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Trabalho de evento-resumo
A homozigous 25 Bp duplication (Nt 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon as a new cause of combined 17alpha-hydroxylase/17,20-lyase deficiency (2005)
Martin, Regina M.; Costa, Elaine F.; Arnhold, Ivo J. P.; Mendonça, Berenice B.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: HIPERTENSÃO (ETIOLOGIA), MUTAÇÃO GENÉTICA, BRASILEIROS, HORMÔNIOS SEXUAIS (ANORMALIDADES)
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ABNT
MARTIN, Regina M. et al. A homozigous 25 Bp duplication (Nt 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon as a new cause of combined 17alpha-hydroxylase/17,20-lyase deficiency. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 04 nov. 2025.
APA
Martin, R. M., Costa, E. F., Arnhold, I. J. P., & Mendonça, B. B. (2005). A homozigous 25 Bp duplication (Nt 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon as a new cause of combined 17alpha-hydroxylase/17,20-lyase deficiency. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Martin RM, Costa EF, Arnhold IJP, Mendonça BB. A homozigous 25 Bp duplication (Nt 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon as a new cause of combined 17alpha-hydroxylase/17,20-lyase deficiency. Program and Abstracts. 2005 ;[citado 2025 nov. 04 ]
Vancouver
Martin RM, Costa EF, Arnhold IJP, Mendonça BB. A homozigous 25 Bp duplication (Nt 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon as a new cause of combined 17alpha-hydroxylase/17,20-lyase deficiency. Program and Abstracts. 2005 ;[citado 2025 nov. 04 ]
Trabalho de evento-resumo
Molecular analysis of the GABA-A receptor alpha-1 subunit gene (GABRA1) and electroencephalographic findings in girls with idiopathic gonadotropin-dependent precocious puberty (2005)
Brito, Vinicius N.; Arnhold, Ivo J. P.; Mendonça, Berenice B.; Guilhoto, Laura M.; Freitas, Karina M.; Latronico, Ana C.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: PUBERDADE PRECOCE (ETIOLOGIA), CRIANÇAS, GONADOTROFINAS, HORMÔNIOS HIPOFISÁRIOS (ANORMALIDADES)
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ABNT
BRITO, Vinicius N. et al. Molecular analysis of the GABA-A receptor alpha-1 subunit gene (GABRA1) and electroencephalographic findings in girls with idiopathic gonadotropin-dependent precocious puberty. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 04 nov. 2025.
APA
Brito, V. N., Arnhold, I. J. P., Mendonça, B. B., Guilhoto, L. M., Freitas, K. M., & Latronico, A. C. (2005). Molecular analysis of the GABA-A receptor alpha-1 subunit gene (GABRA1) and electroencephalographic findings in girls with idiopathic gonadotropin-dependent precocious puberty. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Brito VN, Arnhold IJP, Mendonça BB, Guilhoto LM, Freitas KM, Latronico AC. Molecular analysis of the GABA-A receptor alpha-1 subunit gene (GABRA1) and electroencephalographic findings in girls with idiopathic gonadotropin-dependent precocious puberty. Program and Abstracts. 2005 ;[citado 2025 nov. 04 ]
Vancouver
Brito VN, Arnhold IJP, Mendonça BB, Guilhoto LM, Freitas KM, Latronico AC. Molecular analysis of the GABA-A receptor alpha-1 subunit gene (GABRA1) and electroencephalographic findings in girls with idiopathic gonadotropin-dependent precocious puberty. Program and Abstracts. 2005 ;[citado 2025 nov. 04 ]
Trabalho de evento-resumo
Prevalence of a genetic variant of luteinizing hormone (Tr8Arg and lle 15Thr) in a brazilian population of healthy subjects and in patients with hypogonadotropic hypogonadism (2005)
Berger, Karina; Billerbeck, Ana Elisa C.; Costa, Elaine M. F.; Cavalho, Luciani R.; Arnhold, Ivo J. P.; Mendonça, Berenice B.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: POLIMORFISMO, TÉCNICAS CITOLÓGICAS, BRASILEIROS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERGER, Karina et al. Prevalence of a genetic variant of luteinizing hormone (Tr8Arg and lle 15Thr) in a brazilian population of healthy subjects and in patients with hypogonadotropic hypogonadism. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 04 nov. 2025.
APA
Berger, K., Billerbeck, A. E. C., Costa, E. M. F., Cavalho, L. R., Arnhold, I. J. P., & Mendonça, B. B. (2005). Prevalence of a genetic variant of luteinizing hormone (Tr8Arg and lle 15Thr) in a brazilian population of healthy subjects and in patients with hypogonadotropic hypogonadism. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Berger K, Billerbeck AEC, Costa EMF, Cavalho LR, Arnhold IJP, Mendonça BB. Prevalence of a genetic variant of luteinizing hormone (Tr8Arg and lle 15Thr) in a brazilian population of healthy subjects and in patients with hypogonadotropic hypogonadism. Program and Abstracts. 2005 ;[citado 2025 nov. 04 ]
Vancouver
Berger K, Billerbeck AEC, Costa EMF, Cavalho LR, Arnhold IJP, Mendonça BB. Prevalence of a genetic variant of luteinizing hormone (Tr8Arg and lle 15Thr) in a brazilian population of healthy subjects and in patients with hypogonadotropic hypogonadism. Program and Abstracts. 2005 ;[citado 2025 nov. 04 ]
Trabalho de evento-resumo
The effects of pamindronate treatment in girls with polyostotic fibrous dysplasia in McCune Albrigth syndrome (2005)
Bezerra, Milena G. T.; Brito, Vinicius N.; Arnhold, Ivo J. P.; Mendonça, Berenice B.; Latronico, Ana C.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: DOENÇA RARA, MUTAÇÃO GENÉTICA, FÁRMACOS (SISTEMA REPRODUTOR;EFEITOS ADVERSOS)
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ABNT
BEZERRA, Milena G. T. et al. The effects of pamindronate treatment in girls with polyostotic fibrous dysplasia in McCune Albrigth syndrome. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 04 nov. 2025.
APA
Bezerra, M. G. T., Brito, V. N., Arnhold, I. J. P., Mendonça, B. B., & Latronico, A. C. (2005). The effects of pamindronate treatment in girls with polyostotic fibrous dysplasia in McCune Albrigth syndrome. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Bezerra MGT, Brito VN, Arnhold IJP, Mendonça BB, Latronico AC. The effects of pamindronate treatment in girls with polyostotic fibrous dysplasia in McCune Albrigth syndrome. Program and Abstracts. 2005 ;[citado 2025 nov. 04 ]
Vancouver
Bezerra MGT, Brito VN, Arnhold IJP, Mendonça BB, Latronico AC. The effects of pamindronate treatment in girls with polyostotic fibrous dysplasia in McCune Albrigth syndrome. Program and Abstracts. 2005 ;[citado 2025 nov. 04 ]
Trabalho de evento-resumo
Patients with Noonan syndrome without mutation in PTPN11repond better to GH treatment than patients with PTPN11 mutations (2005)
Jorge. Alexandre A. L.; Ferreira, Lize V.; Souza, Silvia A. L.; Arnhold, Ivo J. P.; Mendonça, Berenice B.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: CRIANÇAS, SEGUIMENTOS, HORMÔNIO DO CRESCIMENTO (TERAPIA), MUTAÇÃO GENÉTICA
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ABNT
JORGE. ALEXANDRE A. L., et al. Patients with Noonan syndrome without mutation in PTPN11repond better to GH treatment than patients with PTPN11 mutations. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 04 nov. 2025.
APA
Jorge. Alexandre A. L.,, Ferreira, L. V., Souza, S. A. L., Arnhold, I. J. P., & Mendonça, B. B. (2005). Patients with Noonan syndrome without mutation in PTPN11repond better to GH treatment than patients with PTPN11 mutations. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Jorge. Alexandre A. L., Ferreira LV, Souza SAL, Arnhold IJP, Mendonça BB. Patients with Noonan syndrome without mutation in PTPN11repond better to GH treatment than patients with PTPN11 mutations. Program and Abstracts. 2005 ;[citado 2025 nov. 04 ]
Vancouver
Jorge. Alexandre A. L., Ferreira LV, Souza SAL, Arnhold IJP, Mendonça BB. Patients with Noonan syndrome without mutation in PTPN11repond better to GH treatment than patients with PTPN11 mutations. Program and Abstracts. 2005 ;[citado 2025 nov. 04 ]
Trabalho de evento-resumo
Growth and bone mineral density in patients with androgem insensitivity syndrome with mutations in the androgen receptor gene (2005)
Danilovic, Debora L. S.; Costa, Elaine M. F.; Melo, Karla; Correa, Rafaela V.; Correa, Pedro H. S.; Mendonça, Berenice B.; Arnhold, Ivo J. P.; Fragoso, Maria Candida B. V.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: ESTRÓGENOS (TERAPIA), DENSIDADE ÓSSEA, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DANILOVIC, Debora L. S. et al. Growth and bone mineral density in patients with androgem insensitivity syndrome with mutations in the androgen receptor gene. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 04 nov. 2025.
APA
Danilovic, D. L. S., Costa, E. M. F., Melo, K., Correa, R. V., Correa, P. H. S., Mendonça, B. B., et al. (2005). Growth and bone mineral density in patients with androgem insensitivity syndrome with mutations in the androgen receptor gene. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Danilovic DLS, Costa EMF, Melo K, Correa RV, Correa PHS, Mendonça BB, Arnhold IJP, Fragoso MCBV. Growth and bone mineral density in patients with androgem insensitivity syndrome with mutations in the androgen receptor gene. Program and Abstracts. 2005 ;[citado 2025 nov. 04 ]
Vancouver
Danilovic DLS, Costa EMF, Melo K, Correa RV, Correa PHS, Mendonça BB, Arnhold IJP, Fragoso MCBV. Growth and bone mineral density in patients with androgem insensitivity syndrome with mutations in the androgen receptor gene. Program and Abstracts. 2005 ;[citado 2025 nov. 04 ]

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