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Artigo de periodico
Potential determinants of thyroid peroxidase antibodies and mortality risk: results from the ELSA-Brasil study (2024)
Meneghini, Vandrize ; Tebar, William Rodrigues ; Santos, Itamar S ; Janovsky, Carolina Porto Silva ; Almeida-Pititto, Bianca de ; Birck, Marina Gabriela; Lotufo, Paulo Andrade ; Goulart, Alessandra Carvalho ; Sgarbi, José Augusto ; Teixeira, Patrícia de Fátima dos Santos; Tunes, Gisela ; Bensenor, Isabela Martins
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidades: FM, FSP, IME, HU
Assuntos: TIREOIDITE AUTOIMUNE, PEROXIDASE, MORTALIDADE, ANÁLISE DE REGRESSÃO E DE CORRELAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MENEGHINI, Vandrize et al. Potential determinants of thyroid peroxidase antibodies and mortality risk: results from the ELSA-Brasil study. Journal of Clinical Endocrinology and Metabolism, v. 109, n. 2, p. e698–e710p, 2024Tradução . . Disponível em: https://doi.org/10.1210/clinem/dgad539. Acesso em: 01 out. 2024.
APA
Meneghini, V., Tebar, W. R., Santos, I. S., Janovsky, C. P. S., Almeida-Pititto, B. de, Birck, M. G., et al. (2024). Potential determinants of thyroid peroxidase antibodies and mortality risk: results from the ELSA-Brasil study. Journal of Clinical Endocrinology and Metabolism, 109( 2), e698–e710p. doi:10.1210/clinem/dgad539
NLM
Meneghini V, Tebar WR, Santos IS, Janovsky CPS, Almeida-Pititto B de, Birck MG, Lotufo PA, Goulart AC, Sgarbi JA, Teixeira P de F dos S, Tunes G, Bensenor IM. Potential determinants of thyroid peroxidase antibodies and mortality risk: results from the ELSA-Brasil study [Internet]. Journal of Clinical Endocrinology and Metabolism. 2024 ; 109( 2): e698–e710p.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/clinem/dgad539
Vancouver
Meneghini V, Tebar WR, Santos IS, Janovsky CPS, Almeida-Pititto B de, Birck MG, Lotufo PA, Goulart AC, Sgarbi JA, Teixeira P de F dos S, Tunes G, Bensenor IM. Potential determinants of thyroid peroxidase antibodies and mortality risk: results from the ELSA-Brasil study [Internet]. Journal of Clinical Endocrinology and Metabolism. 2024 ; 109( 2): e698–e710p.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/clinem/dgad539
Artigo de periodico
Nicotinamide nucleotide transhydrogenase is essential for adrenal steroidogenesis: clinical and in vitro lessons (2023)
Bodoni, Aline Faccioli; Coeli-Lacchini, Fernanda Borchers; Gebenlian, Juliana Lourenço; Sobral, Lays Martin; Garcia, Cristiana Bernadelli ; Silva Junior, Wilson Araújo da ; Peronni, Kamila Chagas; Ramalho, Leandra Naira Zambelli ; Ramalho, Fernando Silva ; Moreira, Ayrton Custódio; Castro, Margaret de ; Leopoldino, Andréia Machado ; Antonini, Sonir Roberto Rauber
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidades: FCFRP, FMRP
Assuntos: MITOCÔNDRIAS, IMUNOHISTOQUÍMICA, ESTRESSE OXIDATIVO, IMUNOFLUORESCÊNCIA, CORTISOL
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ABNT
BODONI, Aline Faccioli et al. Nicotinamide nucleotide transhydrogenase is essential for adrenal steroidogenesis: clinical and in vitro lessons. Journal of Clinical Endocrinology and Metabolism, v. 108, n. 6, p. 1464-1474, 2023Tradução . . Disponível em: https://doi.org/10.1210/clinem/dgac705. Acesso em: 01 out. 2024.
APA
Bodoni, A. F., Coeli-Lacchini, F. B., Gebenlian, J. L., Sobral, L. M., Garcia, C. B., Silva Junior, W. A. da, et al. (2023). Nicotinamide nucleotide transhydrogenase is essential for adrenal steroidogenesis: clinical and in vitro lessons. Journal of Clinical Endocrinology and Metabolism, 108( 6), 1464-1474. doi:10.1210/clinem/dgac705
NLM
Bodoni AF, Coeli-Lacchini FB, Gebenlian JL, Sobral LM, Garcia CB, Silva Junior WA da, Peronni KC, Ramalho LNZ, Ramalho FS, Moreira AC, Castro M de, Leopoldino AM, Antonini SRR. Nicotinamide nucleotide transhydrogenase is essential for adrenal steroidogenesis: clinical and in vitro lessons [Internet]. Journal of Clinical Endocrinology and Metabolism. 2023 ; 108( 6): 1464-1474.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/clinem/dgac705
Vancouver
Bodoni AF, Coeli-Lacchini FB, Gebenlian JL, Sobral LM, Garcia CB, Silva Junior WA da, Peronni KC, Ramalho LNZ, Ramalho FS, Moreira AC, Castro M de, Leopoldino AM, Antonini SRR. Nicotinamide nucleotide transhydrogenase is essential for adrenal steroidogenesis: clinical and in vitro lessons [Internet]. Journal of Clinical Endocrinology and Metabolism. 2023 ; 108( 6): 1464-1474.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/clinem/dgac705
Artigo de periodico
Integrating methylome and transcriptome signatures expands the molecular classification of the pituitary tumors (2022)
Silva Júnior, Rui Milton Patrício da; Bueno, Ana Carolina; Martins, Clarissa Silva; Coelli-Lacchini, Fernanda; Ozaki, Jorge Guilherme Okanobo; Almeida-e-Silva, Danillo Cunha de ; Marrero-Gutiérrez, Junier; Santos, Antônio Carlos dos; Garcia-Peral, Carlos; Machado, Hélio Rubens; Santos, Marcelo Volpon ; Elias, Paula Conde Lamparelli; Moreira, Ayrton Custódio; Colli, Leandro Machado ; Vêncio, Ricardo Zorzetto Nicoliello; Antonini, Sonir Roberto Rauber ; Castro, Margaret de
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidades: FMRP, FFCLRP, BIOINFORMÁTICA
Assuntos: NEOPLASIAS HIPOFISÁRIAS, METILAÇÃO DE DNA, SEQUENCIAMENTO GENÉTICO, RNA
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ABNT
SILVA JÚNIOR, Rui Milton Patrício da et al. Integrating methylome and transcriptome signatures expands the molecular classification of the pituitary tumors. Journal of Clinical Endocrinology and Metabolism, v. 108, n. 6, p. 1452-1463, 2022Tradução . . Disponível em: https://doi.org/10.1210/clinem/dgac703. Acesso em: 01 out. 2024.
APA
Silva Júnior, R. M. P. da, Bueno, A. C., Martins, C. S., Coelli-Lacchini, F., Ozaki, J. G. O., Almeida-e-Silva, D. C. de, et al. (2022). Integrating methylome and transcriptome signatures expands the molecular classification of the pituitary tumors. Journal of Clinical Endocrinology and Metabolism, 108( 6), 1452-1463. doi:10.1210/clinem/dgac703
NLM
Silva Júnior RMP da, Bueno AC, Martins CS, Coelli-Lacchini F, Ozaki JGO, Almeida-e-Silva DC de, Marrero-Gutiérrez J, Santos AC dos, Garcia-Peral C, Machado HR, Santos MV, Elias PCL, Moreira AC, Colli LM, Vêncio RZN, Antonini SRR, Castro M de. Integrating methylome and transcriptome signatures expands the molecular classification of the pituitary tumors [Internet]. Journal of Clinical Endocrinology and Metabolism. 2022 ; 108( 6): 1452-1463.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/clinem/dgac703
Vancouver
Silva Júnior RMP da, Bueno AC, Martins CS, Coelli-Lacchini F, Ozaki JGO, Almeida-e-Silva DC de, Marrero-Gutiérrez J, Santos AC dos, Garcia-Peral C, Machado HR, Santos MV, Elias PCL, Moreira AC, Colli LM, Vêncio RZN, Antonini SRR, Castro M de. Integrating methylome and transcriptome signatures expands the molecular classification of the pituitary tumors [Internet]. Journal of Clinical Endocrinology and Metabolism. 2022 ; 108( 6): 1452-1463.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/clinem/dgac703
Artigo de periodico
Time to diagnosis in cushing’s syndrome: a meta-analysis based on 5367 patients (2020)
Rubinstein, German; Osswald, Andrea; Hoster, Eva; Losa, Marco; Elenkova, Atanaska; Zacharieva, Sabina; Machado, Márcio Carlos; Hanzu, Felicia Alexandra; Zopp, Stephanie; Ritzel, Katrin; Oliveira, Ricardo Santos de
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidades: FMRP, FM
Assuntos: IDADE, ESTATÍSTICA, FATORES SEXUAIS, FATORES ETÁRIOS, DIAGNÓSTICO CLÍNICO
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ABNT
RUBINSTEIN, German et al. Time to diagnosis in cushing’s syndrome: a meta-analysis based on 5367 patients. Journal of Clinical Endocrinology and Metabolism, v. 105, n. 3, p. e12-e22, 2020Tradução . . Disponível em: https://doi.org/10.1210/clinem/dgz136. Acesso em: 01 out. 2024.
APA
Rubinstein, G., Osswald, A., Hoster, E., Losa, M., Elenkova, A., Zacharieva, S., et al. (2020). Time to diagnosis in cushing’s syndrome: a meta-analysis based on 5367 patients. Journal of Clinical Endocrinology and Metabolism, 105( 3), e12-e22. doi:10.1210/clinem/dgz136
NLM
Rubinstein G, Osswald A, Hoster E, Losa M, Elenkova A, Zacharieva S, Machado MC, Hanzu FA, Zopp S, Ritzel K, Oliveira RS de. Time to diagnosis in cushing’s syndrome: a meta-analysis based on 5367 patients [Internet]. Journal of Clinical Endocrinology and Metabolism. 2020 ; 105( 3): e12-e22.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/clinem/dgz136
Vancouver
Rubinstein G, Osswald A, Hoster E, Losa M, Elenkova A, Zacharieva S, Machado MC, Hanzu FA, Zopp S, Ritzel K, Oliveira RS de. Time to diagnosis in cushing’s syndrome: a meta-analysis based on 5367 patients [Internet]. Journal of Clinical Endocrinology and Metabolism. 2020 ; 105( 3): e12-e22.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/clinem/dgz136
Artigo de periodico
Insight into the ontogeny of GnRH neurons from patients born without a nose (2020)
Delaney, Angela; Volochayev, Rita; Meader, Brooke; Lee, Janice; Almpani, Konstantinia; Noukelak, Germaine Y.; Henkind, Jennifer; Chalmers, Laura; Law, Jennifer R.; Williamson, Kathleen A.; Jacobsen, Christina M.; Buitrago, Tatiana Pineda; Perez, Orlando; Cho, Chie-Hee; Kaindl, Angela; Rauch, Anita; Steindl, Katharina; Garcia, Jose Elias; Russell, Bianca E.; Prasad, Rameshwar; Mondal, Uttam K.; Reigstad, Hallvard M.; Clements, Scott; Kim, Susan; Inoue, Kaoru; Arora, Gazal; Salnikov, Kathryn B.; DiOrio, Nicole P.; Prada, Rolando; Capri, Yline; Morioka, Kosuke; Mizota, Michiyo; Zechi-Ceide, Roseli Maria ; Nakata, Nancy Mizue Kokitsu ; Tonello, Cristiano ; Pittoli, Siulan Vendramini Paulovich ; Dalben, Gisele da Silva ; Balasubramanian, Ravikumar; Dwyer, Andrew A.; Seminara, Stephanie B.; Crowley Júnior, William F.; Plummer, Lacey; Hall, Janet E.; Graham Júnior, John M.; Lin, Angela E.; Shaw, Natalie D.
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: HRAC
Assuntos: HORMÔNIO LIBERADOR DE GONADOTROFINAS, AGENESIA, NARIZ (ANATOMIA), MALFORMAÇÕES, FENÓTIPOS
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ABNT
DELANEY, Angela et al. Insight into the ontogeny of GnRH neurons from patients born without a nose. Journal of Clinical Endocrinology and Metabolism, v. 105, n. 5, p. 1538-1551, 2020Tradução . . Disponível em: https://doi.org/10.1210/clinem/dgaa065. Acesso em: 01 out. 2024.
APA
Delaney, A., Volochayev, R., Meader, B., Lee, J., Almpani, K., Noukelak, G. Y., et al. (2020). Insight into the ontogeny of GnRH neurons from patients born without a nose. Journal of Clinical Endocrinology and Metabolism, 105( 5), 1538-1551. doi:10.1210/clinem/dgaa065
NLM
Delaney A, Volochayev R, Meader B, Lee J, Almpani K, Noukelak GY, Henkind J, Chalmers L, Law JR, Williamson KA, Jacobsen CM, Buitrago TP, Perez O, Cho C-H, Kaindl A, Rauch A, Steindl K, Garcia JE, Russell BE, Prasad R, Mondal UK, Reigstad HM, Clements S, Kim S, Inoue K, Arora G, Salnikov KB, DiOrio NP, Prada R, Capri Y, Morioka K, Mizota M, Zechi-Ceide RM, Nakata NMK, Tonello C, Pittoli SVP, Dalben G da S, Balasubramanian R, Dwyer AA, Seminara SB, Crowley Júnior WF, Plummer L, Hall JE, Graham Júnior JM, Lin AE, Shaw ND. Insight into the ontogeny of GnRH neurons from patients born without a nose [Internet]. Journal of Clinical Endocrinology and Metabolism. 2020 ; 105( 5): 1538-1551.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/clinem/dgaa065
Vancouver
Delaney A, Volochayev R, Meader B, Lee J, Almpani K, Noukelak GY, Henkind J, Chalmers L, Law JR, Williamson KA, Jacobsen CM, Buitrago TP, Perez O, Cho C-H, Kaindl A, Rauch A, Steindl K, Garcia JE, Russell BE, Prasad R, Mondal UK, Reigstad HM, Clements S, Kim S, Inoue K, Arora G, Salnikov KB, DiOrio NP, Prada R, Capri Y, Morioka K, Mizota M, Zechi-Ceide RM, Nakata NMK, Tonello C, Pittoli SVP, Dalben G da S, Balasubramanian R, Dwyer AA, Seminara SB, Crowley Júnior WF, Plummer L, Hall JE, Graham Júnior JM, Lin AE, Shaw ND. Insight into the ontogeny of GnRH neurons from patients born without a nose [Internet]. Journal of Clinical Endocrinology and Metabolism. 2020 ; 105( 5): 1538-1551.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/clinem/dgaa065
Artigo de periodico
Landscape of familial isolated and young-onset pituitary adenomas: prospective diagnosis in AIP mutation carriers (2015)
Hernández-Ramirez, Laura C.; Gabrovska, Plamena; Dénes, Judit; Stals, Karen; Trivellin, Giampaolo; Tilley, Daniel; Ferraú, Francesco; Evanson, Jane; Ellard, Sian; Grossman, Ashley B.; Roncaroli, Federico; Gadelha, Mônica R.; Korbonits, Márta; Castro, Margaret de
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: FMRP
Assuntos: GLÂNDULA PITUITÁRIA, ADENOMA, MUTAÇÃO GENÉTICA, HIDROCARBONETOS
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ABNT
HERNÁNDEZ-RAMIREZ, Laura C. et al. Landscape of familial isolated and young-onset pituitary adenomas: prospective diagnosis in AIP mutation carriers. Journal of Clinical Endocrinology and Metabolism, v. 100, n. 9, p. E1242-E1254, 2015Tradução . . Disponível em: https://doi.org/10.1210/jc.2015-1869. Acesso em: 01 out. 2024.
APA
Hernández-Ramirez, L. C., Gabrovska, P., Dénes, J., Stals, K., Trivellin, G., Tilley, D., et al. (2015). Landscape of familial isolated and young-onset pituitary adenomas: prospective diagnosis in AIP mutation carriers. Journal of Clinical Endocrinology and Metabolism, 100( 9), E1242-E1254. doi:10.1210/jc.2015-1869
NLM
Hernández-Ramirez LC, Gabrovska P, Dénes J, Stals K, Trivellin G, Tilley D, Ferraú F, Evanson J, Ellard S, Grossman AB, Roncaroli F, Gadelha MR, Korbonits M, Castro M de. Landscape of familial isolated and young-onset pituitary adenomas: prospective diagnosis in AIP mutation carriers [Internet]. Journal of Clinical Endocrinology and Metabolism. 2015 ; 100( 9): E1242-E1254.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2015-1869
Vancouver
Hernández-Ramirez LC, Gabrovska P, Dénes J, Stals K, Trivellin G, Tilley D, Ferraú F, Evanson J, Ellard S, Grossman AB, Roncaroli F, Gadelha MR, Korbonits M, Castro M de. Landscape of familial isolated and young-onset pituitary adenomas: prospective diagnosis in AIP mutation carriers [Internet]. Journal of Clinical Endocrinology and Metabolism. 2015 ; 100( 9): E1242-E1254.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2015-1869
Artigo de periodico-carta/editorial
Letter to the Editor. [Carta]: comments on "LGR5 activates noncanonical Wnt signaling and inhibits aldosterone production in the human adrenal" by Shaikh L. H., et al (2015)
Leal, Letícia Ferro; Mermejo, Livia M.; Martins, Clarissa S.; Antonini, Sonir Roberto Rauber; Castro, Margaret de
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: FMRP
Assuntos: ALDOSTERONA, SISTEMA ENDÓCRINO, GENES
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ABNT
LEAL, Letícia Ferro et al. Letter to the Editor. [Carta]: comments on "LGR5 activates noncanonical Wnt signaling and inhibits aldosterone production in the human adrenal" by Shaikh L. H., et al. Journal of Clinical Endocrinology and Metabolism. Chevy Chase: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1210/jc.2015-3610. Acesso em: 01 out. 2024. , 2015
APA
Leal, L. F., Mermejo, L. M., Martins, C. S., Antonini, S. R. R., & Castro, M. de. (2015). Letter to the Editor. [Carta]: comments on "LGR5 activates noncanonical Wnt signaling and inhibits aldosterone production in the human adrenal" by Shaikh L. H., et al. Journal of Clinical Endocrinology and Metabolism. Chevy Chase: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1210/jc.2015-3610
NLM
Leal LF, Mermejo LM, Martins CS, Antonini SRR, Castro M de. Letter to the Editor. [Carta]: comments on "LGR5 activates noncanonical Wnt signaling and inhibits aldosterone production in the human adrenal" by Shaikh L. H., et al [Internet]. Journal of Clinical Endocrinology and Metabolism. 2015 ; 100( 12): L125.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2015-3610
Vancouver
Leal LF, Mermejo LM, Martins CS, Antonini SRR, Castro M de. Letter to the Editor. [Carta]: comments on "LGR5 activates noncanonical Wnt signaling and inhibits aldosterone production in the human adrenal" by Shaikh L. H., et al [Internet]. Journal of Clinical Endocrinology and Metabolism. 2015 ; 100( 12): L125.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2015-3610
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
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidades: FM, FMRP
Assuntos: CRIANÇAS, TÉCNICAS GENÉTICAS, PUBERDADE PRECOCE, MUTAÇÃO GENÉTICA
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ABNT
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: 01 out. 2024.
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 2024 out. 01 ] 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 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2013-3126
Artigo de periodico
A Novel ADIPOQ mutation (p.M40K) impairs assembly of high-molecular-weight adiponectin and is associated with early-onset obesity and metabolic syndrome (2014)
Bueno, Ana Carolina; Sun, Kai; Martins, Clarissa Silva; Elias Júnior, Jorge; Miranda, Wallace; Tao, Caroline; Foss-Freitas, Maria Cristina; Barbieri, Marco Antonio; Bettiol, Heloisa; Castro, Margaret de; Scherer, Philipp E.; Antonini, Sonir Roberto Rauber
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: FMRP
Assuntos: GENÉTICA, POLIMORFISMO, HORMÔNIOS (DEFICIÊNCIA), ENDOCRINOLOGIA (METABOLISMO)
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ABNT
BUENO, Ana Carolina et al. A Novel ADIPOQ mutation (p.M40K) impairs assembly of high-molecular-weight adiponectin and is associated with early-onset obesity and metabolic syndrome. Journal of Clinical Endocrinology and Metabolism, v. 99 n.4, p. E683-E693, 2014Tradução . . Disponível em: https://doi.org/10.1210/jc.2013-3009. Acesso em: 01 out. 2024.
APA
Bueno, A. C., Sun, K., Martins, C. S., Elias Júnior, J., Miranda, W., Tao, C., et al. (2014). A Novel ADIPOQ mutation (p.M40K) impairs assembly of high-molecular-weight adiponectin and is associated with early-onset obesity and metabolic syndrome. Journal of Clinical Endocrinology and Metabolism, 99 n.4, E683-E693. doi:10.1210/jc.2013-3009
NLM
Bueno AC, Sun K, Martins CS, Elias Júnior J, Miranda W, Tao C, Foss-Freitas MC, Barbieri MA, Bettiol H, Castro M de, Scherer PE, Antonini SRR. A Novel ADIPOQ mutation (p.M40K) impairs assembly of high-molecular-weight adiponectin and is associated with early-onset obesity and metabolic syndrome [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99 n.4 E683-E693.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2013-3009
Vancouver
Bueno AC, Sun K, Martins CS, Elias Júnior J, Miranda W, Tao C, Foss-Freitas MC, Barbieri MA, Bettiol H, Castro M de, Scherer PE, Antonini SRR. A Novel ADIPOQ mutation (p.M40K) impairs assembly of high-molecular-weight adiponectin and is associated with early-onset obesity and metabolic syndrome [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99 n.4 E683-E693.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2013-3009
Artigo de periodico
Late-night salivary cortisol has a better performance than urinary free cortisol in the diagnosis of Cushing's syndrome (2014)
Elias, Paula Conde Lamparelli; Martinez, Edson Zangiacomi; Barone, Bruno F. C.; Mermejo, Livia M.; Castro, Margaret; Moreira, Ayrton Custódio
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: FMRP
Assuntos: RITMO CIRCADIANO, TÉCNICAS DE DIAGNÓSTICO E PROCEDIMENTOS, SISTEMA ENDÓCRINO (DIAGNÓSTICO), SALIVA (QUÍMICA), REPRODUTIBILIDADE DE RESULTADOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ELIAS, Paula Conde Lamparelli et al. Late-night salivary cortisol has a better performance than urinary free cortisol in the diagnosis of Cushing's syndrome. Journal of Clinical Endocrinology and Metabolism, v. 99, n. 6, p. 2045-2051, 2014Tradução . . Disponível em: https://doi.org/10.1210/jc.2013-4262. Acesso em: 01 out. 2024.
APA
Elias, P. C. L., Martinez, E. Z., Barone, B. F. C., Mermejo, L. M., Castro, M., & Moreira, A. C. (2014). Late-night salivary cortisol has a better performance than urinary free cortisol in the diagnosis of Cushing's syndrome. Journal of Clinical Endocrinology and Metabolism, 99( 6), 2045-2051. doi:10.1210/jc.2013-4262
NLM
Elias PCL, Martinez EZ, Barone BFC, Mermejo LM, Castro M, Moreira AC. Late-night salivary cortisol has a better performance than urinary free cortisol in the diagnosis of Cushing's syndrome [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99( 6): 2045-2051.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2013-4262
Vancouver
Elias PCL, Martinez EZ, Barone BFC, Mermejo LM, Castro M, Moreira AC. Late-night salivary cortisol has a better performance than urinary free cortisol in the diagnosis of Cushing's syndrome [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99( 6): 2045-2051.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2013-4262
Artigo de periodico
ARMC5 mutation are a frequent cause of primary macronodular adrenal hyperplasia (2014)
Alencar, Guilherme Asmar; Lerario, Antonio Marcondes; Nishi, Mirian Yumie; Mariani, Beatriz Marinho de Paula; Almeida, Madson Queiroz; Tremblay, Johanne; Hamet, Pavel; Zerbini, Maria Claudis Nogueira; Gomes, Gilberto Carlos; Bordeau, Isabelle; Pereira, Maria Adelaide Albergaria; Rocha, Manoel de Souza; Chambo, Jose Carlos; Lacroix, Andre; Mendonça, Berenice Bilharinho; Fragoso, Maria Candida B. Villares
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Assuntos: POLIMORFISMO, MUTAÇÃO GENÉTICA, HIPERPLASIA SUPRARRENAL CONGÊNITA
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ABNT
ALENCAR, Guilherme Asmar et al. ARMC5 mutation are a frequent cause of primary macronodular adrenal hyperplasia. Journal of Clinical Endocrinology and Metabolism, v. 99, n. 8, p. E1501-E1509, 2014Tradução . . Disponível em: https://doi.org/10.1210/jc.2013-4237. Acesso em: 01 out. 2024.
APA
Alencar, G. A., Lerario, A. M., Nishi, M. Y., Mariani, B. M. de P., Almeida, M. Q., Tremblay, J., et al. (2014). ARMC5 mutation are a frequent cause of primary macronodular adrenal hyperplasia. Journal of Clinical Endocrinology and Metabolism, 99( 8), E1501-E1509. doi:10.1210/jc.2013-4237
NLM
Alencar GA, Lerario AM, Nishi MY, Mariani BM de P, Almeida MQ, Tremblay J, Hamet P, Zerbini MCN, Gomes GC, Bordeau I, Pereira MAA, Rocha M de S, Chambo JC, Lacroix A, Mendonça BB, Fragoso MCBV. ARMC5 mutation are a frequent cause of primary macronodular adrenal hyperplasia [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99( 8): E1501-E1509.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2013-4237
Vancouver
Alencar GA, Lerario AM, Nishi MY, Mariani BM de P, Almeida MQ, Tremblay J, Hamet P, Zerbini MCN, Gomes GC, Bordeau I, Pereira MAA, Rocha M de S, Chambo JC, Lacroix A, Mendonça BB, Fragoso MCBV. ARMC5 mutation are a frequent cause of primary macronodular adrenal hyperplasia [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99( 8): E1501-E1509.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2013-4237
Artigo de periodico
Isolated GH deficiency due to a GHRH receptor mutation causes hip joint problems and genu valgum, and reduces size but not density of trabecular and mixed bone (2013)
Epitácio-Pereira, Carlos C.; Silva, Gabriella M. F.; Salvatori, Roberto; Santana, João A. M.; Pereira, Francisco A.; Gois-Júnior, Miburge B.; Britto, Allan V. O.; Oliveira, Carla R. P.; Souza, Anita H. O.; Santos, Elenilde G.; Campos, Viviane C.; Pereira, Rossana M. C.; Valença, Eugênia H. O.; Barbosa, Rita A. A.; Farias, Maria Isabel T.; Paula, Francisco Jose Albuquerque de; Ribeiro, Taisa V.; Oliveira, Mario C. P.; Aguiar-Oliveira, Manuel H.
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: FMRP
Assuntos: NANISMO, OSTEOARTRITE DO JOELHO, DENSIDADE ÓSSEA, GLÂNDULA PITUITÁRIA
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ABNT
EPITÁCIO-PEREIRA, Carlos C. et al. Isolated GH deficiency due to a GHRH receptor mutation causes hip joint problems and genu valgum, and reduces size but not density of trabecular and mixed bone. Journal of Clinical Endocrinology and Metabolism, v. 98, n. 11, p. E1710-E1715, 2013Tradução . . Disponível em: https://doi.org/10.1210/jc.2013-2349. Acesso em: 01 out. 2024.
APA
Epitácio-Pereira, C. C., Silva, G. M. F., Salvatori, R., Santana, J. A. M., Pereira, F. A., Gois-Júnior, M. B., et al. (2013). Isolated GH deficiency due to a GHRH receptor mutation causes hip joint problems and genu valgum, and reduces size but not density of trabecular and mixed bone. Journal of Clinical Endocrinology and Metabolism, 98( 11), E1710-E1715. doi:10.1210/jc.2013-2349
NLM
Epitácio-Pereira CC, Silva GMF, Salvatori R, Santana JAM, Pereira FA, Gois-Júnior MB, Britto AVO, Oliveira CRP, Souza AHO, Santos EG, Campos VC, Pereira RMC, Valença EHO, Barbosa RAA, Farias MIT, Paula FJA de, Ribeiro TV, Oliveira MCP, Aguiar-Oliveira MH. Isolated GH deficiency due to a GHRH receptor mutation causes hip joint problems and genu valgum, and reduces size but not density of trabecular and mixed bone [Internet]. Journal of Clinical Endocrinology and Metabolism. 2013 ; 98( 11): E1710-E1715.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2013-2349
Vancouver
Epitácio-Pereira CC, Silva GMF, Salvatori R, Santana JAM, Pereira FA, Gois-Júnior MB, Britto AVO, Oliveira CRP, Souza AHO, Santos EG, Campos VC, Pereira RMC, Valença EHO, Barbosa RAA, Farias MIT, Paula FJA de, Ribeiro TV, Oliveira MCP, Aguiar-Oliveira MH. Isolated GH deficiency due to a GHRH receptor mutation causes hip joint problems and genu valgum, and reduces size but not density of trabecular and mixed bone [Internet]. Journal of Clinical Endocrinology and Metabolism. 2013 ; 98( 11): E1710-E1715.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2013-2349
Artigo de periodico
Lipid peroxidation is associated with the severity of periodontal disease and local inflammatory markers in patients with type 2 diabetes (2012)
Bastos, Alliny S.; Graves, Dana T.; Loureiro, Ana Paula de Melo ; Rossa Júnior, Carlos; Abdalla, Dulcinéia Saes Parra ; Faulin, Tanize do Espirito Santo; Câmara, Niels Olsen Saraiva ; Andriankaja, Oelisoa; Orrico, Silvana R. P.
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidades: ICB, FCF
Assunto: IMUNOLOGIA
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ABNT
BASTOS, Alliny S. et al. Lipid peroxidation is associated with the severity of periodontal disease and local inflammatory markers in patients with type 2 diabetes. Journal of Clinical Endocrinology and Metabolism, v. 97, n. 8, p. e1353-e1362, 2012Tradução . . Disponível em: https://doi.org/10.1210/jc.2011-3397. Acesso em: 01 out. 2024.
APA
Bastos, A. S., Graves, D. T., Loureiro, A. P. de M., Rossa Júnior, C., Abdalla, D. S. P., Faulin, T. do E. S., et al. (2012). Lipid peroxidation is associated with the severity of periodontal disease and local inflammatory markers in patients with type 2 diabetes. Journal of Clinical Endocrinology and Metabolism, 97( 8), e1353-e1362. doi:10.1210/jc.2011-3397
NLM
Bastos AS, Graves DT, Loureiro AP de M, Rossa Júnior C, Abdalla DSP, Faulin T do ES, Câmara NOS, Andriankaja O, Orrico SRP. Lipid peroxidation is associated with the severity of periodontal disease and local inflammatory markers in patients with type 2 diabetes [Internet]. Journal of Clinical Endocrinology and Metabolism. 2012 ; 97( 8): e1353-e1362.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2011-3397
Vancouver
Bastos AS, Graves DT, Loureiro AP de M, Rossa Júnior C, Abdalla DSP, Faulin T do ES, Câmara NOS, Andriankaja O, Orrico SRP. Lipid peroxidation is associated with the severity of periodontal disease and local inflammatory markers in patients with type 2 diabetes [Internet]. Journal of Clinical Endocrinology and Metabolism. 2012 ; 97( 8): e1353-e1362.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2011-3397
Artigo de periodico
Obesity due to Melanocortin 4 Receptor (MC4R) Deficiency Is Associated with Increased Linear Growth and Final Height, Fasting Hyperinsulinemia, and Incompletely Suppressed Growth Hormone Secretion (2011)
Martinelli Junior, Carlos Eduardo; Keogh, Julia M.; Greenfield, Jerry R.; Henning, Elana; Klaauw, Agatha A. van der; Blackwood, Anthea; O’Rahilly, Stephen; Roelfsema, Ferdinand; Camacho-Hübner, Cecilia; Pijl, Hanno; Farooqi, I. Sadaf
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: FMRP
Assuntos: OBESIDADE (GENÉTICA), ANTROPOMETRIA, PROTEÍNAS DE TRANSPORTE, GLICOPROTEÍNAS, INSULINA
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ABNT
MARTINELLI JUNIOR, Carlos Eduardo et al. Obesity due to Melanocortin 4 Receptor (MC4R) Deficiency Is Associated with Increased Linear Growth and Final Height, Fasting Hyperinsulinemia, and Incompletely Suppressed Growth Hormone Secretion. Journal of Clinical Endocrinology and Metabolism, v. 96, n. 1, p. E181-E188, 2011Tradução . . Disponível em: https://doi.org/10.1210/jc.2010-1369. Acesso em: 01 out. 2024.
APA
Martinelli Junior, C. E., Keogh, J. M., Greenfield, J. R., Henning, E., Klaauw, A. A. van der, Blackwood, A., et al. (2011). Obesity due to Melanocortin 4 Receptor (MC4R) Deficiency Is Associated with Increased Linear Growth and Final Height, Fasting Hyperinsulinemia, and Incompletely Suppressed Growth Hormone Secretion. Journal of Clinical Endocrinology and Metabolism, 96( 1), E181-E188. doi:10.1210/jc.2010-1369
NLM
Martinelli Junior CE, Keogh JM, Greenfield JR, Henning E, Klaauw AA van der, Blackwood A, O’Rahilly S, Roelfsema F, Camacho-Hübner C, Pijl H, Farooqi IS. Obesity due to Melanocortin 4 Receptor (MC4R) Deficiency Is Associated with Increased Linear Growth and Final Height, Fasting Hyperinsulinemia, and Incompletely Suppressed Growth Hormone Secretion [Internet]. Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 1): E181-E188.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2010-1369
Vancouver
Martinelli Junior CE, Keogh JM, Greenfield JR, Henning E, Klaauw AA van der, Blackwood A, O’Rahilly S, Roelfsema F, Camacho-Hübner C, Pijl H, Farooqi IS. Obesity due to Melanocortin 4 Receptor (MC4R) Deficiency Is Associated with Increased Linear Growth and Final Height, Fasting Hyperinsulinemia, and Incompletely Suppressed Growth Hormone Secretion [Internet]. Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 1): E181-E188.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2010-1369
Artigo de periodico
18F-FDG-PET/CT Imaging of ACTH-Independent Macronodular Adrenocortical Hyperplasia (AIMAH) Demonstrating Increased 18F-FDG Uptake (2011)
Alencar, Guilherme Asmar; Fragoso, Maria Candida Barisson Villares; Yamaga, Lilian Yuri Itaya; Lerario, Antonio Marcondes; Mendonça, Berenice Bilharinho
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Assuntos: DIAGNÓSTICO DIFERENCIAL, NEOPLASIAS DAS GLÂNDULAS SUPRARRENAIS, TOMOGRAFIA COMPUTADORIZADA POR EMISSÃO DE FÓTON ÚNICO, METÁSTASE NEOPLÁSICA, HIPERPLASIA SUPRARRENAL CONGÊNITA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALENCAR, Guilherme Asmar et al. 18F-FDG-PET/CT Imaging of ACTH-Independent Macronodular Adrenocortical Hyperplasia (AIMAH) Demonstrating Increased 18F-FDG Uptake. Journal of Clinical Endocrinology and Metabolism, v. 96, n. 11, p. 3300-3301, 2011Tradução . . Disponível em: https://doi.org/10.1210/jc.2011-1397. Acesso em: 01 out. 2024.
APA
Alencar, G. A., Fragoso, M. C. B. V., Yamaga, L. Y. I., Lerario, A. M., & Mendonça, B. B. (2011). 18F-FDG-PET/CT Imaging of ACTH-Independent Macronodular Adrenocortical Hyperplasia (AIMAH) Demonstrating Increased 18F-FDG Uptake. Journal of Clinical Endocrinology and Metabolism, 96( 11), 3300-3301. doi:10.1210/jc.2011-1397
NLM
Alencar GA, Fragoso MCBV, Yamaga LYI, Lerario AM, Mendonça BB. 18F-FDG-PET/CT Imaging of ACTH-Independent Macronodular Adrenocortical Hyperplasia (AIMAH) Demonstrating Increased 18F-FDG Uptake [Internet]. Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 11): 3300-3301.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2011-1397
Vancouver
Alencar GA, Fragoso MCBV, Yamaga LYI, Lerario AM, Mendonça BB. 18F-FDG-PET/CT Imaging of ACTH-Independent Macronodular Adrenocortical Hyperplasia (AIMAH) Demonstrating Increased 18F-FDG Uptake [Internet]. Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 11): 3300-3301.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2011-1397
Artigo de periodico
A giant primary hemangioma of the thyroid gland (2011)
Maciel, Léa Maria Zanini; Gomes, Patrícia M.; Magalhães, Patrícia K. R.; Mello-Filho, Francisco Veríssimo; Freitas, Luiz Carlos Conti de
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: FMRP
Assuntos: HEMANGIOMA, GLÂNDULA TIREOIDE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MACIEL, Léa Maria Zanini et al. A giant primary hemangioma of the thyroid gland. Journal of Clinical Endocrinology and Metabolism, v. 96, n. 6, p. 1623-1624, 2011Tradução . . Disponível em: https://doi.org/10.1210/jc.2010-3016. Acesso em: 01 out. 2024.
APA
Maciel, L. M. Z., Gomes, P. M., Magalhães, P. K. R., Mello-Filho, F. V., & Freitas, L. C. C. de. (2011). A giant primary hemangioma of the thyroid gland. Journal of Clinical Endocrinology and Metabolism, 96( 6), 1623-1624. doi:10.1210/jc.2010-3016
NLM
Maciel LMZ, Gomes PM, Magalhães PKR, Mello-Filho FV, Freitas LCC de. A giant primary hemangioma of the thyroid gland [Internet]. Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 6): 1623-1624.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2010-3016
Vancouver
Maciel LMZ, Gomes PM, Magalhães PKR, Mello-Filho FV, Freitas LCC de. A giant primary hemangioma of the thyroid gland [Internet]. Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 6): 1623-1624.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2010-3016
Artigo de periodico
Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency (2011)
França, Marcela M.; Jorge, Alexander A. L.; Alatzoglou, Kyriaki S.; Carvalho, Luciani R. S.; Mendonça, Berenice Bilharinho; Audi, Laura; Carrascosa, Antonio; Dattani, Mehul T.; Arnhold, Ivo J. P.
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Assuntos: MUTAÇÃO GENÉTICA, POLIMORFISMO, HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA), FENÓTIPOS, ELETROFORESE, SEGUIMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FRANÇA, Marcela M. et al. Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency. Journal of Clinical Endocrinology and Metabolism, v. 96, n. 9, p. E1457-1460, 2011Tradução . . Disponível em: https://doi.org/10.1210/jc.2011-0170. Acesso em: 01 out. 2024.
APA
França, M. M., Jorge, A. A. L., Alatzoglou, K. S., Carvalho, L. R. S., Mendonça, B. B., Audi, L., et al. (2011). Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency. Journal of Clinical Endocrinology and Metabolism, 96( 9), E1457-1460. doi:10.1210/jc.2011-0170
NLM
França MM, Jorge AAL, Alatzoglou KS, Carvalho LRS, Mendonça BB, Audi L, Carrascosa A, Dattani MT, Arnhold IJP. Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency [Internet]. Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 9): E1457-1460.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2011-0170
Vancouver
França MM, Jorge AAL, Alatzoglou KS, Carvalho LRS, Mendonça BB, Audi L, Carrascosa A, Dattani MT, Arnhold IJP. Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency [Internet]. Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 9): E1457-1460.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2011-0170
Artigo de periodico
Mineralocorticoid receptor mutations differentially affect individual gene expression profiles in pseudohypoaldosteronism type 1 (2011)
Rosa, Fabio Luiz Fernandes; Hubert, Edwige Ludiwyne; Fagart, Jérome; Tchitchek, Nicolas; Gomes, Débora; Jouanno, Elodie; Benecke, Arndt; Oblin, Marie-Edith Rafestin; jeunemaitre, Xavier; Antonini, Sonir Roberto Rauber; Zennaro, Maria Christina
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: FMRP
Assuntos: ENDOCRINOLOGIA, PEDIATRIA, EXPRESSÃO GÊNICA
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ABNT
ROSA, Fabio Luiz Fernandes et al. Mineralocorticoid receptor mutations differentially affect individual gene expression profiles in pseudohypoaldosteronism type 1. Journal of Clinical Endocrinology and Metabolism, v. 96, n. 3, p. E519-E527, 2011Tradução . . Acesso em: 01 out. 2024.
APA
Rosa, F. L. F., Hubert, E. L., Fagart, J., Tchitchek, N., Gomes, D., Jouanno, E., et al. (2011). Mineralocorticoid receptor mutations differentially affect individual gene expression profiles in pseudohypoaldosteronism type 1. Journal of Clinical Endocrinology and Metabolism, 96( 3), E519-E527.
NLM
Rosa FLF, Hubert EL, Fagart J, Tchitchek N, Gomes D, Jouanno E, Benecke A, Oblin M-ER, jeunemaitre X, Antonini SRR, Zennaro MC. Mineralocorticoid receptor mutations differentially affect individual gene expression profiles in pseudohypoaldosteronism type 1. Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 3): E519-E527.[citado 2024 out. 01 ]
Vancouver
Rosa FLF, Hubert EL, Fagart J, Tchitchek N, Gomes D, Jouanno E, Benecke A, Oblin M-ER, jeunemaitre X, Antonini SRR, Zennaro MC. Mineralocorticoid receptor mutations differentially affect individual gene expression profiles in pseudohypoaldosteronism type 1. Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 3): E519-E527.[citado 2024 out. 01 ]
Artigo de periodico
Wnt/β-catenin pathway deregulation in childhood adrenocortical tumors (2011)
Leal, Letícia Ferro; Mermejo, Lívia Mara; Ramalho, Leandra Naíra Zambelli; Martinelli Junior, Carlos Eduardo; Yunes, Jose Andres; Seidinger, Ana Luiza; Mastellaro, Maria José; Cardinalli, Izilda Aparecida; Brandalise, Silvia Regina; Moreira, Ayrton Custódio; Tone, Luiz Gonzaga; Scrideli, Carlos Alberto; Castro, Margaret de; Antonini, Sonir Roberto Rauber
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: FMRP
Assuntos: CRIANÇAS, NEOPLASIAS DO CÓRTEX SUPRARRENAL, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEAL, Letícia Ferro et al. Wnt/β-catenin pathway deregulation in childhood adrenocortical tumors. Journal of Clinical Endocrinology and Metabolism, v. 96, n. 10, p. 3106-3114, 2011Tradução . . Acesso em: 01 out. 2024.
APA
Leal, L. F., Mermejo, L. M., Ramalho, L. N. Z., Martinelli Junior, C. E., Yunes, J. A., Seidinger, A. L., et al. (2011). Wnt/β-catenin pathway deregulation in childhood adrenocortical tumors. Journal of Clinical Endocrinology and Metabolism, 96( 10), 3106-3114.
NLM
Leal LF, Mermejo LM, Ramalho LNZ, Martinelli Junior CE, Yunes JA, Seidinger AL, Mastellaro MJ, Cardinalli IA, Brandalise SR, Moreira AC, Tone LG, Scrideli CA, Castro M de, Antonini SRR. Wnt/β-catenin pathway deregulation in childhood adrenocortical tumors. Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 10): 3106-3114.[citado 2024 out. 01 ]
Vancouver
Leal LF, Mermejo LM, Ramalho LNZ, Martinelli Junior CE, Yunes JA, Seidinger AL, Mastellaro MJ, Cardinalli IA, Brandalise SR, Moreira AC, Tone LG, Scrideli CA, Castro M de, Antonini SRR. Wnt/β-catenin pathway deregulation in childhood adrenocortical tumors. Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 10): 3106-3114.[citado 2024 out. 01 ]
Artigo de periodico
Wnt/β-catenin pathway deregulation in childhood adrenocortical tumors (2011)
Leal, Letícia F.; Mermejo, Lívia M.; Ramalho, Leandra Naíra Zambelli; Martinelli Junior, Carlos Eduardo; Yunes, José A.; Seidinger, Ana Luiza; Mastellaro, Maria José; Cardinalli, Izilda A.; Brandalise, Silvia R.; Moreira, Ayrton Custódio; Tone, Luiz Gonzaga; Scrideli, Carlos Alberto; Castro, Margaret de; Antonini, Sonir Roberto Rauber
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: FMRP
Assuntos: NEOPLASIAS DO CÓRTEX SUPRARRENAL, CRIANÇAS, MUTAÇÃO GENÉTICA, ESTUDOS DE COORTES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEAL, Letícia F. et al. Wnt/β-catenin pathway deregulation in childhood adrenocortical tumors. Journal of Clinical Endocrinology and Metabolism, v. 96, n. 10, p. 3106-3114, 2011Tradução . . Disponível em: https://doi.org/10.1210/jc.2011-0363. Acesso em: 01 out. 2024.
APA
Leal, L. F., Mermejo, L. M., Ramalho, L. N. Z., Martinelli Junior, C. E., Yunes, J. A., Seidinger, A. L., et al. (2011). Wnt/β-catenin pathway deregulation in childhood adrenocortical tumors. Journal of Clinical Endocrinology and Metabolism, 96( 10), 3106-3114. doi:10.1210/jc.2011-0363
NLM
Leal LF, Mermejo LM, Ramalho LNZ, Martinelli Junior CE, Yunes JA, Seidinger AL, Mastellaro MJ, Cardinalli IA, Brandalise SR, Moreira AC, Tone LG, Scrideli CA, Castro M de, Antonini SRR. Wnt/β-catenin pathway deregulation in childhood adrenocortical tumors [Internet]. Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 10): 3106-3114.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2011-0363
Vancouver
Leal LF, Mermejo LM, Ramalho LNZ, Martinelli Junior CE, Yunes JA, Seidinger AL, Mastellaro MJ, Cardinalli IA, Brandalise SR, Moreira AC, Tone LG, Scrideli CA, Castro M de, Antonini SRR. Wnt/β-catenin pathway deregulation in childhood adrenocortical tumors [Internet]. Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 10): 3106-3114.[citado 2024 out. 01 ] Available from: https://doi.org/10.1210/jc.2011-0363

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