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

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1980 1
1990 1
1995 1
1996 1
2000 2
2002 1
2003 1
2004 1
2005 2
2006 2
2007 1
2008 1
2009 3
2010 1
2011 1
2013 2
2014 4
2015 2
2016 1
2017 5
2018 1
2019 8
2020 4
2021 4
2022 1
2024 0

Text availability

Article attribute

Article type

Publication date

PubMed for id: 1775535

45 results

Results by year

Filters applied: . Clear all
Page 1
Aedes albopictus diversity and relationships in south-western Europe and Brazil by rDNA/mtDNA and phenotypic analyses: ITS-2, a useful marker for spread studies.
Artigas P, Reguera-Gomez M, Valero MA, Osca D, da Silva Pacheco R, Rosa-Freitas MG, Fernandes Silva-do-Nascimento T, Paredes-Esquivel C, Lucientes J, Mas-Coma S, Bargues MD. Artigas P, et al. Parasit Vectors. 2021 Jun 26;14(1):333. doi: 10.1186/s13071-021-04829-9. Parasit Vectors. 2021. PMID: 34174940 Free PMC article.
Glutathione S-transferase, catalase, and mitochondrial superoxide dismutase gene polymorphisms modulate redox potential in systemic lupus erythematosus patients from Manaus, Amazonas, Brazil.
de Oliveira MAA, Mallmann NH, de Souza GKBB, de Jesus Bacha T, Lima ES, de Lima DSN, de Souza Passos LF, de Souza Gonçalves M, de Moura Neto JP. de Oliveira MAA, et al. Clin Rheumatol. 2021 Sep;40(9):3639-3649. doi: 10.1007/s10067-021-05680-0. Epub 2021 Mar 20. Clin Rheumatol. 2021. PMID: 33745084
Mitochondrial dysfunction caused by novel ATAD3A mutations.
Dorison N, Gaignard P, Bayot A, Gelot A, Becker PH, Fourati S, Lebigot E, Charles P, Wai T, Therond P, Slama A. Dorison N, et al. Mol Genet Metab. 2020 Sep-Oct;131(1-2):107-113. doi: 10.1016/j.ymgme.2020.09.002. Epub 2020 Sep 9. Mol Genet Metab. 2020. PMID: 32933822 Free article.
Dystonia-Ataxia with early handwriting deterioration in COQ8A mutation carriers: A case series and literature review.
Galosi S, Barca E, Carrozzo R, Schirinzi T, Quinzii CM, Lieto M, Vasco G, Zanni G, Di Nottia M, Galatolo D, Filla A, Bertini E, Santorelli FM, Leuzzi V, Haas R, Hirano M, Friedman J. Galosi S, et al. Parkinsonism Relat Disord. 2019 Nov;68:8-16. doi: 10.1016/j.parkreldis.2019.09.015. Epub 2019 Sep 28. Parkinsonism Relat Disord. 2019. PMID: 31621627 Review.
45 results