Motor impairment in a rare form of spastic paraplegia (Spoan syndrome): a 10-year follow-up (2019)
- Authors:
- USP affiliated authors: ZATZ, MAYANA - IB ; KOK, FERNANDO - FM ; LANCMAN, SELMA - FM ; CAVALCANTE, PRISCILLA MARIA DE ANDRADE - FM
- Unidades: IB; FM
- DOI: 10.1186/s12883-019-1465-5
- Subjects: DOENÇAS NEURODEGENERATIVAS; DOENÇAS GENÉTICAS; DOENÇAS RARAS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: BMC Neurology
- ISSN: 1471-2377
- Volume/Número/Paginação/Ano: v. 19, art. 256, 2019
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
ABNT
GALVÃO, Cláudia R. C et al. Motor impairment in a rare form of spastic paraplegia (Spoan syndrome): a 10-year follow-up. BMC Neurology, v. 19, 2019Tradução . . Disponível em: https://doi.org/10.1186/s12883-019-1465-5. Acesso em: 10 jan. 2026. -
APA
Galvão, C. R. C., Cavalcante, P. M. A., Olinda, R., Graciani, Z., Zatz, M., Kok, F., et al. (2019). Motor impairment in a rare form of spastic paraplegia (Spoan syndrome): a 10-year follow-up. BMC Neurology, 19. doi:10.1186/s12883-019-1465-5 -
NLM
Galvão CRC, Cavalcante PMA, Olinda R, Graciani Z, Zatz M, Kok F, Santos S, Lancman S. Motor impairment in a rare form of spastic paraplegia (Spoan syndrome): a 10-year follow-up [Internet]. BMC Neurology. 2019 ; 19[citado 2026 jan. 10 ] Available from: https://doi.org/10.1186/s12883-019-1465-5 -
Vancouver
Galvão CRC, Cavalcante PMA, Olinda R, Graciani Z, Zatz M, Kok F, Santos S, Lancman S. Motor impairment in a rare form of spastic paraplegia (Spoan syndrome): a 10-year follow-up [Internet]. BMC Neurology. 2019 ; 19[citado 2026 jan. 10 ] Available from: https://doi.org/10.1186/s12883-019-1465-5 - Avaliação da intervenção com exercícios, alongamento e órtese na função manual de pessoas com síndrome Spoan
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- Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndrome
- A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability
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Informações sobre o DOI: 10.1186/s12883-019-1465-5 (Fonte: oaDOI API)
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