ReP USP - Resultado da busca

Trabalho de evento-resumo periodico
Identification of six new mutations on chilean population with maple syrup urine disease (2017)
Campanholi, Diana; Camelo Júnior, José Simon; Cornejo, Veronica; Schwartz, Ida V. D.; Borges, Ester; Silva Júnior, Wilson Araújo da; Campo, Karen
Source: Journal of Inborn Errors of Metabolism and Screening. Conference titles: International Congress of Inborn Errors of Metabolism. Unidade: FMRP
Subjects: GENÉTICA ANIMAL, GADO NELORE, INTERAÇÃO GENÓTIPO-AMBIENTE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAMPANHOLI, Diana et al. Identification of six new mutations on chilean population with maple syrup urine disease. Journal of Inborn Errors of Metabolism and Screening. Thousand Oaks: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 03 jun. 2024. , 2017
APA
Campanholi, D., Camelo Júnior, J. S., Cornejo, V., Schwartz, I. V. D., Borges, E., Silva Júnior, W. A. da, & Campo, K. (2017). Identification of six new mutations on chilean population with maple syrup urine disease. Journal of Inborn Errors of Metabolism and Screening. Thousand Oaks: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Campanholi D, Camelo Júnior JS, Cornejo V, Schwartz IVD, Borges E, Silva Júnior WA da, Campo K. Identification of six new mutations on chilean population with maple syrup urine disease. Journal of Inborn Errors of Metabolism and Screening. 2017 ; 5 174-175.[citado 2024 jun. 03 ]
Vancouver
Campanholi D, Camelo Júnior JS, Cornejo V, Schwartz IVD, Borges E, Silva Júnior WA da, Campo K. Identification of six new mutations on chilean population with maple syrup urine disease. Journal of Inborn Errors of Metabolism and Screening. 2017 ; 5 174-175.[citado 2024 jun. 03 ]
Trabalho de evento-resumo periodico
Case report of a LAL-D infant presentation: going beyond known boundaries (2017)
Camelo Júnior, José Simon; Monteiro, Jacqueline Pontes; Sawamura, Regina; Bicesto, Marcela; Lourenço, Charles; Gonçalves, Ana Beatriz
Source: Journal of Inborn Errors of Metabolism and Screening. Conference titles: International Congress of Inborn Errors of Metabolism. Unidade: FMRP
Assunto: ERROS INATOS DO METABOLISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAMELO JÚNIOR, José Simon et al. Case report of a LAL-D infant presentation: going beyond known boundaries. Journal of Inborn Errors of Metabolism and Screening. Thousand Oaks: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 03 jun. 2024. , 2017
APA
Camelo Júnior, J. S., Monteiro, J. P., Sawamura, R., Bicesto, M., Lourenço, C., & Gonçalves, A. B. (2017). Case report of a LAL-D infant presentation: going beyond known boundaries. Journal of Inborn Errors of Metabolism and Screening. Thousand Oaks: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Camelo Júnior JS, Monteiro JP, Sawamura R, Bicesto M, Lourenço C, Gonçalves AB. Case report of a LAL-D infant presentation: going beyond known boundaries. Journal of Inborn Errors of Metabolism and Screening. 2017 ; 5 261-262.[citado 2024 jun. 03 ]
Vancouver
Camelo Júnior JS, Monteiro JP, Sawamura R, Bicesto M, Lourenço C, Gonçalves AB. Case report of a LAL-D infant presentation: going beyond known boundaries. Journal of Inborn Errors of Metabolism and Screening. 2017 ; 5 261-262.[citado 2024 jun. 03 ]
Trabalho de evento-resumo periodico
Acute porphyrias in Brazil: the challenges in a chameleonic disorder (2009)
Lourenço, Charles Marques; Pina Neto, João Monteiro de; Mendes, Carla C.; Horta, E.; Carneiro, José; Burin, Maira; Leal, R. C.; Secchin, J.; Giugliani, Roberto; Marques Júnior, Wilson; Bandeira Neto, Abderval Pinto; Ramos, J.
Source: Molecular Genetics snd Metabolism. Conference titles: International Congress of Inborn Errors of Metabolism. Unidade: FMRP
Subjects: URINA, SISTEMA NERVOSO CENTRAL, METABOLISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOURENÇO, Charles Marques et al. Acute porphyrias in Brazil: the challenges in a chameleonic disorder. Molecular Genetics snd Metabolism. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 03 jun. 2024. , 2009
APA
Lourenço, C. M., Pina Neto, J. M. de, Mendes, C. C., Horta, E., Carneiro, J., Burin, M., et al. (2009). Acute porphyrias in Brazil: the challenges in a chameleonic disorder. Molecular Genetics snd Metabolism. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Lourenço CM, Pina Neto JM de, Mendes CC, Horta E, Carneiro J, Burin M, Leal RC, Secchin J, Giugliani R, Marques Júnior W, Bandeira Neto AP, Ramos J. Acute porphyrias in Brazil: the challenges in a chameleonic disorder. Molecular Genetics snd Metabolism. 2009 ; 98( 1-2): 140.[citado 2024 jun. 03 ]
Vancouver
Lourenço CM, Pina Neto JM de, Mendes CC, Horta E, Carneiro J, Burin M, Leal RC, Secchin J, Giugliani R, Marques Júnior W, Bandeira Neto AP, Ramos J. Acute porphyrias in Brazil: the challenges in a chameleonic disorder. Molecular Genetics snd Metabolism. 2009 ; 98( 1-2): 140.[citado 2024 jun. 03 ]
Trabalho de evento-resumo periodico
Cholelithiasis in two MPS VI patients: expanding the phenotype of maroteaux-lamy sindrome (2009)
Lourenço, Charles Marques; Neto, J. C.; Giovanetti, D. F.; Pina Neto, João Monteiro de
Source: Molecular Genetics snd Metabolism. Conference titles: International Congress of Inborn Errors of Metabolism. Unidade: FMRP
Subjects: CÁLCULOS VESICAIS, GLICOSAMINOGLICANAS, COLELITÍASE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOURENÇO, Charles Marques et al. Cholelithiasis in two MPS VI patients: expanding the phenotype of maroteaux-lamy sindrome. Molecular Genetics snd Metabolism. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 03 jun. 2024. , 2009
APA
Lourenço, C. M., Neto, J. C., Giovanetti, D. F., & Pina Neto, J. M. de. (2009). Cholelithiasis in two MPS VI patients: expanding the phenotype of maroteaux-lamy sindrome. Molecular Genetics snd Metabolism. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Lourenço CM, Neto JC, Giovanetti DF, Pina Neto JM de. Cholelithiasis in two MPS VI patients: expanding the phenotype of maroteaux-lamy sindrome. Molecular Genetics snd Metabolism. 2009 ; 98( 1-2): 71.[citado 2024 jun. 03 ]
Vancouver
Lourenço CM, Neto JC, Giovanetti DF, Pina Neto JM de. Cholelithiasis in two MPS VI patients: expanding the phenotype of maroteaux-lamy sindrome. Molecular Genetics snd Metabolism. 2009 ; 98( 1-2): 71.[citado 2024 jun. 03 ]
Trabalho de evento-resumo periodico
Genetic "metabolic" evaluation of intellectual disability: ptoposal of a standard investigation protocol for screening of inborn errors of metabolism as cause of mental retardation (2009)
Lourenço, Charles Marques; Carneiro, José; Burin, Maira; Giugliani, Roberto; Pina Neto, João Monteiro de; Marques Júnior, Wilson
Source: Molecular Genetics snd Metabolism. Conference titles: International Congress of Inborn Errors of Metabolism. Unidade: FMRP
Subjects: RETARDO MENTAL, ESCOLA ESPECIAL, CRIANÇAS, ADULTOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOURENÇO, Charles Marques et al. Genetic "metabolic" evaluation of intellectual disability: ptoposal of a standard investigation protocol for screening of inborn errors of metabolism as cause of mental retardation. Molecular Genetics snd Metabolism. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 03 jun. 2024. , 2009
APA
Lourenço, C. M., Carneiro, J., Burin, M., Giugliani, R., Pina Neto, J. M. de, & Marques Júnior, W. (2009). Genetic "metabolic" evaluation of intellectual disability: ptoposal of a standard investigation protocol for screening of inborn errors of metabolism as cause of mental retardation. Molecular Genetics snd Metabolism. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Lourenço CM, Carneiro J, Burin M, Giugliani R, Pina Neto JM de, Marques Júnior W. Genetic "metabolic" evaluation of intellectual disability: ptoposal of a standard investigation protocol for screening of inborn errors of metabolism as cause of mental retardation. Molecular Genetics snd Metabolism. 2009 ; 98( 1-2): 133-134.[citado 2024 jun. 03 ]
Vancouver
Lourenço CM, Carneiro J, Burin M, Giugliani R, Pina Neto JM de, Marques Júnior W. Genetic "metabolic" evaluation of intellectual disability: ptoposal of a standard investigation protocol for screening of inborn errors of metabolism as cause of mental retardation. Molecular Genetics snd Metabolism. 2009 ; 98( 1-2): 133-134.[citado 2024 jun. 03 ]

USP Schools

ReP

Filtros

Authors

Subjects