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Filtros : "Pasqualin, L. M." "Neuromuscular Disorders" Removido: "Gurgel Giannetti, Juliana" Limpar

Filtros

Trabalho de evento-resumo periodico
Clinical and histological aspects in 17 Brazilian children with sarcoglycanopathy (2011)
Albuquerque, M. A. V.; Martins, C. A.; Pasqualin, L. M.; Zanoteli, E.; Neto, O. L. A.; Resende, M. B. D.; Chadi, G.; Reed, U. C.
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: FM
Subjects: CRIANÇAS, BRASILEIROS, DOENÇAS NEUROMUSCULARES (DIAGNÓSTICO), BIÓPSIA, RESUMOS (EVENTOS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALBUQUERQUE, M. A. V. et al. Clinical and histological aspects in 17 Brazilian children with sarcoglycanopathy. Neuromuscular Disorders. Oxford: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2011.06.848. Acesso em: 11 nov. 2024. , 2011
APA
Albuquerque, M. A. V., Martins, C. A., Pasqualin, L. M., Zanoteli, E., Neto, O. L. A., Resende, M. B. D., et al. (2011). Clinical and histological aspects in 17 Brazilian children with sarcoglycanopathy. Neuromuscular Disorders. Oxford: Faculdade de Medicina, Universidade de São Paulo. doi:10.1016/j.nmd.2011.06.848
NLM
Albuquerque MAV, Martins CA, Pasqualin LM, Zanoteli E, Neto OLA, Resende MBD, Chadi G, Reed UC. Clinical and histological aspects in 17 Brazilian children with sarcoglycanopathy [Internet]. Neuromuscular Disorders. 2011 ; 21( 9-10): 668.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.nmd.2011.06.848
Vancouver
Albuquerque MAV, Martins CA, Pasqualin LM, Zanoteli E, Neto OLA, Resende MBD, Chadi G, Reed UC. Clinical and histological aspects in 17 Brazilian children with sarcoglycanopathy [Internet]. Neuromuscular Disorders. 2011 ; 21( 9-10): 668.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.nmd.2011.06.848
Trabalho de evento-resumo periodico
Congenital muscular dystrophy with intracytoplasmatic aggregates on muscle biopsy caused by mutation on LMNA gene (2011)
Pasqualin, L. M.; Zanoteli, E.; Albuquerque, M. A. V.; Martins, C. A.; Neto, O. L. A.; Resende, M. B. D.; Chadi, G.; Reed, U. C.
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: FM
Subjects: DISTROFIA MUSCULAR, DOENÇAS NEURODEGENERATIVAS, MUTAÇÃO GENÉTICA, RESUMOS (EVENTOS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASQUALIN, L. M. et al. Congenital muscular dystrophy with intracytoplasmatic aggregates on muscle biopsy caused by mutation on LMNA gene. Neuromuscular Disorders. Oxford: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2011.06.831. Acesso em: 11 nov. 2024. , 2011
APA
Pasqualin, L. M., Zanoteli, E., Albuquerque, M. A. V., Martins, C. A., Neto, O. L. A., Resende, M. B. D., et al. (2011). Congenital muscular dystrophy with intracytoplasmatic aggregates on muscle biopsy caused by mutation on LMNA gene. Neuromuscular Disorders. Oxford: Faculdade de Medicina, Universidade de São Paulo. doi:10.1016/j.nmd.2011.06.831
NLM
Pasqualin LM, Zanoteli E, Albuquerque MAV, Martins CA, Neto OLA, Resende MBD, Chadi G, Reed UC. Congenital muscular dystrophy with intracytoplasmatic aggregates on muscle biopsy caused by mutation on LMNA gene [Internet]. Neuromuscular Disorders. 2011 ; 21( 9-10): 663.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.nmd.2011.06.831
Vancouver
Pasqualin LM, Zanoteli E, Albuquerque MAV, Martins CA, Neto OLA, Resende MBD, Chadi G, Reed UC. Congenital muscular dystrophy with intracytoplasmatic aggregates on muscle biopsy caused by mutation on LMNA gene [Internet]. Neuromuscular Disorders. 2011 ; 21( 9-10): 663.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.nmd.2011.06.831

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