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Postnatal cytomegalovirus infection in very low birth weight infants fed with raw maternal milk: incidence, morbidity and correlates in a highly seropositive population (2013)
Mussi-Pinhata, Marisa Márcia; Martins-Celini, Fabia P.; Yamamoto, Aparecida Yulie; Passos, Debora M.; Nascimento, Suely D. do; Lima, Edineia V.; Di Giovanni, Celia M.; Quadrado, Ellen R. S.; Barta, Roberta; Almeida, Maria Fernanda B. de
Source: Program Guide. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FMRP
Subjects: INFECÇÕES POR CYTOMEGALOVIRUS, ALEITAMENTO MATERNO, ESTUDOS DE COORTES
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ABNT
MUSSI-PINHATA, Marisa Márcia et al. Postnatal cytomegalovirus infection in very low birth weight infants fed with raw maternal milk: incidence, morbidity and correlates in a highly seropositive population. 2013, Anais.. The Woodlands: Pediatric Academic Societies, 2013. . Acesso em: 04 out. 2024.
APA
Mussi-Pinhata, M. M., Martins-Celini, F. P., Yamamoto, A. Y., Passos, D. M., Nascimento, S. D. do, Lima, E. V., et al. (2013). Postnatal cytomegalovirus infection in very low birth weight infants fed with raw maternal milk: incidence, morbidity and correlates in a highly seropositive population. In Program Guide. The Woodlands: Pediatric Academic Societies.
NLM
Mussi-Pinhata MM, Martins-Celini FP, Yamamoto AY, Passos DM, Nascimento SD do, Lima EV, Di Giovanni CM, Quadrado ERS, Barta R, Almeida MFB de. Postnatal cytomegalovirus infection in very low birth weight infants fed with raw maternal milk: incidence, morbidity and correlates in a highly seropositive population. Program Guide. 2013 ;[citado 2024 out. 04 ]
Vancouver
Mussi-Pinhata MM, Martins-Celini FP, Yamamoto AY, Passos DM, Nascimento SD do, Lima EV, Di Giovanni CM, Quadrado ERS, Barta R, Almeida MFB de. Postnatal cytomegalovirus infection in very low birth weight infants fed with raw maternal milk: incidence, morbidity and correlates in a highly seropositive population. Program Guide. 2013 ;[citado 2024 out. 04 ]
Trabalho de evento-resumo
Cesarean section is correlated with increased body mass index in childhood in two brazilian birth cohort studies (2012)
Goldani, Helena A. S.; Gutierrez, Manoel R. P.; Bettiol, Heloisa; Silva, Antonio A. M.; Cardoso, Viviane Cunha; Barbieri, Manuela Ramos; Goldani, Marcelo Z.; Barbieri, Marco Antonio
Source: Program Guide. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FMRP
Subjects: CESÁREA (AVALIAÇÃO;RELAÇÃO), ÍNDICE DE MASSA CORPORAL, OBESIDADE, ESTUDOS DE COORTES, INFÂNCIA, CRIANÇAS
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ABNT
GOLDANI, Helena A. S. et al. Cesarean section is correlated with increased body mass index in childhood in two brazilian birth cohort studies. 2012, Anais.. The Woodlands: Pediatric Academic Societies, 2012. . Acesso em: 04 out. 2024.
APA
Goldani, H. A. S., Gutierrez, M. R. P., Bettiol, H., Silva, A. A. M., Cardoso, V. C., Barbieri, M. R., et al. (2012). Cesarean section is correlated with increased body mass index in childhood in two brazilian birth cohort studies. In Program Guide. The Woodlands: Pediatric Academic Societies.
NLM
Goldani HAS, Gutierrez MRP, Bettiol H, Silva AAM, Cardoso VC, Barbieri MR, Goldani MZ, Barbieri MA. Cesarean section is correlated with increased body mass index in childhood in two brazilian birth cohort studies. Program Guide. 2012 ;[citado 2024 out. 04 ]
Vancouver
Goldani HAS, Gutierrez MRP, Bettiol H, Silva AAM, Cardoso VC, Barbieri MR, Goldani MZ, Barbieri MA. Cesarean section is correlated with increased body mass index in childhood in two brazilian birth cohort studies. Program Guide. 2012 ;[citado 2024 out. 04 ]
Trabalho de evento-resumo
Life course risk factos for adult pre-hypertension and hypertension (2012)
Cardoso, Viviane Cunha; Ferraro, Alexandre A.; Cavalli, Ricardo de Carvalho; Silva, Antonio A. M.; Bettiol, Heloisa; Barbieri, Marco Antonio; Gandi, Carlos
Source: Program Guide. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidades: FMRP, FM
Subjects: HIPERTENSÃO, ADULTOS, FATORES DE RISCO, ANTROPOMETRIA, ESTADO NUTRICIONAL
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ABNT
CARDOSO, Viviane Cunha et al. Life course risk factos for adult pre-hypertension and hypertension. 2012, Anais.. The Woodlands: Pediatric Academic Societies, 2012. . Acesso em: 04 out. 2024.
APA
Cardoso, V. C., Ferraro, A. A., Cavalli, R. de C., Silva, A. A. M., Bettiol, H., Barbieri, M. A., & Gandi, C. (2012). Life course risk factos for adult pre-hypertension and hypertension. In Program Guide. The Woodlands: Pediatric Academic Societies.
NLM
Cardoso VC, Ferraro AA, Cavalli R de C, Silva AAM, Bettiol H, Barbieri MA, Gandi C. Life course risk factos for adult pre-hypertension and hypertension. Program Guide. 2012 ;[citado 2024 out. 04 ]
Vancouver
Cardoso VC, Ferraro AA, Cavalli R de C, Silva AAM, Bettiol H, Barbieri MA, Gandi C. Life course risk factos for adult pre-hypertension and hypertension. Program Guide. 2012 ;[citado 2024 out. 04 ]
Trabalho de evento-resumo
Assessement of vitamin A nutritional status in preterm newborn infants (2008)
Weinman, Angela M; Jorge, Salim Moyses; Martins, Antonio Roberto; Camelo, José S.; Martinez, Francisco Eulógio
Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FMRP
Subjects: VITAMINA A, RECÉM-NASCIDO
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ABNT
WEINMAN, Angela M et al. Assessement of vitamin A nutritional status in preterm newborn infants. 2008, Anais.. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2008. . Acesso em: 04 out. 2024.
APA
Weinman, A. M., Jorge, S. M., Martins, A. R., Camelo, J. S., & Martinez, F. E. (2008). Assessement of vitamin A nutritional status in preterm newborn infants. In . Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Weinman AM, Jorge SM, Martins AR, Camelo JS, Martinez FE. Assessement of vitamin A nutritional status in preterm newborn infants. 2008 ;[citado 2024 out. 04 ]
Vancouver
Weinman AM, Jorge SM, Martins AR, Camelo JS, Martinez FE. Assessement of vitamin A nutritional status in preterm newborn infants. 2008 ;[citado 2024 out. 04 ]
Trabalho de evento-resumo
Quantitation of colostrum ingested on the first day of life exclusively breast-fed healthy newborn infants (2008)
Santoro Júnior, Walter; Martinez, Francisco Eulógio
Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FMRP
Subjects: NUTRIÇÃO INFANTIL, RECÉM-NASCIDO
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ABNT
SANTORO JÚNIOR, Walter e MARTINEZ, Francisco Eulógio. Quantitation of colostrum ingested on the first day of life exclusively breast-fed healthy newborn infants. 2008, Anais.. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2008. . Acesso em: 04 out. 2024.
APA
Santoro Júnior, W., & Martinez, F. E. (2008). Quantitation of colostrum ingested on the first day of life exclusively breast-fed healthy newborn infants. In . Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Santoro Júnior W, Martinez FE. Quantitation of colostrum ingested on the first day of life exclusively breast-fed healthy newborn infants. 2008 ;[citado 2024 out. 04 ]
Vancouver
Santoro Júnior W, Martinez FE. Quantitation of colostrum ingested on the first day of life exclusively breast-fed healthy newborn infants. 2008 ;[citado 2024 out. 04 ]
Trabalho de evento-resumo periodico
Trends in prenatal care use and its association with low birthweight (LBW) in southeast Brazil (2004)
Goldani, Marcelo; Barbieri, Marco Antonio; Silva, Antônio; Bettiol, Heloísa
Source: Pediatric Research. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FMRP
Subjects: RECÉM-NASCIDO DE BAIXO PESO, CUIDADO PRÉ-NATAL
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ABNT
GOLDANI, Marcelo et al. Trends in prenatal care use and its association with low birthweight (LBW) in southeast Brazil. Pediatric Research. Philadelphia: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 2004
APA
Goldani, M., Barbieri, M. A., Silva, A., & Bettiol, H. (2004). Trends in prenatal care use and its association with low birthweight (LBW) in southeast Brazil. Pediatric Research. Philadelphia: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Goldani M, Barbieri MA, Silva A, Bettiol H. Trends in prenatal care use and its association with low birthweight (LBW) in southeast Brazil. Pediatric Research. 2004 ; 55( 4): 165A.[citado 2024 out. 04 ]
Vancouver
Goldani M, Barbieri MA, Silva A, Bettiol H. Trends in prenatal care use and its association with low birthweight (LBW) in southeast Brazil. Pediatric Research. 2004 ; 55( 4): 165A.[citado 2024 out. 04 ]
Trabalho de evento-resumo periodico
Factors associated with infant and adolescent mortality (2004)
Andrade, Zuleica; Bettiol, Heloísa; Barbieri, Marco Antonio; Gutierrez, Manoel; Godoi, Dannielle
Source: Pediatric Research. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FMRP
Subjects: MORTALIDADE INFANTIL, ADOLESCENTES (MORTALIDADE)
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ABNT
ANDRADE, Zuleica et al. Factors associated with infant and adolescent mortality. Pediatric Research. Philadelphia: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 2004
APA
Andrade, Z., Bettiol, H., Barbieri, M. A., Gutierrez, M., & Godoi, D. (2004). Factors associated with infant and adolescent mortality. Pediatric Research. Philadelphia: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Andrade Z, Bettiol H, Barbieri MA, Gutierrez M, Godoi D. Factors associated with infant and adolescent mortality. Pediatric Research. 2004 ; 55( 4): 172.[citado 2024 out. 04 ]
Vancouver
Andrade Z, Bettiol H, Barbieri MA, Gutierrez M, Godoi D. Factors associated with infant and adolescent mortality. Pediatric Research. 2004 ; 55( 4): 172.[citado 2024 out. 04 ]
Trabalho de evento-resumo periodico
Why are the low birthweight (LBW) rates in Brazil higher in richer than in poorer municipalities ?: Exploring the epidemiologic paradox of LBW (2004)
Silva, Antônio; Bettiol, Heloísa; Barbieri, Marco Antonio; Pereira, Marcio; Brito, Luiz; Ribeiro, Valdinar; Aragão, Vânia
Source: Pediatric Research. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FMRP
Subjects: RECÉM-NASCIDO DE BAIXO PESO, EPIDEMIOLOGIA
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ABNT
SILVA, Antônio et al. Why are the low birthweight (LBW) rates in Brazil higher in richer than in poorer municipalities ?: Exploring the epidemiologic paradox of LBW. Pediatric Research. Philadelphia: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 2004
APA
Silva, A., Bettiol, H., Barbieri, M. A., Pereira, M., Brito, L., Ribeiro, V., & Aragão, V. (2004). Why are the low birthweight (LBW) rates in Brazil higher in richer than in poorer municipalities ?: Exploring the epidemiologic paradox of LBW. Pediatric Research. Philadelphia: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Silva A, Bettiol H, Barbieri MA, Pereira M, Brito L, Ribeiro V, Aragão V. Why are the low birthweight (LBW) rates in Brazil higher in richer than in poorer municipalities ?: Exploring the epidemiologic paradox of LBW. Pediatric Research. 2004 ; 55( 4): 167A.[citado 2024 out. 04 ]
Vancouver
Silva A, Bettiol H, Barbieri MA, Pereira M, Brito L, Ribeiro V, Aragão V. Why are the low birthweight (LBW) rates in Brazil higher in richer than in poorer municipalities ?: Exploring the epidemiologic paradox of LBW. Pediatric Research. 2004 ; 55( 4): 167A.[citado 2024 out. 04 ]
Trabalho de evento-resumo periodico
Analysis of SP-B and SP-C gene mutation/polymorphisms in paraffin embedded lung tissue and blood fron withs severe respiratory insuficiency (2002)
Lyra, Priscila R.; Diniz, Edna Maria de Albuquerque; Vaz, Flavio Adolfo Costa; Zheng, Chunmiao; DiAngelo, Susan; Lin, Zhenwu; Floros, Joana; Hoffmann, Joseph W.; Mello, Daphne E. de
Source: Pediatric Research. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, POLIMORFISMO (GENÉTICA), INSUFICIÊNCIA RESPIRATÓRIA, CRIANÇAS
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ABNT
LYRA, Priscila R. et al. Analysis of SP-B and SP-C gene mutation/polymorphisms in paraffin embedded lung tissue and blood fron withs severe respiratory insuficiency. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 2002
APA
Lyra, P. R., Diniz, E. M. de A., Vaz, F. A. C., Zheng, C., DiAngelo, S., Lin, Z., et al. (2002). Analysis of SP-B and SP-C gene mutation/polymorphisms in paraffin embedded lung tissue and blood fron withs severe respiratory insuficiency. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.
NLM
Lyra PR, Diniz EM de A, Vaz FAC, Zheng C, DiAngelo S, Lin Z, Floros J, Hoffmann JW, Mello DE de. Analysis of SP-B and SP-C gene mutation/polymorphisms in paraffin embedded lung tissue and blood fron withs severe respiratory insuficiency. Pediatric Research. 2002 ; 51( 4): pt.2. 347A.[citado 2024 out. 04 ]
Vancouver
Lyra PR, Diniz EM de A, Vaz FAC, Zheng C, DiAngelo S, Lin Z, Floros J, Hoffmann JW, Mello DE de. Analysis of SP-B and SP-C gene mutation/polymorphisms in paraffin embedded lung tissue and blood fron withs severe respiratory insuficiency. Pediatric Research. 2002 ; 51( 4): pt.2. 347A.[citado 2024 out. 04 ]
Trabalho de evento-resumo periodico
Chronic lymphocitic thyroiditis: a 17-year follow-up (2001)
Kuperman, Hilton; Szeliga, Daniela V. M.; Passos, Leonardo D.; Lima, Thais M. R.; Manna, Thais D.; Damiani, Durval; Dichtchekenian, Vae; Setian, Nuvarte
Source: Pediatric Research. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FM
Subjects: ENDOCRINOLOGIA, PEDIATRIA, BIOLOGIA
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ABNT
KUPERMAN, Hilton et al. Chronic lymphocitic thyroiditis: a 17-year follow-up. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 2001
APA
Kuperman, H., Szeliga, D. V. M., Passos, L. D., Lima, T. M. R., Manna, T. D., Damiani, D., et al. (2001). Chronic lymphocitic thyroiditis: a 17-year follow-up. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.
NLM
Kuperman H, Szeliga DVM, Passos LD, Lima TMR, Manna TD, Damiani D, Dichtchekenian V, Setian N. Chronic lymphocitic thyroiditis: a 17-year follow-up. Pediatric Research. 2001 ; 49( 4 pt. 2): 163A. res. PI-970.[citado 2024 out. 04 ]
Vancouver
Kuperman H, Szeliga DVM, Passos LD, Lima TMR, Manna TD, Damiani D, Dichtchekenian V, Setian N. Chronic lymphocitic thyroiditis: a 17-year follow-up. Pediatric Research. 2001 ; 49( 4 pt. 2): 163A. res. PI-970.[citado 2024 out. 04 ]
Trabalho de evento-resumo periodico
Maternal uniparental disomy causing homozygosity for a dominat activating mutation in the luteinzing hormone receptor gene (2001)
Latronico, Ana Claudia; Billerbeck, Ana Elisa; Pinto, Emilia M.; D`Alva, Catarina B.; Arnhold, Ivo J. P.; Mendonca, Berenice Bilharinho
Source: Pediatric Research. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FM
Subjects: ENDOCRINOLOGIA, BIOLOGIA
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ABNT
LATRONICO, Ana Claudia et al. Maternal uniparental disomy causing homozygosity for a dominat activating mutation in the luteinzing hormone receptor gene. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 2001
APA
Latronico, A. C., Billerbeck, A. E., Pinto, E. M., D`Alva, C. B., Arnhold, I. J. P., & Mendonca, B. B. (2001). Maternal uniparental disomy causing homozygosity for a dominat activating mutation in the luteinzing hormone receptor gene. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.
NLM
Latronico AC, Billerbeck AE, Pinto EM, D`Alva CB, Arnhold IJP, Mendonca BB. Maternal uniparental disomy causing homozygosity for a dominat activating mutation in the luteinzing hormone receptor gene. Pediatric Research. 2001 ; 49( 4 pt. 2): 140A. res. PI-834.[citado 2024 out. 04 ]
Vancouver
Latronico AC, Billerbeck AE, Pinto EM, D`Alva CB, Arnhold IJP, Mendonca BB. Maternal uniparental disomy causing homozygosity for a dominat activating mutation in the luteinzing hormone receptor gene. Pediatric Research. 2001 ; 49( 4 pt. 2): 140A. res. PI-834.[citado 2024 out. 04 ]
Trabalho de evento-resumo periodico
Non-genetic male pseudohermaphroditism & reduced prenatal growth (2001)
Mendonca, Berenice Bilharinho; Billerbeck, Ana Elisa Correia; Souza, Silvia Leao; Rocha, Catarina B. D`Alva; Arnhold, Ivo Jorge Prado; Zegher, Francis de
Source: Pediatric Research. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FM
Assunto: ENDOCRINOLOGIA
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ABNT
MENDONCA, Berenice Bilharinho et al. Non-genetic male pseudohermaphroditism & reduced prenatal growth. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 2001
APA
Mendonca, B. B., Billerbeck, A. E. C., Souza, S. L., Rocha, C. B. D. `A., Arnhold, I. J. P., & Zegher, F. de. (2001). Non-genetic male pseudohermaphroditism & reduced prenatal growth. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.
NLM
Mendonca BB, Billerbeck AEC, Souza SL, Rocha CBD`A, Arnhold IJP, Zegher F de. Non-genetic male pseudohermaphroditism & reduced prenatal growth. Pediatric Research. 2001 ; 49( 4 pt. 2): 54 res. P3-320.[citado 2024 out. 04 ]
Vancouver
Mendonca BB, Billerbeck AEC, Souza SL, Rocha CBD`A, Arnhold IJP, Zegher F de. Non-genetic male pseudohermaphroditism & reduced prenatal growth. Pediatric Research. 2001 ; 49( 4 pt. 2): 54 res. P3-320.[citado 2024 out. 04 ]
Trabalho de evento-resumo periodico
Male pseudohermaphroditism associated with low birthweight (2001)
Costa, Elaine M. F.; Correa, Rafaela V.; Melo, Karla F. A. S.; Arnhold, Ivo Jorge Prado; Mendonca, Berenice Bilharinho
Source: Pediatric Research. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FM
Assunto: ENDOCRINOLOGIA
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ABNT
COSTA, Elaine M. F. et al. Male pseudohermaphroditism associated with low birthweight. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 2001
APA
Costa, E. M. F., Correa, R. V., Melo, K. F. A. S., Arnhold, I. J. P., & Mendonca, B. B. (2001). Male pseudohermaphroditism associated with low birthweight. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.
NLM
Costa EMF, Correa RV, Melo KFAS, Arnhold IJP, Mendonca BB. Male pseudohermaphroditism associated with low birthweight. Pediatric Research. 2001 ; 49( 4 pt. 2): 57A. res. P3-334.[citado 2024 out. 04 ]
Vancouver
Costa EMF, Correa RV, Melo KFAS, Arnhold IJP, Mendonca BB. Male pseudohermaphroditism associated with low birthweight. Pediatric Research. 2001 ; 49( 4 pt. 2): 57A. res. P3-334.[citado 2024 out. 04 ]
Trabalho de evento-resumo periodico
Preterm rabbitis submitted to prolonged hyperoxia as an animal model for the study of bronchopulmonary dysplasia (2001)
Proenca, Renata S. M.; Okay, Yassuhiko; Vaz, Flávio Adolfo Costa; Mauad, Thais; Rebello, Celso M.; Mataloun, Marta M. G. B.; Gibelli, Maria A. C. B.
Source: Pediatric Research. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FM
Subjects: PEDIATRIA, BRONCOPNEUMONIA ANIMAL (ESTUDO)
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ABNT
PROENCA, Renata S. M. et al. Preterm rabbitis submitted to prolonged hyperoxia as an animal model for the study of bronchopulmonary dysplasia. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 2001
APA
Proenca, R. S. M., Okay, Y., Vaz, F. A. C., Mauad, T., Rebello, C. M., Mataloun, M. M. G. B., & Gibelli, M. A. C. B. (2001). Preterm rabbitis submitted to prolonged hyperoxia as an animal model for the study of bronchopulmonary dysplasia. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.
NLM
Proenca RSM, Okay Y, Vaz FAC, Mauad T, Rebello CM, Mataloun MMGB, Gibelli MACB. Preterm rabbitis submitted to prolonged hyperoxia as an animal model for the study of bronchopulmonary dysplasia. Pediatric Research. 2001 ; 49( 4 pt. 2): 410A res. 2357.[citado 2024 out. 04 ]
Vancouver
Proenca RSM, Okay Y, Vaz FAC, Mauad T, Rebello CM, Mataloun MMGB, Gibelli MACB. Preterm rabbitis submitted to prolonged hyperoxia as an animal model for the study of bronchopulmonary dysplasia. Pediatric Research. 2001 ; 49( 4 pt. 2): 410A res. 2357.[citado 2024 out. 04 ]
Trabalho de evento-resumo periodico
Absence of inactivating mutations in the GH receptor gene (GHR) in children with idiopathic short stature (ISS) and low levels of IGFBP-3 (2001)
Jorge, Alexander A. L.; Lin, Chin J.; Souza, Silvia C. A. L.; arnhold, Ivo Jorge Prado; Mendonca, Berenice Bilharinho
Source: Pediatric Research. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FM
Assunto: ENDOCRINOLOGIA
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ABNT
JORGE, Alexander A. L. et al. Absence of inactivating mutations in the GH receptor gene (GHR) in children with idiopathic short stature (ISS) and low levels of IGFBP-3. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 2001
APA
Jorge, A. A. L., Lin, C. J., Souza, S. C. A. L., arnhold, I. J. P., & Mendonca, B. B. (2001). Absence of inactivating mutations in the GH receptor gene (GHR) in children with idiopathic short stature (ISS) and low levels of IGFBP-3. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.
NLM
Jorge AAL, Lin CJ, Souza SCAL, arnhold IJP, Mendonca BB. Absence of inactivating mutations in the GH receptor gene (GHR) in children with idiopathic short stature (ISS) and low levels of IGFBP-3. Pediatric Research. 2001 ; 49( 4 pt. 2): 69A. res. P1-407.[citado 2024 out. 04 ]
Vancouver
Jorge AAL, Lin CJ, Souza SCAL, arnhold IJP, Mendonca BB. Absence of inactivating mutations in the GH receptor gene (GHR) in children with idiopathic short stature (ISS) and low levels of IGFBP-3. Pediatric Research. 2001 ; 49( 4 pt. 2): 69A. res. P1-407.[citado 2024 out. 04 ]
Trabalho de evento-resumo periodico
Poor reproducibility of IGF-I and IGFBP-3 generation test in children with short stature (2001)
Jorge, Alexander A. L; Souza, Silvia C. A. L.; Arnhold, Ivo J. P.; Mendonca, Berenice Bilharinho
Source: Pediatric Research. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FM
Subjects: ENDOCRINOLOGIA, PEDIATRIA
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ABNT
JORGE, Alexander A. L et al. Poor reproducibility of IGF-I and IGFBP-3 generation test in children with short stature. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 2001
APA
Jorge, A. A. L., Souza, S. C. A. L., Arnhold, I. J. P., & Mendonca, B. B. (2001). Poor reproducibility of IGF-I and IGFBP-3 generation test in children with short stature. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.
NLM
Jorge AAL, Souza SCAL, Arnhold IJP, Mendonca BB. Poor reproducibility of IGF-I and IGFBP-3 generation test in children with short stature. Pediatric Research. 2001 ; 49( 4 pt. 2): 78A. res. PI-461.[citado 2024 out. 04 ]
Vancouver
Jorge AAL, Souza SCAL, Arnhold IJP, Mendonca BB. Poor reproducibility of IGF-I and IGFBP-3 generation test in children with short stature. Pediatric Research. 2001 ; 49( 4 pt. 2): 78A. res. PI-461.[citado 2024 out. 04 ]
Trabalho de evento-resumo periodico
Molecular study of 181 brazilian patients with 21-hydroxylase deficiency: identification of six new mutations (2001)
Bachega, Tania A. S. S.; Billerbeck, Ana E. C.; Madureira, Guiomar; Marcondes, Jose A. M.; Pinto, Emilia M.; Correa, Rafaela P.; Arnhold, Ivo J. P.; Mendonca, Berenice Bilharinho
Source: Pediatric Research. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FM
Subjects: ENDOCRINOLOGIA, METABOLISMO
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ABNT
BACHEGA, Tania A. S. S. et al. Molecular study of 181 brazilian patients with 21-hydroxylase deficiency: identification of six new mutations. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 2001
APA
Bachega, T. A. S. S., Billerbeck, A. E. C., Madureira, G., Marcondes, J. A. M., Pinto, E. M., Correa, R. P., et al. (2001). Molecular study of 181 brazilian patients with 21-hydroxylase deficiency: identification of six new mutations. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.
NLM
Bachega TASS, Billerbeck AEC, Madureira G, Marcondes JAM, Pinto EM, Correa RP, Arnhold IJP, Mendonca BB. Molecular study of 181 brazilian patients with 21-hydroxylase deficiency: identification of six new mutations. Pediatric Research. 2001 ; 49( 4 pt. 2): 113A. res. PI-670.[citado 2024 out. 04 ]
Vancouver
Bachega TASS, Billerbeck AEC, Madureira G, Marcondes JAM, Pinto EM, Correa RP, Arnhold IJP, Mendonca BB. Molecular study of 181 brazilian patients with 21-hydroxylase deficiency: identification of six new mutations. Pediatric Research. 2001 ; 49( 4 pt. 2): 113A. res. PI-670.[citado 2024 out. 04 ]
Trabalho de evento-resumo periodico
Detection of Y-specific sequences in 122 patients with Turner syndrome: nested PCR is not a reliable method (2001)
Nishi, Mirian Yumie; Dominice, Sorahaia; Medeiros, Maria Aparecida; Billerbeck, Ana Elisa Correia; Mendonca, Berenice Bilharinho
Source: Pediatric Research. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FM
Subjects: ENDOCRINOLOGIA, REAÇÃO EM CADEIA POR POLIMERASE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NISHI, Mirian Yumie et al. Detection of Y-specific sequences in 122 patients with Turner syndrome: nested PCR is not a reliable method. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 2001
APA
Nishi, M. Y., Dominice, S., Medeiros, M. A., Billerbeck, A. E. C., & Mendonca, B. B. (2001). Detection of Y-specific sequences in 122 patients with Turner syndrome: nested PCR is not a reliable method. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.
NLM
Nishi MY, Dominice S, Medeiros MA, Billerbeck AEC, Mendonca BB. Detection of Y-specific sequences in 122 patients with Turner syndrome: nested PCR is not a reliable method. Pediatric Research. 2001 ; 49( 4 pt. 2): 55 res. P3-325.[citado 2024 out. 04 ]
Vancouver
Nishi MY, Dominice S, Medeiros MA, Billerbeck AEC, Mendonca BB. Detection of Y-specific sequences in 122 patients with Turner syndrome: nested PCR is not a reliable method. Pediatric Research. 2001 ; 49( 4 pt. 2): 55 res. P3-325.[citado 2024 out. 04 ]
Trabalho de evento-resumo periodico
Diagnotic value of ultrasensitive immunofluorometric gonadotropin assays in hypogonadotropic hypogonadism (2001)
Costa, Elaine M. F.; Mendonca, Berenice Bilharinho; Latronico, Ana Claudia; Arnhold, Ivo J. P.
Source: Pediatric Research. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FM
Subjects: ENDOCRINOLOGIA, GONADOTROFINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COSTA, Elaine M. F. et al. Diagnotic value of ultrasensitive immunofluorometric gonadotropin assays in hypogonadotropic hypogonadism. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 2001
APA
Costa, E. M. F., Mendonca, B. B., Latronico, A. C., & Arnhold, I. J. P. (2001). Diagnotic value of ultrasensitive immunofluorometric gonadotropin assays in hypogonadotropic hypogonadism. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.
NLM
Costa EMF, Mendonca BB, Latronico AC, Arnhold IJP. Diagnotic value of ultrasensitive immunofluorometric gonadotropin assays in hypogonadotropic hypogonadism. Pediatric Research. 2001 ; 49( 4 pt. 2): 138A. res. PI-823.[citado 2024 out. 04 ]
Vancouver
Costa EMF, Mendonca BB, Latronico AC, Arnhold IJP. Diagnotic value of ultrasensitive immunofluorometric gonadotropin assays in hypogonadotropic hypogonadism. Pediatric Research. 2001 ; 49( 4 pt. 2): 138A. res. PI-823.[citado 2024 out. 04 ]
Trabalho de evento-resumo periodico
Nephrogenic diabetes insipidus associated with two different AVP type-2 receptor mutations (2001)
Manna, Thais D.; Guedes, Dulce R.; Damiani, Durval; Setian, Nuvarte; Sarubi, Juliana C.; Boson, Wolfanga; Marco, Luis A. de
Source: Pediatric Research. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FM
Assunto: PEDIATRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MANNA, Thais D. et al. Nephrogenic diabetes insipidus associated with two different AVP type-2 receptor mutations. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 2001
APA
Manna, T. D., Guedes, D. R., Damiani, D., Setian, N., Sarubi, J. C., Boson, W., & Marco, L. A. de. (2001). Nephrogenic diabetes insipidus associated with two different AVP type-2 receptor mutations. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.
NLM
Manna TD, Guedes DR, Damiani D, Setian N, Sarubi JC, Boson W, Marco LA de. Nephrogenic diabetes insipidus associated with two different AVP type-2 receptor mutations. Pediatric Research. 2001 ; 49( 4 pt. 2): 60A. res. P3-357.[citado 2024 out. 04 ]
Vancouver
Manna TD, Guedes DR, Damiani D, Setian N, Sarubi JC, Boson W, Marco LA de. Nephrogenic diabetes insipidus associated with two different AVP type-2 receptor mutations. Pediatric Research. 2001 ; 49( 4 pt. 2): 60A. res. P3-357.[citado 2024 out. 04 ]

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