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Trabalho de evento-resumo periodico
Novel Mutation in Rspo1 in Patient with Disorder of Sexual Development 46, XX Testicular Associated to Hiperceratose Palmoplantaris (2011)
Silva, R.; Domenice, S.; Nishi, M.; Machado, A.; Silva, T.; Santos, M.; Brandão, M.; Mendonça, B.; Costa, E.
Fonte: Hormone Research in Paediatrics. Nome do evento: Annual Meeting of the Sociedad Latino-Americana de Endocrinología Pediátrica (SLEP). Unidade: FM
Assuntos: MUTAÇÃO GENÉTICA, NEOPLASIAS TESTICULARES, DISTÚRBIOS DA FUNÇÃO SOCIAL, CARCINOMA DE CÉLULAS ESCAMOSAS, RESUMOS (EVENTOS)
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ABNT
SILVA, R. et al. Novel Mutation in Rspo1 in Patient with Disorder of Sexual Development 46, XX Testicular Associated to Hiperceratose Palmoplantaris. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf. Acesso em: 19 ago. 2024. , 2011
APA
Silva, R., Domenice, S., Nishi, M., Machado, A., Silva, T., Santos, M., et al. (2011). Novel Mutation in Rspo1 in Patient with Disorder of Sexual Development 46, XX Testicular Associated to Hiperceratose Palmoplantaris. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf
NLM
Silva R, Domenice S, Nishi M, Machado A, Silva T, Santos M, Brandão M, Mendonça B, Costa E. Novel Mutation in Rspo1 in Patient with Disorder of Sexual Development 46, XX Testicular Associated to Hiperceratose Palmoplantaris [Internet]. Hormone Research in Paediatrics. 2011 ; 76( suppl. 4): 22 res. 58.[citado 2024 ago. 19 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf
Vancouver
Silva R, Domenice S, Nishi M, Machado A, Silva T, Santos M, Brandão M, Mendonça B, Costa E. Novel Mutation in Rspo1 in Patient with Disorder of Sexual Development 46, XX Testicular Associated to Hiperceratose Palmoplantaris [Internet]. Hormone Research in Paediatrics. 2011 ; 76( suppl. 4): 22 res. 58.[citado 2024 ago. 19 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf
Artigo de periodico
TCF21 gene analysis in brazilian patients with 46,XY and 46,XX disorders of gonadal development (2007)
Gomes, C.; Domenice, S.; Santos, M.; Arnhold, I.; Mendonça, Berenice Bilharinho de; Costa, E.
Fonte: Hormone research. Nome do evento: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Assuntos: TÉCNICAS DE DIAGNÓSTICO E PROCEDIMENTOS, MUTAÇÃO GENÉTICA (ETIOLOGIA), POLIMORFISMO
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ABNT
GOMES, C. et al. TCF21 gene analysis in brazilian patients with 46,XY and 46,XX disorders of gonadal development. Hormone research, v. 68, p. 12, 2007Tradução . . Acesso em: 19 ago. 2024.
APA
Gomes, C., Domenice, S., Santos, M., Arnhold, I., Mendonça, B. B. de, & Costa, E. (2007). TCF21 gene analysis in brazilian patients with 46,XY and 46,XX disorders of gonadal development. Hormone research, 68, 12.
NLM
Gomes C, Domenice S, Santos M, Arnhold I, Mendonça BB de, Costa E. TCF21 gene analysis in brazilian patients with 46,XY and 46,XX disorders of gonadal development. Hormone research. 2007 ; 68 12.[citado 2024 ago. 19 ]
Vancouver
Gomes C, Domenice S, Santos M, Arnhold I, Mendonça BB de, Costa E. TCF21 gene analysis in brazilian patients with 46,XY and 46,XX disorders of gonadal development. Hormone research. 2007 ; 68 12.[citado 2024 ago. 19 ]
Artigo de periodico
New IVS2-2A>G mutation in the anti-mullerian hormone gene in 46,XY patients with persistent mullerian duct syndrome (PMDS) (2007)
Zaba Neto, A.; Nishi, M.; Costa, E.; Mendonça, Berenice Bilharinho de
Fonte: Hormone research. Nome do evento: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Assuntos: TRANSTORNOS GONADAIS, PROCESSOS PATOLÓGICOS, NEOPLASIAS TESTICULARES
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ABNT
ZABA NETO, A. et al. New IVS2-2A>G mutation in the anti-mullerian hormone gene in 46,XY patients with persistent mullerian duct syndrome (PMDS). Hormone research, v. 68, p. 31, 2007Tradução . . Acesso em: 19 ago. 2024.
APA
Zaba Neto, A., Nishi, M., Costa, E., & Mendonça, B. B. de. (2007). New IVS2-2A>G mutation in the anti-mullerian hormone gene in 46,XY patients with persistent mullerian duct syndrome (PMDS). Hormone research, 68, 31.
NLM
Zaba Neto A, Nishi M, Costa E, Mendonça BB de. New IVS2-2A>G mutation in the anti-mullerian hormone gene in 46,XY patients with persistent mullerian duct syndrome (PMDS). Hormone research. 2007 ; 68 31.[citado 2024 ago. 19 ]
Vancouver
Zaba Neto A, Nishi M, Costa E, Mendonça BB de. New IVS2-2A>G mutation in the anti-mullerian hormone gene in 46,XY patients with persistent mullerian duct syndrome (PMDS). Hormone research. 2007 ; 68 31.[citado 2024 ago. 19 ]
Artigo de periodico
Duplication of the dosage-sensitive sex reversal (DSS) locus in a brazilian patient with partial 46,XY gonadal dysgenesis and gonadoblastoma (2007)
Costa, E.; Domenice, S.; Nishi, M.; Pinto, E.; Mendonça, Berenice Bilharinho de
Fonte: Hormone research. Nome do evento: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Assuntos: CROMOSSOMOS SEXUAIS (DEFICIÊNCIA), TERAPIA, BRASILEIROS
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ABNT
COSTA, E. et al. Duplication of the dosage-sensitive sex reversal (DSS) locus in a brazilian patient with partial 46,XY gonadal dysgenesis and gonadoblastoma. Hormone research, v. 68, p. 6, 2007Tradução . . Acesso em: 19 ago. 2024.
APA
Costa, E., Domenice, S., Nishi, M., Pinto, E., & Mendonça, B. B. de. (2007). Duplication of the dosage-sensitive sex reversal (DSS) locus in a brazilian patient with partial 46,XY gonadal dysgenesis and gonadoblastoma. Hormone research, 68, 6.
NLM
Costa E, Domenice S, Nishi M, Pinto E, Mendonça BB de. Duplication of the dosage-sensitive sex reversal (DSS) locus in a brazilian patient with partial 46,XY gonadal dysgenesis and gonadoblastoma. Hormone research. 2007 ; 68 6.[citado 2024 ago. 19 ]
Vancouver
Costa E, Domenice S, Nishi M, Pinto E, Mendonça BB de. Duplication of the dosage-sensitive sex reversal (DSS) locus in a brazilian patient with partial 46,XY gonadal dysgenesis and gonadoblastoma. Hormone research. 2007 ; 68 6.[citado 2024 ago. 19 ]
Artigo de periodico
Presence of several polyadenylation signal polymorphisms in IGF1 gene of children born small for gestational age (SGA) with and without postnatal catch-up growth (2007)
Coutinho, D.; Coletta, R.; Costa, E.; Boguszewski, M.; Pachi, P.; Damiani, D.; Arnhold, I.; Mendonça, Berenice Bilharinho de; Jorge, A.
Fonte: Hormone research. Nome do evento: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Assuntos: POLIMORFISMO, ALELOPATIA, CRIANÇAS, RECÉM-NASCIDO PEQUENO PARA IDADE GESTACIONAL
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ABNT
COUTINHO, D. et al. Presence of several polyadenylation signal polymorphisms in IGF1 gene of children born small for gestational age (SGA) with and without postnatal catch-up growth. Hormone research, v. 68, p. 8, 2007Tradução . . Acesso em: 19 ago. 2024.
APA
Coutinho, D., Coletta, R., Costa, E., Boguszewski, M., Pachi, P., Damiani, D., et al. (2007). Presence of several polyadenylation signal polymorphisms in IGF1 gene of children born small for gestational age (SGA) with and without postnatal catch-up growth. Hormone research, 68, 8.
NLM
Coutinho D, Coletta R, Costa E, Boguszewski M, Pachi P, Damiani D, Arnhold I, Mendonça BB de, Jorge A. Presence of several polyadenylation signal polymorphisms in IGF1 gene of children born small for gestational age (SGA) with and without postnatal catch-up growth. Hormone research. 2007 ; 68 8.[citado 2024 ago. 19 ]
Vancouver
Coutinho D, Coletta R, Costa E, Boguszewski M, Pachi P, Damiani D, Arnhold I, Mendonça BB de, Jorge A. Presence of several polyadenylation signal polymorphisms in IGF1 gene of children born small for gestational age (SGA) with and without postnatal catch-up growth. Hormone research. 2007 ; 68 8.[citado 2024 ago. 19 ]
Artigo de periodico
Mutations in the SRY gene identified in three patients with 46,XY disorders of sexual development (DSD) due to abnormalities of gonadal development (2007)
Domenice, S.; Nishi, M.; Medeiros, M.; Costa, E.; Mendonça, Berenice Bilharinho de
Fonte: Hormone research. Nome do evento: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Assuntos: MUTAÇÃO GENÉTICA, TERAPIA, ANORMALIDADES CROMOSSÔMICAS, BRASILEIROS
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ABNT
DOMENICE, S. et al. Mutations in the SRY gene identified in three patients with 46,XY disorders of sexual development (DSD) due to abnormalities of gonadal development. Hormone research, v. 68, p. 8, 2007Tradução . . Acesso em: 19 ago. 2024.
APA
Domenice, S., Nishi, M., Medeiros, M., Costa, E., & Mendonça, B. B. de. (2007). Mutations in the SRY gene identified in three patients with 46,XY disorders of sexual development (DSD) due to abnormalities of gonadal development. Hormone research, 68, 8.
NLM
Domenice S, Nishi M, Medeiros M, Costa E, Mendonça BB de. Mutations in the SRY gene identified in three patients with 46,XY disorders of sexual development (DSD) due to abnormalities of gonadal development. Hormone research. 2007 ; 68 8.[citado 2024 ago. 19 ]
Vancouver
Domenice S, Nishi M, Medeiros M, Costa E, Mendonça BB de. Mutations in the SRY gene identified in three patients with 46,XY disorders of sexual development (DSD) due to abnormalities of gonadal development. Hormone research. 2007 ; 68 8.[citado 2024 ago. 19 ]
Artigo de periodico
Frequency of molecular diagnosis in brazilian patients with 46,XY disorders of sexual development (DSD) (2007)
Costa, E.; Domenice, S.; Billerbeck, A.; Melo, K.; Correa, R.; Nishi, M.; Pinto, E.; Gomes, C.; Coletta, R.; Abreu, A.; Brandão, M.; Martin, R.; Marui, S.; Xavier, Ana Claudia Latronico; Arnhold, I.; Mendonça, Berenice Bilharinho de
Fonte: Hormone research. Nome do evento: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Assuntos: CROMOSSOMOS SEXUAIS (DEFICIÊNCIA), TERAPIA, BRASILEIROS
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ABNT
COSTA, E. et al. Frequency of molecular diagnosis in brazilian patients with 46,XY disorders of sexual development (DSD). Hormone research, v. 68, p. 6, 2007Tradução . . Acesso em: 19 ago. 2024.
APA
Costa, E., Domenice, S., Billerbeck, A., Melo, K., Correa, R., Nishi, M., et al. (2007). Frequency of molecular diagnosis in brazilian patients with 46,XY disorders of sexual development (DSD). Hormone research, 68, 6.
NLM
Costa E, Domenice S, Billerbeck A, Melo K, Correa R, Nishi M, Pinto E, Gomes C, Coletta R, Abreu A, Brandão M, Martin R, Marui S, Xavier ACL, Arnhold I, Mendonça BB de. Frequency of molecular diagnosis in brazilian patients with 46,XY disorders of sexual development (DSD). Hormone research. 2007 ; 68 6.[citado 2024 ago. 19 ]
Vancouver
Costa E, Domenice S, Billerbeck A, Melo K, Correa R, Nishi M, Pinto E, Gomes C, Coletta R, Abreu A, Brandão M, Martin R, Marui S, Xavier ACL, Arnhold I, Mendonça BB de. Frequency of molecular diagnosis in brazilian patients with 46,XY disorders of sexual development (DSD). Hormone research. 2007 ; 68 6.[citado 2024 ago. 19 ]
Artigo de periodico
Absence of mutations in DHG gene in brazilian patients with 46,XY disorders of gonadal development (2007)
Gomes, C.; Domenice, S.; Arnhold, I.; Mendonça, Berenice Bilharinho de; Costa, E.
Fonte: Hormone research. Nome do evento: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Assuntos: BRASILEIROS, TRANSTORNOS DA DIFERENCIAÇÃO SEXUAL, MUTAÇÃO GENÉTICA
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ABNT
GOMES, C. et al. Absence of mutations in DHG gene in brazilian patients with 46,XY disorders of gonadal development. Hormone research, v. 68, p. 12, 2007Tradução . . Acesso em: 19 ago. 2024.
APA
Gomes, C., Domenice, S., Arnhold, I., Mendonça, B. B. de, & Costa, E. (2007). Absence of mutations in DHG gene in brazilian patients with 46,XY disorders of gonadal development. Hormone research, 68, 12.
NLM
Gomes C, Domenice S, Arnhold I, Mendonça BB de, Costa E. Absence of mutations in DHG gene in brazilian patients with 46,XY disorders of gonadal development. Hormone research. 2007 ; 68 12.[citado 2024 ago. 19 ]
Vancouver
Gomes C, Domenice S, Arnhold I, Mendonça BB de, Costa E. Absence of mutations in DHG gene in brazilian patients with 46,XY disorders of gonadal development. Hormone research. 2007 ; 68 12.[citado 2024 ago. 19 ]
Trabalho de evento-resumo
Mutational analysis of neuropeptide y-y1 receptor gene (npy-y1) in human idiopathic pubertal disorders (2004)
Freitas, K.; Brito, V.; Costa, E.; Arnhold, I.; Mendonca, B. B.; Latronico, A. C.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: HORMÔNIO DO CRESCIMENTO (SECREÇÃO), PUBERDADE PRECOCE (ANORMALIDADES;GENÉTICAS), SEQUENCIAMENTO GENÉTICO, HORMÔNIOS SEXUAIS (GENÉTICA)
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ABNT
FREITAS, K. et al. Mutational analysis of neuropeptide y-y1 receptor gene (npy-y1) in human idiopathic pubertal disorders. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 19 ago. 2024.
APA
Freitas, K., Brito, V., Costa, E., Arnhold, I., Mendonca, B. B., & Latronico, A. C. (2004). Mutational analysis of neuropeptide y-y1 receptor gene (npy-y1) in human idiopathic pubertal disorders. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Freitas K, Brito V, Costa E, Arnhold I, Mendonca BB, Latronico AC. Mutational analysis of neuropeptide y-y1 receptor gene (npy-y1) in human idiopathic pubertal disorders. Program and Abstracts. 2004 ;[citado 2024 ago. 19 ]
Vancouver
Freitas K, Brito V, Costa E, Arnhold I, Mendonca BB, Latronico AC. Mutational analysis of neuropeptide y-y1 receptor gene (npy-y1) in human idiopathic pubertal disorders. Program and Abstracts. 2004 ;[citado 2024 ago. 19 ]
Trabalho de evento-resumo
The content and expression of nitric oxide (NO) synthase isoforms in bone marrow neutrophils from ovalbumin sensitized rats (1999)
Ferreira, H. H. A.; De Nucci, Gilberto ; De Luca, I. M. S.; Costa, E.; Antunes, E
Fonte: Resumos. Nome do evento: Reunião Anual da Federação de Sociedades de Biologia Experimental. Unidade: ICB
Assunto: FARMACOLOGIA
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ABNT
FERREIRA, H. H. A. et al. The content and expression of nitric oxide (NO) synthase isoforms in bone marrow neutrophils from ovalbumin sensitized rats. 1999, Anais.. São Paulo: FESBE, 1999. . Acesso em: 19 ago. 2024.
APA
Ferreira, H. H. A., De Nucci, G., De Luca, I. M. S., Costa, E., & Antunes, E. (1999). The content and expression of nitric oxide (NO) synthase isoforms in bone marrow neutrophils from ovalbumin sensitized rats. In Resumos. São Paulo: FESBE.
NLM
Ferreira HHA, De Nucci G, De Luca IMS, Costa E, Antunes E. The content and expression of nitric oxide (NO) synthase isoforms in bone marrow neutrophils from ovalbumin sensitized rats. Resumos. 1999 ;[citado 2024 ago. 19 ]
Vancouver
Ferreira HHA, De Nucci G, De Luca IMS, Costa E, Antunes E. The content and expression of nitric oxide (NO) synthase isoforms in bone marrow neutrophils from ovalbumin sensitized rats. Resumos. 1999 ;[citado 2024 ago. 19 ]

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