Congenital Muscular Dystrophy With Dropped Head Linked to the LMNA Gene in a Brazilian Cohort (2014)
- Authors:
- USP affiliated authors: REED, UMBERTINA CONTI - FM ; CHADI, GERSON - FM
- Unidade: FM
- DOI: 10.1016/j.pediatrneurol.2013.11.010
- Subjects: PEDIATRIA; MUTAÇÃO GENÉTICA; DISTROFIA MUSCULAR; DOENÇAS CONGÊNITAS
- Language: Inglês
- Imprenta:
- Publisher place: Chippewa Falls (US)
- Date published: 2014
- Source:
- Título do periódico: Pediatric Neurology
- ISSN: 0887-8994
- Volume/Número/Paginação/Ano: v. 50, n. 4, p. 400-406, 2014
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
PASQUALIN, Lívia M. A. et al. Congenital Muscular Dystrophy With Dropped Head Linked to the LMNA Gene in a Brazilian Cohort. Pediatric Neurology, v. 50, n. 4, p. 400-406, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.pediatrneurol.2013.11.010. Acesso em: 23 abr. 2024. -
APA
Pasqualin, L. M. A., Reed, U. C., Costa, T. V. M. M., Quedas, E., Albuquerque, M. A. .V., Resende, M. B. D., et al. (2014). Congenital Muscular Dystrophy With Dropped Head Linked to the LMNA Gene in a Brazilian Cohort. Pediatric Neurology, 50( 4), 400-406. doi:10.1016/j.pediatrneurol.2013.11.010 -
NLM
Pasqualin LMA, Reed UC, Costa TVMM, Quedas E, Albuquerque MA .V, Resende MBD, Franzon RC, Rutkowski A, Chadi G, Zanoteli E. Congenital Muscular Dystrophy With Dropped Head Linked to the LMNA Gene in a Brazilian Cohort [Internet]. Pediatric Neurology. 2014 ; 50( 4): 400-406.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2013.11.010 -
Vancouver
Pasqualin LMA, Reed UC, Costa TVMM, Quedas E, Albuquerque MA .V, Resende MBD, Franzon RC, Rutkowski A, Chadi G, Zanoteli E. Congenital Muscular Dystrophy With Dropped Head Linked to the LMNA Gene in a Brazilian Cohort [Internet]. Pediatric Neurology. 2014 ; 50( 4): 400-406.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2013.11.010 - Duchenne muscular dystrophy and Duane's syndrome: a rare association [Carta]
- Spinal muscular atrophy: from animal model to clinical trial
- SMN1 gene study for diagnosis of spinal muscular atrophy (SMA)
- Multiplex PCR for identifying DMD gene deletions in children with Duchenne/Becker muscular dystrophy (DMD/BMD)
- Clinical and histological aspects in 17 Brazilian children with sarcoglycanopathy
- Congenital muscular dystrophy with intracytoplasmatic aggregates on muscle biopsy caused by mutation on LMNA gene
- Clinical aspects of patients with sarcoglycanopathies under steroids therapy
- DNM2 mutations in a cohort of sporadic patients with centronuclear myopathy
- Semiologia neuropediátrica: desenvolvimento neuropsicomotor
- Infecções congênitas
Informações sobre o DOI: 10.1016/j.pediatrneurol.2013.11.010 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
