Incidental magnetic resonance imaging findings leading to an unusual diagnosis: Adult onset Krabbe disease (2022)
- Authors:
- Autor USP: KOK, FERNANDO - FM
- Unidade: FM
- DOI: 10.1111/ene.15298
- Subjects: DOENÇAS GENÉTICAS; RESSONÂNCIA MAGNÉTICA; ADULTOS
- Language: Inglês
- Imprenta:
- Source:
- Título: European journal of neurology
- ISSN: 1351-5101
- Volume/Número/Paginação/Ano: v. 29, n. 6, p. 1859-1862, 2022
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
PAIVA, Anderson Rodrigues Brandao et al. Incidental magnetic resonance imaging findings leading to an unusual diagnosis: Adult onset Krabbe disease. European journal of neurology, v. 29, n. 6, p. 1859-1862, 2022Tradução . . Disponível em: https://doi.org/10.1111/ene.15298. Acesso em: 12 fev. 2026. -
APA
Paiva, A. R. B., Fonseca Neto, R. E., Afonso, C. L., Freua, F., Nobrega, P. R., & Kok, F. (2022). Incidental magnetic resonance imaging findings leading to an unusual diagnosis: Adult onset Krabbe disease. European journal of neurology, 29( 6), 1859-1862. doi:10.1111/ene.15298 -
NLM
Paiva ARB, Fonseca Neto RE, Afonso CL, Freua F, Nobrega PR, Kok F. Incidental magnetic resonance imaging findings leading to an unusual diagnosis: Adult onset Krabbe disease [Internet]. European journal of neurology. 2022 ; 29( 6): 1859-1862.[citado 2026 fev. 12 ] Available from: https://doi.org/10.1111/ene.15298 -
Vancouver
Paiva ARB, Fonseca Neto RE, Afonso CL, Freua F, Nobrega PR, Kok F. Incidental magnetic resonance imaging findings leading to an unusual diagnosis: Adult onset Krabbe disease [Internet]. European journal of neurology. 2022 ; 29( 6): 1859-1862.[citado 2026 fev. 12 ] Available from: https://doi.org/10.1111/ene.15298 - 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)
- 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
- When multiple sclerosis and X-linked adrenoleukodystrophy are tangled A challenging case
- Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency [editorial]: A Novel Mutation with Prominent Ataxia
Informações sobre o DOI: 10.1111/ene.15298 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
