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 |
---|---|
2009 | 1 |
2010 | 2 |
2011 | 1 |
2020 | 1 |
2021 | 1 |
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
Studying the "Rigid-Flexible" Properties of Polymeric Micelle Core-Forming Segments with a Hydrophobic Phthalocyanine Probe Using NMR and UV Spectroscopy.
Langmuir. 2021 Apr 13;37(14):4316-4330. doi: 10.1021/acs.langmuir.1c00328. Epub 2021 Apr 1.
Langmuir. 2021.
PMID: 33794644
Free PMC article.
The 5' regulatory sequence of the PMP22 in the patients with Charcot-Marie-Tooth disease.
Sinkiewicz-Darol E, Kabzińska D, Moszyńska I, Kochański A.
Sinkiewicz-Darol E, et al. Among authors: moszynska i.
Acta Biochim Pol. 2010;57(3):373-7. Epub 2010 Sep 15.
Acta Biochim Pol. 2010.
PMID: 20842290
Free article.
Item in Clipboard
Dysmyelinating and demyelinating Charcot-Marie-Tooth disease associated with two myelin protein zero gene mutations.
Drac H, Kabzińska D, Moszyńska I, Strugalska-Cynowska H, Hausmanowa-Petrusewicz I, Kochański A.
Drac H, et al. Among authors: moszynska i.
J Appl Genet. 2011 May;52(2):177-83. doi: 10.1007/s13353-010-0003-3. Epub 2010 Nov 3.
J Appl Genet. 2011.
PMID: 21107784
Item in Clipboard
Hydrophobically Functionalized Poly(Acrylic Acid) Comprising the Ester-Type Labile Spacer: Synthesis and Self-Organization in Water.
Lamch Ł, Ronka S, Moszyńska I, Warszyński P, Wilk KA.
Lamch Ł, et al. Among authors: moszynska i.
Polymers (Basel). 2020 May 22;12(5):1185. doi: 10.3390/polym12051185.
Polymers (Basel). 2020.
PMID: 32455970
Free PMC article.
Item in Clipboard
A newly identified Thr99fsX110 mutation in the PMP22 gene associated with an atypical phenotype of the hereditary neuropathy with liability to pressure palsies.
Moszyńska I, Kabzińska D, Sinkiewicz-Darol E, Kochański A.
Moszyńska I, et al.
Acta Biochim Pol. 2009;56(4):627-30. Epub 2009 Oct 15.
Acta Biochim Pol. 2009.
PMID: 19830275
Free article.
Item in Clipboard
Cite
Cite