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Fernando Freua

Showing results (21-30 of 36) with videos related to

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Brain Sciences|August 26, 2023
Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids (SLIPPERS)-Does it Really Exist?Fernando Freua, João Vitor Mahler, Pedro Lucas Grangeiro de Sá Barreto Lima, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|July 18, 2024
Young-Onset Alzheimer Dementia Due to a Novel Pathogenic <i>Presenilin 1</i> Variant Initially Misdiagnosed as Autoimmune EncephalitisNathalia Rossoni Ronchi, Matheus A Castro, Artur M Coutinho, et al.
Movement Disorders Clinical Practice|January 23, 2024
Gerstmann-Sträussler-Scheinker Disease Presenting as Late-Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with NeuropathologyChristopher D Stephen, Claudio Melo de Gusmao, Sharan R Srinivasan, et al.
Cold Spring Harbor Molecular Case Studies|September 30, 2022
Arginase 1 deficiency presenting as complicated hereditary spastic paraplegiaFernando Freua, Mariana Espíndola de Castro Almeida, Paulo Ribeiro Nóbrega, et al.
Cerebellum (London, England)|June 18, 2025
PHARC (Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa and Cataract) - A Case Report and Clinical-Focused Literature ReviewSergio Roberto Pereira da Silva, Renata Montes Garcia Barbosa, Patricia Pontes Cruz, et al.
Clinical Genetics|August 5, 2024
Clinicogenetic characterization of cerebrotendinous xanthomatosis in BrazilHelena Fussiger, Pedro Lucas G S B Lima, Paulo V S Souza, et al.
Neurology. Genetics|January 31, 2019
<i>PUS3</i> mutations are associated with intellectual disability, leukoencephalopathy, and nephropathyAnderson Rodrigues Brandão de Paiva, David S Lynch, Uirá Souto Melo, et al.
Scientific Reports|November 16, 2021
Clinical and molecular characterization of a large cohort of childhood onset hereditary spastic paraplegiasGabriela Marchisio Giordani, Fabrício Diniz, Helena Fussiger, et al.
Arquivos De Neuro-Psiquiatria|May 18, 2026
Metapneumovirus-associated necrotizing disseminated acute leukoencephalopathySara Caixeta de Souza, Ahmed Haydar, João Lucas Silva Santana, et al.
Brain Sciences|August 26, 2023
Subacute Partially Reversible Leukoencephalopathy Expands the Aicardi-Goutières Syndrome PhenotypeIsabella Peixoto de Barcelos, Clarissa Bueno, Luís Filipe S Godoy, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Brain Sciences|August 26, 2023
Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids (SLIPPERS)-Does it Really Exist?Fernando Freua, João Vitor Mahler, Pedro Lucas Grangeiro de Sá Barreto Lima, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|July 18, 2024
Young-Onset Alzheimer Dementia Due to a Novel Pathogenic <i>Presenilin 1</i> Variant Initially Misdiagnosed as Autoimmune EncephalitisNathalia Rossoni Ronchi, Matheus A Castro, Artur M Coutinho, et al.
Movement Disorders Clinical Practice|January 23, 2024
Gerstmann-Sträussler-Scheinker Disease Presenting as Late-Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with NeuropathologyChristopher D Stephen, Claudio Melo de Gusmao, Sharan R Srinivasan, et al.
Cold Spring Harbor Molecular Case Studies|September 30, 2022
Arginase 1 deficiency presenting as complicated hereditary spastic paraplegiaFernando Freua, Mariana Espíndola de Castro Almeida, Paulo Ribeiro Nóbrega, et al.
Cerebellum (London, England)|June 18, 2025
PHARC (Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa and Cataract) - A Case Report and Clinical-Focused Literature ReviewSergio Roberto Pereira da Silva, Renata Montes Garcia Barbosa, Patricia Pontes Cruz, et al.
Clinical Genetics|August 5, 2024
Clinicogenetic characterization of cerebrotendinous xanthomatosis in BrazilHelena Fussiger, Pedro Lucas G S B Lima, Paulo V S Souza, et al.
Neurology. Genetics|January 31, 2019
<i>PUS3</i> mutations are associated with intellectual disability, leukoencephalopathy, and nephropathyAnderson Rodrigues Brandão de Paiva, David S Lynch, Uirá Souto Melo, et al.
Scientific Reports|November 16, 2021
Clinical and molecular characterization of a large cohort of childhood onset hereditary spastic paraplegiasGabriela Marchisio Giordani, Fabrício Diniz, Helena Fussiger, et al.
Arquivos De Neuro-Psiquiatria|May 18, 2026
Metapneumovirus-associated necrotizing disseminated acute leukoencephalopathySara Caixeta de Souza, Ahmed Haydar, João Lucas Silva Santana, et al.
Brain Sciences|August 26, 2023
Subacute Partially Reversible Leukoencephalopathy Expands the Aicardi-Goutières Syndrome PhenotypeIsabella Peixoto de Barcelos, Clarissa Bueno, Luís Filipe S Godoy, et al.
Pageof 4