ReP USP - Resultado da busca

Trabalho de evento-resumo periodico
Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families (2001)
Paula, Flavia de; Viegas, R.; Kai, A.; Moreira, E S; Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Nigro, Vicenzo; Zatz, Mayana
Source: European Journal of Human Genetics. Conference titles: International Congress of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PAULA, Flavia de et al. Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families. European Journal of Human Genetics. Basingstoke: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2001
APA
Paula, F. de, Viegas, R., Kai, A., Moreira, E. S., Passos-Bueno, M. R., Vainzof, M., et al. (2001). Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families. European Journal of Human Genetics. Basingstoke: Instituto de Biociências, Universidade de São Paulo.
NLM
Paula F de, Viegas R, Kai A, Moreira ES, Passos-Bueno MR, Vainzof M, Nigro V, Zatz M. Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families. European Journal of Human Genetics. 2001 ; 9 396.[citado 2024 nov. 01 ]
Vancouver
Paula F de, Viegas R, Kai A, Moreira ES, Passos-Bueno MR, Vainzof M, Nigro V, Zatz M. Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families. European Journal of Human Genetics. 2001 ; 9 396.[citado 2024 nov. 01 ]
Trabalho de evento-resumo periodico
Muscular dystrophies; same mutation but different clinical courses? The next challenge (2001)
Zatz, Mayana ; Vainzof, Mariz ; Passos-Bueno, Maria Rita
Source: European Journal of Human Genetics. Conference titles: International Congress of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana e VAINZOF, Mariz e PASSOS-BUENO, Maria Rita. Muscular dystrophies; same mutation but different clinical courses? The next challenge. European Journal of Human Genetics. Basingstoke: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2001
APA
Zatz, M., Vainzof, M., & Passos-Bueno, M. R. (2001). Muscular dystrophies; same mutation but different clinical courses? The next challenge. European Journal of Human Genetics. Basingstoke: Instituto de Biociências, Universidade de São Paulo.
NLM
Zatz M, Vainzof M, Passos-Bueno MR. Muscular dystrophies; same mutation but different clinical courses? The next challenge. European Journal of Human Genetics. 2001 ; 9 68-69.[citado 2024 nov. 01 ]
Vancouver
Zatz M, Vainzof M, Passos-Bueno MR. Muscular dystrophies; same mutation but different clinical courses? The next challenge. European Journal of Human Genetics. 2001 ; 9 68-69.[citado 2024 nov. 01 ]
Trabalho de evento-resumo periodico
Protein analysis in autosomal recessive limb-girdle muscular dystrophies (AR-Igmd) (2001)
Vainzof, Mariz ; Moreira, E S; Paula, Flavia de; Pavanello, Rita de Cássia M; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: European Journal of Human Genetics. Conference titles: International Congress of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Protein analysis in autosomal recessive limb-girdle muscular dystrophies (AR-Igmd). European Journal of Human Genetics. Basingstoke: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2001
APA
Vainzof, M., Moreira, E. S., Paula, F. de, Pavanello, R. de C. M., Passos-Bueno, M. R., & Zatz, M. (2001). Protein analysis in autosomal recessive limb-girdle muscular dystrophies (AR-Igmd). European Journal of Human Genetics. Basingstoke: Instituto de Biociências, Universidade de São Paulo.
NLM
Vainzof M, Moreira ES, Paula F de, Pavanello R de CM, Passos-Bueno MR, Zatz M. Protein analysis in autosomal recessive limb-girdle muscular dystrophies (AR-Igmd). European Journal of Human Genetics. 2001 ; 9 396.[citado 2024 nov. 01 ]
Vancouver
Vainzof M, Moreira ES, Paula F de, Pavanello R de CM, Passos-Bueno MR, Zatz M. Protein analysis in autosomal recessive limb-girdle muscular dystrophies (AR-Igmd). European Journal of Human Genetics. 2001 ; 9 396.[citado 2024 nov. 01 ]
Artigo de periodico
High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumours (2001)
Zorick, Todd S.; Mustacchi, Zan; Bando, Sílvia Yumi; Zatz, Mayana ; Moreira-Filho, Carlos Alberto; Olsen, Björn; Passos-Bueno, Maria Rita
Source: European Journal of Human Genetics. Unidade: IB
Assunto: SÍNDROME DE DOWN
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZORICK, Todd S. et al. High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumours. European Journal of Human Genetics, v. 9, p. 811-814, 2001Tradução . . Disponível em: https://doi.org/10.1038/sj.ejhg.5200721. Acesso em: 01 nov. 2024.
APA
Zorick, T. S., Mustacchi, Z., Bando, S. Y., Zatz, M., Moreira-Filho, C. A., Olsen, B., & Passos-Bueno, M. R. (2001). High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumours. European Journal of Human Genetics, 9, 811-814. doi:10.1038/sj.ejhg.5200721
NLM
Zorick TS, Mustacchi Z, Bando SY, Zatz M, Moreira-Filho CA, Olsen B, Passos-Bueno MR. High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumours [Internet]. European Journal of Human Genetics. 2001 ; 9 811-814.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/sj.ejhg.5200721
Vancouver
Zorick TS, Mustacchi Z, Bando SY, Zatz M, Moreira-Filho CA, Olsen B, Passos-Bueno MR. High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumours [Internet]. European Journal of Human Genetics. 2001 ; 9 811-814.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/sj.ejhg.5200721

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