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Artigo de periodico
Role of the Natriuretic Peptide System in Normal Growth and Growth Disorders (2014)
Vasques, G. A.; Arnhold, I. J. P.; Jorge, A. A. L.
Source: Hormone Research in Paediatrics. Unidade: FM
Subjects: FATORES DE RISCO, MODELOS ANIMAIS, PEPTÍDEOS, PEPTÍDEO NATRIURÉTICO ATRIAL
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ABNT
VASQUES, G. A. e ARNHOLD, I. J. P. e JORGE, A. A. L. Role of the Natriuretic Peptide System in Normal Growth and Growth Disorders. Hormone Research in Paediatrics, v. 82, n. 4, p. 222-229, 2014Tradução . . Disponível em: http://www.karger.com/Article/Pdf/365049. Acesso em: 30 set. 2024.
APA
Vasques, G. A., Arnhold, I. J. P., & Jorge, A. A. L. (2014). Role of the Natriuretic Peptide System in Normal Growth and Growth Disorders. Hormone Research in Paediatrics, 82( 4), 222-229. doi:10.1159/000365049
NLM
Vasques GA, Arnhold IJP, Jorge AAL. Role of the Natriuretic Peptide System in Normal Growth and Growth Disorders [Internet]. Hormone Research in Paediatrics. 2014 ; 82( 4): 222-229.[citado 2024 set. 30 ] Available from: http://www.karger.com/Article/Pdf/365049
Vancouver
Vasques GA, Arnhold IJP, Jorge AAL. Role of the Natriuretic Peptide System in Normal Growth and Growth Disorders [Internet]. Hormone Research in Paediatrics. 2014 ; 82( 4): 222-229.[citado 2024 set. 30 ] Available from: http://www.karger.com/Article/Pdf/365049
Artigo de periodico
The Sitting Height/Height Ratio for Age in Healthy and Short Individuals and Its Potential Role in Selecting Short Children for SHOX Analysis (2013)
Malaquias, A. C.; Scalco, R. C.; Fontenele, E. G. P.; Costalonga, E. F.; Baldin, A. D.; Braz, A. F.; Funari, M. F. A.; Nishi, M. Y.; Guerra-Junior, G.; Mendonca, B. B.; Arnhold, I. J. P.; Jorge, A. A. L.
Source: Hormone Research in Paediatrics. Unidade: FM
Subjects: GENES (ANÁLISE), ENDOCRINOPATIAS, INSUFICIÊNCIA DE CRESCIMENTO
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ABNT
MALAQUIAS, A. C. et al. The Sitting Height/Height Ratio for Age in Healthy and Short Individuals and Its Potential Role in Selecting Short Children for SHOX Analysis. Hormone Research in Paediatrics, v. 80, n. 6 p. 449-456, 2013Tradução . . Disponível em: https://doi.org/10.1159/000355411. Acesso em: 30 set. 2024.
APA
Malaquias, A. C., Scalco, R. C., Fontenele, E. G. P., Costalonga, E. F., Baldin, A. D., Braz, A. F., et al. (2013). The Sitting Height/Height Ratio for Age in Healthy and Short Individuals and Its Potential Role in Selecting Short Children for SHOX Analysis. Hormone Research in Paediatrics, 80( 6 p. 449-456). doi:10.1159/000355411
NLM
Malaquias AC, Scalco RC, Fontenele EGP, Costalonga EF, Baldin AD, Braz AF, Funari MFA, Nishi MY, Guerra-Junior G, Mendonca BB, Arnhold IJP, Jorge AAL. The Sitting Height/Height Ratio for Age in Healthy and Short Individuals and Its Potential Role in Selecting Short Children for SHOX Analysis [Internet]. Hormone Research in Paediatrics. 2013 ; 80( 6 p. 449-456):[citado 2024 set. 30 ] Available from: https://doi.org/10.1159/000355411
Vancouver
Malaquias AC, Scalco RC, Fontenele EGP, Costalonga EF, Baldin AD, Braz AF, Funari MFA, Nishi MY, Guerra-Junior G, Mendonca BB, Arnhold IJP, Jorge AAL. The Sitting Height/Height Ratio for Age in Healthy and Short Individuals and Its Potential Role in Selecting Short Children for SHOX Analysis [Internet]. Hormone Research in Paediatrics. 2013 ; 80( 6 p. 449-456):[citado 2024 set. 30 ] Available from: https://doi.org/10.1159/000355411
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: 30 set. 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 set. 30 ] 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 set. 30 ] 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: 30 set. 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 set. 30 ] 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 set. 30 ] 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: 30 set. 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 set. 30 ] 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 set. 30 ] 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)
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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: 30 set. 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 set. 30 ] 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 set. 30 ] 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
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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: 30 set. 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 set. 30 ] 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 set. 30 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Artigo de periodico
Molecular mechanisms of pituitary organogenesis: In search of novel regulatory genes (2010)
Davis, S .W.; Castinetti, F.; Carvalho, L. R.; Ellsworth, B. S.; Potok, M. A.; Lyons, R. H.; Brinkmeier, M. L.; Raetzman, L. T.; Carninci, P.; Mortensen, A. H.; Hayashizaki, Y.; Arnhold, I. J. P.; Mendonça, B. B.; Brue, T.S.A. Campera,∗; Camper, S. A.,∗
Source: Molecular and Cellular Endocrinology. Unidade: FM
Subjects: BIOLOGIA MOLECULAR, MECANISMOS, GLÂNDULA PRITUITÁRIA (FISIOPATOLOGIA), GENES REGULADORES
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ABNT
DAVIS, S .W. et al. Molecular mechanisms of pituitary organogenesis: In search of novel regulatory genes. Molecular and Cellular Endocrinology, v. 323, n. 1, p. 4-19, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2009.12.012. Acesso em: 30 set. 2024.
APA
Davis, S. .W., Castinetti, F., Carvalho, L. R., Ellsworth, B. S., Potok, M. A., Lyons, R. H., et al. (2010). Molecular mechanisms of pituitary organogenesis: In search of novel regulatory genes. Molecular and Cellular Endocrinology, 323( 1), 4-19. doi:10.1016/j.mce.2009.12.012
NLM
Davis S .W, Castinetti F, Carvalho LR, Ellsworth BS, Potok MA, Lyons RH, Brinkmeier ML, Raetzman LT, Carninci P, Mortensen AH, Hayashizaki Y, Arnhold IJP, Mendonça BB, Brue TSAC, Camper SA. Molecular mechanisms of pituitary organogenesis: In search of novel regulatory genes [Internet]. Molecular and Cellular Endocrinology. 2010 ; 323( 1): 4-19.[citado 2024 set. 30 ] Available from: https://doi.org/10.1016/j.mce.2009.12.012
Vancouver
Davis S .W, Castinetti F, Carvalho LR, Ellsworth BS, Potok MA, Lyons RH, Brinkmeier ML, Raetzman LT, Carninci P, Mortensen AH, Hayashizaki Y, Arnhold IJP, Mendonça BB, Brue TSAC, Camper SA. Molecular mechanisms of pituitary organogenesis: In search of novel regulatory genes [Internet]. Molecular and Cellular Endocrinology. 2010 ; 323( 1): 4-19.[citado 2024 set. 30 ] Available from: https://doi.org/10.1016/j.mce.2009.12.012
Artigo de periodico
Mutations of the KISS1 gene in disorders of puberty (2010)
Silveira, L. G.; Noel, S. D.; Silveira-Neto, A. P.; Abreu, A. P.; Brito, V. N.; Santos, M. G; Bianco, S. D. C.; Kuohung, W.; Xu, S.; Gryngarten, M.; Escobar, M. E.; Arnhold, I. J. P.; Mendonca, B. B.; Kaiser, U. B.; Latronico, A. C.
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, GENES (ANÁLISE), PUBERDADE (GENÉTICA), FENÓTIPOS
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ABNT
SILVEIRA, L. G. et al. Mutations of the KISS1 gene in disorders of puberty. Journal of Clinical Endocrinology and Metabolism, v. 95, n. 5, p. 2276-2280, 2010Tradução . . Disponível em: http://jcem.endojournals.org/cgi/reprint/95/5/2276. Acesso em: 30 set. 2024.
APA
Silveira, L. G., Noel, S. D., Silveira-Neto, A. P., Abreu, A. P., Brito, V. N., Santos, M. G., et al. (2010). Mutations of the KISS1 gene in disorders of puberty. Journal of Clinical Endocrinology and Metabolism, 95( 5), 2276-2280. Recuperado de http://jcem.endojournals.org/cgi/reprint/95/5/2276
NLM
Silveira LG, Noel SD, Silveira-Neto AP, Abreu AP, Brito VN, Santos MG, Bianco SDC, Kuohung W, Xu S, Gryngarten M, Escobar ME, Arnhold IJP, Mendonca BB, Kaiser UB, Latronico AC. Mutations of the KISS1 gene in disorders of puberty [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 5): 2276-2280.[citado 2024 set. 30 ] Available from: http://jcem.endojournals.org/cgi/reprint/95/5/2276
Vancouver
Silveira LG, Noel SD, Silveira-Neto AP, Abreu AP, Brito VN, Santos MG, Bianco SDC, Kuohung W, Xu S, Gryngarten M, Escobar ME, Arnhold IJP, Mendonca BB, Kaiser UB, Latronico AC. Mutations of the KISS1 gene in disorders of puberty [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 5): 2276-2280.[citado 2024 set. 30 ] Available from: http://jcem.endojournals.org/cgi/reprint/95/5/2276
Trabalho de evento-resumo periodico
A novel mutation in the CXORF6 gene in patients with undertermined 46.XY disorders of sex development (2008)
Brandão, M. P.; Domenice, S.; Arnhold, I. J. P.; Costa, E. M. F.; Mendonça, B. B.
Source: Arquivos Brasileiros de Endocrinologia e Metabologia. Conference titles: International Congress of Endocrinology. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, POLIMORFISMO, DIFERENÇAS SEXUAIS (PSICOGÊNESE)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BRANDÃO, M. P. et al. A novel mutation in the CXORF6 gene in patients with undertermined 46.XY disorders of sex development. Arquivos Brasileiros de Endocrinologia e Metabologia. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 30 set. 2024. , 2008
APA
Brandão, M. P., Domenice, S., Arnhold, I. J. P., Costa, E. M. F., & Mendonça, B. B. (2008). A novel mutation in the CXORF6 gene in patients with undertermined 46.XY disorders of sex development. Arquivos Brasileiros de Endocrinologia e Metabologia. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
NLM
Brandão MP, Domenice S, Arnhold IJP, Costa EMF, Mendonça BB. A novel mutation in the CXORF6 gene in patients with undertermined 46.XY disorders of sex development. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52 S794.[citado 2024 set. 30 ]
Vancouver
Brandão MP, Domenice S, Arnhold IJP, Costa EMF, Mendonça BB. A novel mutation in the CXORF6 gene in patients with undertermined 46.XY disorders of sex development. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52 S794.[citado 2024 set. 30 ]
Trabalho de evento-resumo periodico
Intragenic delection of the shox gene in a family with Léri-Well dyschondrosteosis detected by multiplex ligation-dependent probe amplification (MLPA) (2008)
Funari, M. F. A.; Jorge, A. A. L.; Arnhold, I. J. P.; Pinto, E. M.; Mendonça, B. B.; Nishi. M. Y.
Source: Arquivos Brasileiros de Endocrinologia e Metabologia. Conference titles: International Congress of Endocrinology. Unidade: FM
Subjects: TÉCNICAS CITOLÓGICAS, AMPLIFICAÇÃO DE GENES, BIOMARCADORES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FUNARI, M. F. A. et al. Intragenic delection of the shox gene in a family with Léri-Well dyschondrosteosis detected by multiplex ligation-dependent probe amplification (MLPA). Arquivos Brasileiros de Endocrinologia e Metabologia. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 30 set. 2024. , 2008
APA
Funari, M. F. A., Jorge, A. A. L., Arnhold, I. J. P., Pinto, E. M., Mendonça, B. B., & Nishi. M. Y.,. (2008). Intragenic delection of the shox gene in a family with Léri-Well dyschondrosteosis detected by multiplex ligation-dependent probe amplification (MLPA). Arquivos Brasileiros de Endocrinologia e Metabologia. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
NLM
Funari MFA, Jorge AAL, Arnhold IJP, Pinto EM, Mendonça BB, Nishi. M. Y. Intragenic delection of the shox gene in a family with Léri-Well dyschondrosteosis detected by multiplex ligation-dependent probe amplification (MLPA). Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52 S794.[citado 2024 set. 30 ]
Vancouver
Funari MFA, Jorge AAL, Arnhold IJP, Pinto EM, Mendonça BB, Nishi. M. Y. Intragenic delection of the shox gene in a family with Léri-Well dyschondrosteosis detected by multiplex ligation-dependent probe amplification (MLPA). Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52 S794.[citado 2024 set. 30 ]
Trabalho de evento-resumo periodico
Effects of prenatal and postnatal androgen excess in gender identity and sexual orientation in adult female patients with classical 21-hydroxylase deficiency (2008)
Inácio, M.; Madureira, G.; Gomes, L. G.; Verduguez, E.; Arnhold, I. J. P.; Mendonça, B. B.; Bachega, T. A. A. S.
Source: Arquivos Brasileiros de Endocrinologia e Metabologia. Conference titles: International Congress of Endocrinology. Unidade: FM
Subjects: HORMÔNIOS (DEFICIÊNCIA), ORIENTAÇÃO SEXUAL, ANDRÓGENOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
INÁCIO, M. et al. Effects of prenatal and postnatal androgen excess in gender identity and sexual orientation in adult female patients with classical 21-hydroxylase deficiency. Arquivos Brasileiros de Endocrinologia e Metabologia. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 30 set. 2024. , 2008
APA
Inácio, M., Madureira, G., Gomes, L. G., Verduguez, E., Arnhold, I. J. P., Mendonça, B. B., & Bachega, T. A. A. S. (2008). Effects of prenatal and postnatal androgen excess in gender identity and sexual orientation in adult female patients with classical 21-hydroxylase deficiency. Arquivos Brasileiros de Endocrinologia e Metabologia. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
NLM
Inácio M, Madureira G, Gomes LG, Verduguez E, Arnhold IJP, Mendonça BB, Bachega TAAS. Effects of prenatal and postnatal androgen excess in gender identity and sexual orientation in adult female patients with classical 21-hydroxylase deficiency. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52 S787.[citado 2024 set. 30 ]
Vancouver
Inácio M, Madureira G, Gomes LG, Verduguez E, Arnhold IJP, Mendonça BB, Bachega TAAS. Effects of prenatal and postnatal androgen excess in gender identity and sexual orientation in adult female patients with classical 21-hydroxylase deficiency. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52 S787.[citado 2024 set. 30 ]
Trabalho de evento-resumo periodico
An activating mutation of the Kiss-1 gene in a boy with gonadotropin-dependent precocious pubertry (2007)
Silveira, L. G.; Santos, M. A. G.; Brito, V. N.; Lima-Valassi, H. P.; Arnhold, I. J. P.; Mendonça, B. B.; Latronico, A. C
Source: Clinics. Conference titles: Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do HC-FMUSP". Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, PUBERDADE PRECOCE, FENÓTIPOS, GONADOTROFINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVEIRA, L. G. et al. An activating mutation of the Kiss-1 gene in a boy with gonadotropin-dependent precocious pubertry. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 30 set. 2024. , 2007
APA
Silveira, L. G., Santos, M. A. G., Brito, V. N., Lima-Valassi, H. P., Arnhold, I. J. P., Mendonça, B. B., & Latronico, A. C. (2007). An activating mutation of the Kiss-1 gene in a boy with gonadotropin-dependent precocious pubertry. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
NLM
Silveira LG, Santos MAG, Brito VN, Lima-Valassi HP, Arnhold IJP, Mendonça BB, Latronico AC. An activating mutation of the Kiss-1 gene in a boy with gonadotropin-dependent precocious pubertry. Clinics. 2007 ; 62 S94.[citado 2024 set. 30 ]
Vancouver
Silveira LG, Santos MAG, Brito VN, Lima-Valassi HP, Arnhold IJP, Mendonça BB, Latronico AC. An activating mutation of the Kiss-1 gene in a boy with gonadotropin-dependent precocious pubertry. Clinics. 2007 ; 62 S94.[citado 2024 set. 30 ]
Artigo de periodico
Analysis of LH determination 2 hours after depot leuprolide acetate in monitoring gonadotropin-dependent precocious puberty treatment (2007)
Cukier, P.; Xavier, Ana Claudia Latronico; Arnhold, I. J. P.; Mendonça, Berenice Bilharinho de; Brito, V. Nahime
Source: Hormone research. Conference titles: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Subjects: PUBERDADE PRECOCE (TERAPIA), SEGUIMENTOS, SENSIBILIDADE E ESPECIFICIDADE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CUKIER, P. et al. Analysis of LH determination 2 hours after depot leuprolide acetate in monitoring gonadotropin-dependent precocious puberty treatment. Hormone research, v. 68, p. 7, 2007Tradução . . Acesso em: 30 set. 2024.
APA
Cukier, P., Xavier, A. C. L., Arnhold, I. J. P., Mendonça, B. B. de, & Brito, V. N. (2007). Analysis of LH determination 2 hours after depot leuprolide acetate in monitoring gonadotropin-dependent precocious puberty treatment. Hormone research, 68, 7.
NLM
Cukier P, Xavier ACL, Arnhold IJP, Mendonça BB de, Brito VN. Analysis of LH determination 2 hours after depot leuprolide acetate in monitoring gonadotropin-dependent precocious puberty treatment. Hormone research. 2007 ; 68 7.[citado 2024 set. 30 ]
Vancouver
Cukier P, Xavier ACL, Arnhold IJP, Mendonça BB de, Brito VN. Analysis of LH determination 2 hours after depot leuprolide acetate in monitoring gonadotropin-dependent precocious puberty treatment. Hormone research. 2007 ; 68 7.[citado 2024 set. 30 ]
Trabalho de evento-resumo periodico
IGF-I response of fibroblasts from Noonan syndrome patients harboring constitutionaly active SHP-2 protein (2006)
Jorge, A. A. L.; Montenegro, L. R.; Arnhold, I. J. P.; Mendonça, Berenice Bilharinho de
Source: Journal of pediatric endocrinology and metabolism. Conference titles: Annual Meeting of the Sociedad Latinoamericana de Endocrinologia Pediátrica (SLEP). Unidade: FM
Subjects: FIBROBLASTOS (ANÁLISE), CRESCIMENTO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JORGE, A. A. L. et al. IGF-I response of fibroblasts from Noonan syndrome patients harboring constitutionaly active SHP-2 protein. Journal of pediatric endocrinology and metabolism. London: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 30 set. 2024. , 2006
APA
Jorge, A. A. L., Montenegro, L. R., Arnhold, I. J. P., & Mendonça, B. B. de. (2006). IGF-I response of fibroblasts from Noonan syndrome patients harboring constitutionaly active SHP-2 protein. Journal of pediatric endocrinology and metabolism. London: Faculdade de Medicina, Universidade de São Paulo.
NLM
Jorge AAL, Montenegro LR, Arnhold IJP, Mendonça BB de. IGF-I response of fibroblasts from Noonan syndrome patients harboring constitutionaly active SHP-2 protein. Journal of pediatric endocrinology and metabolism. 2006 ; 19( suppl.3): 1067.[citado 2024 set. 30 ]
Vancouver
Jorge AAL, Montenegro LR, Arnhold IJP, Mendonça BB de. IGF-I response of fibroblasts from Noonan syndrome patients harboring constitutionaly active SHP-2 protein. Journal of pediatric endocrinology and metabolism. 2006 ; 19( suppl.3): 1067.[citado 2024 set. 30 ]
Trabalho de evento-resumo periodico
Frequency of SHOX mutations in idiopathic short stature (ISS) (2006)
Jorge, A. A. L.; Souza, S. C.; Liborio, D. C. C.; Nishi, M. Y.; Billerbeck, A. E.; Arnhold, I. J. P.; Mendonça, Berenice Bilharinho de
Source: Journal of pediatric endocrinology and metabolism. Conference titles: Annual Meeting of the Sociedad Latinoamericana de Endocrinologia Pediátrica (SLEP). Unidade: FM
Assunto: MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JORGE, A. A. L. et al. Frequency of SHOX mutations in idiopathic short stature (ISS). Journal of pediatric endocrinology and metabolism. London: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 30 set. 2024. , 2006
APA
Jorge, A. A. L., Souza, S. C., Liborio, D. C. C., Nishi, M. Y., Billerbeck, A. E., Arnhold, I. J. P., & Mendonça, B. B. de. (2006). Frequency of SHOX mutations in idiopathic short stature (ISS). Journal of pediatric endocrinology and metabolism. London: Faculdade de Medicina, Universidade de São Paulo.
NLM
Jorge AAL, Souza SC, Liborio DCC, Nishi MY, Billerbeck AE, Arnhold IJP, Mendonça BB de. Frequency of SHOX mutations in idiopathic short stature (ISS). Journal of pediatric endocrinology and metabolism. 2006 ; 19( suppl.3): 1063.[citado 2024 set. 30 ]
Vancouver
Jorge AAL, Souza SC, Liborio DCC, Nishi MY, Billerbeck AE, Arnhold IJP, Mendonça BB de. Frequency of SHOX mutations in idiopathic short stature (ISS). Journal of pediatric endocrinology and metabolism. 2006 ; 19( suppl.3): 1063.[citado 2024 set. 30 ]
Artigo de periodico
Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion (2006)
Abrão, Milena Garcia; Leitet, M. V.; Carvalho, L. R.; Billerbeck, A. E. C.; Nishi, M. Y.; Barbosa, A. S.; Martin, R. M.; Arnhold, I. J. P.; Mendonça, Berenice Bilharinho
Source: Clinical Endocrinology. Unidade: FM
Subjects: ENDOCRINOLOGIA, HORMÔNIOS HIPOFISÁRIOS (DEFICIÊNCIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABRÃO, Milena Garcia et al. Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion. Clinical Endocrinology, v. 65, n. 3, p. 294-300, 2006Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2006.02592.x. Acesso em: 30 set. 2024.
APA
Abrão, M. G., Leitet, M. V., Carvalho, L. R., Billerbeck, A. E. C., Nishi, M. Y., Barbosa, A. S., et al. (2006). Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion. Clinical Endocrinology, 65( 3), 294-300. doi:10.1111/j.1365-2265.2006.02592.x
NLM
Abrão MG, Leitet MV, Carvalho LR, Billerbeck AEC, Nishi MY, Barbosa AS, Martin RM, Arnhold IJP, Mendonça BB. Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion [Internet]. Clinical Endocrinology. 2006 ; 65( 3): 294-300.[citado 2024 set. 30 ] Available from: https://doi.org/10.1111/j.1365-2265.2006.02592.x
Vancouver
Abrão MG, Leitet MV, Carvalho LR, Billerbeck AEC, Nishi MY, Barbosa AS, Martin RM, Arnhold IJP, Mendonça BB. Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion [Internet]. Clinical Endocrinology. 2006 ; 65( 3): 294-300.[citado 2024 set. 30 ] Available from: https://doi.org/10.1111/j.1365-2265.2006.02592.x
Trabalho de evento-resumo periodico
Final height in patients with gonadotropin-dependent precocious puberty treated with depot GnRH agonists (2006)
Brito, V. N.; Cukier, P.; Teles, M. G.; Mendonça, Berenice Bilharinho de; Arnhold, I. J. P.
Source: Journal of pediatric endocrinology and metabolism. Conference titles: Annual Meeting of the Sociedad Latinoamericana de Endocrinologia Pediátrica (SLEP). Unidade: FM
Subjects: GONADOTROFINAS, PUBERDADE PRECOCE, RESUMOS (CONGRESSOS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BRITO, V. N. et al. Final height in patients with gonadotropin-dependent precocious puberty treated with depot GnRH agonists. Journal of pediatric endocrinology and metabolism. London: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 30 set. 2024. , 2006
APA
Brito, V. N., Cukier, P., Teles, M. G., Mendonça, B. B. de, & Arnhold, I. J. P. (2006). Final height in patients with gonadotropin-dependent precocious puberty treated with depot GnRH agonists. Journal of pediatric endocrinology and metabolism. London: Faculdade de Medicina, Universidade de São Paulo.
NLM
Brito VN, Cukier P, Teles MG, Mendonça BB de, Arnhold IJP. Final height in patients with gonadotropin-dependent precocious puberty treated with depot GnRH agonists. Journal of pediatric endocrinology and metabolism. 2006 ; 19( suppl.3): 1085.[citado 2024 set. 30 ]
Vancouver
Brito VN, Cukier P, Teles MG, Mendonça BB de, Arnhold IJP. Final height in patients with gonadotropin-dependent precocious puberty treated with depot GnRH agonists. Journal of pediatric endocrinology and metabolism. 2006 ; 19( suppl.3): 1085.[citado 2024 set. 30 ]
Trabalho de evento-resumo periodico
EEG and mutational analysis of the GABA-A receptor 1 subunit gene (GABRA1) in girls with idiopathic gonadotropin dependent precocious puberty (2005)
Guilhoto, Laura Maria de Figueiredo Ferreira; Brito, V. N.; Mendonça, B. B.; Freitas, K. C. M.; Arnhold, I. J. P.; Latronico, A. C.; Grossmann, R M
Source: Epilepsia. Conference titles: International Epilepsy Congress. Unidade: HU
Subjects: EPILEPSIA, NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUILHOTO, Laura Maria de Figueiredo Ferreira et al. EEG and mutational analysis of the GABA-A receptor 1 subunit gene (GABRA1) in girls with idiopathic gonadotropin dependent precocious puberty. Epilepsia. Amsterdam: Raven Press. Disponível em: http://www.blackwell-synergy.com/toc/epi/46/s6;jsessionid=b90sFo4zGi8doyTUFB. Acesso em: 30 set. 2024. , 2005
APA
Guilhoto, L. M. de F. F., Brito, V. N., Mendonça, B. B., Freitas, K. C. M., Arnhold, I. J. P., Latronico, A. C., & Grossmann, R. M. (2005). EEG and mutational analysis of the GABA-A receptor 1 subunit gene (GABRA1) in girls with idiopathic gonadotropin dependent precocious puberty. Epilepsia. Amsterdam: Raven Press. Recuperado de http://www.blackwell-synergy.com/toc/epi/46/s6;jsessionid=b90sFo4zGi8doyTUFB
NLM
Guilhoto LM de FF, Brito VN, Mendonça BB, Freitas KCM, Arnhold IJP, Latronico AC, Grossmann RM. EEG and mutational analysis of the GABA-A receptor 1 subunit gene (GABRA1) in girls with idiopathic gonadotropin dependent precocious puberty [Internet]. Epilepsia. 2005 ; 46 255 res. p769.[citado 2024 set. 30 ] Available from: http://www.blackwell-synergy.com/toc/epi/46/s6;jsessionid=b90sFo4zGi8doyTUFB
Vancouver
Guilhoto LM de FF, Brito VN, Mendonça BB, Freitas KCM, Arnhold IJP, Latronico AC, Grossmann RM. EEG and mutational analysis of the GABA-A receptor 1 subunit gene (GABRA1) in girls with idiopathic gonadotropin dependent precocious puberty [Internet]. Epilepsia. 2005 ; 46 255 res. p769.[citado 2024 set. 30 ] Available from: http://www.blackwell-synergy.com/toc/epi/46/s6;jsessionid=b90sFo4zGi8doyTUFB
Trabalho de evento-resumo periodico
Complete deletion of the PROP1 gene in two sibling with combined pituitary hormone deficiency (CPHD) (2004)
Abrao, M. G.; Carvalho, L.; Leite, M. V.; Nishi, M.; Barbosa, A.; Arnhold, I. J. P.; Mendonça, B. B.
Source: Journal of pediatric endocrinology and metabolism. Conference titles: Annual Meeting of the Sociedad Latinoamericana de Endocrinologia Pediátrica (SLEP). Unidade: FM
Subjects: HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA), DELEÇÃO DE GENES, GLÂNDULA PITUITÁRIA (FISIOPATOLOGIA), AMPLIFICAÇÃO DE GENES, RESUMOS (CONGRESSOS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABRAO, M. G. et al. Complete deletion of the PROP1 gene in two sibling with combined pituitary hormone deficiency (CPHD). Journal of pediatric endocrinology and metabolism. London: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 30 set. 2024. , 2004
APA
Abrao, M. G., Carvalho, L., Leite, M. V., Nishi, M., Barbosa, A., Arnhold, I. J. P., & Mendonça, B. B. (2004). Complete deletion of the PROP1 gene in two sibling with combined pituitary hormone deficiency (CPHD). Journal of pediatric endocrinology and metabolism. London: Faculdade de Medicina, Universidade de São Paulo.
NLM
Abrao MG, Carvalho L, Leite MV, Nishi M, Barbosa A, Arnhold IJP, Mendonça BB. Complete deletion of the PROP1 gene in two sibling with combined pituitary hormone deficiency (CPHD). Journal of pediatric endocrinology and metabolism. 2004 ; 17( suppl.5): 1345.[citado 2024 set. 30 ]
Vancouver
Abrao MG, Carvalho L, Leite MV, Nishi M, Barbosa A, Arnhold IJP, Mendonça BB. Complete deletion of the PROP1 gene in two sibling with combined pituitary hormone deficiency (CPHD). Journal of pediatric endocrinology and metabolism. 2004 ; 17( suppl.5): 1345.[citado 2024 set. 30 ]

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