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 |
---|---|
2011 | 1 |
2015 | 1 |
2020 | 1 |
2021 | 2 |
2023 | 2 |
2024 | 1 |
Search Results
7 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
Safety and efficacy of gene therapy with onasemnogene abeparvovec in the treatment of spinal muscular atrophy: A systematic review and meta-analysis.
J Paediatr Child Health. 2023 Mar;59(3):431-438. doi: 10.1111/jpc.16340. Epub 2023 Feb 1.
J Paediatr Child Health. 2023.
PMID: 36722610
Review.
HPDL deficiency causes a neuromuscular disease by impairing the mitochondrial respiration.
Sun Y, Wei X, Fang F, Shen Y, Wei H, Li J, Ye X, Zhan Y, Ye X, Liu X, Yang W, Li Y, Geng X, Huang X, Ruan Y, Qin Z, Yi S, Lyu J, Fang H, Yu Y.
Sun Y, et al. Among authors: ruan y.
J Genet Genomics. 2021 Aug 20;48(8):727-736. doi: 10.1016/j.jgg.2021.01.009. Epub 2021 Jun 17.
J Genet Genomics. 2021.
PMID: 34334354
Item in Clipboard
Phenotypic and genotypic characterization of NPRL3-related epilepsy: Two case reports and literature review.
Yang D, Wang J, Qin Z, Feng J, Mao C, Chen Y, Huang X, Ruan Y.
Yang D, et al. Among authors: ruan y.
Epilepsia Open. 2024 Feb;9(1):33-40. doi: 10.1002/epi4.12856. Epub 2023 Nov 28.
Epilepsia Open. 2024.
PMID: 37902097
Free PMC article.
Review.
Item in Clipboard
Streptococcal infection and immune response in children with Tourette's syndrome.
Li E, Ruan Y, Chen Q, Cui X, Lv L, Zheng P, Wang L.
Li E, et al. Among authors: ruan y.
Childs Nerv Syst. 2015 Jul;31(7):1157-63. doi: 10.1007/s00381-015-2692-8. Epub 2015 May 1.
Childs Nerv Syst. 2015.
PMID: 25930720
Item in Clipboard
Case Report: Christianson Syndrome Caused by SLC9A6 Mutation: From Case to Genotype-Phenotype Analysis.
Lan Y, Yi S, Li M, Wang J, Yang Q, Yi S, Chen F, Huang L, Ruan Y, Shen Y, Luo J, Qin Z.
Lan Y, et al. Among authors: ruan y.
Front Genet. 2021 Dec 20;12:783841. doi: 10.3389/fgene.2021.783841. eCollection 2021.
Front Genet. 2021.
PMID: 34987551
Free PMC article.
Item in Clipboard
A graphene oxide-aided triple helical aggregation-induced emission biosensor for highly specific detection of charged collagen peptides.
Sun X, Qiao Y, Li W, Sui Y, Ruan Y, Xiao J.
Sun X, et al. Among authors: ruan y.
J Mater Chem B. 2020 Jul 28;8(28):6027-6033. doi: 10.1039/d0tb00476f. Epub 2020 Jun 22.
J Mater Chem B. 2020.
PMID: 32568343
Item in Clipboard
[Diagnostic value of serum Cystatin C in renal function impairments in children with viral encephalitis].
Ruan YY, Feng JT, Huang ZQ, Qin WL, Mou JF.
Ruan YY, et al.
Zhongguo Dang Dai Er Ke Za Zhi. 2011 Feb;13(2):119-22.
Zhongguo Dang Dai Er Ke Za Zhi. 2011.
PMID: 21342620
Free article.
Chinese.
Item in Clipboard
Cite
Cite