Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ivana Rocha, Raslan"'
Publikováno v:
Revista de Saúde, Vol 12, Iss 1, Pp 42-45 (2021)
Tem como objetivo mostrar à comunidade científica um caso de cerebelite pós-infecciosa com achado radiográfico indicativo de deficiência de vitamina B12, a partir da avaliação do prontuário da paciente. Relatamos o caso de uma criança de 8 a
Externí odkaz:
https://doaj.org/article/016553456aa74eb68bec4c533c47e23b
Autor:
Luane Abdalla, Gouvêa, Ivana Rocha, Raslan, Augusto Bragança Reis, Rosa, Thiago Yoshinaga Tonholo, Silva, Rejane Macedo, Campos, Marcelo de Melo, Aragão, Orlando Graziani Povoas, Barsottini, José Luiz, Pedroso
Publikováno v:
The Cerebellum. 22:316-318
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e56c3b359fa25bdb3a5acc6be9b642e
https://doi.org/10.1007/s12311-022-01380-w
https://doi.org/10.1007/s12311-022-01380-w
Publikováno v:
Revista de Saúde. 12:42-45
Tem como objetivo mostrar à comunidade científica um caso de cerebelite pós-infecciosa com achado radiográfico indicativo de deficiência de vitamina B12, a partir da avaliação do prontuário da paciente. Relatamos o caso de uma criança de 8 a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ab38a09c8d24ad9cb07d54489b2b1aa
https://doi.org/10.21727/rs.v12i1.2475
https://doi.org/10.21727/rs.v12i1.2475
Publikováno v:
Neurol Clin Pract
Purpose of ReviewThis review proposes a clinical classification for congenital ataxias based on clinical features, neuroimaging, and course of the disease.Recent FindingsCongenital ataxias are an unusual group of neurologic disorders, with heterogene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c342050566aa8459150da9ac7b94795
https://doi.org/10.1212/cpj.0000000000000966
https://doi.org/10.1212/cpj.0000000000000966
Autor:
Fernando Kok, José Luiz Pedroso, Janneke H M Schuurs-Hoeijmakers, Orlando Graziani Povoas Barsottini, Marcondes C. França, João Bosco Oliveira, Ivana Rocha Raslan, Rolph Pfundt
Publikováno v:
Parkinsonism & Related Disorders, 92, pp. 33-35
Parkinsonism & Related Disorders, 92, 33-35
Parkinsonism & Related Disorders, 92, 33-35
Item does not contain fulltext
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1531a4bf4faa4670ebb918d123067fe3
https://repository.ubn.ru.nl/handle/2066/244073
https://repository.ubn.ru.nl/handle/2066/244073
Autor:
Orlando Graziani Povoas Barsottini, Paula Camila Alves de Assis Pereira Matos, Carolina Sanchez Aranda, José Luiz Pedroso, Juliana Harumi Arita, Karyme Hussein Daghastanli, Vinícius Boaratti Ciarlariello, Ivana Rocha Raslan, Augusto Bragança Reis Rosa
Publikováno v:
Mov Disord Clin Pract
Background Ataxia telangiectasia is one of the most common causes of autosomal recessive cerebellar ataxias. However, absence of telangiectasia, normal levels of alpha-fetoprotein and negative genetic test may direct to alternative diagnosis with sim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::827a75754fc1d9abd1e2932c50f63478
https://europepmc.org/articles/PMC7780949/
https://europepmc.org/articles/PMC7780949/