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Artigo de periodico
Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma (2014)
Danilovic, Debora L. S.; Lima, Erika U.; Domingues, Regina B.; Brandao, Lenine G.; Hoff, Ana O.; Marui, Suemi
Source: European Journal of Endocrinology. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, NEOPLASIAS DA TIREOIDE (DIAGNÓSTICO), PROGNÓSTICO, CARCINOMA DE CÉLULAS ESCAMOSAS
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ABNT
DANILOVIC, Debora L. S. et al. Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma. European Journal of Endocrinology, v. 170, n. 4, p. 619-625, 2014Tradução . . Disponível em: https://doi.org/10.1530/EJE-13-0944. Acesso em: 09 nov. 2024.
APA
Danilovic, D. L. S., Lima, E. U., Domingues, R. B., Brandao, L. G., Hoff, A. O., & Marui, S. (2014). Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma. European Journal of Endocrinology, 170( 4), 619-625. doi:10.1530/EJE-13-0944
NLM
Danilovic DLS, Lima EU, Domingues RB, Brandao LG, Hoff AO, Marui S. Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma [Internet]. European Journal of Endocrinology. 2014 ; 170( 4): 619-625.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1530/EJE-13-0944
Vancouver
Danilovic DLS, Lima EU, Domingues RB, Brandao LG, Hoff AO, Marui S. Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma [Internet]. European Journal of Endocrinology. 2014 ; 170( 4): 619-625.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1530/EJE-13-0944
Artigo de periodico
Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways (2014)
Canton, Ana P. M.; Costa, Sílvia S.; Rodrigues, Tatiane C.; Bertola, Debora R.; Malaquias, Alexsandra C.; Correa, Fernanda A.; Arnhold, Ivo J. P.; Rosenberg, Carla ; Jorge, Alexander A. L.
Source: European Journal of Endocrinology. Unidades: IB, FM
Subjects: GENES, IDADE GESTACIONAL, CRESCIMENTO E DESENVOLVIMENTO
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CANTON, Ana P. M. et al. Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways. European Journal of Endocrinology, v. 171, n. 2, p. 253-262, 2014Tradução . . Disponível em: https://doi.org/10.1530/eje-14-0232. Acesso em: 09 nov. 2024.
APA
Canton, A. P. M., Costa, S. S., Rodrigues, T. C., Bertola, D. R., Malaquias, A. C., Correa, F. A., et al. (2014). Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways. European Journal of Endocrinology, 171( 2), 253-262. doi:10.1530/eje-14-0232
NLM
Canton APM, Costa SS, Rodrigues TC, Bertola DR, Malaquias AC, Correa FA, Arnhold IJP, Rosenberg C, Jorge AAL. Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways [Internet]. European Journal of Endocrinology. 2014 ; 171( 2): 253-262.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1530/eje-14-0232
Vancouver
Canton APM, Costa SS, Rodrigues TC, Bertola DR, Malaquias AC, Correa FA, Arnhold IJP, Rosenberg C, Jorge AAL. Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways [Internet]. European Journal of Endocrinology. 2014 ; 171( 2): 253-262.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1530/eje-14-0232
Artigo de periodico
Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients (2012)
Fragoso, Maria Candida B. V.; Almeida, Madson Queiroz; Mazzuco, Tania L.; Mariani, Beatriz M. P.; Brito, Luciana P.; Gonçalves, Talita Cardoso; Alencar, Guilherme A.; Lima, Lorena de O.; Faria, Andre M.; Bourdeau, Isabelle; Lucon, Antonio M.; Freire, Daniel S.; Latronico, Ana Claudia; Mendonca, Berenice B.; Lacroix, Andre; Lerario, Antonio M.
Source: European Journal of Endocrinology. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, NEOPLASIAS DAS GLÂNDULAS SUPRARRENAIS, PROGNÓSTICO, CRIANÇAS, ADULTOS, EXPRESSÃO GÊNICA, ESTUDOS DE COORTES, BRASIL
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FRAGOSO, Maria Candida B. V. et al. Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients. European Journal of Endocrinology, v. 166, n. 1, p. 61-67, 2012Tradução . . Disponível em: https://doi.org/10.1530/EJE-11-0964. Acesso em: 09 nov. 2024.
APA
Fragoso, M. C. B. V., Almeida, M. Q., Mazzuco, T. L., Mariani, B. M. P., Brito, L. P., Gonçalves, T. C., et al. (2012). Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients. European Journal of Endocrinology, 166( 1), 61-67. doi:10.1530/EJE-11-0964
NLM
Fragoso MCBV, Almeida MQ, Mazzuco TL, Mariani BMP, Brito LP, Gonçalves TC, Alencar GA, Lima L de O, Faria AM, Bourdeau I, Lucon AM, Freire DS, Latronico AC, Mendonca BB, Lacroix A, Lerario AM. Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients [Internet]. European Journal of Endocrinology. 2012 ; 166( 1): 61-67.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1530/EJE-11-0964
Vancouver
Fragoso MCBV, Almeida MQ, Mazzuco TL, Mariani BMP, Brito LP, Gonçalves TC, Alencar GA, Lima L de O, Faria AM, Bourdeau I, Lucon AM, Freire DS, Latronico AC, Mendonca BB, Lacroix A, Lerario AM. Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients [Internet]. European Journal of Endocrinology. 2012 ; 166( 1): 61-67.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1530/EJE-11-0964
Artigo de periodico
Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver–Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11 (2012)
Montenegro, Luciana R.; Leal, Andrea C.; Coutinho, Debora C.; Valassi, Helena P. L.; Nishi, Mirian Y.; Arnhold, Ivo J. P.; Mendonca, Berenice B.; Jorge, Alexander A. L.
Source: European Journal of Endocrinology. Unidade: FM
Subjects: METABOLISMO (QUÍMICA), PROLIFERAÇÃO CELULAR, CULTURA DE CÉLULAS, FENÓTIPOS, REAÇÃO EM CADEIA POR POLIMERASE, ANORMALIDADES MUSCULOSQUELÉTICAS (GENÉTICA), BIOQUÍMICA CLÍNICA
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ABNT
MONTENEGRO, Luciana R. et al. Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver–Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11. European Journal of Endocrinology, v. 166, n. 3, p. 543-550, 2012Tradução . . Disponível em: https://doi.org/10.1530/EJE-11-0964. Acesso em: 09 nov. 2024.
APA
Montenegro, L. R., Leal, A. C., Coutinho, D. C., Valassi, H. P. L., Nishi, M. Y., Arnhold, I. J. P., et al. (2012). Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver–Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11. European Journal of Endocrinology, 166( 3), 543-550. doi:10.1530/EJE-11-0964
NLM
Montenegro LR, Leal AC, Coutinho DC, Valassi HPL, Nishi MY, Arnhold IJP, Mendonca BB, Jorge AAL. Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver–Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11 [Internet]. European Journal of Endocrinology. 2012 ; 166( 3): 543-550.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1530/EJE-11-0964
Vancouver
Montenegro LR, Leal AC, Coutinho DC, Valassi HPL, Nishi MY, Arnhold IJP, Mendonca BB, Jorge AAL. Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver–Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11 [Internet]. European Journal of Endocrinology. 2012 ; 166( 3): 543-550.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1530/EJE-11-0964
Artigo de periodico
Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism (2011)
Beneduzzi, Daiane; Iyer, Anita K.; Trarbach, Ericka Barbosa; Silveira-Neto, Acacio P.; Silveira, Letícia G.; Tusset, Cintia; Yip, Kathleen; Mendonça, Berenice B,; Mellon, Pamela L.; Latronico, Ana Claudia
Source: European Journal of Endocrinology. Unidade: FM
Subjects: HIPOGONADISMO (GENÉTICO;CONGÊNITO), PUBERDADE (DESENVOLVIMENTO), HORMÔNIO LUTEINIZANTE (SECREÇÃO), HIPOTÁLAMO (FISIOPATOLOGIA), GENES, HORMÔNIO FOLÍCULO-ESTIMULANTE (SECREÇÃO)
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ABNT
BENEDUZZI, Daiane et al. Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism. European Journal of Endocrinology, v. 165, n. 2, p. 145-150, 2011Tradução . . Disponível em: https://doi.org/10.1530/EJE-11-0199. Acesso em: 09 nov. 2024.
APA
Beneduzzi, D., Iyer, A. K., Trarbach, E. B., Silveira-Neto, A. P., Silveira, L. G., Tusset, C., et al. (2011). Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism. European Journal of Endocrinology, 165( 2), 145-150. doi:10.1530/EJE-11-0199
NLM
Beneduzzi D, Iyer AK, Trarbach EB, Silveira-Neto AP, Silveira LG, Tusset C, Yip K, Mendonça BB, Mellon PL, Latronico AC. Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism [Internet]. European Journal of Endocrinology. 2011 ; 165( 2): 145-150.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1530/EJE-11-0199
Vancouver
Beneduzzi D, Iyer AK, Trarbach EB, Silveira-Neto AP, Silveira LG, Tusset C, Yip K, Mendonça BB, Mellon PL, Latronico AC. Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism [Internet]. European Journal of Endocrinology. 2011 ; 165( 2): 145-150.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1530/EJE-11-0199
Artigo de periodico
Thyroid and the environment: exposure to excessive nutritional iodine increases the prevalence of thyroid disorders in São Paulo, Brazil (2008)
Camargo, Rosalinda Y. A.; Tomimori, Eduardo K.; Neves, Solange C.; Rubio, Ileana G. S.; Galrão, Ana Luiza; Knobel, Meyer; Medeiros-Neto, Geraldo
Source: European Journal of Endocrinology. Unidade: FM
Subjects: DOENÇAS DA TIREOIDE (DIAGNÓSTICO), EXPOSIÇÃO AMBIENTAL, MEIO AMBIENTE, IODO (EFEITOS ADVERSOS), HIPERTIREOIDISMO (DIETOTERAPIA), SÃO PAULO, BRASIL
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CAMARGO, Rosalinda Y. A. et al. Thyroid and the environment: exposure to excessive nutritional iodine increases the prevalence of thyroid disorders in São Paulo, Brazil. European Journal of Endocrinology, v. 159, n. 3, p. 293-299, 2008Tradução . . Disponível em: https://doi.org/10.1530/EJE-08-0192. Acesso em: 09 nov. 2024.
APA
Camargo, R. Y. A., Tomimori, E. K., Neves, S. C., Rubio, I. G. S., Galrão, A. L., Knobel, M., & Medeiros-Neto, G. (2008). Thyroid and the environment: exposure to excessive nutritional iodine increases the prevalence of thyroid disorders in São Paulo, Brazil. European Journal of Endocrinology, 159( 3), 293-299. doi:10.1530/EJE-08-0192
NLM
Camargo RYA, Tomimori EK, Neves SC, Rubio IGS, Galrão AL, Knobel M, Medeiros-Neto G. Thyroid and the environment: exposure to excessive nutritional iodine increases the prevalence of thyroid disorders in São Paulo, Brazil [Internet]. European Journal of Endocrinology. 2008 ; 159( 3): 293-299.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1530/EJE-08-0192
Vancouver
Camargo RYA, Tomimori EK, Neves SC, Rubio IGS, Galrão AL, Knobel M, Medeiros-Neto G. Thyroid and the environment: exposure to excessive nutritional iodine increases the prevalence of thyroid disorders in São Paulo, Brazil [Internet]. European Journal of Endocrinology. 2008 ; 159( 3): 293-299.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1530/EJE-08-0192
Artigo de periodico
Multiple endocrine neoplasia type 1 in Brazil: MEN1 founding mutation, clinical features, and bone mineral density profile (2008)
Lourenço Jr, D. M.; Toledo, R. A.; Mackowiak, I. I.; Coutinho, F. L.; Cavalcanti, M. G.; Correia-Deur, J. E. M.; Montenegro, F.; Siqueira, S. A. C.; Margarido, L. C.; Machado, M. C.; Toledo, S. P. A.
Source: European Journal of Endocrinology. Unidade: FM
Subjects: NEOPLASIA ENDÓCRINA MÚLTIPLA (GENÉTICA;EPIDEMIOLOGIA), DENSIDADE ÓSSEA, ANÁLISE ESTATÍSTICA DE DADOS, FENÓTIPOS, PROLIFERAÇÃO CELULAR, GENOMAS
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ABNT
LOURENÇO JR, D. M. et al. Multiple endocrine neoplasia type 1 in Brazil: MEN1 founding mutation, clinical features, and bone mineral density profile. European Journal of Endocrinology, v. 159, n. 3, p. 259-274, 2008Tradução . . Disponível em: https://doi.org/10.1530/EJE-08-0153. Acesso em: 09 nov. 2024.
APA
Lourenço Jr, D. M., Toledo, R. A., Mackowiak, I. I., Coutinho, F. L., Cavalcanti, M. G., Correia-Deur, J. E. M., et al. (2008). Multiple endocrine neoplasia type 1 in Brazil: MEN1 founding mutation, clinical features, and bone mineral density profile. European Journal of Endocrinology, 159( 3), 259-274. doi:10.1530/EJE-08-0153
NLM
Lourenço Jr DM, Toledo RA, Mackowiak II, Coutinho FL, Cavalcanti MG, Correia-Deur JEM, Montenegro F, Siqueira SAC, Margarido LC, Machado MC, Toledo SPA. Multiple endocrine neoplasia type 1 in Brazil: MEN1 founding mutation, clinical features, and bone mineral density profile [Internet]. European Journal of Endocrinology. 2008 ; 159( 3): 259-274.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1530/EJE-08-0153
Vancouver
Lourenço Jr DM, Toledo RA, Mackowiak II, Coutinho FL, Cavalcanti MG, Correia-Deur JEM, Montenegro F, Siqueira SAC, Margarido LC, Machado MC, Toledo SPA. Multiple endocrine neoplasia type 1 in Brazil: MEN1 founding mutation, clinical features, and bone mineral density profile [Internet]. European Journal of Endocrinology. 2008 ; 159( 3): 259-274.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1530/EJE-08-0153
Artigo de periodico
A new species of Halicyclops (Copepoda, Cyclopoida, Cyclopidae) from cenotes of the Yucatan Peninsula, Mexico, with an identification Key for the species of the genus from the Caribbean region and adjacent areas (1998)
Rocha, Carlos Eduardo Falavigna da; Iliffe, Thomas M.; Reid, Janet Warner; Suárez-Morales, Eduardo
Source: Sarsia. Unidade: IB
Subjects: COPEPODA, FAUNA
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ROCHA, Carlos Eduardo Falavigna da et al. A new species of Halicyclops (Copepoda, Cyclopoida, Cyclopidae) from cenotes of the Yucatan Peninsula, Mexico, with an identification Key for the species of the genus from the Caribbean region and adjacent areas. Sarsia, v. 83, p. 387-399, 1998Tradução . . Disponível em: https://doi.org/10.1080/00364827.1998.10413698. Acesso em: 09 nov. 2024.
APA
Rocha, C. E. F. da, Iliffe, T. M., Reid, J. W., & Suárez-Morales, E. (1998). A new species of Halicyclops (Copepoda, Cyclopoida, Cyclopidae) from cenotes of the Yucatan Peninsula, Mexico, with an identification Key for the species of the genus from the Caribbean region and adjacent areas. Sarsia, 83, 387-399. doi:10.1080/00364827.1998.10413698
NLM
Rocha CEF da, Iliffe TM, Reid JW, Suárez-Morales E. A new species of Halicyclops (Copepoda, Cyclopoida, Cyclopidae) from cenotes of the Yucatan Peninsula, Mexico, with an identification Key for the species of the genus from the Caribbean region and adjacent areas [Internet]. Sarsia. 1998 ; 83 387-399.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1080/00364827.1998.10413698
Vancouver
Rocha CEF da, Iliffe TM, Reid JW, Suárez-Morales E. A new species of Halicyclops (Copepoda, Cyclopoida, Cyclopidae) from cenotes of the Yucatan Peninsula, Mexico, with an identification Key for the species of the genus from the Caribbean region and adjacent areas [Internet]. Sarsia. 1998 ; 83 387-399.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1080/00364827.1998.10413698

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