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Trabalho de evento-resumo periodico
Novel Mutations in the Growth Hormone Secretagogue Receptor Gene (GHSR) Associated with Constitutional Delay in Growth and Puberty (CDGP) (2010)
Pugliese-Pires, P. N.; Fortin, J.P.; Zhu , Y.; Mendonça, B. B.; Arnhold, I. J. P.; Kopin, A.; Jorge, A. A. L.
Source: Hormone Research in Paediatrics. Conference titles: Annual meeting of the Sociedad Latino-Americana de Endocrinología Pediátrica (SLEP). Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, HORMÔNIO DE CRESCIMENTO, PUBERDADE, GENES (SECREÇÃO)
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ABNT
PUGLIESE-PIRES, P. N. et al. Novel Mutations in the Growth Hormone Secretagogue Receptor Gene (GHSR) Associated with Constitutional Delay in Growth and Puberty (CDGP). Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf. Acesso em: 13 jun. 2024. , 2010
APA
Pugliese-Pires, P. N., Fortin, J. P., Zhu , Y., Mendonça, B. B., Arnhold, I. J. P., Kopin, A., & Jorge, A. A. L. (2010). Novel Mutations in the Growth Hormone Secretagogue Receptor Gene (GHSR) Associated with Constitutional Delay in Growth and Puberty (CDGP). Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
NLM
Pugliese-Pires PN, Fortin JP, Zhu Y, Mendonça BB, Arnhold IJP, Kopin A, Jorge AAL. Novel Mutations in the Growth Hormone Secretagogue Receptor Gene (GHSR) Associated with Constitutional Delay in Growth and Puberty (CDGP) [Internet]. Hormone Research in Paediatrics. 2010 ; 74( suppl. 1): 1.[citado 2024 jun. 13 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Vancouver
Pugliese-Pires PN, Fortin JP, Zhu Y, Mendonça BB, Arnhold IJP, Kopin A, Jorge AAL. Novel Mutations in the Growth Hormone Secretagogue Receptor Gene (GHSR) Associated with Constitutional Delay in Growth and Puberty (CDGP) [Internet]. Hormone Research in Paediatrics. 2010 ; 74( suppl. 1): 1.[citado 2024 jun. 13 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Trabalho de evento-resumo periodico
A Novel Mutation in CBX2 Gene in a Brazilian Patient with 46,XY Disorders of Sex Development (DSD) Due to Gonadal Dysgenesis (2010)
Gomes, C. R.; Domenice, S.; Mendonça, B. B.; Arnhold, I. J. P.; Costa, E. M. F.
Source: Hormone Research in Paediatrics. Conference titles: Annual meeting of the Sociedad Latino-Americana de Endocrinología Pediátrica (SLEP). Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, TRANSTORNOS GONADAIS (FISIOPATOLOGIA), DESENVOLVIMENTO PSICOSSEXUAL, POLIMORFISMO, GENES (ANÁLISE)
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ABNT
GOMES, C. R. et al. A Novel Mutation in CBX2 Gene in a Brazilian Patient with 46,XY Disorders of Sex Development (DSD) Due to Gonadal Dysgenesis. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf. Acesso em: 13 jun. 2024. , 2010
APA
Gomes, C. R., Domenice, S., Mendonça, B. B., Arnhold, I. J. P., & Costa, E. M. F. (2010). A Novel Mutation in CBX2 Gene in a Brazilian Patient with 46,XY Disorders of Sex Development (DSD) Due to Gonadal Dysgenesis. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
NLM
Gomes CR, Domenice S, Mendonça BB, Arnhold IJP, Costa EMF. A Novel Mutation in CBX2 Gene in a Brazilian Patient with 46,XY Disorders of Sex Development (DSD) Due to Gonadal Dysgenesis [Internet]. Hormone Research in Paediatrics. 2010 ; 74( suppl. 1): 6.[citado 2024 jun. 13 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Vancouver
Gomes CR, Domenice S, Mendonça BB, Arnhold IJP, Costa EMF. A Novel Mutation in CBX2 Gene in a Brazilian Patient with 46,XY Disorders of Sex Development (DSD) Due to Gonadal Dysgenesis [Internet]. Hormone Research in Paediatrics. 2010 ; 74( suppl. 1): 6.[citado 2024 jun. 13 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Trabalho de evento-resumo periodico
Novel Mutations (p.G6R and p.R511W) in IGF1R Gene in Children Born Small for Gestational Age (SGA) Without Catch-up Growth (2010)
Coutinho, D. C.; Leal, A. C.; Ribeiro, L. M.; Mendonça, B. B.; Arnhold, I. J. P.; Jorge, A. A. L.
Source: Hormone Research in Paediatrics. Conference titles: Annual meeting of the Sociedad Latino-Americana de Endocrinología Pediátrica (SLEP). Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, HORMÔNIO DE CRESCIMENTO, CRIANÇAS, GENES (ANÁLISE), FATORES DE CRESCIMENTO
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ABNT
COUTINHO, D. C. et al. Novel Mutations (p.G6R and p.R511W) in IGF1R Gene in Children Born Small for Gestational Age (SGA) Without Catch-up Growth. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf. Acesso em: 13 jun. 2024. , 2010
APA
Coutinho, D. C., Leal, A. C., Ribeiro, L. M., Mendonça, B. B., Arnhold, I. J. P., & Jorge, A. A. L. (2010). Novel Mutations (p.G6R and p.R511W) in IGF1R Gene in Children Born Small for Gestational Age (SGA) Without Catch-up Growth. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
NLM
Coutinho DC, Leal AC, Ribeiro LM, Mendonça BB, Arnhold IJP, Jorge AAL. Novel Mutations (p.G6R and p.R511W) in IGF1R Gene in Children Born Small for Gestational Age (SGA) Without Catch-up Growth [Internet]. Hormone Research in Paediatrics. 2010 ; 74( suppl. 1): 2.[citado 2024 jun. 13 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Vancouver
Coutinho DC, Leal AC, Ribeiro LM, Mendonça BB, Arnhold IJP, Jorge AAL. Novel Mutations (p.G6R and p.R511W) in IGF1R Gene in Children Born Small for Gestational Age (SGA) Without Catch-up Growth [Internet]. Hormone Research in Paediatrics. 2010 ; 74( suppl. 1): 2.[citado 2024 jun. 13 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Trabalho de evento-resumo periodico
Growth Hormone (GH) Pharmacogenetics: Positive Influence of GH Receptor (GHR) Exon 3 Deleted Allele (d3) on First-year Growth Velocity and Final Height in Patients with Turner Syndrome (TS) Treated with Recombinant Human GH (rhGH) (2010)
Braz, A. F.; Costalonga, E. F.; Malaquias, A. C.; Mendonça, B. B.; Arnhold, I. J. P.; Jorge, A. A. L.
Source: Hormone Research in Paediatrics. Conference titles: Annual meeting of the Sociedad Latino-Americana de Endocrinología Pediátrica (SLEP). Unidade: FM
Subjects: HORMÔNIO LIBERADOR DE HORMÔNIO DE CRESCIMENTO (ANÁLISE), HORMÔNIO DE CRESCIMENTO (GENÉTICA), ENDOCRINOPATIAS (DIAGNÓSTICO;FISIOPATOLOGIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BRAZ, A. F. et al. Growth Hormone (GH) Pharmacogenetics: Positive Influence of GH Receptor (GHR) Exon 3 Deleted Allele (d3) on First-year Growth Velocity and Final Height in Patients with Turner Syndrome (TS) Treated with Recombinant Human GH (rhGH). Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf. Acesso em: 13 jun. 2024. , 2010
APA
Braz, A. F., Costalonga, E. F., Malaquias, A. C., Mendonça, B. B., Arnhold, I. J. P., & Jorge, A. A. L. (2010). Growth Hormone (GH) Pharmacogenetics: Positive Influence of GH Receptor (GHR) Exon 3 Deleted Allele (d3) on First-year Growth Velocity and Final Height in Patients with Turner Syndrome (TS) Treated with Recombinant Human GH (rhGH). Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
NLM
Braz AF, Costalonga EF, Malaquias AC, Mendonça BB, Arnhold IJP, Jorge AAL. Growth Hormone (GH) Pharmacogenetics: Positive Influence of GH Receptor (GHR) Exon 3 Deleted Allele (d3) on First-year Growth Velocity and Final Height in Patients with Turner Syndrome (TS) Treated with Recombinant Human GH (rhGH) [Internet]. Hormone Research in Paediatrics. 2010 ; 74( suppl. 1): 4.[citado 2024 jun. 13 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Vancouver
Braz AF, Costalonga EF, Malaquias AC, Mendonça BB, Arnhold IJP, Jorge AAL. Growth Hormone (GH) Pharmacogenetics: Positive Influence of GH Receptor (GHR) Exon 3 Deleted Allele (d3) on First-year Growth Velocity and Final Height in Patients with Turner Syndrome (TS) Treated with Recombinant Human GH (rhGH) [Internet]. Hormone Research in Paediatrics. 2010 ; 74( suppl. 1): 4.[citado 2024 jun. 13 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Trabalho de evento-resumo periodico
Long Term Glucocorticoid Exposition Does Not Play the Major Role in the Development of Obesity and Metabolic Syndrome in Classical Form of 21-Hydroxylase Deficiency (2010)
Moreira, R. P. P.; Brito, V. N.; Gomes, L. G.; Madureira, G.; Mendonça, B. B.; Bachega, T. A. S. S.
Source: Hormone Research in Paediatrics. Conference titles: Annual meeting of the Sociedad Latino-Americana de Endocrinología Pediátrica (SLEP). Unidade: FM
Subjects: HIDROXILASE (DEFICIÊNCIA), SEGUIMENTOS, METABOLISMO BASAL (PATOLOGIA), CORTISOL (ANÁLISE)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOREIRA, R. P. P. et al. Long Term Glucocorticoid Exposition Does Not Play the Major Role in the Development of Obesity and Metabolic Syndrome in Classical Form of 21-Hydroxylase Deficiency. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf. Acesso em: 13 jun. 2024. , 2010
APA
Moreira, R. P. P., Brito, V. N., Gomes, L. G., Madureira, G., Mendonça, B. B., & Bachega, T. A. S. S. (2010). Long Term Glucocorticoid Exposition Does Not Play the Major Role in the Development of Obesity and Metabolic Syndrome in Classical Form of 21-Hydroxylase Deficiency. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
NLM
Moreira RPP, Brito VN, Gomes LG, Madureira G, Mendonça BB, Bachega TASS. Long Term Glucocorticoid Exposition Does Not Play the Major Role in the Development of Obesity and Metabolic Syndrome in Classical Form of 21-Hydroxylase Deficiency [Internet]. Hormone Research in Paediatrics. 2010 ; 74( suppl. 1): 12.[citado 2024 jun. 13 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Vancouver
Moreira RPP, Brito VN, Gomes LG, Madureira G, Mendonça BB, Bachega TASS. Long Term Glucocorticoid Exposition Does Not Play the Major Role in the Development of Obesity and Metabolic Syndrome in Classical Form of 21-Hydroxylase Deficiency [Internet]. Hormone Research in Paediatrics. 2010 ; 74( suppl. 1): 12.[citado 2024 jun. 13 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Trabalho de evento-resumo periodico
Quality of Life in a Large Cohort of Patients with 46,XX and 46,XY Disorders of Sex Development (DSD) (2010)
Amaral, R. C.; Brito, V. N.; Domenice, S.; Olvieira, A.; Sircil, M. H.; Mendonça, B. B.; Arnhold, I. J. P.; Costa, E. M. F.; Inacio, M.
Source: Hormone Research in Paediatrics. Conference titles: Annual meeting of the Sociedad Latino-Americana de Endocrinología Pediátrica (SLEP). Unidade: FM
Subjects: GENÉTICA MOLECULAR, QUALIDADE DE VIDA, INFERTILIDADE FEMININA, DESENVOLVIMENTO PSICOSSEXUAL (CRESCIMENTO E DESENVOLVIMENTO), ESTUDOS DE COORTES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AMARAL, R. C. et al. Quality of Life in a Large Cohort of Patients with 46,XX and 46,XY Disorders of Sex Development (DSD). Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf. Acesso em: 13 jun. 2024. , 2010
APA
Amaral, R. C., Brito, V. N., Domenice, S., Olvieira, A., Sircil, M. H., Mendonça, B. B., et al. (2010). Quality of Life in a Large Cohort of Patients with 46,XX and 46,XY Disorders of Sex Development (DSD). Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
NLM
Amaral RC, Brito VN, Domenice S, Olvieira A, Sircil MH, Mendonça BB, Arnhold IJP, Costa EMF, Inacio M. Quality of Life in a Large Cohort of Patients with 46,XX and 46,XY Disorders of Sex Development (DSD) [Internet]. Hormone Research in Paediatrics. 2010 ; 74( suppl. 1): 7.[citado 2024 jun. 13 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Vancouver
Amaral RC, Brito VN, Domenice S, Olvieira A, Sircil MH, Mendonça BB, Arnhold IJP, Costa EMF, Inacio M. Quality of Life in a Large Cohort of Patients with 46,XX and 46,XY Disorders of Sex Development (DSD) [Internet]. Hormone Research in Paediatrics. 2010 ; 74( suppl. 1): 7.[citado 2024 jun. 13 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Trabalho de evento-resumo periodico
Contiguous Gene Syndrome Caused by an Interstitial Deletion in the Short Arm of X-chromosome Diagnosed by MLPA (2010)
Alves, B. B.; Silveira, L. F. G.; Teles, M.; Nishi, M. Y.; Funari, M. F. A.; Mendonça, B. B.
Source: Hormone Research in Paediatrics. Conference titles: Annual meeting of the Sociedad Latino-Americana de Endocrinología Pediátrica (SLEP). Unidade: FM
Subjects: DELEÇÃO DE GENES, DOENÇAS GENÉTICAS (DIAGNÓSTICO), CROMOSSOMO X (PATOLOGIA), FENÓTIPOS (ANORMALIDADES)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALVES, B. B. et al. Contiguous Gene Syndrome Caused by an Interstitial Deletion in the Short Arm of X-chromosome Diagnosed by MLPA. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf. Acesso em: 13 jun. 2024. , 2010
APA
Alves, B. B., Silveira, L. F. G., Teles, M., Nishi, M. Y., Funari, M. F. A., & Mendonça, B. B. (2010). Contiguous Gene Syndrome Caused by an Interstitial Deletion in the Short Arm of X-chromosome Diagnosed by MLPA. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
NLM
Alves BB, Silveira LFG, Teles M, Nishi MY, Funari MFA, Mendonça BB. Contiguous Gene Syndrome Caused by an Interstitial Deletion in the Short Arm of X-chromosome Diagnosed by MLPA [Internet]. Hormone Research in Paediatrics. 2010 ; 74( suppl. 1): 21.[citado 2024 jun. 13 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Vancouver
Alves BB, Silveira LFG, Teles M, Nishi MY, Funari MFA, Mendonça BB. Contiguous Gene Syndrome Caused by an Interstitial Deletion in the Short Arm of X-chromosome Diagnosed by MLPA [Internet]. Hormone Research in Paediatrics. 2010 ; 74( suppl. 1): 21.[citado 2024 jun. 13 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf

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