ReP USP - Resultado da busca

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.
Source: Program and Abstracts. Conference titles: International Congress of Endocrinology. Unidade: FM
Subjects: HORMÔNIO DO CRESCIMENTO (SECREÇÃO), PUBERDADE PRECOCE (ANORMALIDADES;GENÉTICAS), SEQUENCIAMENTO GENÉTICO, HORMÔNIOS SEXUAIS (GENÉTICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 03 nov. 2025.
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 2025 nov. 03 ]
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 2025 nov. 03 ]
Trabalho de evento-resumo
Mutational analysis of the gaba-a receptor alpha1 subunit gene (gabra 1) in girls familial and sporadic idiophatic gonadotrpin-dependent precocious puberty (2004)
Brito, V.; Mendonca, B. B.; Freitas, k.; Arnhold, I.; Latronico, A. C.
Source: Program and Abstracts. Conference titles: International Congress of Endocrinology. Unidade: FM
Subjects: HORMÔNIO DO CRESCIMENTO (FISIOPATOLOGIA), PUBERDADE PRECOCE, POLIMORFISMO, GENES SUPRESSORES DE TUMOR (METABOLISMO), GONADOTROFINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BRITO, V. et al. Mutational analysis of the gaba-a receptor alpha1 subunit gene (gabra 1) in girls familial and sporadic idiophatic gonadotrpin-dependent precocious puberty. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 03 nov. 2025.
APA
Brito, V., Mendonca, B. B., Freitas, k., Arnhold, I., & Latronico, A. C. (2004). Mutational analysis of the gaba-a receptor alpha1 subunit gene (gabra 1) in girls familial and sporadic idiophatic gonadotrpin-dependent precocious puberty. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Brito V, Mendonca BB, Freitas k., Arnhold I, Latronico AC. Mutational analysis of the gaba-a receptor alpha1 subunit gene (gabra 1) in girls familial and sporadic idiophatic gonadotrpin-dependent precocious puberty. Program and Abstracts. 2004 ;[citado 2025 nov. 03 ]
Vancouver
Brito V, Mendonca BB, Freitas k., Arnhold I, Latronico AC. Mutational analysis of the gaba-a receptor alpha1 subunit gene (gabra 1) in girls familial and sporadic idiophatic gonadotrpin-dependent precocious puberty. Program and Abstracts. 2004 ;[citado 2025 nov. 03 ]
Trabalho de evento-resumo
Diagnosis and treatment of girls with gonadotropin-independent precocious puberty due to automous ovarian cysts (2004)
d`Alva, C.; Latronico, A.; Brito, V.; Teles, M.; Arnhold, I.; Mendonca, B. B.
Source: Program and Abstracts. Conference titles: International Congress of Endocrinology. Unidade: FM
Subjects: PUBERDADE PRECOCE (ETIOLOGIA;GENÉTICA;DIAGNÓSTICO;TERAPIA), HORMÔNIOS SEXUAIS FEMININOS (GENÉTICA;ANORMALIDADES), CISTOS OVARIANOS (ETIOLOGIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
D`ALVA, C. et al. Diagnosis and treatment of girls with gonadotropin-independent precocious puberty due to automous ovarian cysts. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 03 nov. 2025.
APA
d`Alva, C., Latronico, A., Brito, V., Teles, M., Arnhold, I., & Mendonca, B. B. (2004). Diagnosis and treatment of girls with gonadotropin-independent precocious puberty due to automous ovarian cysts. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
d`Alva C, Latronico A, Brito V, Teles M, Arnhold I, Mendonca BB. Diagnosis and treatment of girls with gonadotropin-independent precocious puberty due to automous ovarian cysts. Program and Abstracts. 2004 ;[citado 2025 nov. 03 ]
Vancouver
d`Alva C, Latronico A, Brito V, Teles M, Arnhold I, Mendonca BB. Diagnosis and treatment of girls with gonadotropin-independent precocious puberty due to automous ovarian cysts. Program and Abstracts. 2004 ;[citado 2025 nov. 03 ]
Trabalho de evento-resumo
Final heigth in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency treated with cortisone acetate (2004)
Parente, E.; Marquezine, E.; Rodrigues, a.; Maureira, G.; Brenlha, E. M.; Ueti, R.; Arnhold, I.; Mendonca, B. B.; Bachega, T. A. S.
Source: Program and Abstracts. Conference titles: International Congress of Endocrinology. Unidade: FM
Subjects: CORTISOL (APLICAÇÕES TERAPÊUTICAS), HORMÔNIOS (DEFICIÊNCIA), TERAPIAS COMPLEMENTARES, HIPERPLASIA SUPRARRENAL CONGÊNITA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PARENTE, E. et al. Final heigth in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency treated with cortisone acetate. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 03 nov. 2025.
APA
Parente, E., Marquezine, E., Rodrigues, a., Maureira, G., Brenlha, E. M., Ueti, R., et al. (2004). Final heigth in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency treated with cortisone acetate. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Parente E, Marquezine E, Rodrigues a., Maureira G, Brenlha EM, Ueti R, Arnhold I, Mendonca BB, Bachega TAS. Final heigth in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency treated with cortisone acetate. Program and Abstracts. 2004 ;[citado 2025 nov. 03 ]
Vancouver
Parente E, Marquezine E, Rodrigues a., Maureira G, Brenlha EM, Ueti R, Arnhold I, Mendonca BB, Bachega TAS. Final heigth in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency treated with cortisone acetate. Program and Abstracts. 2004 ;[citado 2025 nov. 03 ]

USP Schools

ReP

Filtros

Authors

Subjects