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Artigo de periodico
Effects of glucocorticoids on interstitial glucose concentrations in individuals with hematologic cancer and without known diagnosis of diabetes: a pilot study (2022)
Toyoshima, Marcos Tadashi Kakitani ; Cukier, Priscilla; Souza, Alexandre Barbosa Câmara de ; Pereira, Juliana; Hoff, Ana Oliveira; Nery, Marcia
Source: Einstein-sao paulo. Unidade: FM
Subjects: HORMÔNIOS GLICOCORTICOIDES, DIABETES MELLITUS, NEOPLASIAS, HEMATOLOGIA
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TOYOSHIMA, Marcos Tadashi Kakitani et al. Effects of glucocorticoids on interstitial glucose concentrations in individuals with hematologic cancer and without known diagnosis of diabetes: a pilot study. Einstein-sao paulo, v. 20, 2022Tradução . . Disponível em: https://doi.org/10.31744/einstein_journal/2022AO8031. Acesso em: 25 out. 2025.
APA
Toyoshima, M. T. K., Cukier, P., Souza, A. B. C. de, Pereira, J., Hoff, A. O., & Nery, M. (2022). Effects of glucocorticoids on interstitial glucose concentrations in individuals with hematologic cancer and without known diagnosis of diabetes: a pilot study. Einstein-sao paulo, 20. doi:10.31744/einstein_journal/2022AO8031
NLM
Toyoshima MTK, Cukier P, Souza ABC de, Pereira J, Hoff AO, Nery M. Effects of glucocorticoids on interstitial glucose concentrations in individuals with hematologic cancer and without known diagnosis of diabetes: a pilot study [Internet]. Einstein-sao paulo. 2022 ; 20[citado 2025 out. 25 ] Available from: https://doi.org/10.31744/einstein_journal/2022AO8031
Vancouver
Toyoshima MTK, Cukier P, Souza ABC de, Pereira J, Hoff AO, Nery M. Effects of glucocorticoids on interstitial glucose concentrations in individuals with hematologic cancer and without known diagnosis of diabetes: a pilot study [Internet]. Einstein-sao paulo. 2022 ; 20[citado 2025 out. 25 ] Available from: https://doi.org/10.31744/einstein_journal/2022AO8031
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
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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: 25 out. 2025.
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 2025 out. 25 ] 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 2025 out. 25 ] Available from: https://doi.org/10.1159/000477584
Artigo de periodico
New digital tool to facilitate subcutaneous insulin therapy orders: an inpatient insulin dose calculator (2015)
Toyoshima, Marcos Tadashi Kakitani; Souza, Alexandre Barbosa Câmara de ; Admoni, Sharon Nina; Cukier, Priscilla; Lottenberg, Simão Augusto; Latronico, Ana Claudia; Nery, Márcia
Source: Diabetology and Metabolic Syndrome. Unidade: FM
Subjects: INSULINA (APLICAÇÕES TERAPÊUTICAS), PACIENTES HOSPITALIZADOS, DIABETES MELLITUS (TERAPIA)
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TOYOSHIMA, Marcos Tadashi Kakitani et al. New digital tool to facilitate subcutaneous insulin therapy orders: an inpatient insulin dose calculator. Diabetology and Metabolic Syndrome, v. 7, p. 6 , 2015Tradução . . Disponível em: https://doi.org/10.1186/s13098-015-0111-7. Acesso em: 25 out. 2025.
APA
Toyoshima, M. T. K., Souza, A. B. C. de, Admoni, S. N., Cukier, P., Lottenberg, S. A., Latronico, A. C., & Nery, M. (2015). New digital tool to facilitate subcutaneous insulin therapy orders: an inpatient insulin dose calculator. Diabetology and Metabolic Syndrome, 7, 6 . doi:10.1186/s13098-015-0111-7
NLM
Toyoshima MTK, Souza ABC de, Admoni SN, Cukier P, Lottenberg SA, Latronico AC, Nery M. New digital tool to facilitate subcutaneous insulin therapy orders: an inpatient insulin dose calculator [Internet]. Diabetology and Metabolic Syndrome. 2015 ; 7 6 .[citado 2025 out. 25 ] Available from: https://doi.org/10.1186/s13098-015-0111-7
Vancouver
Toyoshima MTK, Souza ABC de, Admoni SN, Cukier P, Lottenberg SA, Latronico AC, Nery M. New digital tool to facilitate subcutaneous insulin therapy orders: an inpatient insulin dose calculator [Internet]. Diabetology and Metabolic Syndrome. 2015 ; 7 6 .[citado 2025 out. 25 ] Available from: https://doi.org/10.1186/s13098-015-0111-7
Artigo de periodico
Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3 (2014)
Macedo, Delanie B.; Abreu, Ana Paula; Reis, Ana Claudia S.; Montenegro, Luciana R.; Dauber, Andrew; Beneduzzi, Daiane; Cukier, Priscilla; Silveira, Leticia F. G.; Teles, Milena G.; Carroll, Rona S.; Guerra Junior, Gil; Guaragna Filho, Guilherme; Gucev, Zoran; Arnhold, Ivo J. P.; Castro, Margaret de; Moreira, Ayrton C.; Martinelli Jr., Carlos Eduardo; Hirschhorn, Joel N.; Mendonca, Berenice B.; Brito, Vinicius N.; Antonini, Sonir R.; Kaiser, Ursula B.; Latronico, Ana Claudia
Source: Journal of Clinical Endocrinology and Metabolism. Unidades: FM, FMRP
Subjects: CRIANÇAS, TÉCNICAS GENÉTICAS, PUBERDADE PRECOCE, MUTAÇÃO GENÉTICA
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MACEDO, Delanie B. et al. Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3. Journal of Clinical Endocrinology and Metabolism, v. 99, n. 6, p. E1097-E1103, 2014Tradução . . Disponível em: https://doi.org/10.1210/jc.2013-3126. Acesso em: 25 out. 2025.
APA
Macedo, D. B., Abreu, A. P., Reis, A. C. S., Montenegro, L. R., Dauber, A., Beneduzzi, D., et al. (2014). Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3. Journal of Clinical Endocrinology and Metabolism, 99( 6), E1097-E1103. doi:10.1210/jc.2013-3126
NLM
Macedo DB, Abreu AP, Reis ACS, Montenegro LR, Dauber A, Beneduzzi D, Cukier P, Silveira LFG, Teles MG, Carroll RS, Guerra Junior G, Guaragna Filho G, Gucev Z, Arnhold IJP, Castro M de, Moreira AC, Martinelli Jr. CE, Hirschhorn JN, Mendonca BB, Brito VN, Antonini SR, Kaiser UB, Latronico AC. Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3 [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99( 6): E1097-E1103.[citado 2025 out. 25 ] Available from: https://doi.org/10.1210/jc.2013-3126
Vancouver
Macedo DB, Abreu AP, Reis ACS, Montenegro LR, Dauber A, Beneduzzi D, Cukier P, Silveira LFG, Teles MG, Carroll RS, Guerra Junior G, Guaragna Filho G, Gucev Z, Arnhold IJP, Castro M de, Moreira AC, Martinelli Jr. CE, Hirschhorn JN, Mendonca BB, Brito VN, Antonini SR, Kaiser UB, Latronico AC. Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3 [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99( 6): E1097-E1103.[citado 2025 out. 25 ] Available from: https://doi.org/10.1210/jc.2013-3126
Artigo de periodico
The benign spectrum of hypothalamic hamartomas: Infrequent epilepsy and normal cognition in patients presenting with central precocious puberty (2013)
Cukier, Priscilla; Castro, Luiz Henrique Martins; Banaskiwitz, Natalie; Teles, Leandro Roberto; Ferreira, Luiz Roberto Kobuti; Adda, Carla Cristina; Leite, Claudia da Costa; Mendonça, Berenice Bilharinho; Latronico, Ana Claudia; Brito, Vinicius Nahime
Source: Seizure. Unidade: FM
Subjects: COGNIÇÃO (AVALIAÇÃO), EPILEPSIA, PUBERDADE PRECOCE, DISTÚRBIOS DO COMPORTAMENTO
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ABNT
CUKIER, Priscilla et al. The benign spectrum of hypothalamic hamartomas: Infrequent epilepsy and normal cognition in patients presenting with central precocious puberty. Seizure, v. 22, n. 1, p. 28\201332, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.seizure.2012.09.013. Acesso em: 25 out. 2025.
APA
Cukier, P., Castro, L. H. M., Banaskiwitz, N., Teles, L. R., Ferreira, L. R. K., Adda, C. C., et al. (2013). The benign spectrum of hypothalamic hamartomas: Infrequent epilepsy and normal cognition in patients presenting with central precocious puberty. Seizure, 22( 1), 28\201332. doi:10.1016/j.seizure.2012.09.013
NLM
Cukier P, Castro LHM, Banaskiwitz N, Teles LR, Ferreira LRK, Adda CC, Leite C da C, Mendonça BB, Latronico AC, Brito VN. The benign spectrum of hypothalamic hamartomas: Infrequent epilepsy and normal cognition in patients presenting with central precocious puberty [Internet]. Seizure. 2013 ; 22( 1): 28\201332.[citado 2025 out. 25 ] Available from: https://doi.org/10.1016/j.seizure.2012.09.013
Vancouver
Cukier P, Castro LHM, Banaskiwitz N, Teles LR, Ferreira LRK, Adda CC, Leite C da C, Mendonça BB, Latronico AC, Brito VN. The benign spectrum of hypothalamic hamartomas: Infrequent epilepsy and normal cognition in patients presenting with central precocious puberty [Internet]. Seizure. 2013 ; 22( 1): 28\201332.[citado 2025 out. 25 ] Available from: https://doi.org/10.1016/j.seizure.2012.09.013
Artigo de periodico
Molecular and gene network analysis of thyroid transcription factor 1(TFF1) and enhanced at puberty (EAP1) gene in patients with GnRH-dependent pubertal disorders (2013)
Cukier, Priscilla; Wright, Hollis; Rulfs, Tomke; Silveira, Leticia Ferreira Gontijo; Teles, Milena Gurgel; Mendonça, Berenice Bilharinho de; Arnhold, Ivo J. P.; Heger, Sabine; Xavier, Ana Claudia Latronico; Ojeba, Sergio R.; Brito, Vinicius Nahime
Source: Hormone Research in Paediatrics. Unidade: FM
Subjects: PUBERDADE (ANORMALIDADES), GONADOTROFINAS, EXPRESSÃO GÊNICA, HIPOGONADISMO
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ABNT
CUKIER, Priscilla et al. Molecular and gene network analysis of thyroid transcription factor 1(TFF1) and enhanced at puberty (EAP1) gene in patients with GnRH-dependent pubertal disorders. Hormone Research in Paediatrics, v. 80, n. 2, p. 257-266, 2013Tradução . . Disponível em: http://www.karger.com/Article/FullText/354643. Acesso em: 25 out. 2025.
APA
Cukier, P., Wright, H., Rulfs, T., Silveira, L. F. G., Teles, M. G., Mendonça, B. B. de, et al. (2013). Molecular and gene network analysis of thyroid transcription factor 1(TFF1) and enhanced at puberty (EAP1) gene in patients with GnRH-dependent pubertal disorders. Hormone Research in Paediatrics, 80( 2), 257-266. Recuperado de http://www.karger.com/Article/FullText/354643
NLM
Cukier P, Wright H, Rulfs T, Silveira LFG, Teles MG, Mendonça BB de, Arnhold IJP, Heger S, Xavier ACL, Ojeba SR, Brito VN. Molecular and gene network analysis of thyroid transcription factor 1(TFF1) and enhanced at puberty (EAP1) gene in patients with GnRH-dependent pubertal disorders [Internet]. Hormone Research in Paediatrics. 2013 ; 80( 2): 257-266.[citado 2025 out. 25 ] Available from: http://www.karger.com/Article/FullText/354643
Vancouver
Cukier P, Wright H, Rulfs T, Silveira LFG, Teles MG, Mendonça BB de, Arnhold IJP, Heger S, Xavier ACL, Ojeba SR, Brito VN. Molecular and gene network analysis of thyroid transcription factor 1(TFF1) and enhanced at puberty (EAP1) gene in patients with GnRH-dependent pubertal disorders [Internet]. Hormone Research in Paediatrics. 2013 ; 80( 2): 257-266.[citado 2025 out. 25 ] Available from: http://www.karger.com/Article/FullText/354643
Artigo de periodico
Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3 (2013)
Abreu, Ana Paula; Dauber, Andrew; Macedo, Delanie B.; Noel, Sekoni D.; Brito, Vinicius N.; Gill, John C.; Cukier, Priscilla; Thompson, Iain R.; Navarro, Victor M.; Gagliardi, Priscila C.; Rodrigues, Tânia; Kochi, Cristiane; Longui, Carlos Alberto; Beckers, Dominique; Zegher, Francis de; Montenegro, Luciana R.; Mendonca, Berenice B.; Carroll, Rona S.; Hirschhorn, Joel N.; Latronico, Ana Claudia; Kaiser, Ursula B.
Source: The New England Journal of Medicine. Unidade: FM
Subjects: PUBERDADE PRECOCE, MUTAÇÃO GENÉTICA, GONADOTROFINAS, REAÇÃO EM CADEIA POR POLIMERASE, BIOLOGIA MOLECULAR, ANÁLISE SEQUENCIAL
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ABNT
ABREU, Ana Paula et al. Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3. The New England Journal of Medicine, v. 368, n. 26, p. 2467-2475, 2013Tradução . . Disponível em: http://www.nejm.org/doi/full/10.1056/NEJMoa1302160. Acesso em: 25 out. 2025.
APA
Abreu, A. P., Dauber, A., Macedo, D. B., Noel, S. D., Brito, V. N., Gill, J. C., et al. (2013). Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3. The New England Journal of Medicine, 368( 26), 2467-2475. doi:10.1056/NEJMoa1302160
NLM
Abreu AP, Dauber A, Macedo DB, Noel SD, Brito VN, Gill JC, Cukier P, Thompson IR, Navarro VM, Gagliardi PC, Rodrigues T, Kochi C, Longui CA, Beckers D, Zegher F de, Montenegro LR, Mendonca BB, Carroll RS, Hirschhorn JN, Latronico AC, Kaiser UB. Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3 [Internet]. The New England Journal of Medicine. 2013 ; 368( 26): 2467-2475.[citado 2025 out. 25 ] Available from: http://www.nejm.org/doi/full/10.1056/NEJMoa1302160
Vancouver
Abreu AP, Dauber A, Macedo DB, Noel SD, Brito VN, Gill JC, Cukier P, Thompson IR, Navarro VM, Gagliardi PC, Rodrigues T, Kochi C, Longui CA, Beckers D, Zegher F de, Montenegro LR, Mendonca BB, Carroll RS, Hirschhorn JN, Latronico AC, Kaiser UB. Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3 [Internet]. The New England Journal of Medicine. 2013 ; 368( 26): 2467-2475.[citado 2025 out. 25 ] Available from: http://www.nejm.org/doi/full/10.1056/NEJMoa1302160
Trabalho de evento-resumo periodico
Loss-of-function mutations in a gene cause central precocius puberty (2013)
Abreu, Ana Paula; Dauber, Andrew; Macedo, Delaine Bulcão; Noel, Sekoni D.; Brito, Vinicius Nahime; Gill, John C.; Cukier, Priscilla; Thompson, Ian; Navarro, Victor M.; Gagliardi, Priscila C.; Rodrigues, Tânia M.; Kochi, Cristiane; Longui, Carlos A.; Beckers, Dominique; Zegher, Francis de; Montenegro, Luciana R.; Mendonça, Berenice Bilharinho de; Carroll, Rona S.; Hirschhorn, Joel N.; Xavier, Ana Claudia Latronico; Kaiser, Ursula B.
Source: Hormone Research in Paediatrics. Conference titles: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting. Unidade: FM
Subjects: PUBERDADE PRECOCE, TRANSTORNOS DO CRESCIMENTO, ENDOCRINOPATIAS
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ABNT
ABREU, Ana Paula et al. Loss-of-function mutations in a gene cause central precocius puberty. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 25 out. 2025. , 2013
APA
Abreu, A. P., Dauber, A., Macedo, D. B., Noel, S. D., Brito, V. N., Gill, J. C., et al. (2013). Loss-of-function mutations in a gene cause central precocius puberty. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Abreu AP, Dauber A, Macedo DB, Noel SD, Brito VN, Gill JC, Cukier P, Thompson I, Navarro VM, Gagliardi PC, Rodrigues TM, Kochi C, Longui CA, Beckers D, Zegher F de, Montenegro LR, Mendonça BB de, Carroll RS, Hirschhorn JN, Xavier ACL, Kaiser UB. Loss-of-function mutations in a gene cause central precocius puberty. Hormone Research in Paediatrics. 2013 ; 80 35.[citado 2025 out. 25 ]
Vancouver
Abreu AP, Dauber A, Macedo DB, Noel SD, Brito VN, Gill JC, Cukier P, Thompson I, Navarro VM, Gagliardi PC, Rodrigues TM, Kochi C, Longui CA, Beckers D, Zegher F de, Montenegro LR, Mendonça BB de, Carroll RS, Hirschhorn JN, Xavier ACL, Kaiser UB. Loss-of-function mutations in a gene cause central precocius puberty. Hormone Research in Paediatrics. 2013 ; 80 35.[citado 2025 out. 25 ]
Trabalho de evento-resumo periodico
Effectiveness of leuprolide acetate 3-month depot (11.25 mg) in the treatment of patients with central precocious puberty: experience of (2012)
Brito, Vinicius Nahime; Cukier, Priscilla; Lima, Lorena Oliveira; Silveira, Leticia F. Gontijo; Teles, Milena; Mendonça, Berenice B.; Arnhold, Ivo J. Prado; Latronico, Ana Claudia
Source: Hormone research in paediatrics. Conference titles: 51th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE). Unidade: FM
Subjects: PUBERDADE PRECOSE, TESTOSTERONA (NÍVEL), NEUROENDORCRINOLOGIA, HORMÔNOS (USO TERAPÊUTICO), RESUMOS (EVENTOS)
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ABNT
BRITO, Vinicius Nahime et al. Effectiveness of leuprolide acetate 3-month depot (11.25 mg) in the treatment of patients with central precocious puberty: experience of. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000343184. Acesso em: 25 out. 2025. , 2012
APA
Brito, V. N., Cukier, P., Lima, L. O., Silveira, L. F. G., Teles, M., Mendonça, B. B., et al. (2012). Effectiveness of leuprolide acetate 3-month depot (11.25 mg) in the treatment of patients with central precocious puberty: experience of. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. doi:10.1159/000343184
NLM
Brito VN, Cukier P, Lima LO, Silveira LFG, Teles M, Mendonça BB, Arnhold IJP, Latronico AC. Effectiveness of leuprolide acetate 3-month depot (11.25 mg) in the treatment of patients with central precocious puberty: experience of [Internet]. Hormone research in paediatrics. 2012 ;78( suppl. 1): 232.[citado 2025 out. 25 ] Available from: https://doi.org/10.1159/000343184
Vancouver
Brito VN, Cukier P, Lima LO, Silveira LFG, Teles M, Mendonça BB, Arnhold IJP, Latronico AC. Effectiveness of leuprolide acetate 3-month depot (11.25 mg) in the treatment of patients with central precocious puberty: experience of [Internet]. Hormone research in paediatrics. 2012 ;78( suppl. 1): 232.[citado 2025 out. 25 ] Available from: https://doi.org/10.1159/000343184
Artigo de periodico
Possible role of a radiation-induced p53 mutation in a Nelson’s syndrome patient with a fatal outcome (2011)
Pinto, Emilia Modolo; Siqueira, Sheila A. C.; Cukier, Priscilla; Fragoso, Maria C. B. V.; Lin, Chin Jia; Mendonca, Berenice Bilharinho de
Source: Pituitary. Unidade: FM
Subjects: NEOPLASIAS DAS GLÂNDULAS SUPRARRENAIS, GLÂNDULA PRITUITÁRIA (FISIOPATOLOGIA;EFEITOS DE RADIAÇÃO;;COMPLICAÇÕES), ADNEOMA (MORTALIDADE)
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ABNT
PINTO, Emilia Modolo et al. Possible role of a radiation-induced p53 mutation in a Nelson’s syndrome patient with a fatal outcome. Pituitary, v. 14, p. 400-404, 2011Tradução . . Disponível em: https://doi.org/10.1007/s11102-009-0194-y. Acesso em: 25 out. 2025.
APA
Pinto, E. M., Siqueira, S. A. C., Cukier, P., Fragoso, M. C. B. V., Lin, C. J., & Mendonca, B. B. de. (2011). Possible role of a radiation-induced p53 mutation in a Nelson’s syndrome patient with a fatal outcome. Pituitary, 14, 400-404. doi:10.1007/s11102-009-0194-y
NLM
Pinto EM, Siqueira SAC, Cukier P, Fragoso MCBV, Lin CJ, Mendonca BB de. Possible role of a radiation-induced p53 mutation in a Nelson’s syndrome patient with a fatal outcome [Internet]. Pituitary. 2011 ; 14 400-404.[citado 2025 out. 25 ] Available from: https://doi.org/10.1007/s11102-009-0194-y
Vancouver
Pinto EM, Siqueira SAC, Cukier P, Fragoso MCBV, Lin CJ, Mendonca BB de. Possible role of a radiation-induced p53 mutation in a Nelson’s syndrome patient with a fatal outcome [Internet]. Pituitary. 2011 ; 14 400-404.[citado 2025 out. 25 ] Available from: https://doi.org/10.1007/s11102-009-0194-y
Tese (Doutorado)
Estudo dos genes TTF-1 e EAP1 em pacientes com distúrbios puberais centrais e avaliação neurológica e neurocognitiva de pacientes com hamartoma hipotalâmico (2010)
Cukier, Priscilla; Brito, Vinicius Nahime de (Orientador)
Unidade: FM
Subjects: PUBERDADE PRECOCE, HIPOGONADISMO, NEOPLASIAS, MANIFESTAÇÕES NEUROLÓGICAS, EPILEPSIA, GENES
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ABNT
CUKIER, Priscilla. Estudo dos genes TTF-1 e EAP1 em pacientes com distúrbios puberais centrais e avaliação neurológica e neurocognitiva de pacientes com hamartoma hipotalâmico. 2010. Tese (Doutorado) – Universidade de São Paulo, São Paulo, 2010. Disponível em: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-01022011-173710/. Acesso em: 25 out. 2025.
APA
Cukier, P. (2010). Estudo dos genes TTF-1 e EAP1 em pacientes com distúrbios puberais centrais e avaliação neurológica e neurocognitiva de pacientes com hamartoma hipotalâmico (Tese (Doutorado). Universidade de São Paulo, São Paulo. Recuperado de http://www.teses.usp.br/teses/disponiveis/5/5135/tde-01022011-173710/
NLM
Cukier P. Estudo dos genes TTF-1 e EAP1 em pacientes com distúrbios puberais centrais e avaliação neurológica e neurocognitiva de pacientes com hamartoma hipotalâmico [Internet]. 2010 ;[citado 2025 out. 25 ] Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-01022011-173710/
Vancouver
Cukier P. Estudo dos genes TTF-1 e EAP1 em pacientes com distúrbios puberais centrais e avaliação neurológica e neurocognitiva de pacientes com hamartoma hipotalâmico [Internet]. 2010 ;[citado 2025 out. 25 ] Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-01022011-173710/
Trabalho de evento-resumo periodico
Familial central precocious puberty: prevalence, segregation analysis and penetrance rate (2010)
Cukier, Priscilla; Silveira, Leticia F. G.; Otto, Paulo A ; Arnhold, Ivo J. P; Mendonca, Berenice Bilharinho; Gagliardi, Priscila; Beckers, Domenique; Pasqualini, Titania; Latronico, Ana Claudia; Brito, Vinicius N
Source: Endocrine Reviews. Conference titles: Meeting and Expo of the Endocrine Society. Unidades: IB, FM
Assunto: PUBERDADE (PREVALÊNCIA;GENÉTICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CUKIER, Priscilla et al. Familial central precocious puberty: prevalence, segregation analysis and penetrance rate. Endocrine Reviews. Chevy Chase: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 25 out. 2025. , 2010
APA
Cukier, P., Silveira, L. F. G., Otto, P. A., Arnhold, I. J. P., Mendonca, B. B., Gagliardi, P., et al. (2010). Familial central precocious puberty: prevalence, segregation analysis and penetrance rate. Endocrine Reviews. Chevy Chase: Instituto de Biociências, Universidade de São Paulo.
NLM
Cukier P, Silveira LFG, Otto PA, Arnhold IJP, Mendonca BB, Gagliardi P, Beckers D, Pasqualini T, Latronico AC, Brito VN. Familial central precocious puberty: prevalence, segregation analysis and penetrance rate. Endocrine Reviews. 2010 ; 31( Ju 2010):[citado 2025 out. 25 ]
Vancouver
Cukier P, Silveira LFG, Otto PA, Arnhold IJP, Mendonca BB, Gagliardi P, Beckers D, Pasqualini T, Latronico AC, Brito VN. Familial central precocious puberty: prevalence, segregation analysis and penetrance rate. Endocrine Reviews. 2010 ; 31( Ju 2010):[citado 2025 out. 25 ]
Artigo de periodico
Nelson's Syndrome: a case report (2007)
Cukier, Priscilla; Duch, Flávia Moretti; Teixeira, Manoel Jacobsen; Fragoso, Maria Candida B. V.; Pereira, Maria Adelaide A.; Freire, Daniel Soares; Fonoff, Erich Talamoni; Costa, Márcia Helena Soares; Domenice, Sorahia; Lucon, Antonio Marmo; Mendonça, Berenice B. de
Source: Arquivos brasileiros de endocrinologia e metabologia. Unidade: FM
Subjects: OBESIDADE (METABOLISMO), DOENÇAS METABÓLICAS, GLÂNDULAS SUPRARRENAIS, CONDUTAS TERAPÊUTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CUKIER, Priscilla et al. Nelson's Syndrome: a case report. Arquivos brasileiros de endocrinologia e metabologia, v. 51, n. 1, p. 116-124, 2007Tradução . . Disponível em: https://doi.org/10.1590/S0004-27302007000100019. Acesso em: 25 out. 2025.
APA
Cukier, P., Duch, F. M., Teixeira, M. J., Fragoso, M. C. B. V., Pereira, M. A. A., Freire, D. S., et al. (2007). Nelson's Syndrome: a case report. Arquivos brasileiros de endocrinologia e metabologia, 51( 1), 116-124. doi:10.1590/S0004-27302007000100019
NLM
Cukier P, Duch FM, Teixeira MJ, Fragoso MCBV, Pereira MAA, Freire DS, Fonoff ET, Costa MHS, Domenice S, Lucon AM, Mendonça BB de. Nelson's Syndrome: a case report [Internet]. Arquivos brasileiros de endocrinologia e metabologia. 2007 ; 51( 1): 116-124.[citado 2025 out. 25 ] Available from: https://doi.org/10.1590/S0004-27302007000100019
Vancouver
Cukier P, Duch FM, Teixeira MJ, Fragoso MCBV, Pereira MAA, Freire DS, Fonoff ET, Costa MHS, Domenice S, Lucon AM, Mendonça BB de. Nelson's Syndrome: a case report [Internet]. Arquivos brasileiros de endocrinologia e metabologia. 2007 ; 51( 1): 116-124.[citado 2025 out. 25 ] Available from: https://doi.org/10.1590/S0004-27302007000100019
Artigo de periodico
Use of nonradioactive labeling to detect large gene rearrangements in 21-hydroxylase deficiency (2004)
Cukier, Priscilla; Bachega, Tania A. S. S.; Mendonça, Berenice B.; Billerbeck, Ana Elisa C.
Source: Revista do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CUKIER, Priscilla et al. Use of nonradioactive labeling to detect large gene rearrangements in 21-hydroxylase deficiency. Revista do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, v. 59, n. 6, p. 369-374, 2004Tradução . . Disponível em: https://doi.org/10.1590/s0041-87812004000600010. Acesso em: 25 out. 2025.
APA
Cukier, P., Bachega, T. A. S. S., Mendonça, B. B., & Billerbeck, A. E. C. (2004). Use of nonradioactive labeling to detect large gene rearrangements in 21-hydroxylase deficiency. Revista do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, 59( 6), 369-374. doi:10.1590/s0041-87812004000600010
NLM
Cukier P, Bachega TASS, Mendonça BB, Billerbeck AEC. Use of nonradioactive labeling to detect large gene rearrangements in 21-hydroxylase deficiency [Internet]. Revista do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo. 2004 ; 59( 6): 369-374.[citado 2025 out. 25 ] Available from: https://doi.org/10.1590/s0041-87812004000600010
Vancouver
Cukier P, Bachega TASS, Mendonça BB, Billerbeck AEC. Use of nonradioactive labeling to detect large gene rearrangements in 21-hydroxylase deficiency [Internet]. Revista do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo. 2004 ; 59( 6): 369-374.[citado 2025 out. 25 ] Available from: https://doi.org/10.1590/s0041-87812004000600010

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