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 |
---|---|
2006 | 1 |
2019 | 1 |
2024 | 0 |
Search Results
2 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
Prevalence, Type, and Molecular Spectrum of NF1 Mutations in Patients with Neurofibromatosis Type 1 and Congenital Heart Disease.
Genes (Basel). 2019 Sep 4;10(9):675. doi: 10.3390/genes10090675.
Genes (Basel). 2019.
PMID: 31487937
Free PMC article.
Frequency and phenotypes of LRRK2 G2019S mutation in Italian patients with Parkinson's disease.
Marongiu R, Ghezzi D, Ialongo T, Soleti F, Elia A, Cavone S, Albanese A, Altavista MC, Barone P, Brusa L, Cortelli P, Petrozzi L, Scaglione C, Stanzione P, Tinazzi M, Zeviani M, Dallapiccola B, Bentivoglio AR, Valente EM, Garavaglia B; Italian PD Study Group.
Marongiu R, et al. Among authors: cavone s.
Mov Disord. 2006 Aug;21(8):1232-5. doi: 10.1002/mds.20890.
Mov Disord. 2006.
PMID: 16622859
Item in Clipboard
Cite
Cite