Doenças neuromusculares (2017)
- Authors:
- USP affiliated authors: REED, UMBERTINA CONTI - FM ; ZANOTELI, EDMAR - FM
- Unidade: FM
- Subjects: NEURÔNIOS; ATROFIA MUSCULAR; DOENÇAS NEUROMUSCULARES
- Language: Português
- Imprenta:
- ISBN: 9788538807421
- Source:
- Título do periódico: Tratado de neurologia infantil
-
ABNT
FONSECA, Alulin Tácio Quadros Santos Monteiro e ZANOTELI, Edmar e REED, Umbertina Conti. Doenças neuromusculares. Tratado de neurologia infantil. Tradução . São Paulo: Atheneu, 2017. . . Acesso em: 25 abr. 2024. -
APA
Fonseca, A. T. Q. S. M., Zanoteli, E., & Reed, U. C. (2017). Doenças neuromusculares. In Tratado de neurologia infantil. São Paulo: Atheneu. -
NLM
Fonseca ATQSM, Zanoteli E, Reed UC. Doenças neuromusculares. In: Tratado de neurologia infantil. São Paulo: Atheneu; 2017. [citado 2024 abr. 25 ] -
Vancouver
Fonseca ATQSM, Zanoteli E, Reed UC. Doenças neuromusculares. In: Tratado de neurologia infantil. São Paulo: Atheneu; 2017. [citado 2024 abr. 25 ] - Clinical and imaging hallmarks of the MYH7-related myopathy with severe axial involvement
- Atypical phenotype in a case of MYH7 congenital myopathy
- A novel acta 1 mutation in a patient with nemaline myopathy
- Clinical and histological features of brazilian patients with nemaline myopathy
- RYR1-related exertional rhabdomyolysis: Expanding spectrum and diagnostic challenges
- Congenital fiber type disproportion caused by TPM3 mutation: a report of two atypical cases
- Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy
- Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0 [Carta]
- Muscle biopsy with dystrophic pattern and rimmed vacuoles: GNE myopathy in a Brazilian patient
- Phenotypic Intermediate Forms Overlapping to Emery-Dreifuss and Limb Girdle Muscular Dystrophies Caused by Lamin A/C Gene Mutations
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas