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Artigo de periodico
Rs4862705 in the melatonin receptor 1A gene is associated with renal function decline in type 1 diabetes individuals (2024)
Daher, Gustavo; Bezerra, Daniele Pereira Santos ; Cavaleiro, Ana Mercedes de Sousa ; Pelaes, Tatiana Souza ; Admoni, Sharon Nina ; Perez, Ricardo Vessoni ; Machado, Cleide Guimarães ; Amaral, Fernanda Gaspar do ; Giannella, Maria Lucia Cardillo Correa ; Cipolla Neto, José
Source: Frontiers in Endocrinology. Unidades: ICB, FM
Subjects: FISIOLOGIA, MELATONINA, ANTIOXIDANTES, DIABETES MELLITUS, POLIMORFISMO, ESTRESSE OXIDATIVO, ESTUDOS TRANSVERSAIS, ESTUDOS LONGITUDINAIS, NEFROPATIAS
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ABNT
DAHER, Gustavo et al. Rs4862705 in the melatonin receptor 1A gene is associated with renal function decline in type 1 diabetes individuals. Frontiers in Endocrinology, 2024Tradução . . Disponível em: https://doi.org/10.3389/fendo.2024.1331012. Acesso em: 15 abr. 2026.
APA
Daher, G., Bezerra, D. P. S., Cavaleiro, A. M. de S., Pelaes, T. S., Admoni, S. N., Perez, R. V., et al. (2024). Rs4862705 in the melatonin receptor 1A gene is associated with renal function decline in type 1 diabetes individuals. Frontiers in Endocrinology. doi:10.3389/fendo.2024.1331012
NLM
Daher G, Bezerra DPS, Cavaleiro AM de S, Pelaes TS, Admoni SN, Perez RV, Machado CG, Amaral FG do, Giannella MLCC, Cipolla Neto J. Rs4862705 in the melatonin receptor 1A gene is associated with renal function decline in type 1 diabetes individuals [Internet]. Frontiers in Endocrinology. 2024 ;[citado 2026 abr. 15 ] Available from: https://doi.org/10.3389/fendo.2024.1331012
Vancouver
Daher G, Bezerra DPS, Cavaleiro AM de S, Pelaes TS, Admoni SN, Perez RV, Machado CG, Amaral FG do, Giannella MLCC, Cipolla Neto J. Rs4862705 in the melatonin receptor 1A gene is associated with renal function decline in type 1 diabetes individuals [Internet]. Frontiers in Endocrinology. 2024 ;[citado 2026 abr. 15 ] Available from: https://doi.org/10.3389/fendo.2024.1331012
Artigo de periodico
Variant rs17619600 in the gene encoding serotonin receptor 2B (HTR2B) increases the risk of gestational diabetes mellitus: a case-control study (2023)
Penno, Juliana Regina Chamlian Zucare; Bezerra, Daniele Pereira Santos ; Cavaleiro, Ana Mercedes de Sousa; Oliveira, Ana Maria da Silva Sousa; Zaccara, Tatiana Assunção ; Costa, Rafaela Alkmin da ; Francisco, Rossana Pulcineli Vieira ; Giannella, Maria Lucia Cardillo Correa
Source: European journal of medical research. Unidade: FM
Subjects: POLIMORFISMO, DIABETES MELLITUS, COMPLICAÇÕES NA GRAVIDEZ, FATORES DE RISCO
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ABNT
PENNO, Juliana Regina Chamlian Zucare et al. Variant rs17619600 in the gene encoding serotonin receptor 2B (HTR2B) increases the risk of gestational diabetes mellitus: a case-control study. European journal of medical research, v. 28, n. 1, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/54739. Acesso em: 15 abr. 2026.
APA
Penno, J. R. C. Z., Bezerra, D. P. S., Cavaleiro, A. M. de S., Oliveira, A. M. da S. S., Zaccara, T. A., Costa, R. A. da, et al. (2023). Variant rs17619600 in the gene encoding serotonin receptor 2B (HTR2B) increases the risk of gestational diabetes mellitus: a case-control study. European journal of medical research, 28( 1). doi:10.1186/s40001-023-01211-6
NLM
Penno JRCZ, Bezerra DPS, Cavaleiro AM de S, Oliveira AM da SS, Zaccara TA, Costa RA da, Francisco RPV, Giannella MLCC. Variant rs17619600 in the gene encoding serotonin receptor 2B (HTR2B) increases the risk of gestational diabetes mellitus: a case-control study [Internet]. European journal of medical research. 2023 ; 28( 1):[citado 2026 abr. 15 ] Available from: https://observatorio.fm.usp.br/handle/OPI/54739
Vancouver
Penno JRCZ, Bezerra DPS, Cavaleiro AM de S, Oliveira AM da SS, Zaccara TA, Costa RA da, Francisco RPV, Giannella MLCC. Variant rs17619600 in the gene encoding serotonin receptor 2B (HTR2B) increases the risk of gestational diabetes mellitus: a case-control study [Internet]. European journal of medical research. 2023 ; 28( 1):[citado 2026 abr. 15 ] Available from: https://observatorio.fm.usp.br/handle/OPI/54739
Artigo de periodico
Alcohol use disorder is associated with upregulation of MicroRNA‐34a and MicroRNA‐34c in Hippocampal postmortem tissue (2021)
Bezerra, Daniele Perreira Santos ; Cavaleiro, Ana Mercedes de Sousa ; Santos, Aritania Sousa ; Suemoto, Claudia Kimie ; Pasqualucci, Carlos Augusto ; Jacob Filho, Wilson ; Leite, Renata Elaine Paraizo ; Passarelli, Marisa ; Marie, Suely Kazue Nagahashi ; Machado, Ubiratan Fabres ; Giannella, Maria Lucia Cardillo Correa
Source: Alcoholism: Clinical and Experimental Research. Unidades: FM, ICB
Subjects: FISIOLOGIA, EPIGÊNESE GENÉTICA, ETANOL, HIPOCAMPO, MICRORNAS, EXPRESSÃO GÊNICA, ÁLCOOL, DOENÇA DE ALZHEIMER
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ABNT
BEZERRA, Daniele Perreira Santos et al. Alcohol use disorder is associated with upregulation of MicroRNA‐34a and MicroRNA‐34c in Hippocampal postmortem tissue. Alcoholism: Clinical and Experimental Research, v. 45, n. 1, p. 64-68, 2021Tradução . . Disponível em: https://doi.org/10.1111/acer.14505. Acesso em: 15 abr. 2026.
APA
Bezerra, D. P. S., Cavaleiro, A. M. de S., Santos, A. S., Suemoto, C. K., Pasqualucci, C. A., Jacob Filho, W., et al. (2021). Alcohol use disorder is associated with upregulation of MicroRNA‐34a and MicroRNA‐34c in Hippocampal postmortem tissue. Alcoholism: Clinical and Experimental Research, 45( 1), 64-68. doi:10.1111/acer.14505
NLM
Bezerra DPS, Cavaleiro AM de S, Santos AS, Suemoto CK, Pasqualucci CA, Jacob Filho W, Leite REP, Passarelli M, Marie SKN, Machado UF, Giannella MLCC. Alcohol use disorder is associated with upregulation of MicroRNA‐34a and MicroRNA‐34c in Hippocampal postmortem tissue [Internet]. Alcoholism: Clinical and Experimental Research. 2021 ; 45( 1): 64-68.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1111/acer.14505
Vancouver
Bezerra DPS, Cavaleiro AM de S, Santos AS, Suemoto CK, Pasqualucci CA, Jacob Filho W, Leite REP, Passarelli M, Marie SKN, Machado UF, Giannella MLCC. Alcohol use disorder is associated with upregulation of MicroRNA‐34a and MicroRNA‐34c in Hippocampal postmortem tissue [Internet]. Alcoholism: Clinical and Experimental Research. 2021 ; 45( 1): 64-68.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1111/acer.14505
Artigo de periodico
Leukotriene pathway activation associates with poor glycemic control and with cardiovascular autonomic neuropathy in type 1 diabetes (2020)
Bezerra, Daniele Perreira dos Santos ; Ribeiro Junior, Luciano Filgueiras; Monteiro, Maria Beatriz ; Admoni, Sharon Nina ; Perez, Ricardo Vessoni ; Cavaleiro, Ana Mercedes de Sousa; Machado, Cleide Guimarães; Machado, Ubiratan Fabres ; Passarelli, Marisa ; Jancar, Sonia ; Giannella, Maria Lucia Correa
Source: Mediators of Inflammation. Unidades: FM, ICB
Subjects: FISIOLOGIA, IMUNOLOGIA, GLICEMIA, LEUCOTRIENOS, SISTEMA NERVOSO AUTÔNOMO, NEUROPATIAS DIABÉTICAS, DIABETES MELLITUS, EXPRESSÃO GÊNICA, NEFROPATIAS, INFLAMAÇÃO
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ABNT
BEZERRA, Daniele Perreira dos Santos et al. Leukotriene pathway activation associates with poor glycemic control and with cardiovascular autonomic neuropathy in type 1 diabetes. Mediators of Inflammation, p. 9 , 2020Tradução . . Disponível em: https://doi.org/10.1155/2020/5704713. Acesso em: 15 abr. 2026.
APA
Bezerra, D. P. dos S., Ribeiro Junior, L. F., Monteiro, M. B., Admoni, S. N., Perez, R. V., Cavaleiro, A. M. de S., et al. (2020). Leukotriene pathway activation associates with poor glycemic control and with cardiovascular autonomic neuropathy in type 1 diabetes. Mediators of Inflammation, 9 . doi:10.1155/2020/5704713
NLM
Bezerra DP dos S, Ribeiro Junior LF, Monteiro MB, Admoni SN, Perez RV, Cavaleiro AM de S, Machado CG, Machado UF, Passarelli M, Jancar S, Giannella MLC. Leukotriene pathway activation associates with poor glycemic control and with cardiovascular autonomic neuropathy in type 1 diabetes [Internet]. Mediators of Inflammation. 2020 ; 9 .[citado 2026 abr. 15 ] Available from: https://doi.org/10.1155/2020/5704713
Vancouver
Bezerra DP dos S, Ribeiro Junior LF, Monteiro MB, Admoni SN, Perez RV, Cavaleiro AM de S, Machado CG, Machado UF, Passarelli M, Jancar S, Giannella MLC. Leukotriene pathway activation associates with poor glycemic control and with cardiovascular autonomic neuropathy in type 1 diabetes [Internet]. Mediators of Inflammation. 2020 ; 9 .[citado 2026 abr. 15 ] Available from: https://doi.org/10.1155/2020/5704713
Artigo de periodico
Allelic variations in genes belonging to glutathione system increase proliferative retinopathy risk in type 1 diabetes individuals (2019)
Perez, Ricardo Vessoni; Machado, Cleide Guimaraes; Santos-bezerra, Daniele Pereira; Admoni, Sharon Nina; Patente, Thiago Andrade; Monteiro, Maria Beatriz; Cavaleiro, Ana Mercedes de Sousa; Queiroz, Marcia Silva; Nery, Marcia; Giannella, Maria Lúcia Cardillo Côrrea
Source: Gene. Unidade: FM
Subjects: DIABETES MELLITUS INSULINO-DEPENDENTE, DOENÇAS RETINIANAS, ESTRESSE OXIDATIVO, ESTUDOS TRANSVERSAIS, OLIGOPEPTÍDEOS
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ABNT
PEREZ, Ricardo Vessoni et al. Allelic variations in genes belonging to glutathione system increase proliferative retinopathy risk in type 1 diabetes individuals. Gene, v. 703, p. 120-124, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.gene.2019.04.015. Acesso em: 15 abr. 2026.
APA
Perez, R. V., Machado, C. G., Santos-bezerra, D. P., Admoni, S. N., Patente, T. A., Monteiro, M. B., et al. (2019). Allelic variations in genes belonging to glutathione system increase proliferative retinopathy risk in type 1 diabetes individuals. Gene, 703, 120-124. doi:10.1016/j.gene.2019.04.015
NLM
Perez RV, Machado CG, Santos-bezerra DP, Admoni SN, Patente TA, Monteiro MB, Cavaleiro AM de S, Queiroz MS, Nery M, Giannella MLCC. Allelic variations in genes belonging to glutathione system increase proliferative retinopathy risk in type 1 diabetes individuals [Internet]. Gene. 2019 ; 703 120-124.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1016/j.gene.2019.04.015
Vancouver
Perez RV, Machado CG, Santos-bezerra DP, Admoni SN, Patente TA, Monteiro MB, Cavaleiro AM de S, Queiroz MS, Nery M, Giannella MLCC. Allelic variations in genes belonging to glutathione system increase proliferative retinopathy risk in type 1 diabetes individuals [Internet]. Gene. 2019 ; 703 120-124.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1016/j.gene.2019.04.015
Artigo de periodico-carta/editorial
Glutathione peroxidase 4 functional variant rs713041 modulates the risk for cardiovascular autonomic neuropathy in individuals with type 1 diabetes [Carta] (2019)
Admoni, Sharon Nina; Santos-Bezerra, Daniele Pereira ; Perez, Ricardo Vessoni ; Patente, Thiago Andrade ; Monteiro, Maria Beatriz; Cavaleiro, Ana Mercedes; Parisi, Maria Candida; Moura Neto, Arnaldo; Pavin, Elizabeth João ; Giannella, Maria Lúcia Cardillo Côrrea
Source: Diabetes & vascular disease research. Unidade: FM
Subjects: PEROXIDASE, CÓDIGO GENÉTICO, DIABETES MELLITUS NÃO INSULINO-DEPENDENTE, NEUROPATIAS DIABÉTICAS, DOENÇAS CARDIOVASCULARES, ESTRESSE OXIDATIVO
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ABNT
ADMONI, Sharon Nina et al. Glutathione peroxidase 4 functional variant rs713041 modulates the risk for cardiovascular autonomic neuropathy in individuals with type 1 diabetes [Carta]. Diabetes & vascular disease research. London: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1177/1479164118820641. Acesso em: 15 abr. 2026. , 2019
APA
Admoni, S. N., Santos-Bezerra, D. P., Perez, R. V., Patente, T. A., Monteiro, M. B., Cavaleiro, A. M., et al. (2019). Glutathione peroxidase 4 functional variant rs713041 modulates the risk for cardiovascular autonomic neuropathy in individuals with type 1 diabetes [Carta]. Diabetes & vascular disease research. London: Faculdade de Medicina, Universidade de São Paulo. doi:10.1177/1479164118820641
NLM
Admoni SN, Santos-Bezerra DP, Perez RV, Patente TA, Monteiro MB, Cavaleiro AM, Parisi MC, Moura Neto A, Pavin EJ, Giannella MLCC. Glutathione peroxidase 4 functional variant rs713041 modulates the risk for cardiovascular autonomic neuropathy in individuals with type 1 diabetes [Carta] [Internet]. Diabetes & vascular disease research. 2019 ; 16( 3): 297-299.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1177/1479164118820641
Vancouver
Admoni SN, Santos-Bezerra DP, Perez RV, Patente TA, Monteiro MB, Cavaleiro AM, Parisi MC, Moura Neto A, Pavin EJ, Giannella MLCC. Glutathione peroxidase 4 functional variant rs713041 modulates the risk for cardiovascular autonomic neuropathy in individuals with type 1 diabetes [Carta] [Internet]. Diabetes & vascular disease research. 2019 ; 16( 3): 297-299.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1177/1479164118820641
Artigo de periodico
Association between the CYBA and NOX4 genes of NADPH oxidase and its relationship with metabolic syndrome in non-alcoholic fatty liver disease in Brazilian population (2018)
Rabelo, Fabiola; Cavaleiro, Ana Mercedes; Carrilho, Flair Jose; Correa-giannella, Maria Lucia; Oliveira, Claudia P.
Source: Hepatobiliary & pancreatic diseases international. Unidade: FM
Subjects: HEPATOPATIAS, SÍNDROME X METABÓLICA, POLIMORFISMO, ESTRESSE OXIDATIVO
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ABNT
RABELO, Fabiola et al. Association between the CYBA and NOX4 genes of NADPH oxidase and its relationship with metabolic syndrome in non-alcoholic fatty liver disease in Brazilian population. Hepatobiliary & pancreatic diseases international, v. 17, n. 4, p. 330-335, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.hbpd.2018.06.005. Acesso em: 15 abr. 2026.
APA
Rabelo, F., Cavaleiro, A. M., Carrilho, F. J., Correa-giannella, M. L., & Oliveira, C. P. (2018). Association between the CYBA and NOX4 genes of NADPH oxidase and its relationship with metabolic syndrome in non-alcoholic fatty liver disease in Brazilian population. Hepatobiliary & pancreatic diseases international, 17( 4), 330-335. doi:10.1016/j.hbpd.2018.06.005
NLM
Rabelo F, Cavaleiro AM, Carrilho FJ, Correa-giannella ML, Oliveira CP. Association between the CYBA and NOX4 genes of NADPH oxidase and its relationship with metabolic syndrome in non-alcoholic fatty liver disease in Brazilian population [Internet]. Hepatobiliary & pancreatic diseases international. 2018 ; 17( 4): 330-335.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1016/j.hbpd.2018.06.005
Vancouver
Rabelo F, Cavaleiro AM, Carrilho FJ, Correa-giannella ML, Oliveira CP. Association between the CYBA and NOX4 genes of NADPH oxidase and its relationship with metabolic syndrome in non-alcoholic fatty liver disease in Brazilian population [Internet]. Hepatobiliary & pancreatic diseases international. 2018 ; 17( 4): 330-335.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1016/j.hbpd.2018.06.005
Artigo de periodico
Dietary advanced glycated end-products and medicines influence the expression of SIRT1 and DDOST in peripheral mononuclear cells from long-term type 1 diabetes patients (2018)
Bezerra, Daniele Pereira dos Santos; Lima, Adriana Machado Saldiba de; Caillaud, Maria Beatriz Camargo Monteiro; Adnomi, Sharon Nina; Perez, Ricardo Vessoni; Machado, Cleide Guimarães; Shimizu, Maria Heloisa Massalo; Cavaleiro, Ana Mercedes de Sousa; Thieme, Karina ; Queiroz, Márcia Silva; Machado, Ubiratan Fabres ; Gianella Neto, Daniel; Passarelli, Marisa; Giannella, Maria Lúcia Cardillo Corrêa
Source: Diabetes & vascular disease research. Unidades: FM, ICB
Subjects: DIABETES MELLITUS INSULINO-DEPENDENTE, DOENÇAS VASCULARES, ESTRESSE OXIDATIVO, ESTATINAS, INIBIDORES DE ENZIMAS, ATIVAÇÃO ENZIMÁTICA, REAÇÃO EM CADEIA POR POLIMERASE, EXPRESSÃO GÊNICA, ANGIOTENSINAS
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ABNT
BEZERRA, Daniele Pereira dos Santos et al. Dietary advanced glycated end-products and medicines influence the expression of SIRT1 and DDOST in peripheral mononuclear cells from long-term type 1 diabetes patients. Diabetes & vascular disease research, v. 15, n. 1, p. 81-89, 2018Tradução . . Disponível em: https://doi.org/10.1177/1479164117733918. Acesso em: 15 abr. 2026.
APA
Bezerra, D. P. dos S., Lima, A. M. S. de, Caillaud, M. B. C. M., Adnomi, S. N., Perez, R. V., Machado, C. G., et al. (2018). Dietary advanced glycated end-products and medicines influence the expression of SIRT1 and DDOST in peripheral mononuclear cells from long-term type 1 diabetes patients. Diabetes & vascular disease research, 15( 1), 81-89. doi:10.1177/1479164117733918
NLM
Bezerra DP dos S, Lima AMS de, Caillaud MBCM, Adnomi SN, Perez RV, Machado CG, Shimizu MHM, Cavaleiro AM de S, Thieme K, Queiroz MS, Machado UF, Gianella Neto D, Passarelli M, Giannella MLCC. Dietary advanced glycated end-products and medicines influence the expression of SIRT1 and DDOST in peripheral mononuclear cells from long-term type 1 diabetes patients [Internet]. Diabetes & vascular disease research. 2018 ; 15( 1): 81-89.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1177/1479164117733918
Vancouver
Bezerra DP dos S, Lima AMS de, Caillaud MBCM, Adnomi SN, Perez RV, Machado CG, Shimizu MHM, Cavaleiro AM de S, Thieme K, Queiroz MS, Machado UF, Gianella Neto D, Passarelli M, Giannella MLCC. Dietary advanced glycated end-products and medicines influence the expression of SIRT1 and DDOST in peripheral mononuclear cells from long-term type 1 diabetes patients [Internet]. Diabetes & vascular disease research. 2018 ; 15( 1): 81-89.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1177/1479164117733918
Trabalho de evento-resumo periodico
Influence of UCP3 gene polymorphisms on metabolic syndrome and cardiovascular risk in patients with in non-alcoholic fatty liver disease (2017)
Toda, K. S.; Stefano, J. T.; Costa, F. B.; Cavaleiro, A. M.; Mazo, D. F.; Carrilho, F. J.; Correa-Giannella, M. L.; Oliveira, C. P.
Source: Journal of hepatology. Conference titles: Annual meeting of the European Association for the Study of the Liver. Unidade: FM
Subjects: FÍGADO GORDUROSO, POLIMORFISMO, SÍNDROME X METABÓLICA
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ABNT
TODA, K. S. et al. Influence of UCP3 gene polymorphisms on metabolic syndrome and cardiovascular risk in patients with in non-alcoholic fatty liver disease. Journal of hepatology. Amsterdam: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/S0168-8278(17)30612-8. Acesso em: 15 abr. 2026. , 2017
APA
Toda, K. S., Stefano, J. T., Costa, F. B., Cavaleiro, A. M., Mazo, D. F., Carrilho, F. J., et al. (2017). Influence of UCP3 gene polymorphisms on metabolic syndrome and cardiovascular risk in patients with in non-alcoholic fatty liver disease. Journal of hepatology. Amsterdam: Faculdade de Medicina, Universidade de São Paulo. doi:10.1016/S0168-8278(17)30612-8
NLM
Toda KS, Stefano JT, Costa FB, Cavaleiro AM, Mazo DF, Carrilho FJ, Correa-Giannella ML, Oliveira CP. Influence of UCP3 gene polymorphisms on metabolic syndrome and cardiovascular risk in patients with in non-alcoholic fatty liver disease [Internet]. Journal of hepatology. 2017 ; 66 S167.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1016/S0168-8278(17)30612-8
Vancouver
Toda KS, Stefano JT, Costa FB, Cavaleiro AM, Mazo DF, Carrilho FJ, Correa-Giannella ML, Oliveira CP. Influence of UCP3 gene polymorphisms on metabolic syndrome and cardiovascular risk in patients with in non-alcoholic fatty liver disease [Internet]. Journal of hepatology. 2017 ; 66 S167.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1016/S0168-8278(17)30612-8
Artigo de periodico
Hormetic modulation of hepatic insulin sensitivity by advanced glycation end products (2017)
Fabre, Nelly Takashima; Thieme, Karina ; Silva, Karolline Santana da; Catanozi, Sergio ; Cavaleiro, Ana Mercedes de Sousa ; Pinto Júnior, Danilo Antônio Correa; Okamoto, Maristela Mitiko ; Morais, Mychel Raony Paiva Teixeira ; Falquetto, Bárbara ; Zorn, Telma Maria Tenório; Machado, Ubiratan Fabres ; Passarelli, Marisa ; Corrêa-Giannella, Maria Lucia Cardillo
Source: Molecular and Cellular Endocrinology. Unidades: FM, ICB
Subjects: FÍGADO, DOENÇA CRÔNICA, INSULINA (RESISTÊNCIA), RATOS
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ABNT
FABRE, Nelly Takashima et al. Hormetic modulation of hepatic insulin sensitivity by advanced glycation end products. Molecular and Cellular Endocrinology, v. 447, p. 116-124, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2017.02.035. Acesso em: 15 abr. 2026.
APA
Fabre, N. T., Thieme, K., Silva, K. S. da, Catanozi, S., Cavaleiro, A. M. de S., Pinto Júnior, D. A. C., et al. (2017). Hormetic modulation of hepatic insulin sensitivity by advanced glycation end products. Molecular and Cellular Endocrinology, 447, 116-124. doi:10.1016/j.mce.2017.02.035
NLM
Fabre NT, Thieme K, Silva KS da, Catanozi S, Cavaleiro AM de S, Pinto Júnior DAC, Okamoto MM, Morais MRPT, Falquetto B, Zorn TMT, Machado UF, Passarelli M, Corrêa-Giannella MLC. Hormetic modulation of hepatic insulin sensitivity by advanced glycation end products [Internet]. Molecular and Cellular Endocrinology. 2017 ; 447 116-124.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1016/j.mce.2017.02.035
Vancouver
Fabre NT, Thieme K, Silva KS da, Catanozi S, Cavaleiro AM de S, Pinto Júnior DAC, Okamoto MM, Morais MRPT, Falquetto B, Zorn TMT, Machado UF, Passarelli M, Corrêa-Giannella MLC. Hormetic modulation of hepatic insulin sensitivity by advanced glycation end products [Internet]. Molecular and Cellular Endocrinology. 2017 ; 447 116-124.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1016/j.mce.2017.02.035
Artigo de periodico
Association of single nucleotide polymorphisms in the gene encoding GLUT1 and diabetic nephropathy in Brazilian patients with type 1 diabetes mellitus (2015)
Marques, T.; Patente, T. A.; Monteiro, M. B.; Cavaleiro, A. M.; Queiroz, M. S.; Nery, M.; Azevedo, M.J. de; Canani, L. H.; Parisi, M. C.; Moura-Neto, A.; Passarelli, M.; Gianella-Neto, D.; Machado, Ubiratan Fabres ; Corrêa-Giannella, M. L.
Source: Clinica Chimica Acta. Unidades: ICB, FM
Subjects: NEFROPATIAS, POLIMORFISMO, DIABETES MELLITUS (COMPLICAÇÕES)
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ABNT
MARQUES, T. et al. Association of single nucleotide polymorphisms in the gene encoding GLUT1 and diabetic nephropathy in Brazilian patients with type 1 diabetes mellitus. Clinica Chimica Acta, v. 444, p. 170-175, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.cca.2015.02.025. Acesso em: 15 abr. 2026.
APA
Marques, T., Patente, T. A., Monteiro, M. B., Cavaleiro, A. M., Queiroz, M. S., Nery, M., et al. (2015). Association of single nucleotide polymorphisms in the gene encoding GLUT1 and diabetic nephropathy in Brazilian patients with type 1 diabetes mellitus. Clinica Chimica Acta, 444, 170-175. doi:10.1016/j.cca.2015.02.025
NLM
Marques T, Patente TA, Monteiro MB, Cavaleiro AM, Queiroz MS, Nery M, Azevedo MJ de, Canani LH, Parisi MC, Moura-Neto A, Passarelli M, Gianella-Neto D, Machado UF, Corrêa-Giannella ML. Association of single nucleotide polymorphisms in the gene encoding GLUT1 and diabetic nephropathy in Brazilian patients with type 1 diabetes mellitus [Internet]. Clinica Chimica Acta. 2015 ; 444 170-175.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1016/j.cca.2015.02.025
Vancouver
Marques T, Patente TA, Monteiro MB, Cavaleiro AM, Queiroz MS, Nery M, Azevedo MJ de, Canani LH, Parisi MC, Moura-Neto A, Passarelli M, Gianella-Neto D, Machado UF, Corrêa-Giannella ML. Association of single nucleotide polymorphisms in the gene encoding GLUT1 and diabetic nephropathy in Brazilian patients with type 1 diabetes mellitus [Internet]. Clinica Chimica Acta. 2015 ; 444 170-175.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1016/j.cca.2015.02.025
Artigo de periodico
Association of a variant in the regulatory region of NADPH oxidase 4 gene and metabolic syndrome in patients with chronic hepatitis C (2015)
Siqueira, Erika Rabelo Forte de; Pereira, Luciano Beltrao; Stefano, Jose Tadeu; Patente, Thiago; Cavaleiro, Ana Mercedes; Vasconcelos, Luydson Richardson Silva; Carmo, Rodrigo Feliciano; Pereira, Leila Maria Moreira Beltrao; Carrilho, Flair Jose; Corrêa-Giannella, Maria Lucia; Oliveira, Claudia P.
Source: European Journal of Medical Research. Unidade: FM
Subjects: HEPATIE C, POLIMORFISMO, SÍNDROME X METABÓLICA, HEPATITE CRÔNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SIQUEIRA, Erika Rabelo Forte de et al. Association of a variant in the regulatory region of NADPH oxidase 4 gene and metabolic syndrome in patients with chronic hepatitis C. European Journal of Medical Research, v. 20, n. 45, p. 6 (online), 2015Tradução . . Disponível em: http://www.eurjmedres.com/content/pdf/s40001-015-0136-2.pdf. Acesso em: 15 abr. 2026.
APA
Siqueira, E. R. F. de, Pereira, L. B., Stefano, J. T., Patente, T., Cavaleiro, A. M., Vasconcelos, L. R. S., et al. (2015). Association of a variant in the regulatory region of NADPH oxidase 4 gene and metabolic syndrome in patients with chronic hepatitis C. European Journal of Medical Research, 20( 45), 6 (online). doi:10.1186/s40001-015-0136-2
NLM
Siqueira ERF de, Pereira LB, Stefano JT, Patente T, Cavaleiro AM, Vasconcelos LRS, Carmo RF, Pereira LMMB, Carrilho FJ, Corrêa-Giannella ML, Oliveira CP. Association of a variant in the regulatory region of NADPH oxidase 4 gene and metabolic syndrome in patients with chronic hepatitis C [Internet]. European Journal of Medical Research. 2015 ; 20( 45): 6 (online).[citado 2026 abr. 15 ] Available from: http://www.eurjmedres.com/content/pdf/s40001-015-0136-2.pdf
Vancouver
Siqueira ERF de, Pereira LB, Stefano JT, Patente T, Cavaleiro AM, Vasconcelos LRS, Carmo RF, Pereira LMMB, Carrilho FJ, Corrêa-Giannella ML, Oliveira CP. Association of a variant in the regulatory region of NADPH oxidase 4 gene and metabolic syndrome in patients with chronic hepatitis C [Internet]. European Journal of Medical Research. 2015 ; 20( 45): 6 (online).[citado 2026 abr. 15 ] Available from: http://www.eurjmedres.com/content/pdf/s40001-015-0136-2.pdf
Artigo de periodico
Hyperinsulinism/hyperammonemia (HI/HA) syndrome due to a mutation in the glutamate dehydrogenase gene (2012)
Corrêa-Giannella, Maria Lúcia; Freire, Daniel Soares; Cavaleiro, Ana Mercedes; Fortes, Maria Angela Zanella; Giorgi, Ricardo Rodrigues; Pereira, Maria Adelaide Albergaria
Source: Arquivos brasileiros de endocrinologia e metabologia. Unidade: FM
Subjects: SEQUENCIAMENTO GENÉTICO, PANCREATOPATIAS (ENZIMOLOGIA), DOENÇAS HEREDITÁRIAS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CORRÊA-GIANNELLA, Maria Lúcia et al. Hyperinsulinism/hyperammonemia (HI/HA) syndrome due to a mutation in the glutamate dehydrogenase gene. Arquivos brasileiros de endocrinologia e metabologia, v. 56, n. 8, p. 485-489, 2012Tradução . . Disponível em: https://doi.org/10.1590/S0004-27302012000800004. Acesso em: 15 abr. 2026.
APA
Corrêa-Giannella, M. L., Freire, D. S., Cavaleiro, A. M., Fortes, M. A. Z., Giorgi, R. R., & Pereira, M. A. A. (2012). Hyperinsulinism/hyperammonemia (HI/HA) syndrome due to a mutation in the glutamate dehydrogenase gene. Arquivos brasileiros de endocrinologia e metabologia, 56( 8), 485-489. doi:10.1590/S0004-27302012000800004
NLM
Corrêa-Giannella ML, Freire DS, Cavaleiro AM, Fortes MAZ, Giorgi RR, Pereira MAA. Hyperinsulinism/hyperammonemia (HI/HA) syndrome due to a mutation in the glutamate dehydrogenase gene [Internet]. Arquivos brasileiros de endocrinologia e metabologia. 2012 ; 56( 8): 485-489.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1590/S0004-27302012000800004
Vancouver
Corrêa-Giannella ML, Freire DS, Cavaleiro AM, Fortes MAZ, Giorgi RR, Pereira MAA. Hyperinsulinism/hyperammonemia (HI/HA) syndrome due to a mutation in the glutamate dehydrogenase gene [Internet]. Arquivos brasileiros de endocrinologia e metabologia. 2012 ; 56( 8): 485-489.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1590/S0004-27302012000800004
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)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 15 abr. 2026.
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 2026 abr. 15 ] 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 2026 abr. 15 ] Available from: https://doi.org/10.1007/s11102-009-0194-y
Artigo de periodico
Steatosis in chronic hepatitis C: the role of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphysm and microsomal triglyceride transfer protein (MTP)- 493G/T polymorphism (2011)
Siqueira, Erika Rabelo F.; Oliveira, Claudia P.; Corrêa-Giannella, Maria Lucia; Stefano, Jose Tadeu; Cavaleiro, Ana Mercedes; Fortes, Maria Angela Z.; Muniz, Maria T.; Silva, Felipe S.; Pereira, Leila; Carrilho, Flair J.
Source: Hepatology. Conference titles: Annual Meeting of the American Association for the Study of Liver Diseases. Unidade: FM
Subjects: HEPATITE C (ENZIMOLOGIA), POLIMORFISMO, REAÇÃO EM CADEIA POR POLIMERASE, HEPATITE CRÔNICA, BIOMARCADORES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SIQUEIRA, Erika Rabelo F. et al. Steatosis in chronic hepatitis C: the role of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphysm and microsomal triglyceride transfer protein (MTP)- 493G/T polymorphism. Hepatology, v. 54, n. 4 (Suppl), p. 1329A, 2011Tradução . . Disponível em: https://doi.org/10.1002/hep.v54.1s. Acesso em: 15 abr. 2026.
APA
Siqueira, E. R. F., Oliveira, C. P., Corrêa-Giannella, M. L., Stefano, J. T., Cavaleiro, A. M., Fortes, M. A. Z., et al. (2011). Steatosis in chronic hepatitis C: the role of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphysm and microsomal triglyceride transfer protein (MTP)- 493G/T polymorphism. Hepatology, 54( 4 (Suppl), 1329A. doi:10.1002/hep.v54.1s
NLM
Siqueira ERF, Oliveira CP, Corrêa-Giannella ML, Stefano JT, Cavaleiro AM, Fortes MAZ, Muniz MT, Silva FS, Pereira L, Carrilho FJ. Steatosis in chronic hepatitis C: the role of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphysm and microsomal triglyceride transfer protein (MTP)- 493G/T polymorphism [Internet]. Hepatology. 2011 ; 54( 4 (Suppl): 1329A.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1002/hep.v54.1s
Vancouver
Siqueira ERF, Oliveira CP, Corrêa-Giannella ML, Stefano JT, Cavaleiro AM, Fortes MAZ, Muniz MT, Silva FS, Pereira L, Carrilho FJ. Steatosis in chronic hepatitis C: the role of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphysm and microsomal triglyceride transfer protein (MTP)- 493G/T polymorphism [Internet]. Hepatology. 2011 ; 54( 4 (Suppl): 1329A.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1002/hep.v54.1s
Trabalho de evento-resumo periodico
Na DPH oxidase 4 and P22PHOX (CYBA) gene polymorphisms as risk factors dor arterial hypertension and overt nephrolopathy in type 1 diabetes (2010)
Monteiro, M B; Vieira, S M S; Rocha, T; Cavaleiro, Ana Mercedes de Sousa; Nery, M; Queiroz, M; Dib, S A; Vendramini, M F; Azevedo, M J; Giannella-Neto, D; Canani, L H; Giannella, Maria Lúcia Cardillo Côrrea
Source: Clinics. Conference titles: Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP". Unidade: FM
Subjects: POLIMORFISMO, FATORES DE RISCO, HIPERTENSÃO, NEFROPATIAS, DIABETES MELLITUS, RESUMOS (EVENTOS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MONTEIRO, M B et al. Na DPH oxidase 4 and P22PHOX (CYBA) gene polymorphisms as risk factors dor arterial hypertension and overt nephrolopathy in type 1 diabetes. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 15 abr. 2026. , 2010
APA
Monteiro, M. B., Vieira, S. M. S., Rocha, T., Cavaleiro, A. M. de S., Nery, M., Queiroz, M., et al. (2010). Na DPH oxidase 4 and P22PHOX (CYBA) gene polymorphisms as risk factors dor arterial hypertension and overt nephrolopathy in type 1 diabetes. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
NLM
Monteiro MB, Vieira SMS, Rocha T, Cavaleiro AM de S, Nery M, Queiroz M, Dib SA, Vendramini MF, Azevedo MJ, Giannella-Neto D, Canani LH, Giannella MLCC. Na DPH oxidase 4 and P22PHOX (CYBA) gene polymorphisms as risk factors dor arterial hypertension and overt nephrolopathy in type 1 diabetes. Clinics. 2010 ; 65 S69.[citado 2026 abr. 15 ]
Vancouver
Monteiro MB, Vieira SMS, Rocha T, Cavaleiro AM de S, Nery M, Queiroz M, Dib SA, Vendramini MF, Azevedo MJ, Giannella-Neto D, Canani LH, Giannella MLCC. Na DPH oxidase 4 and P22PHOX (CYBA) gene polymorphisms as risk factors dor arterial hypertension and overt nephrolopathy in type 1 diabetes. Clinics. 2010 ; 65 S69.[citado 2026 abr. 15 ]
Artigo de periodico
A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0 (2010)
Soggia, Ana Priscila; Correa-Giannella, Maria Lúcia; Fortes, Maria Angela Henriques; Luna, Ana Mercedes Cavaleiro; Pereira, Maria Adelaide Albergaria
Source: BMC Medical Genetics. Unidade: FM
Subjects: GLICOGENOSE, MUTAÇÃO GENÉTICA (ENZIMOLOGIA), CRIANÇAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOGGIA, Ana Priscila et al. A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0. BMC Medical Genetics, v. 11, n. 3, p. 1-5, 2010Tradução . . Disponível em: https://doi.org/10.1186/1471-2350-11-3. Acesso em: 15 abr. 2026.
APA
Soggia, A. P., Correa-Giannella, M. L., Fortes, M. A. H., Luna, A. M. C., & Pereira, M. A. A. (2010). A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0. BMC Medical Genetics, 11( 3), 1-5. doi:10.1186/1471-2350-11-3
NLM
Soggia AP, Correa-Giannella ML, Fortes MAH, Luna AMC, Pereira MAA. A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0 [Internet]. BMC Medical Genetics. 2010 ; 11( 3): 1-5.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1186/1471-2350-11-3
Vancouver
Soggia AP, Correa-Giannella ML, Fortes MAH, Luna AMC, Pereira MAA. A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0 [Internet]. BMC Medical Genetics. 2010 ; 11( 3): 1-5.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1186/1471-2350-11-3
Artigo de periodico
Association of polymorphisms of glutamate-cystein ligase and microsomal triglyceride transfer protein genes in non-alcoholic fatty liver disease (2010)
Oliveira, Claudia Pinto Marques Souza de ; Stefano, José Tadeu; Cavaleiro, Ana Mercedes; Fortes, Maria Angela Henriques Zanella; Vieira, Suzana Maria; Lima, Vicência Mara Rodrigues; Santos, Telma Eugenio; Santos, Virginia Nascimento; Salgado, Ana Lucia Farias de Azevedo; Parise, Edson Roberto; Alves, Venâncio Avancini Ferreira; Carrilho, Flair José; Giannella, Maria Lúcia Cardillo Côrrea
Source: Journal of Gastroenterology and Hepatology. Unidade: FM
Subjects: POLIMORFISMO, FÍGADO GORDUROSO (GENÉTICA), ESTRESSE OXIDATIVO, LIPÍDEOS (ANÁLISE), GLUTAMATOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Claudia Pinto Marques Souza de et al. Association of polymorphisms of glutamate-cystein ligase and microsomal triglyceride transfer protein genes in non-alcoholic fatty liver disease. Journal of Gastroenterology and Hepatology, v. 25, n. 2, p. 357-361, 2010Tradução . . Disponível em: https://doi.org/10.1111/j.1440-1746.2009.06001.x. Acesso em: 15 abr. 2026.
APA
Oliveira, C. P. M. S. de, Stefano, J. T., Cavaleiro, A. M., Fortes, M. A. H. Z., Vieira, S. M., Lima, V. M. R., et al. (2010). Association of polymorphisms of glutamate-cystein ligase and microsomal triglyceride transfer protein genes in non-alcoholic fatty liver disease. Journal of Gastroenterology and Hepatology, 25( 2), 357-361. doi:10.1111/j.1440-1746.2009.06001.x
NLM
Oliveira CPMS de, Stefano JT, Cavaleiro AM, Fortes MAHZ, Vieira SM, Lima VMR, Santos TE, Santos VN, Salgado ALF de A, Parise ER, Alves VAF, Carrilho FJ, Giannella MLCC. Association of polymorphisms of glutamate-cystein ligase and microsomal triglyceride transfer protein genes in non-alcoholic fatty liver disease [Internet]. Journal of Gastroenterology and Hepatology. 2010 ; 25( 2): 357-361.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1111/j.1440-1746.2009.06001.x
Vancouver
Oliveira CPMS de, Stefano JT, Cavaleiro AM, Fortes MAHZ, Vieira SM, Lima VMR, Santos TE, Santos VN, Salgado ALF de A, Parise ER, Alves VAF, Carrilho FJ, Giannella MLCC. Association of polymorphisms of glutamate-cystein ligase and microsomal triglyceride transfer protein genes in non-alcoholic fatty liver disease [Internet]. Journal of Gastroenterology and Hepatology. 2010 ; 25( 2): 357-361.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1111/j.1440-1746.2009.06001.x
Artigo de periodico
Hepatocyte growth factor-regulated tyrosine kinase substrate (HGS) and guanylate kinase 1 (GUK1) are differentially expressed in GH-secreting adenomas (2006)
Rocha, Anderson Alves da; Giorgi, Ricardo Rodrigues; Sá, Sandra Valeria de; Cavaleiro, Ana Mercedes; Correa-Giannella, Maria Lucia; Fortes, Maria Angela Henriques Zanella; Cavaleiro, Ana Mercedes; Machado, Marcio Carlos; Cescato, Valter Angelo; Bronstein, Marcello Delano; Giannella Neto, Daniel
Source: Pituitary. Unidade: FM
Subjects: ADENOMA (SECREÇÃO), FÍGADO (FISIOPATOLOGIA), HEPATOPATIAS (ENZIMOLOGIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ROCHA, Anderson Alves da et al. Hepatocyte growth factor-regulated tyrosine kinase substrate (HGS) and guanylate kinase 1 (GUK1) are differentially expressed in GH-secreting adenomas. Pituitary, v. 9, p. 83-92, 2006Tradução . . Disponível em: https://doi.org/10.1007/s11102-006-9277-1. Acesso em: 15 abr. 2026.
APA
Rocha, A. A. da, Giorgi, R. R., Sá, S. V. de, Cavaleiro, A. M., Correa-Giannella, M. L., Fortes, M. A. H. Z., et al. (2006). Hepatocyte growth factor-regulated tyrosine kinase substrate (HGS) and guanylate kinase 1 (GUK1) are differentially expressed in GH-secreting adenomas. Pituitary, 9, 83-92. doi:10.1007/s11102-006-9277-1
NLM
Rocha AA da, Giorgi RR, Sá SV de, Cavaleiro AM, Correa-Giannella ML, Fortes MAHZ, Cavaleiro AM, Machado MC, Cescato VA, Bronstein MD, Giannella Neto D. Hepatocyte growth factor-regulated tyrosine kinase substrate (HGS) and guanylate kinase 1 (GUK1) are differentially expressed in GH-secreting adenomas [Internet]. Pituitary. 2006 ; 9 83-92.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1007/s11102-006-9277-1
Vancouver
Rocha AA da, Giorgi RR, Sá SV de, Cavaleiro AM, Correa-Giannella ML, Fortes MAHZ, Cavaleiro AM, Machado MC, Cescato VA, Bronstein MD, Giannella Neto D. Hepatocyte growth factor-regulated tyrosine kinase substrate (HGS) and guanylate kinase 1 (GUK1) are differentially expressed in GH-secreting adenomas [Internet]. Pituitary. 2006 ; 9 83-92.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1007/s11102-006-9277-1

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