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Akademický článek

Ensino de Artes Visuais em um contexto de pandemia: interlocuções para o Ensino Remoto Emergencial

Autor: Fabrício Andrade Pereira, Ivana Rocha

Publikováno v: Palíndromo, Vol 14, Iss 33 (2022)

O artigo discute o Ensino de Artes Visuais, a partir de uma escola em Betim-MG, durante a pandemia causada pelo novo coronavírus. As atividades oferecidas, em um primeiro momento, podem ser tomadas como ponto de partida para refletir sobre os desafi

Externí odkaz: https://doaj.org/article/2230877aa30d47ff83b8190e2ae6adfa

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Akademický článek

Cerebelite pós-infecciosa com neuroimagem atípica: Relato de caso

Autor: Gabriela Manso Freitas, Sarah Lages Coelho, 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

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Akademický článek

Beyond Typical Ataxia Telangiectasia: How to Identify the Ataxia Telangiectasia‐Like Disorders.

Autor: Raslan, Ivana Rocha¹ (AUTHOR), Pereira Matos, Paula Camila Alves¹ (AUTHOR), Boaratti Ciarlariello, Vinícius¹ (AUTHOR), Daghastanli, Karyme Hussein¹ (AUTHOR), Rosa, Augusto Bragança Reis¹ (AUTHOR), Arita, Juliana Harumi² (AUTHOR), Aranda, Carolina Sanchez³ (AUTHOR), Barsottini, Orlando Graziani Povoas¹ (AUTHOR) orlandobarsottini@gmail.com, Pedroso, José Luiz¹ (AUTHOR)

Publikováno v: Movement Disorders Clinical Practice. Jan2021, Vol. 8 Issue 1, p118-125. 8p.

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Spinocerebellar Ataxia Type 5 (SCA5) Mimicking Cerebral Palsy: a Very Early Onset Autosomal Dominant Hereditary Ataxia

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

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Cerebelite pós infecciosa com neuroimagem simulando deficiência de vitamina B12, uma associação atípica

Autor: Ivana Rocha Raslan, Gabriela Manso Freitas, Sarah Lages Coelho

Publikováno v: Revista de Saúde. 12:42-45

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4ab38a09c8d24ad9cb07d54489b2b1aa
https://doi.org/10.21727/rs.v12i1.2475

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A Proposed Clinical Classification and a Diagnostic Approach for Congenital Ataxias

Autor: Orlando Graziani Povoas Barsottini, Ivana Rocha Raslan, José Luiz Pedroso

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

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TRAUMATISMO ESPINAL

Autor: Ivana Rocha Pinto, Heriberto Bailaba

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6b02bd2fd91034f9f83211eeed209c7f
https://doi.org/10.56088/hinc.978-65-993721-3-1.008

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Quadrupedal gait and cerebellar hypoplasia, the Uner Tan syndrome, caused by ITPR1 gene mutation

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

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Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1531a4bf4faa4670ebb918d123067fe3
https://repository.ubn.ru.nl/handle/2066/244073

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Beyond Typical Ataxia Telangiectasia: How to Identify the Ataxia Telangiectasia‐Like Disorders

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/

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Akademický článek

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