Hypoglycemia in Patients With LAMA2-CMD (2023)
- Authors:
- USP affiliated authors: REED, UMBERTINA CONTI - FM ; ZANOTELI, EDMAR - FM
- Unidade: FM
- DOI: 10.1016/j.pediatrneurol.2023.01.017
- Subjects: HIPOGLICEMIA; FATORES DE RISCO; ESTUDOS RETROSPECTIVOS
- Language: Inglês
- Imprenta:
- Source:
- Título: Pediatric neurology
- ISSN: 0887-8994
- Volume/Número/Paginação/Ano: v. 143, p. 1-5, 2023
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
CAMELO, Clara Gontijo et al. Hypoglycemia in Patients With LAMA2-CMD. Pediatric neurology, v. 143, p. 1-5, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/53952. Acesso em: 27 fev. 2026. -
APA
Camelo, C. G., Moreno, C. de A. M., Artilheiro, M. C., Silva, A. M. S., Fonseca, A. T. Q. S. M., Holanda, R. M. de, et al. (2023). Hypoglycemia in Patients With LAMA2-CMD. Pediatric neurology, 143, 1-5. doi:10.1016/j.pediatrneurol.2023.01.017 -
NLM
Camelo CG, Moreno C de AM, Artilheiro MC, Silva AMS, Fonseca ATQSM, Holanda RM de, Reed UC, Zanoteli E. Hypoglycemia in Patients With LAMA2-CMD [Internet]. Pediatric neurology. 2023 ; 143 1-5.[citado 2026 fev. 27 ] Available from: https://observatorio.fm.usp.br/handle/OPI/53952 -
Vancouver
Camelo CG, Moreno C de AM, Artilheiro MC, Silva AMS, Fonseca ATQSM, Holanda RM de, Reed UC, Zanoteli E. Hypoglycemia in Patients With LAMA2-CMD [Internet]. Pediatric neurology. 2023 ; 143 1-5.[citado 2026 fev. 27 ] Available from: https://observatorio.fm.usp.br/handle/OPI/53952 - Common and variable clinical, histological, and imaging findings of recessive RYR1-related centronuclear myopathy patients
- The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations
- Clinical and molecular findings in a cohort of ANO5-related myopathy
- Muscle biopsy with dystrophic pattern and rimmed vacuoles: GNE myopathy in a Brazilian patient
- Theraputic advances in 5q-linked spinal muscular atrophy
- Phenotypic Intermediate Forms Overlapping to Emery-Dreifuss and Limb Girdle Muscular Dystrophies Caused by Lamin A/C Gene Mutations
- Clinical and imaging hallmarks of the MYH7-related myopathy with severe axial involvement
- Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy
- Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0 [Carta]
- A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms
Informações sobre o DOI: 10.1016/j.pediatrneurol.2023.01.017 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
