ReP USP - Resultado da busca

Artigo de periodico
Immunological evaluation of young unvaccinated patients with Turner syndrome after COVID-19 (2023)
Castro, Mateus V. de ; Silva, Monize V. R ; Oliveira, Luana de Mendonça ; Gozzi-Silva, Sarah C; Naslavsky, Michel ; Scliar, Marilia O ; Magalhães, Monize L ; Rocha, Katia M. da ; Nunes, Kelly ; Castelli, Erick C; Magawa, Jhosiene Y; Santos, Keity S ; Cunha-Neto, Edecio ; Sato, Maria N; Zatz, Mayana
Source: International Journal of Infectious Diseases. Unidades: ICB, IB, FM
Subjects: IMUNOLOGIA, VACINAS, COVID-19, CROMOSSOMO X
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTRO, Mateus V. de et al. Immunological evaluation of young unvaccinated patients with Turner syndrome after COVID-19. International Journal of Infectious Diseases, v. 129, p. 207-215, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.ijid.2023.01.042. Acesso em: 09 ago. 2024.
APA
Castro, M. V. de, Silva, M. V. R., Oliveira, L. de M., Gozzi-Silva, S. C., Naslavsky, M., Scliar, M. O., et al. (2023). Immunological evaluation of young unvaccinated patients with Turner syndrome after COVID-19. International Journal of Infectious Diseases, 129, 207-215. doi:10.1016/j.ijid.2023.01.042
NLM
Castro MV de, Silva MVR, Oliveira L de M, Gozzi-Silva SC, Naslavsky M, Scliar MO, Magalhães ML, Rocha KM da, Nunes K, Castelli EC, Magawa JY, Santos KS, Cunha-Neto E, Sato MN, Zatz M. Immunological evaluation of young unvaccinated patients with Turner syndrome after COVID-19 [Internet]. International Journal of Infectious Diseases. 2023 ; 129 207-215.[citado 2024 ago. 09 ] Available from: https://doi.org/10.1016/j.ijid.2023.01.042
Vancouver
Castro MV de, Silva MVR, Oliveira L de M, Gozzi-Silva SC, Naslavsky M, Scliar MO, Magalhães ML, Rocha KM da, Nunes K, Castelli EC, Magawa JY, Santos KS, Cunha-Neto E, Sato MN, Zatz M. Immunological evaluation of young unvaccinated patients with Turner syndrome after COVID-19 [Internet]. International Journal of Infectious Diseases. 2023 ; 129 207-215.[citado 2024 ago. 09 ] Available from: https://doi.org/10.1016/j.ijid.2023.01.042
Artigo de periodico
Germline variants of Brazilian women with breast cancer and detection of a novel pathogenic ATM deletion in early-onset breast cancer (2021)
Bandeira, Gabriel; Rocha, Katia; Lazar, Monize; Ezquina, Suzana; Yamamoto, Guilherme ; Varela, Monica; Takahashi, Vanessa; Aguena, Meire; Gollop, Thomaz; Zatz, Mayana ; Passos-Bueno, Maria Rita ; Krepischi, Ana Cristina Victorino ; Okamoto, Oswaldo Keith
Source: Breast Cancer. Unidades: IB, BIOINFORMÁTICA, FM
Subjects: NEOPLASIAS MAMÁRIAS, NEOPLASIAS OVARIANAS, DOENÇAS HEREDITÁRIAS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BANDEIRA, Gabriel et al. Germline variants of Brazilian women with breast cancer and detection of a novel pathogenic ATM deletion in early-onset breast cancer. Breast Cancer, v. 28, n. 2, p. 346-354, 2021Tradução . . Disponível em: https://doi.org/10.1007/s12282-020-01165-1. Acesso em: 09 ago. 2024.
APA
Bandeira, G., Rocha, K., Lazar, M., Ezquina, S., Yamamoto, G., Varela, M., et al. (2021). Germline variants of Brazilian women with breast cancer and detection of a novel pathogenic ATM deletion in early-onset breast cancer. Breast Cancer, 28( 2), 346-354. doi:10.1007/s12282-020-01165-1
NLM
Bandeira G, Rocha K, Lazar M, Ezquina S, Yamamoto G, Varela M, Takahashi V, Aguena M, Gollop T, Zatz M, Passos-Bueno MR, Krepischi ACV, Okamoto OK. Germline variants of Brazilian women with breast cancer and detection of a novel pathogenic ATM deletion in early-onset breast cancer [Internet]. Breast Cancer. 2021 ; 28( 2): 346-354.[citado 2024 ago. 09 ] Available from: https://doi.org/10.1007/s12282-020-01165-1
Vancouver
Bandeira G, Rocha K, Lazar M, Ezquina S, Yamamoto G, Varela M, Takahashi V, Aguena M, Gollop T, Zatz M, Passos-Bueno MR, Krepischi ACV, Okamoto OK. Germline variants of Brazilian women with breast cancer and detection of a novel pathogenic ATM deletion in early-onset breast cancer [Internet]. Breast Cancer. 2021 ; 28( 2): 346-354.[citado 2024 ago. 09 ] Available from: https://doi.org/10.1007/s12282-020-01165-1
Artigo de periodico
Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH) (2016)
Moreira, Eloisa S; Silva, Isabela M.W; Lourenço, Naila; Moreira, Danielle P; Ribeiro, Cintia M; Martins, Ana Luiza B; Griesi-Oliveira, Karina; Lazar, Monize; Costa, Sílvia S; Naslavsky, Michel ; Rocha, Kátia M; Aguena, Meire; Fett-Conte, Agnes C; Zatz, Mayana ; Rosenberg, Carla ; Zachi, Elaine C; Bertola, Débora R; Vadasz, Estevão; Passos-Bueno, Maria Rita
Source: Research in Autism Spectrum Disorders. Unidade: IB
Subjects: AUTISMO, DOENÇAS GENÉTICAS, SEQUENCIAMENTO GENÉTICO, SEQUENCIAMENTO GENÉTICO, INTERAÇÃO SOCIAL (COMPORTAMENTO SOCIAL), TRANSTORNOS GLOBAIS DO DESENVOLVIMENTO INFANTIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOREIRA, Eloisa S et al. Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH). Research in Autism Spectrum Disorders, v. 23, p. 145-151, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.rasd.2015.12.012. Acesso em: 09 ago. 2024.
APA
Moreira, E. S., Silva, I. M. W., Lourenço, N., Moreira, D. P., Ribeiro, C. M., Martins, A. L. B., et al. (2016). Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH). Research in Autism Spectrum Disorders, 23, 145-151. doi:10.1016/j.rasd.2015.12.012
NLM
Moreira ES, Silva IMW, Lourenço N, Moreira DP, Ribeiro CM, Martins ALB, Griesi-Oliveira K, Lazar M, Costa SS, Naslavsky M, Rocha KM, Aguena M, Fett-Conte AC, Zatz M, Rosenberg C, Zachi EC, Bertola DR, Vadasz E, Passos-Bueno MR. Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH) [Internet]. Research in Autism Spectrum Disorders. 2016 ; 23 145-151.[citado 2024 ago. 09 ] Available from: https://doi.org/10.1016/j.rasd.2015.12.012
Vancouver
Moreira ES, Silva IMW, Lourenço N, Moreira DP, Ribeiro CM, Martins ALB, Griesi-Oliveira K, Lazar M, Costa SS, Naslavsky M, Rocha KM, Aguena M, Fett-Conte AC, Zatz M, Rosenberg C, Zachi EC, Bertola DR, Vadasz E, Passos-Bueno MR. Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH) [Internet]. Research in Autism Spectrum Disorders. 2016 ; 23 145-151.[citado 2024 ago. 09 ] Available from: https://doi.org/10.1016/j.rasd.2015.12.012
Artigo de periodico
Schinzel–Giedion syndrome in two Brazilian patients: report of a novel mutation in SETBP1 and literature review of the clinical features (2015)
Carvalho, Ellaine; Honjo, Rachel; Magalhães, Monize; Yamamoto, Guilherme; Rocha, Katia; Naslavsky, Michel ; Zatz, Mayana ; Passos-Bueno, Maria Rita ; Kim, Chong
Source: American Journal of Medical Genetics. Unidades: IB, FM
Subjects: GENÉTICA MÉDICA, DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARVALHO, Ellaine et al. Schinzel–Giedion syndrome in two Brazilian patients: report of a novel mutation in SETBP1 and literature review of the clinical features. American Journal of Medical Genetics, p. on-line., 2015Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.36789. Acesso em: 09 ago. 2024.
APA
Carvalho, E., Honjo, R., Magalhães, M., Yamamoto, G., Rocha, K., Naslavsky, M., et al. (2015). Schinzel–Giedion syndrome in two Brazilian patients: report of a novel mutation in SETBP1 and literature review of the clinical features. American Journal of Medical Genetics, on-line. doi:10.1002/ajmg.a.36789
NLM
Carvalho E, Honjo R, Magalhães M, Yamamoto G, Rocha K, Naslavsky M, Zatz M, Passos-Bueno MR, Kim C. Schinzel–Giedion syndrome in two Brazilian patients: report of a novel mutation in SETBP1 and literature review of the clinical features [Internet]. American Journal of Medical Genetics. 2015 ; on-line.[citado 2024 ago. 09 ] Available from: https://doi.org/10.1002/ajmg.a.36789
Vancouver
Carvalho E, Honjo R, Magalhães M, Yamamoto G, Rocha K, Naslavsky M, Zatz M, Passos-Bueno MR, Kim C. Schinzel–Giedion syndrome in two Brazilian patients: report of a novel mutation in SETBP1 and literature review of the clinical features [Internet]. American Journal of Medical Genetics. 2015 ; on-line.[citado 2024 ago. 09 ] Available from: https://doi.org/10.1002/ajmg.a.36789
Artigo de periodico
Centro de Estudos do Genoma Humano: Seis anos de experiência no diagnóstico molecular da Síndrome de Rett (2012)
Splendore, Alessandra; Rocha, Kátia Maria da; Takahashi, Vanessa Naomi Van Opstal; Zatz, Mayana ; Passos-Bueno, Maria Rita
Source: Revista Neurosciências. Unidade: IB
Subjects: SÍNDROME DE RETT, MUTAÇÃO GENÉTICA, RETARDO MENTAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SPLENDORE, Alessandra et al. Centro de Estudos do Genoma Humano: Seis anos de experiência no diagnóstico molecular da Síndrome de Rett. Revista Neurosciências, v. 20, n. 2, p. 194-199, 2012Tradução . . Disponível em: https://doi.org/10.4181/RNC.2012.20.688.6p. Acesso em: 09 ago. 2024.
APA
Splendore, A., Rocha, K. M. da, Takahashi, V. N. V. O., Zatz, M., & Passos-Bueno, M. R. (2012). Centro de Estudos do Genoma Humano: Seis anos de experiência no diagnóstico molecular da Síndrome de Rett. Revista Neurosciências, 20( 2), 194-199. doi:10.4181/RNC.2012.20.688.6p
NLM
Splendore A, Rocha KM da, Takahashi VNVO, Zatz M, Passos-Bueno MR. Centro de Estudos do Genoma Humano: Seis anos de experiência no diagnóstico molecular da Síndrome de Rett [Internet]. Revista Neurosciências. 2012 ; 20( 2): 194-199.[citado 2024 ago. 09 ] Available from: https://doi.org/10.4181/RNC.2012.20.688.6p
Vancouver
Splendore A, Rocha KM da, Takahashi VNVO, Zatz M, Passos-Bueno MR. Centro de Estudos do Genoma Humano: Seis anos de experiência no diagnóstico molecular da Síndrome de Rett [Internet]. Revista Neurosciências. 2012 ; 20( 2): 194-199.[citado 2024 ago. 09 ] Available from: https://doi.org/10.4181/RNC.2012.20.688.6p
Trabalho de evento-resumo periodico
How to deal with unexpected mutations in healthy persons (2011)
Zatz, Mayana ; Pavanello, R C M; Lazar, M; Rocha, K. M; Takahashi, V. N; Vainzof, Mariz
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: IB
Subjects: PERDA AUDITIVA, MUTAÇÃO GENÉTICA, ACONSELHAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. How to deal with unexpected mutations in healthy persons. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2011.06.823. Acesso em: 09 ago. 2024. , 2011
APA
Zatz, M., Pavanello, R. C. M., Lazar, M., Rocha, K. M., Takahashi, V. N., & Vainzof, M. (2011). How to deal with unexpected mutations in healthy persons. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. doi:10.1016/j.nmd.2011.06.823
NLM
Zatz M, Pavanello RCM, Lazar M, Rocha KM, Takahashi VN, Vainzof M. How to deal with unexpected mutations in healthy persons [Internet]. Neuromuscular Disorders. 2011 ; 21( 9-10): 660.[citado 2024 ago. 09 ] Available from: https://doi.org/10.1016/j.nmd.2011.06.823
Vancouver
Zatz M, Pavanello RCM, Lazar M, Rocha KM, Takahashi VN, Vainzof M. How to deal with unexpected mutations in healthy persons [Internet]. Neuromuscular Disorders. 2011 ; 21( 9-10): 660.[citado 2024 ago. 09 ] Available from: https://doi.org/10.1016/j.nmd.2011.06.823

USP Schools

ReP

Filtros

Authors

USP affiliated authors

Date published

Subjects

Source title

Funding Agencies

Indexado em