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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2017 | 4 |
2018 | 2 |
2019 | 1 |
2024 | 0 |
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6 results
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Page 1
Flavonoids, Thyroid Iodide Uptake and Thyroid Cancer-A Review.
Int J Mol Sci. 2017 Jun 12;18(6):1247. doi: 10.3390/ijms18061247.
Int J Mol Sci. 2017.
PMID: 28604619
Free PMC article.
Review.
Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: Genetic evaluation of a possible new syndrome.
Richieri-Costa A, Zechi-Ceide RM, Candido-Souza RM, Monteiro RAC, Tonello C, de Freitas ML, Kokitsu-Nakata NM, Vendramini-Pittoli S, Mazzeu JF, Overes M, Ali-Amin R, van Slegtenhorst M, Hoefsloot LH, Jehee FS.
Richieri-Costa A, et al. Among authors: de freitas ml.
Am J Med Genet A. 2019 Nov;179(11):2170-2177. doi: 10.1002/ajmg.a.61305. Epub 2019 Jul 28.
Am J Med Genet A. 2019.
PMID: 31353810
Item in Clipboard
Influence of Stem Cell Therapy on Thyroid Function and Reactive Oxygen Species Production in Diabetic Rats.
da Silva DLSG, de Freitas ML, Cahil GM, de São José VS, Neto FM, Cardoso RC, da Costa VMC, Fortunato RS, de Carvalho DP, Medei EH, Ferreira ACF.
da Silva DLSG, et al.
Horm Metab Res. 2018 Apr;50(4):331-339. doi: 10.1055/a-0588-7944. Epub 2018 Apr 5.
Horm Metab Res. 2018.
PMID: 29621815
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Rutin Scavenges Reactive Oxygen Species, Inactivates 5'-Adenosine Monophosphate-Activated Protein Kinase, and Increases Sodium-Iodide Symporter Expression in Thyroid PCCL3 Cells.
Gonçalves CFL, de Freitas ML, Fortunato RS, Miranda-Alves L, Carvalho DP, Ferreira ACF.
Gonçalves CFL, et al.
Thyroid. 2018 Feb;28(2):265-275. doi: 10.1089/thy.2016.0585. Epub 2017 Dec 21.
Thyroid. 2018.
PMID: 29160164
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Dual molecular diagnosis contributes to atypical Prader-Willi phenotype in monozygotic twins.
Jehee FS, de Oliveira VT, Gurgel-Giannetti J, Pietra RX, Rubatino FVM, Carobin NV, Vianna GS, de Freitas ML, Fernandes KS, Ribeiro BSV, Brüggenwirth HT, Ali-Amin R; Baylor-Hopkins Center for Mendelian Genomics; White JJ, Akdemir ZC, Jhangiani SN, Gibbs RA, Lupski JR, Varela MC, Koiffmann C, Rosenberg C, Carvalho CMB.
Jehee FS, et al. Among authors: de freitas ml.
Am J Med Genet A. 2017 Sep;173(9):2451-2455. doi: 10.1002/ajmg.a.38315. Epub 2017 Jun 20.
Am J Med Genet A. 2017.
PMID: 28631899
Free PMC article.
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Major Contribution of Genomic Copy Number Variation in Syndromic Congenital Heart Disease: The Use of MLPA as the First Genetic Test.
Monteiro RAC, de Freitas ML, Vianna GS, de Oliveira VT, Pietra RX, Ferreira LCA, Rocha PPO, da S Gonçalves M, da C César G, de S Lima J, Medeiros PFV, Mazzeu JF, Jehee FS.
Monteiro RAC, et al. Among authors: de freitas ml.
Mol Syndromol. 2017 Aug;8(5):227-235. doi: 10.1159/000477226. Epub 2017 Jun 14.
Mol Syndromol. 2017.
PMID: 28878606
Free PMC article.
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