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Artigo de periodico
Identification of SHOX gene deletions in patients with disproportional short stature or Léri-Weill dyschondrosteosis: comparison between the fish technique and microsatellite study (2007)
Funari, M.; Jorge, A.; Souza, S.; Mendonça, Berenice Bilharinho de; Nishi, M.
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, PESO-ESTATURA, BIOMARCADORES
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ABNT
FUNARI, M. et al. Identification of SHOX gene deletions in patients with disproportional short stature or Léri-Weill dyschondrosteosis: comparison between the fish technique and microsatellite study. Hormone research, v. 68, p. 11, 2007Tradução . . Acesso em: 15 jun. 2024.
APA
Funari, M., Jorge, A., Souza, S., Mendonça, B. B. de, & Nishi, M. (2007). Identification of SHOX gene deletions in patients with disproportional short stature or Léri-Weill dyschondrosteosis: comparison between the fish technique and microsatellite study. Hormone research, 68, 11.
NLM
Funari M, Jorge A, Souza S, Mendonça BB de, Nishi M. Identification of SHOX gene deletions in patients with disproportional short stature or Léri-Weill dyschondrosteosis: comparison between the fish technique and microsatellite study. Hormone research. 2007 ; 68 11.[citado 2024 jun. 15 ]
Vancouver
Funari M, Jorge A, Souza S, Mendonça BB de, Nishi M. Identification of SHOX gene deletions in patients with disproportional short stature or Léri-Weill dyschondrosteosis: comparison between the fish technique and microsatellite study. Hormone research. 2007 ; 68 11.[citado 2024 jun. 15 ]
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: 15 jun. 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 jun. 15 ]
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 jun. 15 ]
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: 15 jun. 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 jun. 15 ]
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 jun. 15 ]
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: 15 jun. 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 jun. 15 ]
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 jun. 15 ]
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: 15 jun. 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 jun. 15 ]
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 jun. 15 ]
Artigo de periodico
Mutation in PTPN11 gene are a common cause of noonan syndrome (NS) but are not a selective IGF-1 receptor kinase inhibitor (NVP-AEW541) suppresses proliferation of the human adrenocortical cancer cell line NCI H295 due to apoptosis induction (2007)
Almeida, M. Queiroz; Gerdulo, M.; Jorge, A. Lima Augusto; Nishi, M. Yumie; Lerario, A.; Fragoso, M. Barrison Villares; Mendonça, Berenice Bilharinho de; Xavier, Ana Claudia Latronico
Fonte: Hormone research. Nome do evento: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Assuntos: MUTATAÇÃO GENÉTICA, APOPTOSE, NEOPLASIAS DAS GLÂNDULAS SUPRARRENAIS
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ABNT
ALMEIDA, M. Queiroz et al. Mutation in PTPN11 gene are a common cause of noonan syndrome (NS) but are not a selective IGF-1 receptor kinase inhibitor (NVP-AEW541) suppresses proliferation of the human adrenocortical cancer cell line NCI H295 due to apoptosis induction. Hormone research, v. 68, p. 24, 2007Tradução . . Acesso em: 15 jun. 2024.
APA
Almeida, M. Q., Gerdulo, M., Jorge, A. L. A., Nishi, M. Y., Lerario, A., Fragoso, M. B. V., et al. (2007). Mutation in PTPN11 gene are a common cause of noonan syndrome (NS) but are not a selective IGF-1 receptor kinase inhibitor (NVP-AEW541) suppresses proliferation of the human adrenocortical cancer cell line NCI H295 due to apoptosis induction. Hormone research, 68, 24.
NLM
Almeida MQ, Gerdulo M, Jorge ALA, Nishi MY, Lerario A, Fragoso MBV, Mendonça BB de, Xavier ACL. Mutation in PTPN11 gene are a common cause of noonan syndrome (NS) but are not a selective IGF-1 receptor kinase inhibitor (NVP-AEW541) suppresses proliferation of the human adrenocortical cancer cell line NCI H295 due to apoptosis induction. Hormone research. 2007 ; 68 24.[citado 2024 jun. 15 ]
Vancouver
Almeida MQ, Gerdulo M, Jorge ALA, Nishi MY, Lerario A, Fragoso MBV, Mendonça BB de, Xavier ACL. Mutation in PTPN11 gene are a common cause of noonan syndrome (NS) but are not a selective IGF-1 receptor kinase inhibitor (NVP-AEW541) suppresses proliferation of the human adrenocortical cancer cell line NCI H295 due to apoptosis induction. Hormone research. 2007 ; 68 24.[citado 2024 jun. 15 ]
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: 15 jun. 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 jun. 15 ]
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 jun. 15 ]
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: 15 jun. 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 jun. 15 ]
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 jun. 15 ]
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
Fonte: Hormone research. Nome do evento: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Assuntos: PUBERDADE PRECOCE (TERAPIA), SEGUIMENTOS, SENSIBILIDADE E ESPECIFICIDADE
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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: 15 jun. 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 jun. 15 ]
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 jun. 15 ]
Artigo de periodico
Found in children with idiopathic short stature and NS-associated signs (2007)
Ferreira, L.; Montenegro, L.; 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, PESO-ESTATURA, CRIANÇAS, MUTAÇÃO GENÉTICA
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ABNT
FERREIRA, L. et al. Found in children with idiopathic short stature and NS-associated signs. Hormone research, v. 68, p. 10, 2007Tradução . . Acesso em: 15 jun. 2024.
APA
Ferreira, L., Montenegro, L., Arnhold, I., Mendonça, B. B. de, & Jorge, A. (2007). Found in children with idiopathic short stature and NS-associated signs. Hormone research, 68, 10.
NLM
Ferreira L, Montenegro L, Arnhold I, Mendonça BB de, Jorge A. Found in children with idiopathic short stature and NS-associated signs. Hormone research. 2007 ; 68 10.[citado 2024 jun. 15 ]
Vancouver
Ferreira L, Montenegro L, Arnhold I, Mendonça BB de, Jorge A. Found in children with idiopathic short stature and NS-associated signs. Hormone research. 2007 ; 68 10.[citado 2024 jun. 15 ]
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: 15 jun. 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 jun. 15 ]
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 jun. 15 ]

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