When multiple sclerosis and X-linked adrenoleukodystrophy are tangled A challenging case (2018)
- Authors:
- Autor USP: KOK, FERNANDO - FM
- Unidade: FM
- DOI: 10.1212/CPJ.0000000000000431
- Subjects: ESCLEROSE MÚLTIPLA; DOENÇAS DO SISTEMA NERVOSO; BIOMARCADORES
- Language: Inglês
- Imprenta:
- Publisher place: Philadelphia
- Date published: 2018
- Source:
- Título: Neurology-clinical practice
- ISSN: 2163-0402
- Volume/Número/Paginação/Ano: v. 8, n. 2, p. 156-158, 2018
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
PAIVA, Anderson Rodrigues Brandao de et al. When multiple sclerosis and X-linked adrenoleukodystrophy are tangled A challenging case. Neurology-clinical practice. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1212/CPJ.0000000000000431. Acesso em: 11 fev. 2026. , 2018 -
APA
Paiva, A. R. B. de, Kok, F., Pucci Filho Carlos Rory,, Porto, A. M., Feltrin, F. S., & Camargo, C. H. F. (2018). When multiple sclerosis and X-linked adrenoleukodystrophy are tangled A challenging case. Neurology-clinical practice. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. doi:10.1212/CPJ.0000000000000431 -
NLM
Paiva ARB de, Kok F, Pucci Filho Carlos Rory, Porto AM, Feltrin FS, Camargo CHF. When multiple sclerosis and X-linked adrenoleukodystrophy are tangled A challenging case [Internet]. Neurology-clinical practice. 2018 ; 8( 2): 156-158.[citado 2026 fev. 11 ] Available from: https://doi.org/10.1212/CPJ.0000000000000431 -
Vancouver
Paiva ARB de, Kok F, Pucci Filho Carlos Rory, Porto AM, Feltrin FS, Camargo CHF. When multiple sclerosis and X-linked adrenoleukodystrophy are tangled A challenging case [Internet]. Neurology-clinical practice. 2018 ; 8( 2): 156-158.[citado 2026 fev. 11 ] Available from: https://doi.org/10.1212/CPJ.0000000000000431 - Clinical presentation of a complex neurodevelopmental disorder caused by mutations in ADNP
- Santos syndrome is caused by mutation in the WNT7A gene
- A novel complex neurological phenotype due to a homozygous mutation in FDX2
- Typical clinical and neuroimaging features in Sjögren-Larsson syndrome [Editorial]
- Leukodystrophy with premature ovarian failure: Think on vanishing white matter disease (VWMD)
- Incidental magnetic resonance imaging findings leading to an unusual diagnosis: Adult onset Krabbe disease
- Extreme Clinical Variability Among Carriers of Pathogenic Variant in SSBP1 [Carta]
- Haploidentical bone marrow transplantation with post transplant cyclophosphamide for patients with X-linked adrenoleukodystrophy: a suitable choice in an urgent situation
- A case of mitochondrial DNA depletion syndrome type 11-expanding the genotype and phenotype
- Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency [editorial]: A Novel Mutation with Prominent Ataxia
Informações sobre o DOI: 10.1212/CPJ.0000000000000431 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas