Zobrazeno 1 - 4
of 4
pro vyhledávání: '"F. G. M. Naylor"'
Autor:
Monica S. Haddad, P. Puglia Jr., Jessie M. Navarro, G. Gronich, H. B. Scapolan, F. S. Aloe, M. M. Vilela, F. G. M. Naylor, A. Cukiert, R. Mariano Jr.
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 49, Iss 3, Pp 326-329 (1991)
A epilepsia reflexa ao comer é forma rara de epilepsia reflexa. Um paciente de 24 anos com crises parciais complexas reflexas ao comer foi submetido a avaliações clínica, neurológica, neurorradiológica e eletrencefalográfica. O exame, neuroló
Externí odkaz:
https://doaj.org/article/6aad70cbdd1d4dca9041187033adee41
Autor:
A. Cukiert, F. G. M. Naylor, H. B. Scapolan, M. M. Vilela, F. S. Aloe, J. O. Siffert, Ana M. Tsanaglis, Monica Haddad, Teresa C. Machado, Mary Carvalho-Alegro, J. A. Levy, L. Marques-Assis
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 47, Iss 3, Pp 346-351 (1989)
Two brothers presented to us with a progressive myoclonic syndrome with slight cerebellar symptoms. Neurological examination disclosed moderate cerebellar signs and pale optic discs; asymmetric, asynchronous and arhythmic myoclonus, an arthresthesic
Externí odkaz:
https://doaj.org/article/c56b778804ab416f9cece5077ddff461
Autor:
L Squassante Capeline, G S Lobo Oishi, P S De Souza, F G M Naylor, F J N Mancuso, A S Bulle Oliveira, V Ambrosio Moises
Publikováno v:
European Heart Journal. 43
Background Transthyretin Amyloidosis (ATTR) is a rare genetic cause of potentially fatal infiltrative cardiomyopathy. This is the commonest form of inherited restrictive cardiomyopathy. The Transthyretin (TTR) gene is located on chromosome 18q12.1 wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1603f53baef257c08d9a7be7faa4dd5
https://doi.org/10.1093/eurheartj/ehac544.1776
https://doi.org/10.1093/eurheartj/ehac544.1776
Autor:
Ana M. Tsanaglis, Mary Carvalho-Alegro, H.B. Scapolan, J. O. Siffert, F. G. M. Naylor, Arthur Cukiert, Maria Marluce dos Santos Vilela, Flávio Alóe, Mônica Santoro Haddad, Teresa C. Machado, Luís Marques-Assis, José Antonio Levy
Publikováno v:
Arquivos de Neuro-Psiquiatria v.47 n.3 1989
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Vol 47, Iss 3, Pp 346-351 (1989)
Arquivos de Neuro-Psiquiatria, Volume: 47, Issue: 3, Pages: 346-351, Published: SEP 1989
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Vol 47, Iss 3, Pp 346-351 (1989)
Arquivos de Neuro-Psiquiatria, Volume: 47, Issue: 3, Pages: 346-351, Published: SEP 1989
Two brothers presented to us with a progressive myoclonic syndrome with slight cerebellar symptoms. Neurological examination disclosed moderate cerebellar signs and pale optic discs; asymmetric, asynchronous and arhythmic myoclonus, an arthresthesic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e104df32a8ab437ae2980117fa3f15b
https://pubmed.ncbi.nlm.nih.gov/2619613
https://pubmed.ncbi.nlm.nih.gov/2619613