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Artigo de periodico
Long-term outcomes of Patients with Central Precocious Puberty due to Hypothalamic Hamartoma after GnRHa Treatment: anthropometric, Metabolic, and Reproductive Aspects (2018)
Ramos, Carolina O.; Xavier, Ana C Latronico; Cukier, Priscilla; Macedo, Delanie B.; Bessa, Danielle S.; Cunha-Silva, Marina; Arnhold, Ivo J.; Mendonça, Berenice Bilharinho de; Brito, Vinicius N
Source: Neuroendocrinology. Unidade: FM
Subjects: PUBERDADE PRECOCE, TRANSTORNOS GONADAIS, EPILEPSIA, CRIANÇAS, ÍNDICE DE MASSA CORPORAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAMOS, Carolina O. et al. Long-term outcomes of Patients with Central Precocious Puberty due to Hypothalamic Hamartoma after GnRHa Treatment: anthropometric, Metabolic, and Reproductive Aspects. Neuroendocrinology, v. 106, n. 3, p. 203-210, 2018Tradução . . Disponível em: https://doi.org/10.1159/000477584. Acesso em: 03 nov. 2024.
APA
Ramos, C. O., Xavier, A. C. L., Cukier, P., Macedo, D. B., Bessa, D. S., Cunha-Silva, M., et al. (2018). Long-term outcomes of Patients with Central Precocious Puberty due to Hypothalamic Hamartoma after GnRHa Treatment: anthropometric, Metabolic, and Reproductive Aspects. Neuroendocrinology, 106( 3), 203-210. doi:10.1159/000477584
NLM
Ramos CO, Xavier ACL, Cukier P, Macedo DB, Bessa DS, Cunha-Silva M, Arnhold IJ, Mendonça BB de, Brito VN. Long-term outcomes of Patients with Central Precocious Puberty due to Hypothalamic Hamartoma after GnRHa Treatment: anthropometric, Metabolic, and Reproductive Aspects [Internet]. Neuroendocrinology. 2018 ; 106( 3): 203-210.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1159/000477584
Vancouver
Ramos CO, Xavier ACL, Cukier P, Macedo DB, Bessa DS, Cunha-Silva M, Arnhold IJ, Mendonça BB de, Brito VN. Long-term outcomes of Patients with Central Precocious Puberty due to Hypothalamic Hamartoma after GnRHa Treatment: anthropometric, Metabolic, and Reproductive Aspects [Internet]. Neuroendocrinology. 2018 ; 106( 3): 203-210.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1159/000477584
Artigo de periodico
Methylome profiling of healthy and central precocious puberty girls (2018)
Bessa, Danielle S.; Mendonca, Berenice B.; Xavier, Ana Claudia Latronico
Source: Clinical epigenetics. Unidade: FM
Subjects: METILAÇÃO DE DNA, PUBERDADE PRECOCE, MULHERES, EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BESSA, Danielle S. e MENDONCA, Berenice B. e XAVIER, Ana Claudia Latronico. Methylome profiling of healthy and central precocious puberty girls. Clinical epigenetics, v. 10, 2018Tradução . . Disponível em: https://doi.org/10.1186/s13148-018-0581-1. Acesso em: 03 nov. 2024.
APA
Bessa, D. S., Mendonca, B. B., & Xavier, A. C. L. (2018). Methylome profiling of healthy and central precocious puberty girls. Clinical epigenetics, 10. doi:10.1186/s13148-018-0581-1
NLM
Bessa DS, Mendonca BB, Xavier ACL. Methylome profiling of healthy and central precocious puberty girls [Internet]. Clinical epigenetics. 2018 ; 10[citado 2024 nov. 03 ] Available from: https://doi.org/10.1186/s13148-018-0581-1
Vancouver
Bessa DS, Mendonca BB, Xavier ACL. Methylome profiling of healthy and central precocious puberty girls [Internet]. Clinical epigenetics. 2018 ; 10[citado 2024 nov. 03 ] Available from: https://doi.org/10.1186/s13148-018-0581-1
Artigo de periodico
High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic (2017)
Bessa, Danielle S.; Montenegro, Luciana Ribeiro; Mendonça, Berenice Bilharinho de; Xavier, Ana Claudia Latronico
Source: Neuroendocrinology. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, PUBERDADE PRECOCE, DOENÇAS HEREDITÁRIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BESSA, Danielle S. et al. High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic. Neuroendocrinology, v. 105, n. 1, p. 17-25, 2017Tradução . . Disponível em: https://doi.org/10.1159/000446963. Acesso em: 03 nov. 2024.
APA
Bessa, D. S., Montenegro, L. R., Mendonça, B. B. de, & Xavier, A. C. L. (2017). High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic. Neuroendocrinology, 105( 1), 17-25. doi:10.1159/000446963
NLM
Bessa DS, Montenegro LR, Mendonça BB de, Xavier ACL. High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic [Internet]. Neuroendocrinology. 2017 ; 105( 1): 17-25.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1159/000446963
Vancouver
Bessa DS, Montenegro LR, Mendonça BB de, Xavier ACL. High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic [Internet]. Neuroendocrinology. 2017 ; 105( 1): 17-25.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1159/000446963
Artigo de periodico
Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty (2017)
Dauber, Andrew; Cunha-Silva, Marina; Macedo, Delanie B.; Brito, Vinicius N.; Abreu, Ana Paula; Roberts, Stephanie A.; Montenegro, Luciana R.; Andrew, Melissa; Kirby, Andrew; Weirauch, Matthew T.; Labilloy, Guillaume; Bessa, Danielle S.; Carroll, Rona S.; Jacobs, Dakota C.; Chappell, Patrick E.; Mendonca, Berenice B.; Haig, David; Kaiser, Ursula B.; Latronico, Ana Claudia
Source: Journal of clinical endocrinology and metabolism. Unidade: FM
Subjects: PUBERDADE PRECOCE, REAÇÃO EM CADEIA POR POLIMERASE, HIPOTÁLAMO, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DAUBER, Andrew et al. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty. Journal of clinical endocrinology and metabolism, v. 102, n. 5, p. 1557-1567, 2017Tradução . . Disponível em: https://doi.org/10.1210/jc.2016-3677. Acesso em: 03 nov. 2024.
APA
Dauber, A., Cunha-Silva, M., Macedo, D. B., Brito, V. N., Abreu, A. P., Roberts, S. A., et al. (2017). Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty. Journal of clinical endocrinology and metabolism, 102( 5), 1557-1567. doi:10.1210/jc.2016-3677
NLM
Dauber A, Cunha-Silva M, Macedo DB, Brito VN, Abreu AP, Roberts SA, Montenegro LR, Andrew M, Kirby A, Weirauch MT, Labilloy G, Bessa DS, Carroll RS, Jacobs DC, Chappell PE, Mendonca BB, Haig D, Kaiser UB, Latronico AC. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty [Internet]. Journal of clinical endocrinology and metabolism. 2017 ; 102( 5): 1557-1567.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1210/jc.2016-3677
Vancouver
Dauber A, Cunha-Silva M, Macedo DB, Brito VN, Abreu AP, Roberts SA, Montenegro LR, Andrew M, Kirby A, Weirauch MT, Labilloy G, Bessa DS, Carroll RS, Jacobs DC, Chappell PE, Mendonca BB, Haig D, Kaiser UB, Latronico AC. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty [Internet]. Journal of clinical endocrinology and metabolism. 2017 ; 102( 5): 1557-1567.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1210/jc.2016-3677

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