Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

161 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Physical Activity at Different Life Stages and Its Consequence on the Initial Immunization and Inflammatory Response Against COVID-19.
Rossi PAQ, Gomes R, Nascimento Salazar TCD, Lustosa Barros EM, Vasconcelos S, da Silva AS, Pereira EM, Melo VB, Fonseca MHG, Teixeira CR, Furtado GP, Pontes LQ, Khouri R, Vasconcelos B, Almeida SS, Werneck GL, Rossi FE, Santos MAPD. Rossi PAQ, et al. Among authors: pereira em. J Phys Act Health. 2024 Apr 24:1-9. doi: 10.1123/jpah.2023-0370. Online ahead of print. J Phys Act Health. 2024. PMID: 38663845
Familial lecithin-cholesterol acyltransferase deficiency: If so rare, why so frequent in the state of Piauí, northeastern Brazil?
de Serpa Brandão RMS, Britto FB, do Monte Neto JT, Lima MC, do Monte SJH, de Sousa Lima AV, Pereira EM, da Silva HJN, Oliveira DMTE, Coelho AGB, da Silva AS. de Serpa Brandão RMS, et al. Among authors: pereira em. Mol Genet Metab Rep. 2022 Jan 3;30:100840. doi: 10.1016/j.ymgmr.2021.100840. eCollection 2022 Mar. Mol Genet Metab Rep. 2022. PMID: 35242572 Free PMC article.
CD77 levels over enzyme replacement treatment in Fabry Disease Family (V269M).
Pereira EM, Silva ASD, Silva RND, Monte Neto JT, Nascimento FFD, Sousa JLM, Costa Filho HCSAL, Sales Filho HLA, Labilloy A, Monte SJHD. Pereira EM, et al. J Bras Nefrol. 2018 Oct-Dec;40(4):333-338. doi: 10.1590/2175-8239-JBN-3910. Epub 2018 Jun 4. J Bras Nefrol. 2018. PMID: 29927462 Free PMC article.
Podocyturia in Fabry disease.
Pereira EM, Silva AS, Labilloy A, Monte Neto JT, Monte SJ. Pereira EM, et al. J Bras Nefrol. 2016 Mar;38(1):49-53. doi: 10.5935/0101-2800.20160008. J Bras Nefrol. 2016. PMID: 27049364 Free article. English, Portuguese.
Fetal Alcohol Spectrum Disorders.
Pereira EM. Pereira EM. Pediatr Rev. 2024 May 1;45(5):303-304. doi: 10.1542/pir.2023-006038. Pediatr Rev. 2024. PMID: 38689104 No abstract available.
Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma.
Ma M, Ganapathi M, Zheng Y, Tan KL, Kanca O, Bove KE, Quintanilla N, Sag SO, Temel SG, LeDuc CA, McPartland AJ, Pereira EM, Shen Y, Hagen J, Thomas CP, Nguyen Galván NT, Pan X, Lu S, Rosenfeld JA, Calame DG, Wangler MF, Lupski JR, Pehlivan D, Hertel PM, Chung WK, Bellen HJ. Ma M, et al. Among authors: pereira em. Genet Med. 2024 Mar 21;26(7):101125. doi: 10.1016/j.gim.2024.101125. Online ahead of print. Genet Med. 2024. PMID: 38522068
Trisomy 21.
Pereira EM. Pereira EM. Pediatr Rev. 2024 Feb 1;45(2):116-117. doi: 10.1542/pir.2022-005887. Pediatr Rev. 2024. PMID: 38296776 No abstract available.
161 results