Search Page
Save citations to file
Email citations
Email address has not been verified. Go to
My NCBI account settings
to confirm your email and then refresh this page.
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 |
---|---|
2019 | 2 |
2025 | 1 |
Search Results
3 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
Genomics of rare genetic diseases-experiences from India.
Hum Genomics. 2019 Sep 25;14(1):52. doi: 10.1186/s40246-019-0215-5.
Hum Genomics. 2019.
PMID: 31554517
Free PMC article.
Review.
A novel cathepsin D mutation in 2 siblings with late infantile neuronal ceroid lipofuscinosis.
Thottath J, Vellarikkal SK, Jayarajan R, Verma A, Manamel M, Singh A, Rajendran VR, Sivasubbu S, Scaria V.
Thottath J, et al.
Neurol Genet. 2019 Apr 11;5(3):e302. doi: 10.1212/NXG.0000000000000302. eCollection 2019 Jun.
Neurol Genet. 2019.
PMID: 31086824
Free PMC article.
No abstract available.
Item in Clipboard
Differential practice of peer review and peer feedback between National Health Service (NHS) imaging departments and teleradiology companies; how big is the gap?
Balasubramaniam R, Drinkwater K, Beavon M, Greenhalgh R; Collaborating authors.
Balasubramaniam R, et al.
Clin Radiol. 2025 Jun;85:106919. doi: 10.1016/j.crad.2025.106919. Epub 2025 Apr 2.
Clin Radiol. 2025.
PMID: 40311541
Item in Clipboard
Cite
Cite
ARTICLE TYPE
ARTICLE LANGUAGE
AGE
Filters on the sidebar will be reset to the default list and any currently applied filters will be cleared.