Barros, Claudia, Cardeal, Marina, Fireman, Moacir A.T, Oliveira, Acary S.B, Kiyomoto, Beatriz H, Gabbai, Alberto A
Publikováno v:
In BBA - Molecular Basis of Disease 2002 1588(1):65-70
Autor:
Zanoteli, Edmar, Guimarães, Antônio S., Martins, Ricardo J., Yamashita, Helio K., Toledo, Carlos S., Oliveira, Acary S.B., Gabbai, Alberto A.
Publikováno v:
In Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endodontology July 2000 90(1):118-121
Autor:
Wajchenberg, Marcelo, Astur, Nelson, Fernandes, Eloy A., Paredes-Gamero, Edgar J., Luciano, Rafael P., Schmidt, Beny, Oliveira, Acary S.B., Martins, Delio E.
Publikováno v:
Journal of Pediatric Orthopaedics B; Jul2019, Vol. 28 Issue 4, p362-367, 6p