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Artigo de periodico
Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry (2022)
Lawrence, Neil; Bacila, Irina; Dawson, Jeremy; Bryce, Jillian; Ali, Salma R; Akker, Erica L. T. van den; Bachega, Tania Aparecida Sartori Sanchez ; Baronio, Federico; Birkebaek, Niels H; Bonfig, Walter
Fonte: Clinical endocrinology. Unidade: FM
Assuntos: HIPERPLASIAS, BIOMARCADORES, CORTISOL, ESTUDOS RETROSPECTIVOS
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ABNT
LAWRENCE, Neil et al. Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry. Clinical endocrinology, v. 97, n. 5, p. 551-561, 2022Tradução . . Disponível em: https://doi.org/10.1111/cen.14796. Acesso em: 22 out. 2025.
APA
Lawrence, N., Bacila, I., Dawson, J., Bryce, J., Ali, S. R., Akker, E. L. T. van den, et al. (2022). Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry. Clinical endocrinology, 97( 5), 551-561. doi:10.1111/cen.14796
NLM
Lawrence N, Bacila I, Dawson J, Bryce J, Ali SR, Akker ELT van den, Bachega TASS, Baronio F, Birkebaek NH, Bonfig W. Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry [Internet]. Clinical endocrinology. 2022 ; 97( 5): 551-561.[citado 2025 out. 22 ] Available from: https://doi.org/10.1111/cen.14796
Vancouver
Lawrence N, Bacila I, Dawson J, Bryce J, Ali SR, Akker ELT van den, Bachega TASS, Baronio F, Birkebaek NH, Bonfig W. Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry [Internet]. Clinical endocrinology. 2022 ; 97( 5): 551-561.[citado 2025 out. 22 ] Available from: https://doi.org/10.1111/cen.14796
Artigo de periodico
Revisiting the role of surgery in the treatment of Graves' disease (2022)
Cohen, Oded; Ronen, Ohad; Khafif, Avi; Rodrigo, Juan P; Simo, Ricard; Pace-asciak, Pia; Randolph, Gregory; Mikkelsen, Lauge H; Kowalski, Luiz Paulo ; Olsen, Kerry D
Fonte: Clinical endocrinology. Unidade: FM
Assuntos: TIREOIDECTOMIA, DOENÇAS AUTOIMUNES, DOENÇA DE GRAVES, COMPLICAÇÕES PÓS-OPERATÓRIAS
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ABNT
COHEN, Oded et al. Revisiting the role of surgery in the treatment of Graves' disease. Clinical endocrinology, v. 96, n. 6, p. 747-757, 2022Tradução . . Disponível em: https://doi.org/10.1111/cen.14653. Acesso em: 22 out. 2025.
APA
Cohen, O., Ronen, O., Khafif, A., Rodrigo, J. P., Simo, R., Pace-asciak, P., et al. (2022). Revisiting the role of surgery in the treatment of Graves' disease. Clinical endocrinology, 96( 6), 747-757. doi:10.1111/cen.14653
NLM
Cohen O, Ronen O, Khafif A, Rodrigo JP, Simo R, Pace-asciak P, Randolph G, Mikkelsen LH, Kowalski LP, Olsen KD. Revisiting the role of surgery in the treatment of Graves' disease [Internet]. Clinical endocrinology. 2022 ; 96( 6): 747-757.[citado 2025 out. 22 ] Available from: https://doi.org/10.1111/cen.14653
Vancouver
Cohen O, Ronen O, Khafif A, Rodrigo JP, Simo R, Pace-asciak P, Randolph G, Mikkelsen LH, Kowalski LP, Olsen KD. Revisiting the role of surgery in the treatment of Graves' disease [Internet]. Clinical endocrinology. 2022 ; 96( 6): 747-757.[citado 2025 out. 22 ] Available from: https://doi.org/10.1111/cen.14653
Artigo de periodico
Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes (2018)
Correa, Fernanda A.; Jorge, Alexander Augusto de Lima; Mendonça, Berenice Bilharinho de
Fonte: Clinical endocrinology. Unidade: FM
Assuntos: DOENÇAS CONGÊNITAS, HORMÔNIOS HIPOFISÁRIOS, MUTAÇÃO GENÉTICA
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ABNT
CORREA, Fernanda A. e JORGE, Alexander Augusto de Lima e MENDONÇA, Berenice Bilharinho de. Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes. Clinical endocrinology, v. 88, n. 3, p. 425-431, 2018Tradução . . Disponível em: https://doi.org/10.1111/cen.13535. Acesso em: 22 out. 2025.
APA
Correa, F. A., Jorge, A. A. de L., & Mendonça, B. B. de. (2018). Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes. Clinical endocrinology, 88( 3), 425-431. doi:10.1111/cen.13535
NLM
Correa FA, Jorge AA de L, Mendonça BB de. Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes [Internet]. Clinical endocrinology. 2018 ; 88( 3): 425-431.[citado 2025 out. 22 ] Available from: https://doi.org/10.1111/cen.13535
Vancouver
Correa FA, Jorge AA de L, Mendonça BB de. Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes [Internet]. Clinical endocrinology. 2018 ; 88( 3): 425-431.[citado 2025 out. 22 ] Available from: https://doi.org/10.1111/cen.13535
Artigo de periodico
Long-term outcomes and molecular analysis of a large cohort of patients with 46,XY disorder of sex development due to partial gonadal dysgenesis (2018)
Gomes, Nathalia L.; Mendonça, Berenice Bilharinho de
Fonte: Clinical endocrinology. Unidade: FM
Assuntos: MUTAÇÃO GENÉTICA, TESTOSTERONA, GENITÁLIA MASCULINA
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ABNT
GOMES, Nathalia L. e MENDONÇA, Berenice Bilharinho de. Long-term outcomes and molecular analysis of a large cohort of patients with 46,XY disorder of sex development due to partial gonadal dysgenesis. Clinical endocrinology, v. 89, n. 2, p. 164-177, 2018Tradução . . Disponível em: https://doi.org/10.1111/cen.13717. Acesso em: 22 out. 2025.
APA
Gomes, N. L., & Mendonça, B. B. de. (2018). Long-term outcomes and molecular analysis of a large cohort of patients with 46,XY disorder of sex development due to partial gonadal dysgenesis. Clinical endocrinology, 89( 2), 164-177. doi:10.1111/cen.13717
NLM
Gomes NL, Mendonça BB de. Long-term outcomes and molecular analysis of a large cohort of patients with 46,XY disorder of sex development due to partial gonadal dysgenesis [Internet]. Clinical endocrinology. 2018 ; 89( 2): 164-177.[citado 2025 out. 22 ] Available from: https://doi.org/10.1111/cen.13717
Vancouver
Gomes NL, Mendonça BB de. Long-term outcomes and molecular analysis of a large cohort of patients with 46,XY disorder of sex development due to partial gonadal dysgenesis [Internet]. Clinical endocrinology. 2018 ; 89( 2): 164-177.[citado 2025 out. 22 ] Available from: https://doi.org/10.1111/cen.13717
Artigo de periodico
Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations (2017)
Madeira, Joao Lo; Jorge, Alexander Augusto de Lima; Mendonça, Berenice Bilharinho de
Fonte: Clinical endocrinology. Unidade: FM
Assuntos: HORMÔNIOS HIPOFISÁRIOS, SEQUENCIAMENTO GENÉTICO, BRASILEIROS, ESTUDOS DE COORTES, MUTAÇÃO GENÉTICA
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ABNT
MADEIRA, Joao Lo e JORGE, Alexander Augusto de Lima e MENDONÇA, Berenice Bilharinho de. Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations. Clinical endocrinology, v. 87, n. 6, p. 725-732, 2017Tradução . . Disponível em: https://doi.org/10.1111/cen.13430. Acesso em: 22 out. 2025.
APA
Madeira, J. L., Jorge, A. A. de L., & Mendonça, B. B. de. (2017). Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations. Clinical endocrinology, 87( 6), 725-732. doi:10.1111/cen.13430
NLM
Madeira JL, Jorge AA de L, Mendonça BB de. Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations [Internet]. Clinical endocrinology. 2017 ; 87( 6): 725-732.[citado 2025 out. 22 ] Available from: https://doi.org/10.1111/cen.13430
Vancouver
Madeira JL, Jorge AA de L, Mendonça BB de. Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations [Internet]. Clinical endocrinology. 2017 ; 87( 6): 725-732.[citado 2025 out. 22 ] Available from: https://doi.org/10.1111/cen.13430
Artigo de periodico
Relatively high frequency of non-synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly (2013)
França, Marcela M.; Jorge, Alexander A. L.; Carvalho, Luciani R. S.; Costalonga, Everlayny F.; Otto, Aline P.; Correa, Fernanda A.; Mendonca, Berenice B.; Arnhold, Ivo J. P.
Fonte: Clinical endocrinology. Unidade: FM
Assuntos: HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA), MUTAÇÃO GENÉTICA, IMAGEM POR RESSONÂNCIA MAGNÉTICA, GLÂNDULA PITUITÁRIA
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ABNT
FRANÇA, Marcela M. et al. Relatively high frequency of non-synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly. Clinical endocrinology, v. 78, n. 4, p. 551-557, 2013Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/cen.12044/pdf. Acesso em: 22 out. 2025.
APA
França, M. M., Jorge, A. A. L., Carvalho, L. R. S., Costalonga, E. F., Otto, A. P., Correa, F. A., et al. (2013). Relatively high frequency of non-synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly. Clinical endocrinology, 78( 4), 551-557. doi:10.1111/cen.12044
NLM
França MM, Jorge AAL, Carvalho LRS, Costalonga EF, Otto AP, Correa FA, Mendonca BB, Arnhold IJP. Relatively high frequency of non-synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly [Internet]. Clinical endocrinology. 2013 ; 78( 4): 551-557.[citado 2025 out. 22 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/cen.12044/pdf
Vancouver
França MM, Jorge AAL, Carvalho LRS, Costalonga EF, Otto AP, Correa FA, Mendonca BB, Arnhold IJP. Relatively high frequency of non-synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly [Internet]. Clinical endocrinology. 2013 ; 78( 4): 551-557.[citado 2025 out. 22 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/cen.12044/pdf
Artigo de periodico
Analysis of the insulin-like growth factor 1 receptor gene in children born small for gestational age: in vitro characterization of a novel mutation (p. Arg511 Trp) (2013)
Leal, Andrea C.; Montenegro, Luciana R.; Saito, Renata F.; Ribeiro, Tamaya C.; Coutinho, Debora C.; Mendonca, Berenice B.; Arnhold, Ivo J. P.; Jorge, Alexander A. L.
Fonte: Clinical endocrinology. Unidade: FM
Assuntos: HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA), MUTAÇÃO, ESTUDOS DE COORTES, IDADE GESTACIONAL, FIBROBLASTOS
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ABNT
LEAL, Andrea C. et al. Analysis of the insulin-like growth factor 1 receptor gene in children born small for gestational age: in vitro characterization of a novel mutation (p. Arg511 Trp). Clinical endocrinology, v. 78, n. 4, p. 558-563, 2013Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/cen.12048/pdf. Acesso em: 22 out. 2025.
APA
Leal, A. C., Montenegro, L. R., Saito, R. F., Ribeiro, T. C., Coutinho, D. C., Mendonca, B. B., et al. (2013). Analysis of the insulin-like growth factor 1 receptor gene in children born small for gestational age: in vitro characterization of a novel mutation (p. Arg511 Trp). Clinical endocrinology, 78( 4), 558-563. doi:10.1111/cen.12048
NLM
Leal AC, Montenegro LR, Saito RF, Ribeiro TC, Coutinho DC, Mendonca BB, Arnhold IJP, Jorge AAL. Analysis of the insulin-like growth factor 1 receptor gene in children born small for gestational age: in vitro characterization of a novel mutation (p. Arg511 Trp) [Internet]. Clinical endocrinology. 2013 ; 78( 4): 558-563.[citado 2025 out. 22 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/cen.12048/pdf
Vancouver
Leal AC, Montenegro LR, Saito RF, Ribeiro TC, Coutinho DC, Mendonca BB, Arnhold IJP, Jorge AAL. Analysis of the insulin-like growth factor 1 receptor gene in children born small for gestational age: in vitro characterization of a novel mutation (p. Arg511 Trp) [Internet]. Clinical endocrinology. 2013 ; 78( 4): 558-563.[citado 2025 out. 22 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/cen.12048/pdf
Artigo de periodico
Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1 (2010)
Trarbach, Ericka Barbosa; Teles, Milena Gurgel; Costa, Elaine Maria Frade; Abreu, Ana Paula; Garmes, Heraldo Mendes; Guerra Junior, Gil; Baptista, Maria Tereza Matias; Castro, Margaret de; Mendonca, Berenice Bilharinho; Latronico, Ana Claudia
Fonte: Clinical endocrinology. Unidade: FM
Assuntos: FATORES DE CRESCIMENTO, DELEÇÃO DE GENES, RASTREAMENTO, FIBROBLASTOS, HIPOGONADISMO
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ABNT
TRARBACH, Ericka Barbosa et al. Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1. Clinical endocrinology, v. 72, n. 3, p. 371-376, 2010Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2009.03642.x. Acesso em: 22 out. 2025.
APA
Trarbach, E. B., Teles, M. G., Costa, E. M. F., Abreu, A. P., Garmes, H. M., Guerra Junior, G., et al. (2010). Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1. Clinical endocrinology, 72( 3), 371-376. doi:10.1111/j.1365-2265.2009.03642.x
NLM
Trarbach EB, Teles MG, Costa EMF, Abreu AP, Garmes HM, Guerra Junior G, Baptista MTM, Castro M de, Mendonca BB, Latronico AC. Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1 [Internet]. Clinical endocrinology. 2010 ; 72( 3): 371-376.[citado 2025 out. 22 ] Available from: https://doi.org/10.1111/j.1365-2265.2009.03642.x
Vancouver
Trarbach EB, Teles MG, Costa EMF, Abreu AP, Garmes HM, Guerra Junior G, Baptista MTM, Castro M de, Mendonca BB, Latronico AC. Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1 [Internet]. Clinical endocrinology. 2010 ; 72( 3): 371-376.[citado 2025 out. 22 ] Available from: https://doi.org/10.1111/j.1365-2265.2009.03642.x
Artigo de periodico
46,XY disorders of sex developement (DSD) (2009)
Mendonça, Berenice Bilharinho; Domenice, Sorahia; Arnhold, Ivo J. P.; Costa, Elaine M. F.
Fonte: Clinical endocrinology. Unidade: FM
Assuntos: TRANSTORNOS GONADAIS, DESENVOLVIMENTO PSICOSSOCIAL, TRANSTORNOS DA DIFERENCIAÇÃO SEXUAL (CONGÊNITO), FENÓTIPOS, PSEUDO-HERMAFRODITISMO
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ABNT
MENDONÇA, Berenice Bilharinho et al. 46,XY disorders of sex developement (DSD). Clinical endocrinology, v. 70, n. 2, p. 173-187, 2009Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2007.02993.x-i1. Acesso em: 22 out. 2025.
APA
Mendonça, B. B., Domenice, S., Arnhold, I. J. P., & Costa, E. M. F. (2009). 46,XY disorders of sex developement (DSD). Clinical endocrinology, 70( 2), 173-187. doi:10.1111/j.1365-2265.2007.02993.x-i1
NLM
Mendonça BB, Domenice S, Arnhold IJP, Costa EMF. 46,XY disorders of sex developement (DSD) [Internet]. Clinical endocrinology. 2009 ; 70( 2): 173-187.[citado 2025 out. 22 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.02993.x-i1
Vancouver
Mendonça BB, Domenice S, Arnhold IJP, Costa EMF. 46,XY disorders of sex developement (DSD) [Internet]. Clinical endocrinology. 2009 ; 70( 2): 173-187.[citado 2025 out. 22 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.02993.x-i1

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