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 |
---|---|
2018 | 1 |
2019 | 1 |
2020 | 1 |
2021 | 1 |
2022 | 1 |
2023 | 2 |
2024 | 1 |
Search Results
6 results
Results by year
Filters applied: . Clear all
Page 1
CXCL9 inhibition does not ameliorate disease in murine models of both primary and secondary hemophagocytic lymphohistiocytosis.
Sci Rep. 2023 Jul 29;13(1):12298. doi: 10.1038/s41598-023-39601-9.
Sci Rep. 2023.
PMID: 37516815
Free PMC article.
Commentary: Schizophrenia prevention and prodromal psychosis in children and adolescents.
Taylor JH, Huque ZM.
Taylor JH, et al.
J Child Psychol Psychiatry. 2021 May;62(5):674-676. doi: 10.1111/jcpp.13408. Epub 2021 Mar 6.
J Child Psychol Psychiatry. 2021.
PMID: 33675238
Item in Clipboard
The Expansion of Genetic Testing in Cardiovascular Medicine: Preparing the Cardiology Community for the Changing Landscape.
Reza N, Alford RL, Belmont JW, Marston N.
Reza N, et al.
Curr Cardiol Rep. 2024 Mar;26(3):135-146. doi: 10.1007/s11886-023-02003-4. Epub 2024 Jan 26.
Curr Cardiol Rep. 2024.
PMID: 38277082
Free PMC article.
Review.
Item in Clipboard
Impact of Race, Gender, and Socioeconomic Status on Symptom Severity at Time of Urologic Referral.
Ko JS, Corbett C, Fischer KM, Berry A, Weiss DA, Long CJ, Zderic SA, Van Batavia JP.
Ko JS, et al.
J Racial Ethn Health Disparities. 2023 Aug;10(4):1735-1744. doi: 10.1007/s40615-022-01357-9. Epub 2022 Aug 12.
J Racial Ethn Health Disparities. 2023.
PMID: 35960437
Item in Clipboard
Natural history of multiple sulfatase deficiency: Retrospective phenotyping and functional variant analysis to characterize an ultra-rare disease.
Adang LA, Schlotawa L, Groeschel S, Kehrer C, Harzer K, Staretz-Chacham O, Silva TO, Schwartz IVD, Gärtner J, De Castro M, Costin C, Montgomery EF, Dierks T, Radhakrishnan K, Ahrens-Nicklas RC.
Adang LA, et al.
J Inherit Metab Dis. 2020 Nov;43(6):1298-1309. doi: 10.1002/jimd.12298. Epub 2020 Aug 20.
J Inherit Metab Dis. 2020.
PMID: 32749716
Free PMC article.
Item in Clipboard
Anomalies of the genitourinary tract in children with 22q11.2 deletion syndrome.
Van Batavia JP, Crowley TB, Burrows E, Zackai EH, Sanna-Cherchi S, McDonald-McGinn DM, Kolon TF.
Van Batavia JP, et al.
Am J Med Genet A. 2019 Mar;179(3):381-385. doi: 10.1002/ajmg.a.61020. Epub 2018 Dec 24.
Am J Med Genet A. 2019.
PMID: 30582277
Free PMC article.
Item in Clipboard
Cite
Cite