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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: 14 nov. 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 nov. 14 ] 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 nov. 14 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Artigo de periodico
A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism (2010)
Teles, M. G.; Trarbach, E. B.; Noel, S. D.; Guerra Junior, G.; Beneduzzi, D.; Bianco, S. D.; Jorge, Alexander A. L.; Mukherjee, A.; Baptista, M. T.; Costa, E. M.; Castro, M. de; Mendonça, B. B.; Kaiser, U. B.; Latronico, A. C.
Source: European Journal of Endocrinology. Unidade: FM
Subjects: ENDOCRINOPATIAS (PATOLOGIA;FISIOPATOLOGIA), MUTAÇÃO GENÉTICA, DOENÇAS PULMONARES INTERSTICIAIS, SISTEMA IMUNE (FISIOPATOLOGIA)
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ABNT
TELES, M. G. et al. A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism. European Journal of Endocrinology, v. 163, n. 1, p. 29-34, 2010Tradução . . Disponível em: https://doi.org/10.1530/EJE-10-0012. Acesso em: 14 nov. 2024.
APA
Teles, M. G., Trarbach, E. B., Noel, S. D., Guerra Junior, G., Beneduzzi, D., Bianco, S. D., et al. (2010). A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism. European Journal of Endocrinology, 163( 1), 29-34. doi:10.1530/EJE-10-0012
NLM
Teles MG, Trarbach EB, Noel SD, Guerra Junior G, Beneduzzi D, Bianco SD, Jorge AAL, Mukherjee A, Baptista MT, Costa EM, Castro M de, Mendonça BB, Kaiser UB, Latronico AC. A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism [Internet]. European Journal of Endocrinology. 2010 ; 163( 1): 29-34.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1530/EJE-10-0012
Vancouver
Teles MG, Trarbach EB, Noel SD, Guerra Junior G, Beneduzzi D, Bianco SD, Jorge AAL, Mukherjee A, Baptista MT, Costa EM, Castro M de, Mendonça BB, Kaiser UB, Latronico AC. A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism [Internet]. European Journal of Endocrinology. 2010 ; 163( 1): 29-34.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1530/EJE-10-0012
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: 14 nov. 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 nov. 14 ] 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 nov. 14 ] 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: 14 nov. 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 nov. 14 ] 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 nov. 14 ] 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: 14 nov. 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 nov. 14 ] 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 nov. 14 ] 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)
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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: 14 nov. 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 nov. 14 ] 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 nov. 14 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Trabalho de evento-resumo
TAC3/TACR3 mutations reveal preferential activation of GnRH release by neurokinin B in neonatal life followed by reversal in adulthood (2010)
Gianetti, E.; Tusset, C.; Noel, S.; Au, M.G.; Dwyer, A. A.; Hughes, V. A.; Abreu, A. P.; Carrol, J.; Trarbach, E.; Silveira, L. F. G.; Costa, E. M. F; Mendonça, B. B.; Castro, Margaret de; Lofrano, A.; Hall, J. E.; Bolu, E.; Ozata, M.; Quinton, R.; Amory, J. K.; Stewart, S. E.; Arlt, W.; Cole, T. R.; Crowley, W. F.; Kaiser, B. B.; Latronico, S. B.; Seminara, S. B.
Source: Advance Program. Conference titles: Annual Meeting and Expo of the Endocrine Society (ENDO). Unidade: FMRP
Subjects: NEUROENDOCRINOLOGIA, HIPOGONADISMO
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ABNT
GIANETTI, E. et al. TAC3/TACR3 mutations reveal preferential activation of GnRH release by neurokinin B in neonatal life followed by reversal in adulthood. 2010, Anais.. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2010. . Acesso em: 14 nov. 2024.
APA
Gianetti, E., Tusset, C., Noel, S., Au, M. G., Dwyer, A. A., Hughes, V. A., et al. (2010). TAC3/TACR3 mutations reveal preferential activation of GnRH release by neurokinin B in neonatal life followed by reversal in adulthood. In Advance Program. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Gianetti E, Tusset C, Noel S, Au MG, Dwyer AA, Hughes VA, Abreu AP, Carrol J, Trarbach E, Silveira LFG, Costa EMF, Mendonça BB, Castro M de, Lofrano A, Hall JE, Bolu E, Ozata M, Quinton R, Amory JK, Stewart SE, Arlt W, Cole TR, Crowley WF, Kaiser BB, Latronico SB, Seminara SB. TAC3/TACR3 mutations reveal preferential activation of GnRH release by neurokinin B in neonatal life followed by reversal in adulthood. Advance Program. 2010 ;[citado 2024 nov. 14 ]
Vancouver
Gianetti E, Tusset C, Noel S, Au MG, Dwyer AA, Hughes VA, Abreu AP, Carrol J, Trarbach E, Silveira LFG, Costa EMF, Mendonça BB, Castro M de, Lofrano A, Hall JE, Bolu E, Ozata M, Quinton R, Amory JK, Stewart SE, Arlt W, Cole TR, Crowley WF, Kaiser BB, Latronico SB, Seminara SB. TAC3/TACR3 mutations reveal preferential activation of GnRH release by neurokinin B in neonatal life followed by reversal in adulthood. Advance Program. 2010 ;[citado 2024 nov. 14 ]
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: 14 nov. 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 nov. 14 ] 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 nov. 14 ] 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)
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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: 14 nov. 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 nov. 14 ] 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 nov. 14 ] 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: 14 nov. 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 nov. 14 ] 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 nov. 14 ] Available from: https://doi.org/10.1016/j.mce.2009.12.012
Trabalho de evento-resumo
Association of CYP3A7, POR, SRD5A2 and HSD17B5 gene polymorphisms with the prader score in females with classical form of CAH (2010)
Kaupert, L. C.; Moreira, R. P. P.; Mello, M. P. de; Lemos-Marini, S. H. V.; Guerra Junior, G; Brito, V. N.; Gomes, L. G.; Castro, Margaret de; Mendonça, B. B.; Bachega, T. A. S. S.
Source: Advance Program. Conference titles: Annual Meeting and Expo of the Endocrine Society (ENDO). Unidade: FMRP
Subjects: POLIMORFISMO, ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KAUPERT, L. C. et al. Association of CYP3A7, POR, SRD5A2 and HSD17B5 gene polymorphisms with the prader score in females with classical form of CAH. 2010, Anais.. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2010. . Acesso em: 14 nov. 2024.
APA
Kaupert, L. C., Moreira, R. P. P., Mello, M. P. de, Lemos-Marini, S. H. V., Guerra Junior, G., Brito, V. N., et al. (2010). Association of CYP3A7, POR, SRD5A2 and HSD17B5 gene polymorphisms with the prader score in females with classical form of CAH. In Advance Program. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Kaupert LC, Moreira RPP, Mello MP de, Lemos-Marini SHV, Guerra Junior G, Brito VN, Gomes LG, Castro M de, Mendonça BB, Bachega TASS. Association of CYP3A7, POR, SRD5A2 and HSD17B5 gene polymorphisms with the prader score in females with classical form of CAH. Advance Program. 2010 ;[citado 2024 nov. 14 ]
Vancouver
Kaupert LC, Moreira RPP, Mello MP de, Lemos-Marini SHV, Guerra Junior G, Brito VN, Gomes LG, Castro M de, Mendonça BB, Bachega TASS. Association of CYP3A7, POR, SRD5A2 and HSD17B5 gene polymorphisms with the prader score in females with classical form of CAH. Advance Program. 2010 ;[citado 2024 nov. 14 ]

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