ReP USP - Resultado da busca

Artigo de periodico
Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD) (2004)
Tonini, M. M. O.; Passos-Bueno, Maria Rita ; Cerqueira, A.; Matioli, Sergio Russo ; Pavanello, Rita de Cássia M.; Zatz, Mayana
Source: Neuromuscular Disorders. Unidade: IB
Subjects: BIOLOGIA, GENÉTICA MÉDICA, MALFORMAÇÕES, DOENÇAS MUSCULOSQUELÉTICAS, DOENÇAS NEUROMUSCULARES, DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TONINI, M. M. O. et al. Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD). Neuromuscular Disorders, v. 14, n. 1, p. 33-38, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2003.07.001. Acesso em: 17 jul. 2024.
APA
Tonini, M. M. O., Passos-Bueno, M. R., Cerqueira, A., Matioli, S. R., Pavanello, R. de C. M., & Zatz, M. (2004). Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD). Neuromuscular Disorders, 14( 1), 33-38. doi:10.1016/j.nmd.2003.07.001
NLM
Tonini MMO, Passos-Bueno MR, Cerqueira A, Matioli SR, Pavanello R de CM, Zatz M. Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD) [Internet]. Neuromuscular Disorders. 2004 ; 14( 1): 33-38.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1016/j.nmd.2003.07.001
Vancouver
Tonini MMO, Passos-Bueno MR, Cerqueira A, Matioli SR, Pavanello R de CM, Zatz M. Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD) [Internet]. Neuromuscular Disorders. 2004 ; 14( 1): 33-38.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1016/j.nmd.2003.07.001
Artigo de periodico
Calpainopathy: focus on a pediatric population (2003)
Kolski, H.; Edmonton, A. B.; Vajsar, J.; Paula, F de; Zatz, Mayana
Source: Journal of Child Neurology. Unidade: IB
Subjects: DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KOLSKI, H. et al. Calpainopathy: focus on a pediatric population. Journal of Child Neurology, v. 18, n. 3, p. 212, 2003Tradução . . Acesso em: 17 jul. 2024.
APA
Kolski, H., Edmonton, A. B., Vajsar, J., Paula, F. de, & Zatz, M. (2003). Calpainopathy: focus on a pediatric population. Journal of Child Neurology, 18( 3), 212.
NLM
Kolski H, Edmonton AB, Vajsar J, Paula F de, Zatz M. Calpainopathy: focus on a pediatric population. Journal of Child Neurology. 2003 ; 18( 3): 212.[citado 2024 jul. 17 ]
Vancouver
Kolski H, Edmonton AB, Vajsar J, Paula F de, Zatz M. Calpainopathy: focus on a pediatric population. Journal of Child Neurology. 2003 ; 18( 3): 212.[citado 2024 jul. 17 ]
Artigo de periodico
The 10 autosomal recessive limb-girdle muscular dystrophies (2003)
Zatz, Mayana ; Paula, Flavia de; Starling, Alessandra; Vainzof, Mariz
Source: Neuromuscular Disorders. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. The 10 autosomal recessive limb-girdle muscular dystrophies. Neuromuscular Disorders, v. 13, n. 7-8, p. 532-544, 2003Tradução . . Disponível em: https://doi.org/10.1016/s0960-8966(03)00100-7. Acesso em: 17 jul. 2024.
APA
Zatz, M., Paula, F. de, Starling, A., & Vainzof, M. (2003). The 10 autosomal recessive limb-girdle muscular dystrophies. Neuromuscular Disorders, 13( 7-8), 532-544. doi:10.1016/s0960-8966(03)00100-7
NLM
Zatz M, Paula F de, Starling A, Vainzof M. The 10 autosomal recessive limb-girdle muscular dystrophies [Internet]. Neuromuscular Disorders. 2003 ; 13( 7-8): 532-544.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1016/s0960-8966(03)00100-7
Vancouver
Zatz M, Paula F de, Starling A, Vainzof M. The 10 autosomal recessive limb-girdle muscular dystrophies [Internet]. Neuromuscular Disorders. 2003 ; 13( 7-8): 532-544.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1016/s0960-8966(03)00100-7
Artigo de periodico
Telethonin protein expression in neuromuscular disorders (2002)
Vainzof, Mariz ; Moreira, Eloisa S.; Suzuki, Oscar T.; Faulkner, Georgine; Valle, Georgio; Beggs, Alan H.; Carpen, Olli; Ribeiro, Alberto de Freitas ; Zanoteli, Edmar; Gurgel-Gianneti, Juliana; Tsanaclis, Ana Maria Crous; Silva, Helga Cristina Almeida da; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Biochimica et Biophysica Acta. Unidades: IB, FM
Subjects: DISTROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Telethonin protein expression in neuromuscular disorders. Biochimica et Biophysica Acta, v. 1588, n. 1, p. 33-40, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0925-4439(02)00113-8. Acesso em: 17 jul. 2024.
APA
Vainzof, M., Moreira, E. S., Suzuki, O. T., Faulkner, G., Valle, G., Beggs, A. H., et al. (2002). Telethonin protein expression in neuromuscular disorders. Biochimica et Biophysica Acta, 1588( 1), 33-40. doi:10.1016/s0925-4439(02)00113-8
NLM
Vainzof M, Moreira ES, Suzuki OT, Faulkner G, Valle G, Beggs AH, Carpen O, Ribeiro A de F, Zanoteli E, Gurgel-Gianneti J, Tsanaclis AMC, Silva HCA da, Passos-Bueno MR, Zatz M. Telethonin protein expression in neuromuscular disorders [Internet]. Biochimica et Biophysica Acta. 2002 ; 1588( 1): 33-40.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1016/s0925-4439(02)00113-8
Vancouver
Vainzof M, Moreira ES, Suzuki OT, Faulkner G, Valle G, Beggs AH, Carpen O, Ribeiro A de F, Zanoteli E, Gurgel-Gianneti J, Tsanaclis AMC, Silva HCA da, Passos-Bueno MR, Zatz M. Telethonin protein expression in neuromuscular disorders [Internet]. Biochimica et Biophysica Acta. 2002 ; 1588( 1): 33-40.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1016/s0925-4439(02)00113-8
Artigo de periodico
Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? (2002)
Tonini, M. M. O.; Passos-Bueno, Maria Rita ; Cerqueira, A.; Pavanello, Rita de Cássia M.; Vainzof, Mariz ; Dubowitz, Victor; Zatz, Mayana
Source: Neuromuscular Disorders. Unidade: IB
Assunto: DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TONINI, M. M. O. et al. Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye?. Neuromuscular Disorders, v. 12, n. 6, p. 554-557, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0960-8966(02)00014-7. Acesso em: 17 jul. 2024.
APA
Tonini, M. M. O., Passos-Bueno, M. R., Cerqueira, A., Pavanello, R. de C. M., Vainzof, M., Dubowitz, V., & Zatz, M. (2002). Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? Neuromuscular Disorders, 12( 6), 554-557. doi:10.1016/s0960-8966(02)00014-7
NLM
Tonini MMO, Passos-Bueno MR, Cerqueira A, Pavanello R de CM, Vainzof M, Dubowitz V, Zatz M. Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? [Internet]. Neuromuscular Disorders. 2002 ; 12( 6): 554-557.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1016/s0960-8966(02)00014-7
Vancouver
Tonini MMO, Passos-Bueno MR, Cerqueira A, Pavanello R de CM, Vainzof M, Dubowitz V, Zatz M. Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? [Internet]. Neuromuscular Disorders. 2002 ; 12( 6): 554-557.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1016/s0960-8966(02)00014-7
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: 17 jul. 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 jul. 17 ] 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 jul. 17 ] Available from: https://doi.org/10.1038/sj.ejhg.5200721
Artigo de periodico
Genetic counseling for childless women at risk for Duchenne muscular dystrophy (1999)
Eggers, Sabine; Pavanello, Rita de Cássia M.; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: GENÉTICA MÉDICA, DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
EGGERS, Sabine et al. Genetic counseling for childless women at risk for Duchenne muscular dystrophy. American Journal of Medical Genetics, v. 86, p. 447-453, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p. Acesso em: 17 jul. 2024.
APA
Eggers, S., Pavanello, R. de C. M., Passos-Bueno, M. R., & Zatz, M. (1999). Genetic counseling for childless women at risk for Duchenne muscular dystrophy. American Journal of Medical Genetics, 86, 447-453. doi:10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p
NLM
Eggers S, Pavanello R de CM, Passos-Bueno MR, Zatz M. Genetic counseling for childless women at risk for Duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1999 ; 86 447-453.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p
Vancouver
Eggers S, Pavanello R de CM, Passos-Bueno MR, Zatz M. Genetic counseling for childless women at risk for Duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1999 ; 86 447-453.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p

USP Schools

ReP

Filtros

Authors

USP affiliated authors

Subjects

Non normalized affiliation