ReP USP - Resultado da busca

Parte de monografia/livro
Host genetic susceptibility to ZIKV congenital syndrome: a tale of twins (2021)
Caires Junior, Luiz Carlos de; Goulart, Ernesto ; Zatz, Mayana
Source: Zika Virus Biology, Transmission, and Pathways: The Neuroscience of Zika. Unidades: IEE, IB
Subjects: GÊMEOS, ZIKA VÍRUS, GENÉTICA, MICROCEFALIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAIRES JUNIOR, Luiz Carlos de e GOULART, Ernesto e ZATZ, Mayana. Host genetic susceptibility to ZIKV congenital syndrome: a tale of twins. Zika Virus Biology, Transmission, and Pathways: The Neuroscience of Zika. Tradução . Cambridge: Instituto de Energia e Ambiente, Universidade de São Paulo, 2021. v. 1. p. 179-187. Disponível em: https://doi.org/10.1016/B978-0-12-820268-5.00016-X. Acesso em: 27 set. 2024.
APA
Caires Junior, L. C. de, Goulart, E., & Zatz, M. (2021). Host genetic susceptibility to ZIKV congenital syndrome: a tale of twins. In Zika Virus Biology, Transmission, and Pathways: The Neuroscience of Zika (Vol. 1, p. 179-187). Cambridge: Instituto de Energia e Ambiente, Universidade de São Paulo. doi:10.1016/B978-0-12-820268-5.00016-X
NLM
Caires Junior LC de, Goulart E, Zatz M. Host genetic susceptibility to ZIKV congenital syndrome: a tale of twins [Internet]. In: Zika Virus Biology, Transmission, and Pathways: The Neuroscience of Zika. Cambridge: Instituto de Energia e Ambiente, Universidade de São Paulo; 2021. p. 179-187.[citado 2024 set. 27 ] Available from: https://doi.org/10.1016/B978-0-12-820268-5.00016-X
Vancouver
Caires Junior LC de, Goulart E, Zatz M. Host genetic susceptibility to ZIKV congenital syndrome: a tale of twins [Internet]. In: Zika Virus Biology, Transmission, and Pathways: The Neuroscience of Zika. Cambridge: Instituto de Energia e Ambiente, Universidade de São Paulo; 2021. p. 179-187.[citado 2024 set. 27 ] Available from: https://doi.org/10.1016/B978-0-12-820268-5.00016-X
Parte de monografia/livro
Mayana Zatz: Brazil [Entrevista a Lucia Mendonça Previato] (2013)
Zatz, Mayana
Source: Women Scientists in the Americas. Their inspiring stories. Unidade: IB
Subjects: ENTREVISTA JORNALÍSTICA, MULHERES NA CIÊNCIA, CÉLULAS-TRONCO, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana. Mayana Zatz: Brazil [Entrevista a Lucia Mendonça Previato]. Women Scientists in the Americas. Their inspiring stories. Tradução . Tlalpan: IANAS, 2013. . Disponível em: http://www.nationalacademies.org/includes/IANAS%20Book.pdf. Acesso em: 27 set. 2024.
APA
Zatz, M. (2013). Mayana Zatz: Brazil [Entrevista a Lucia Mendonça Previato]. In Women Scientists in the Americas. Their inspiring stories. Tlalpan: IANAS. Recuperado de http://www.nationalacademies.org/includes/IANAS%20Book.pdf
NLM
Zatz M. Mayana Zatz: Brazil [Entrevista a Lucia Mendonça Previato] [Internet]. In: Women Scientists in the Americas. Their inspiring stories. Tlalpan: IANAS; 2013. [citado 2024 set. 27 ] Available from: http://www.nationalacademies.org/includes/IANAS%20Book.pdf
Vancouver
Zatz M. Mayana Zatz: Brazil [Entrevista a Lucia Mendonça Previato] [Internet]. In: Women Scientists in the Americas. Their inspiring stories. Tlalpan: IANAS; 2013. [citado 2024 set. 27 ] Available from: http://www.nationalacademies.org/includes/IANAS%20Book.pdf
Parte de monografia/livro
Muscular dystrophies and protein mutations (2007)
Vainzof, Mariz ; Zatz, Mayana
Source: Protein misfolding, aggregation, and conformational diseases. Part B: molecular mechanisms of conformational diseases. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES, MUTAÇÃO GENÉTICA, PROTEÍNAS MUSCULARES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz e ZATZ, Mayana. Muscular dystrophies and protein mutations. Protein misfolding, aggregation, and conformational diseases. Part B: molecular mechanisms of conformational diseases. Tradução . New York: Springer Science, 2007. . . Acesso em: 27 set. 2024.
APA
Vainzof, M., & Zatz, M. (2007). Muscular dystrophies and protein mutations. In Protein misfolding, aggregation, and conformational diseases. Part B: molecular mechanisms of conformational diseases. New York: Springer Science.
NLM
Vainzof M, Zatz M. Muscular dystrophies and protein mutations. In: Protein misfolding, aggregation, and conformational diseases. Part B: molecular mechanisms of conformational diseases. New York: Springer Science; 2007. [citado 2024 set. 27 ]
Vancouver
Vainzof M, Zatz M. Muscular dystrophies and protein mutations. In: Protein misfolding, aggregation, and conformational diseases. Part B: molecular mechanisms of conformational diseases. New York: Springer Science; 2007. [citado 2024 set. 27 ]
Parte de monografia/livro
Facioscapulohumel muscular dystrophy: gender differences and genetic counselling in a complex disorder (2004)
Tonini, Maria Manuela de Oliveira; Zatz, Mayana
Source: FSHD facioscapulohumel muscular dystrophy: clinical medicine and molecular cell biology. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TONINI, Maria Manuela de Oliveira e ZATZ, Mayana. Facioscapulohumel muscular dystrophy: gender differences and genetic counselling in a complex disorder. FSHD facioscapulohumel muscular dystrophy: clinical medicine and molecular cell biology. Tradução . London: BIOS Scientific Publishers, 2004. . . Acesso em: 27 set. 2024.
APA
Tonini, M. M. de O., & Zatz, M. (2004). Facioscapulohumel muscular dystrophy: gender differences and genetic counselling in a complex disorder. In FSHD facioscapulohumel muscular dystrophy: clinical medicine and molecular cell biology. London: BIOS Scientific Publishers.
NLM
Tonini MM de O, Zatz M. Facioscapulohumel muscular dystrophy: gender differences and genetic counselling in a complex disorder. In: FSHD facioscapulohumel muscular dystrophy: clinical medicine and molecular cell biology. London: BIOS Scientific Publishers; 2004. [citado 2024 set. 27 ]
Vancouver
Tonini MM de O, Zatz M. Facioscapulohumel muscular dystrophy: gender differences and genetic counselling in a complex disorder. In: FSHD facioscapulohumel muscular dystrophy: clinical medicine and molecular cell biology. London: BIOS Scientific Publishers; 2004. [citado 2024 set. 27 ]
Parte de monografia/livro
Immunological methods for the analysis of protein expression in neuromuscular diseases (2003)
Vainzof, Mariz ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Neurogenetics : methods and protocols. Methods in molecular biology, v. 217. Unidade: IB
Subjects: DISTROFIA MUSCULAR, GENÓTIPOS, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz e PASSOS-BUENO, Maria Rita e ZATZ, Mayana. Immunological methods for the analysis of protein expression in neuromuscular diseases. Neurogenetics : methods and protocols. Methods in molecular biology, v. 217. Tradução . Totowa, N.J.: Humana Press, 2003. . . Acesso em: 27 set. 2024.
APA
Vainzof, M., Passos-Bueno, M. R., & Zatz, M. (2003). Immunological methods for the analysis of protein expression in neuromuscular diseases. In Neurogenetics : methods and protocols. Methods in molecular biology, v. 217. Totowa, N.J.: Humana Press.
NLM
Vainzof M, Passos-Bueno MR, Zatz M. Immunological methods for the analysis of protein expression in neuromuscular diseases. In: Neurogenetics : methods and protocols. Methods in molecular biology, v. 217. Totowa, N.J.: Humana Press; 2003. [citado 2024 set. 27 ]
Vancouver
Vainzof M, Passos-Bueno MR, Zatz M. Immunological methods for the analysis of protein expression in neuromuscular diseases. In: Neurogenetics : methods and protocols. Methods in molecular biology, v. 217. Totowa, N.J.: Humana Press; 2003. [citado 2024 set. 27 ]
Parte de monografia/livro
Human prion protein gene mutation at codon 183 associated with an atypical form of prion disease (1998)
Nitrini, Ricardo; Rosemberg, Sérgio; Passos-Bueno, Maria Rita ; Silva, Luís S Teixeira; Iughetti, Paula; Papadopoulos, Maria; Carrilho, P M; Caramelli, Paulo; Albrecht, Steffen; Zatz, Mayana ; LeBanc, Andréa
Source: Prions and brain diseases in animals and humans. Unidades: FM, IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NITRINI, Ricardo et al. Human prion protein gene mutation at codon 183 associated with an atypical form of prion disease. Prions and brain diseases in animals and humans. Tradução . New York: Plenum Press, 1998. . . Acesso em: 27 set. 2024.
APA
Nitrini, R., Rosemberg, S., Passos-Bueno, M. R., Silva, L. S. T., Iughetti, P., Papadopoulos, M., et al. (1998). Human prion protein gene mutation at codon 183 associated with an atypical form of prion disease. In Prions and brain diseases in animals and humans. New York: Plenum Press.
NLM
Nitrini R, Rosemberg S, Passos-Bueno MR, Silva LST, Iughetti P, Papadopoulos M, Carrilho PM, Caramelli P, Albrecht S, Zatz M, LeBanc A. Human prion protein gene mutation at codon 183 associated with an atypical form of prion disease. In: Prions and brain diseases in animals and humans. New York: Plenum Press; 1998. [citado 2024 set. 27 ]
Vancouver
Nitrini R, Rosemberg S, Passos-Bueno MR, Silva LST, Iughetti P, Papadopoulos M, Carrilho PM, Caramelli P, Albrecht S, Zatz M, LeBanc A. Human prion protein gene mutation at codon 183 associated with an atypical form of prion disease. In: Prions and brain diseases in animals and humans. New York: Plenum Press; 1998. [citado 2024 set. 27 ]
Parte de monografia/livro
Genetic and linkage analysis in autosomal recessive limb-girdle muscular dystrophy (1996)
Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Zatz, Mayana
Source: Handbook of Muscle Disease. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita e VAINZOF, Mariz e ZATZ, Mayana. Genetic and linkage analysis in autosomal recessive limb-girdle muscular dystrophy. Handbook of Muscle Disease. Tradução . New York: Marcel Dekker, 1996. . . Acesso em: 27 set. 2024.
APA
Passos-Bueno, M. R., Vainzof, M., & Zatz, M. (1996). Genetic and linkage analysis in autosomal recessive limb-girdle muscular dystrophy. In Handbook of Muscle Disease. New York: Marcel Dekker.
NLM
Passos-Bueno MR, Vainzof M, Zatz M. Genetic and linkage analysis in autosomal recessive limb-girdle muscular dystrophy. In: Handbook of Muscle Disease. New York: Marcel Dekker; 1996. [citado 2024 set. 27 ]
Vancouver
Passos-Bueno MR, Vainzof M, Zatz M. Genetic and linkage analysis in autosomal recessive limb-girdle muscular dystrophy. In: Handbook of Muscle Disease. New York: Marcel Dekker; 1996. [citado 2024 set. 27 ]
Parte de monografia/livro
Autosomal recessive limb-girdle muscular dystrophies (1996)
Zatz, Mayana ; Vainzof, Mariz ; Passos-Bueno, Maria Rita ; Akiyama, J; Marie, Suely Kazue Nagahashi
Source: Handbook of Muscle Disease. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. Autosomal recessive limb-girdle muscular dystrophies. Handbook of Muscle Disease. Tradução . New York: Marcel Dekker, 1996. . . Acesso em: 27 set. 2024.
APA
Zatz, M., Vainzof, M., Passos-Bueno, M. R., Akiyama, J., & Marie, S. K. N. (1996). Autosomal recessive limb-girdle muscular dystrophies. In Handbook of Muscle Disease. New York: Marcel Dekker.
NLM
Zatz M, Vainzof M, Passos-Bueno MR, Akiyama J, Marie SKN. Autosomal recessive limb-girdle muscular dystrophies. In: Handbook of Muscle Disease. New York: Marcel Dekker; 1996. [citado 2024 set. 27 ]
Vancouver
Zatz M, Vainzof M, Passos-Bueno MR, Akiyama J, Marie SKN. Autosomal recessive limb-girdle muscular dystrophies. In: Handbook of Muscle Disease. New York: Marcel Dekker; 1996. [citado 2024 set. 27 ]
Parte de monografia/livro
Distrophin and dna findings in duchenne and becker carriers (1996)
Vainzof, Mariz ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Handbook of Muscle Disease. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz e PASSOS-BUENO, Maria Rita e ZATZ, Mayana. Distrophin and dna findings in duchenne and becker carriers. Handbook of Muscle Disease. Tradução . New York: Marcel Dekker, 1996. . . Acesso em: 27 set. 2024.
APA
Vainzof, M., Passos-Bueno, M. R., & Zatz, M. (1996). Distrophin and dna findings in duchenne and becker carriers. In Handbook of Muscle Disease. New York: Marcel Dekker.
NLM
Vainzof M, Passos-Bueno MR, Zatz M. Distrophin and dna findings in duchenne and becker carriers. In: Handbook of Muscle Disease. New York: Marcel Dekker; 1996. [citado 2024 set. 27 ]
Vancouver
Vainzof M, Passos-Bueno MR, Zatz M. Distrophin and dna findings in duchenne and becker carriers. In: Handbook of Muscle Disease. New York: Marcel Dekker; 1996. [citado 2024 set. 27 ]
Parte de monografia/livro
New and unexpected findings following dna and dystrophin studies in brazilian dmd / bmd patients (1993)
Zatz, Mayana ; Vainzof, Mariz ; Passos-Bueno, Maria Rita
Source: Systeme Nerveux, Muscles et Maladies Systemiques. 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. New and unexpected findings following dna and dystrophin studies in brazilian dmd / bmd patients. Systeme Nerveux, Muscles et Maladies Systemiques. Tradução . Paris: Expansion Scientifique Francaise, 1993. . . Acesso em: 27 set. 2024.
APA
Zatz, M., Vainzof, M., & Passos-Bueno, M. R. (1993). New and unexpected findings following dna and dystrophin studies in brazilian dmd / bmd patients. In Systeme Nerveux, Muscles et Maladies Systemiques. Paris: Expansion Scientifique Francaise.
NLM
Zatz M, Vainzof M, Passos-Bueno MR. New and unexpected findings following dna and dystrophin studies in brazilian dmd / bmd patients. In: Systeme Nerveux, Muscles et Maladies Systemiques. Paris: Expansion Scientifique Francaise; 1993. [citado 2024 set. 27 ]
Vancouver
Zatz M, Vainzof M, Passos-Bueno MR. New and unexpected findings following dna and dystrophin studies in brazilian dmd / bmd patients. In: Systeme Nerveux, Muscles et Maladies Systemiques. Paris: Expansion Scientifique Francaise; 1993. [citado 2024 set. 27 ]
Parte de monografia/livro
Mazindol and growth-hormone in duchenne dystrophy (1989)
Zatz, Mayana ; Rapaport, D; Vainzof, Mariz ; Pavanello, R C M; Rocha, J M L; Otto, Paulo A
Source: Myelopathies, Neuropathies et Myopathis: Acquisitions Recents; Advances in Neuromuscular Diseases. Unidade: IB
Subjects: DISTROFIA MUSCULAR, HORMÔNIO DO CRESCIMENTO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. Mazindol and growth-hormone in duchenne dystrophy. Myelopathies, Neuropathies et Myopathis: Acquisitions Recents; Advances in Neuromuscular Diseases. Tradução . Paris: Expansion Scientifique Francaise, 1989. . . Acesso em: 27 set. 2024.
APA
Zatz, M., Rapaport, D., Vainzof, M., Pavanello, R. C. M., Rocha, J. M. L., & Otto, P. A. (1989). Mazindol and growth-hormone in duchenne dystrophy. In Myelopathies, Neuropathies et Myopathis: Acquisitions Recents; Advances in Neuromuscular Diseases. Paris: Expansion Scientifique Francaise.
NLM
Zatz M, Rapaport D, Vainzof M, Pavanello RCM, Rocha JML, Otto PA. Mazindol and growth-hormone in duchenne dystrophy. In: Myelopathies, Neuropathies et Myopathis: Acquisitions Recents; Advances in Neuromuscular Diseases. Paris: Expansion Scientifique Francaise; 1989. [citado 2024 set. 27 ]
Vancouver
Zatz M, Rapaport D, Vainzof M, Pavanello RCM, Rocha JML, Otto PA. Mazindol and growth-hormone in duchenne dystrophy. In: Myelopathies, Neuropathies et Myopathis: Acquisitions Recents; Advances in Neuromuscular Diseases. Paris: Expansion Scientifique Francaise; 1989. [citado 2024 set. 27 ]

USP Schools

ReP

Filtros

Authors

USP affiliated authors

Date published

Subjects

Source title

Publisher