Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2022 | 2 |
2023 | 3 |
2024 | 0 |
Search Results
5 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Narrative Review: Update on the Molecular Diagnosis of Fragile X Syndrome.
Int J Mol Sci. 2023 May 24;24(11):9206. doi: 10.3390/ijms24119206.
Int J Mol Sci. 2023.
PMID: 37298158
Free PMC article.
Review.
Mitochondrial Dysfunction, Oxidative Stress, and Therapeutic Strategies in Diabetes, Obesity, and Cardiovascular Disease.
Cojocaru KA, Luchian I, Goriuc A, Antoci LM, Ciobanu CG, Popescu R, Vlad CE, Blaj M, Foia LG.
Cojocaru KA, et al. Among authors: ciobanu cg.
Antioxidants (Basel). 2023 Mar 7;12(3):658. doi: 10.3390/antiox12030658.
Antioxidants (Basel). 2023.
PMID: 36978905
Free PMC article.
Review.
Item in Clipboard
Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype-Phenotype Correlation.
Gavril EC, Popescu R, Nucă I, Ciobanu CG, Butnariu LI, Rusu C, Pânzaru MC.
Gavril EC, et al. Among authors: ciobanu cg.
Genes (Basel). 2022 Nov 10;13(11):2083. doi: 10.3390/genes13112083.
Genes (Basel). 2022.
PMID: 36360320
Free PMC article.
Item in Clipboard
Genotype-Phenotype Correlations in 2q37-Deletion Syndrome: An Update of the Clinical Spectrum and Literature Review.
Gavril EC, Nucă I, Pânzaru MC, Ivanov AV, Mihai CT, Antoci LM, Ciobanu CG, Rusu C, Popescu R.
Gavril EC, et al. Among authors: ciobanu cg.
Genes (Basel). 2023 Feb 11;14(2):465. doi: 10.3390/genes14020465.
Genes (Basel). 2023.
PMID: 36833393
Free PMC article.
Review.
Item in Clipboard
Genetic Polymorphisms in a Familial Hypercholesterolemia Population from North-Eastern Europe.
Maștaleru A, Cojocariu SA, Oancea A, Constantin MML, Roca M, Zota IM, Abdulan I, Rusu C, Popescu R, Antoci LM, Ciobanu CG, Costache AD, Cojocaru E, Mitu F.
Maștaleru A, et al. Among authors: ciobanu cg.
J Pers Med. 2022 Mar 9;12(3):429. doi: 10.3390/jpm12030429.
J Pers Med. 2022.
PMID: 35330428
Free PMC article.
Item in Clipboard
Cite
Cite