Brain MRI Abnormalities, Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy - a Genotype/Phenotype Correlation (2023)
- Authors:
- USP affiliated authors: LUCATO, LEANDRO TAVARES - FM ; REED, UMBERTINA CONTI - FM ; ZANOTELI, EDMAR - FM ; CAMELO, CLARA GONTIJO - FM
- Unidade: FM
- DOI: 10.3233/JND-221638
- Subjects: DISTROFIA MUSCULAR; MALFORMAÇÕES; CÉREBRO; VARIAÇÃO GENÉTICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of neuromuscular diseases
- ISSN: 2214-3599
- Volume/Número/Paginação/Ano: v. 10, n. 4, p. 483-492, 2023
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
CAMELO, Clara Gontijo et al. Brain MRI Abnormalities, Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy - a Genotype/Phenotype Correlation. Journal of neuromuscular diseases, v. 10, n. 4, p. 483-492, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/56122. Acesso em: 15 fev. 2026. -
APA
Camelo, C. G., Artilheiro, M. C., Moreno, C. A. M., Ferraciolli, S. F., Silva, A. M. S. da, Fernandes, T. R., et al. (2023). Brain MRI Abnormalities, Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy - a Genotype/Phenotype Correlation. Journal of neuromuscular diseases, 10( 4), 483-492. doi:10.3233/JND-221638 -
NLM
Camelo CG, Artilheiro MC, Moreno CAM, Ferraciolli SF, Silva AMS da, Fernandes TR, Lucato LT, Rocha AJ, Reed UC, Zanoteli E. Brain MRI Abnormalities, Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy - a Genotype/Phenotype Correlation [Internet]. Journal of neuromuscular diseases. 2023 ; 10( 4): 483-492.[citado 2026 fev. 15 ] Available from: https://observatorio.fm.usp.br/handle/OPI/56122 -
Vancouver
Camelo CG, Artilheiro MC, Moreno CAM, Ferraciolli SF, Silva AMS da, Fernandes TR, Lucato LT, Rocha AJ, Reed UC, Zanoteli E. Brain MRI Abnormalities, Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy - a Genotype/Phenotype Correlation [Internet]. Journal of neuromuscular diseases. 2023 ; 10( 4): 483-492.[citado 2026 fev. 15 ] Available from: https://observatorio.fm.usp.br/handle/OPI/56122 - Common and variable clinical, histological, and imaging findings of recessive RYR1-related centronuclear myopathy patients
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Informações sobre o DOI: 10.3233/JND-221638 (Fonte: oaDOI API)
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