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 |
---|---|
2017 | 3 |
2018 | 2 |
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
Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias.
Genes (Basel). 2017 Oct 18;8(10):276. doi: 10.3390/genes8100276.
Genes (Basel). 2017.
PMID: 29057844
Free PMC article.
Review.
The expression of the MSC-marker CD73 and of NF2/Merlin are correlated in meningiomas.
Kirches E, Steffen T, Waldt N, Hebert E, Pachow D, Wilisch-Neumann A, Keilhoff G, Schneider T, Braunsdorf WEK, Warnke JP, Mawrin C.
Kirches E, et al. Among authors: hebert e.
J Neurooncol. 2018 Jun;138(2):251-259. doi: 10.1007/s11060-018-2807-7. Epub 2018 Feb 21.
J Neurooncol. 2018.
PMID: 29468444
Item in Clipboard
Novel GCH1 Compound Heterozygosity Mutation in Infancy-Onset Generalized Dystonia.
Flotats-Bastardas M, Hebert E, Raspall-Chaure M, Munell F, Macaya A, Lohmann K.
Flotats-Bastardas M, et al. Among authors: hebert e.
Neuropediatrics. 2018 Aug;49(4):296-297. doi: 10.1055/s-0038-1626709. Epub 2018 Feb 22.
Neuropediatrics. 2018.
PMID: 29471552
No abstract available.
Item in Clipboard
In-depth Characterization of the Homodimerization Domain of the Transcription Factor THAP1 and Dystonia-Causing Mutations Therein.
Richter A, Hollstein R, Hebert E, Vulinovic F, Eckhold J, Osmanovic A, Depping R, Kaiser FJ, Lohmann K.
Richter A, et al. Among authors: hebert e.
J Mol Neurosci. 2017 May;62(1):11-16. doi: 10.1007/s12031-017-0904-2. Epub 2017 Mar 15.
J Mol Neurosci. 2017.
PMID: 28299530
Item in Clipboard
Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans.
Lohmann K, Masuho I, Patil DN, Baumann H, Hebert E, Steinrücke S, Trujillano D, Skamangas NK, Dobricic V, Hüning I, Gillessen-Kaesbach G, Westenberger A, Savic-Pavicevic D, Münchau A, Oprea G, Klein C, Rolfs A, Martemyanov KA.
Lohmann K, et al. Among authors: hebert e.
Hum Mol Genet. 2017 Mar 15;26(6):1078-1086. doi: 10.1093/hmg/ddx018.
Hum Mol Genet. 2017.
PMID: 28087732
Free PMC article.
Item in Clipboard
Cite
Cite