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Parkinson disease: α-synuclein mutational screening and new clinical insight into the p.E46K mutation.
Pimentel MM, Rodrigues FC, Leite MA, Campos Júnior M, Rosso AL, Nicaretta DH, Pereira JS, Silva DJ, Della Coletta MV, Vasconcellos LF, Abreu GM, Dos Santos JM, Santos-Rebouças CB. Pimentel MM, et al. Among authors: abreu gm. Parkinsonism Relat Disord. 2015 Jun;21(6):586-9. doi: 10.1016/j.parkreldis.2015.03.011. Epub 2015 Mar 14. Parkinsonism Relat Disord. 2015. PMID: 25817515
The association of the fat mass and obesity-associated gene (FTO) rs9939609 polymorphism and the severe obesity in a Brazilian population.
da Fonseca ACP, Abreu GM, Zembrzuski VM, Campos Junior M, Carneiro JRI, Nogueira Neto JF, Cabello GMK, Cabello PH. da Fonseca ACP, et al. Among authors: abreu gm. Diabetes Metab Syndr Obes. 2019 May 23;12:667-684. doi: 10.2147/DMSO.S199542. eCollection 2019. Diabetes Metab Syndr Obes. 2019. PMID: 31213864 Free PMC article.
SH2B1 variants as potential causes of non-syndromic monogenic obesity in a Brazilian cohort.
da Fonseca ACP, Assis ISS, Salum KCR, Palhinha L, Abreu GM, Zembrzuski VM, Campos Junior M, Nogueira Neto JF, Mattos FCC, Cambraia A, Rosado EL, Maya-Monteiro CM, Cabello PH, Carneiro JRI, Bozza PT. da Fonseca ACP, et al. Among authors: abreu gm. Eat Weight Disord. 2022 Dec;27(8):3665-3674. doi: 10.1007/s40519-022-01506-3. Epub 2022 Nov 27. Eat Weight Disord. 2022. PMID: 36436143
Effects of Supplementation of Murici (Byrsonima crassifolia) and Taperebá (Spondias mombin) Pulp Extracts on Food Intake, Body Parameters, and Oxidative Stress Markers in Healthy Rats.
Almeida CORP, Martinez RM, Souza VR, Lima TPB, Nascimento BA, Noblat GA, Abreu GM, Pereira AD, Figueiredo MS, Teodoro AJ. Almeida CORP, et al. Among authors: abreu gm. J Med Food. 2024 Jan;27(1):47-59. doi: 10.1089/jmf.2022.0158. Epub 2023 Dec 29. J Med Food. 2024. PMID: 38156814
Identification of Variants Responsible for Monogenic Forms of Diabetes in Brazil.
Abreu GM, Tarantino RM, da Fonseca ACP, Andrade JRFO, de Souza RB, Soares CAPD, Cambraia A, Cabello PH, Rodacki M, Zajdenverg L, Zembrzuski VM, Campos Junior M. Abreu GM, et al. Front Endocrinol (Lausanne). 2022 May 3;13:827325. doi: 10.3389/fendo.2022.827325. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35592779 Free PMC article.
PDX1-MODY: A rare missense mutation as a cause of monogenic diabetes.
Abreu GM Miss, Tarantino RM, da Fonseca ACP, de Souza RB, Soares CAPD, Cabello PH, Rodacki M, Zajdenverg L, Zembrzuski VM, Campos Junior M. Abreu GM Miss, et al. Eur J Med Genet. 2021 May;64(5):104194. doi: 10.1016/j.ejmg.2021.104194. Epub 2021 Mar 18. Eur J Med Genet. 2021. PMID: 33746035
A Rare Potential Pathogenic Variant in the BDNF Gene is Found in a Brazilian Patient with Severe Childhood-Onset Obesity.
da Fonseca ACP, Abreu GM, Palhinha L, Zembrzuski VM, Campos Junior M, Carneiro JRI, Nogueira Neto JF, Magno FCCM, Rosado EL, Maya-Monteiro CM, de Cabello GMK, Cabello PH, Bozza PT. da Fonseca ACP, et al. Among authors: abreu gm. Diabetes Metab Syndr Obes. 2021 Jan 6;14:11-22. doi: 10.2147/DMSO.S267202. eCollection 2021. Diabetes Metab Syndr Obes. 2021. PMID: 33442278 Free PMC article.
Identification of a Rare and Potential Pathogenic MC4R Variant in a Brazilian Patient With Adulthood-Onset Severe Obesity.
Salum KCR, de Souza GO, Abreu GM, Campos Junior M, Kohlrausch FB, Carneiro JRI, Nogueira Neto JF, Magno FCCM, Rosado EL, Palhinha L, Maya-Monteiro CM, de Cabello GMK, Cabello PH, Bozza PT, Zembrzuski VM, da Fonseca ACP. Salum KCR, et al. Among authors: abreu gm. Front Genet. 2020 Dec 9;11:608840. doi: 10.3389/fgene.2020.608840. eCollection 2020. Front Genet. 2020. PMID: 33362866 Free PMC article.
17 results