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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: campos junior m. 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
CHCHD2 mutational screening in Brazilian patients with familial Parkinson's disease.
Voigt DD, Nascimento CM, de Souza RB, Cabello Acero PH, Campos Júnior M, da Silva CP, Pereira JS, Rosso AL, Araujo Leite MA, Vasconcellos LFR, Della Coletta MV, da Silva DJ, Nicaretta DH, Gonçalves AP, Dos Santos JM, Calassara V, Santos-Rebouças CB, Pimentel MMG. Voigt DD, et al. Among authors: campos junior m. Neurobiol Aging. 2019 Feb;74:236.e7-236.e8. doi: 10.1016/j.neurobiolaging.2018.09.026. Epub 2018 Sep 27. Neurobiol Aging. 2019. PMID: 30342766
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: campos junior m. 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: campos junior m. 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
The first case of NEUROD1-MODY reported in Latin America.
Abreu GM, Tarantino RM, Cabello PH, Zembrzuski VM, da Fonseca ACP, Rodacki M, Zajdenverg L, Campos Junior M. Abreu GM, et al. Among authors: campos junior m. Mol Genet Genomic Med. 2019 Dec;7(12):e989. doi: 10.1002/mgg3.989. Epub 2019 Oct 2. Mol Genet Genomic Med. 2019. PMID: 31578821 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. Among authors: campos junior m. 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
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