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Trabalho de evento-resumo periodico
Analysis of Sox9 gene expression regulatory region in 46,XY DSD patients without campomelic dysplasia (2013)
Fanelli, Marina; Silva, Rosana B. Silva; Domenice, Sorahia.; Mendonça, Berenice Bilharinho de; Costa, Elaine M. F.
Source: Hormone Research in Paediatrics. Conference titles: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting. Unidade: FM
Subjects: GENES (ANÁLISE), TRANSTORNOS GONADAIS, ENDOCRINOPATIAS
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ABNT
FANELLI, Marina et al. Analysis of Sox9 gene expression regulatory region in 46,XY DSD patients without campomelic dysplasia. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000353762. Acesso em: 05 nov. 2024. , 2013
APA
Fanelli, M., Silva, R. B. S., Domenice, S., Mendonça, B. B. de, & Costa, E. M. F. (2013). Analysis of Sox9 gene expression regulatory region in 46,XY DSD patients without campomelic dysplasia. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. doi:10.1159/000353762
NLM
Fanelli M, Silva RBS, Domenice S, Mendonça BB de, Costa EMF. Analysis of Sox9 gene expression regulatory region in 46,XY DSD patients without campomelic dysplasia [Internet]. Hormone Research in Paediatrics. 2013 ; 80 185.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000353762
Vancouver
Fanelli M, Silva RBS, Domenice S, Mendonça BB de, Costa EMF. Analysis of Sox9 gene expression regulatory region in 46,XY DSD patients without campomelic dysplasia [Internet]. Hormone Research in Paediatrics. 2013 ; 80 185.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000353762
Trabalho de evento-resumo periodico
Polymorphism rs8081612 in the mitogen-activated protein 3 kinase 3 (MAP3K3) gene is associated with children height ina brazilian cohort (2013)
Fontenele, Eveline Gadelha Pereira; d'Alva, Catarina B.; Pinheiro, Daniel P.; Trarbarch,Ericka; Mendonça, Berenice Bilharinho de; Moraes, Maria Elisabete A.; Jorge, Alexander Augusto de Lima
Source: Hormone Research in Paediatrics. Conference titles: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting. Unidade: FM
Subjects: GENES (ANÁLISE), PESOS E MEDIDAS CORPORAIS, POLIMORFISMO, CRIANÇAS, BRASIL
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ABNT
FONTENELE, Eveline Gadelha Pereira et al. Polymorphism rs8081612 in the mitogen-activated protein 3 kinase 3 (MAP3K3) gene is associated with children height ina brazilian cohort. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000353762. Acesso em: 05 nov. 2024. , 2013
APA
Fontenele, E. G. P., d'Alva, C. B., Pinheiro, D. P., Trarbarch, E., Mendonça, B. B. de, Moraes, M. E. A., & Jorge, A. A. de L. (2013). Polymorphism rs8081612 in the mitogen-activated protein 3 kinase 3 (MAP3K3) gene is associated with children height ina brazilian cohort. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. doi:10.1159/000353762
NLM
Fontenele EGP, d'Alva CB, Pinheiro DP, Trarbarch E, Mendonça BB de, Moraes MEA, Jorge AA de L. Polymorphism rs8081612 in the mitogen-activated protein 3 kinase 3 (MAP3K3) gene is associated with children height ina brazilian cohort [Internet]. Hormone Research in Paediatrics. 2013 ; 80 295.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000353762
Vancouver
Fontenele EGP, d'Alva CB, Pinheiro DP, Trarbarch E, Mendonça BB de, Moraes MEA, Jorge AA de L. Polymorphism rs8081612 in the mitogen-activated protein 3 kinase 3 (MAP3K3) gene is associated with children height ina brazilian cohort [Internet]. Hormone Research in Paediatrics. 2013 ; 80 295.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000353762
Trabalho de evento-resumo periodico
The sitting heigh/height ratio for age is a simple and useful tool to select children with idiopathic short stature for SHOX studies (2013)
Malaquias, Alexsandra C.; Fontenele, Eveline G. P.; Costalonga, Everlayny F.; Scalcao, Renata C.; Funari, Mariana F. A.; Nishi, Mirian; Arnhold, Ivo J.P.; Jorge, Alexander Augusto de Lima; Mendonça, Berenice Bilharinho de
Source: Hormone Research in Paediatrics. Conference titles: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting. Unidade: FM
Subjects: ENDOCRINOPATIAS, INSUFICIÊNCIA DE CRESCIMENTO, GENES (ANÁLISE)
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ABNT
MALAQUIAS, Alexsandra C. et al. The sitting heigh/height ratio for age is a simple and useful tool to select children with idiopathic short stature for SHOX studies. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000353762. Acesso em: 05 nov. 2024. , 2013
APA
Malaquias, A. C., Fontenele, E. G. P., Costalonga, E. F., Scalcao, R. C., Funari, M. F. A., Nishi, M., et al. (2013). The sitting heigh/height ratio for age is a simple and useful tool to select children with idiopathic short stature for SHOX studies. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. doi:10.1159/000353762
NLM
Malaquias AC, Fontenele EGP, Costalonga EF, Scalcao RC, Funari MFA, Nishi M, Arnhold IJP, Jorge AA de L, Mendonça BB de. The sitting heigh/height ratio for age is a simple and useful tool to select children with idiopathic short stature for SHOX studies [Internet]. Hormone Research in Paediatrics. 2013 ; 80 161.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000353762
Vancouver
Malaquias AC, Fontenele EGP, Costalonga EF, Scalcao RC, Funari MFA, Nishi M, Arnhold IJP, Jorge AA de L, Mendonça BB de. The sitting heigh/height ratio for age is a simple and useful tool to select children with idiopathic short stature for SHOX studies [Internet]. Hormone Research in Paediatrics. 2013 ; 80 161.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000353762
Artigo de periodico
Novel mutation in the gonadotropin-releasing hormone receptor (GNRHR) gene in a patient with normosmic isolated hypogonadotropic hypogonadism (2012)
Beneduzzi, Daiane; Trarbach, Ericka B; Xavier, Ana Claudia Latronico; Mendonça, Berenice Bilharinho de; Silveira, Letícia F G
Source: Arquivos Brasileiros de Endocrinologia & Metabologia. Unidade: FM
Subjects: HIPOGONADISMO, MUTAÇÃO GENÉTICA, GENES (ANÁLISE), GONADOTROFINAS, AMPLIFICAÇÃO DE GENES, SEQUENCIAMENTO GENÉTICO
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ABNT
BENEDUZZI, Daiane et al. Novel mutation in the gonadotropin-releasing hormone receptor (GNRHR) gene in a patient with normosmic isolated hypogonadotropic hypogonadism. Arquivos Brasileiros de Endocrinologia & Metabologia, v. 56, n. 8, p. 540-544, 2012Tradução . . Disponível em: https://doi.org/10.1590/s0004-27302012000800013. Acesso em: 05 nov. 2024.
APA
Beneduzzi, D., Trarbach, E. B., Xavier, A. C. L., Mendonça, B. B. de, & Silveira, L. F. G. (2012). Novel mutation in the gonadotropin-releasing hormone receptor (GNRHR) gene in a patient with normosmic isolated hypogonadotropic hypogonadism. Arquivos Brasileiros de Endocrinologia & Metabologia, 56( 8), 540-544. doi:10.1590/s0004-27302012000800013
NLM
Beneduzzi D, Trarbach EB, Xavier ACL, Mendonça BB de, Silveira LFG. Novel mutation in the gonadotropin-releasing hormone receptor (GNRHR) gene in a patient with normosmic isolated hypogonadotropic hypogonadism [Internet]. Arquivos Brasileiros de Endocrinologia & Metabologia. 2012 ; 56( 8): 540-544.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1590/s0004-27302012000800013
Vancouver
Beneduzzi D, Trarbach EB, Xavier ACL, Mendonça BB de, Silveira LFG. Novel mutation in the gonadotropin-releasing hormone receptor (GNRHR) gene in a patient with normosmic isolated hypogonadotropic hypogonadism [Internet]. Arquivos Brasileiros de Endocrinologia & Metabologia. 2012 ; 56( 8): 540-544.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1590/s0004-27302012000800013
Artigo de periodico
Novel inactivating mutations in the GH secretagogue receptor gene in patients with constitutional delay of growth and puberty (2011)
Pires, Patricia N. Pugliese; Fortin, Jean-Philippe; Arthur, Thais; Xavier, Ana Claudia Latronico; Mendonça, Berenice Bilharinho de; Villares, Sandra Mara F; Arnhold, Ivo J. P; Kopin, Alan S; Jorge, Alexander Augusto de Lima
Source: European journal of endocrinology. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, GENES (ANÁLISE), PUBERDADE, CRESCIMENTO, RECEPTORES
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ABNT
PIRES, Patricia N. Pugliese et al. Novel inactivating mutations in the GH secretagogue receptor gene in patients with constitutional delay of growth and puberty. European journal of endocrinology, v. 165, n. 2, p. 233-241, 2011Tradução . . Disponível em: https://doi.org/10.1530/EJE-11-016. Acesso em: 05 nov. 2024.
APA
Pires, P. N. P., Fortin, J. -P., Arthur, T., Xavier, A. C. L., Mendonça, B. B. de, Villares, S. M. F., et al. (2011). Novel inactivating mutations in the GH secretagogue receptor gene in patients with constitutional delay of growth and puberty. European journal of endocrinology, 165( 2), 233-241. doi:10.1530/EJE-11-016
NLM
Pires PNP, Fortin J-P, Arthur T, Xavier ACL, Mendonça BB de, Villares SMF, Arnhold IJP, Kopin AS, Jorge AA de L. Novel inactivating mutations in the GH secretagogue receptor gene in patients with constitutional delay of growth and puberty [Internet]. European journal of endocrinology. 2011 ; 165( 2): 233-241.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1530/EJE-11-016
Vancouver
Pires PNP, Fortin J-P, Arthur T, Xavier ACL, Mendonça BB de, Villares SMF, Arnhold IJP, Kopin AS, Jorge AA de L. Novel inactivating mutations in the GH secretagogue receptor gene in patients with constitutional delay of growth and puberty [Internet]. European journal of endocrinology. 2011 ; 165( 2): 233-241.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1530/EJE-11-016
Trabalho de evento-resumo periodico
Considerable frequency of novel GLI2 missense witations in patientes with hypopituitarism without holoprosencephaly (2011)
França, Marcela; Jorge, Alexander; Otto, Aline; Carvalho, Luciani; Mendonça, Berenice Bilharinho de; Arnhold, Ivo J. P
Conference titles: Annual meeting of the european. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, GENES (ANÁLISE), GLÂNDULA PITUITÁRIA (GENÉTICA;FISIOPATOLOGIA), RESUMOS (EVENTOS)
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ABNT
FRANÇA, Marcela et al. Considerable frequency of novel GLI2 missense witations in patientes with hypopituitarism without holoprosencephaly. . Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=334325&Ausgabe=255336&ProduktNr=224036&filename=334325.pdf. Acesso em: 05 nov. 2024. , 2011
APA
França, M., Jorge, A., Otto, A., Carvalho, L., Mendonça, B. B. de, & Arnhold, I. J. P. (2011). Considerable frequency of novel GLI2 missense witations in patientes with hypopituitarism without holoprosencephaly. Basel: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=334325&Ausgabe=255336&ProduktNr=224036&filename=334325.pdf
NLM
França M, Jorge A, Otto A, Carvalho L, Mendonça BB de, Arnhold IJP. Considerable frequency of novel GLI2 missense witations in patientes with hypopituitarism without holoprosencephaly [Internet]. 2011 ; 76 25.[citado 2024 nov. 05 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=334325&Ausgabe=255336&ProduktNr=224036&filename=334325.pdf
Vancouver
França M, Jorge A, Otto A, Carvalho L, Mendonça BB de, Arnhold IJP. Considerable frequency of novel GLI2 missense witations in patientes with hypopituitarism without holoprosencephaly [Internet]. 2011 ; 76 25.[citado 2024 nov. 05 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=334325&Ausgabe=255336&ProduktNr=224036&filename=334325.pdf
Artigo de periodico
TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood (2010)
Gianetti, Elena; Tusset, Cintia; Noel, Sekoni D.; Au, Margaret G.; Dwyer, Andrew A.; Hughes, Virginia A.; Abreu, Ana Paula; Carroll, Jessica; Trarbach, Ericka; Silveira, Leticia F. G.; Costa, Elaine M. F.; Mendonça, Berenice Bilharinho de; Castro, Margaret de; Lofrano, Adriana; Hall, Janet E.; Bolu, Erol; Ozata, Metin; Quinton, Richard; Amory, John K.; Stewart, Susan E.; Arlt, Wiebke; Cole, Trevor R.; Crowley, William F.; Kaiser, Ursula B.; Latronico, Ana Claudia; Seminara, Stephanie B.
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, GENES (ANÁLISE), GONADOTROFINAS (METABOLISMO), FENÓTIPOS, HIPOGONADISMO
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ABNT
GIANETTI, Elena et al. TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood. Journal of Clinical Endocrinology and Metabolism, v. 95, n. 5, p. 2857-2867, 2010Tradução . . Disponível em: https://doi.org/10.1210/jc.2009-2320. Acesso em: 05 nov. 2024.
APA
Gianetti, E., Tusset, C., Noel, S. D., Au, M. G., Dwyer, A. A., Hughes, V. A., et al. (2010). TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood. Journal of Clinical Endocrinology and Metabolism, 95( 5), 2857-2867. doi:10.1210/jc.2009-2320
NLM
Gianetti E, Tusset C, Noel SD, Au MG, Dwyer AA, Hughes VA, Abreu AP, Carroll J, Trarbach E, Silveira LFG, Costa EMF, Mendonça BB de, Castro M de, Lofrano A, Hall JE, Bolu E, Ozata M, Quinton R, Amory JK, Stewart SE, Arlt W, Cole TR, Crowley WF, Kaiser UB, Latronico AC, Seminara SB. TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 5): 2857-2867.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1210/jc.2009-2320
Vancouver
Gianetti E, Tusset C, Noel SD, Au MG, Dwyer AA, Hughes VA, Abreu AP, Carroll J, Trarbach E, Silveira LFG, Costa EMF, Mendonça BB de, Castro M de, Lofrano A, Hall JE, Bolu E, Ozata M, Quinton R, Amory JK, Stewart SE, Arlt W, Cole TR, Crowley WF, Kaiser UB, Latronico AC, Seminara SB. TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 5): 2857-2867.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1210/jc.2009-2320
Trabalho de evento-resumo periodico
The presence of clitoomegaly in nonclassical form of 21-hydroxylase deficiency is modulated by the cag polymorphic tract of androgen receptor gene (2010)
Moura, V O; Pacheco, M; Kaupert, L; Gomes, L G; Marcondes, J A M; Mendonça, Berenice Bilharinho de; Bachega, Tânia Aparecida Sartori Sanchez
Source: Clinics. Conference titles: Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP". Unidade: FM
Subjects: HIDROXILASE (DEFICIÊNCIA), POLIMORFISMO, ANDRÓGENOS, RECEPTORES, GENES (ANÁLISE), RESUMOS (EVENTOS)
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ABNT
MOURA, V O et al. The presence of clitoomegaly in nonclassical form of 21-hydroxylase deficiency is modulated by the cag polymorphic tract of androgen receptor gene. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2010
APA
Moura, V. O., Pacheco, M., Kaupert, L., Gomes, L. G., Marcondes, J. A. M., Mendonça, B. B. de, & Bachega, T. A. S. S. (2010). The presence of clitoomegaly in nonclassical form of 21-hydroxylase deficiency is modulated by the cag polymorphic tract of androgen receptor gene. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
NLM
Moura VO, Pacheco M, Kaupert L, Gomes LG, Marcondes JAM, Mendonça BB de, Bachega TASS. The presence of clitoomegaly in nonclassical form of 21-hydroxylase deficiency is modulated by the cag polymorphic tract of androgen receptor gene. Clinics. 2010 ; 65 S70.[citado 2024 nov. 05 ]
Vancouver
Moura VO, Pacheco M, Kaupert L, Gomes LG, Marcondes JAM, Mendonça BB de, Bachega TASS. The presence of clitoomegaly in nonclassical form of 21-hydroxylase deficiency is modulated by the cag polymorphic tract of androgen receptor gene. Clinics. 2010 ; 65 S70.[citado 2024 nov. 05 ]

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