Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

56 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Duchenne and Becker muscular dystrophies: an Estonian experience.
Talkop UA, Klaassen T, Piirsoo A, Sander V, Napa A, Essenson E, Tammur J, Talvik T. Talkop UA, et al. Among authors: piirsoo a. Brain Dev. 1999 Jun;21(4):244-7. doi: 10.1016/s0387-7604(99)00016-9. Brain Dev. 1999. PMID: 10392746
Four siblings with Hallervorden-Spatz disease.
Vaher U, Napa A, Nurmiste A, Piirsoo A, Sibul H, Talvik T. Vaher U, et al. Among authors: piirsoo a. Brain Dev. 2001 Jul;23(4):236-9. doi: 10.1016/s0387-7604(01)00184-x. Brain Dev. 2001. PMID: 11377002
De novo SCN8A mutation identified by whole-exome sequencing in a boy with neonatal epileptic encephalopathy, multiple congenital anomalies, and movement disorders.
Vaher U, Nõukas M, Nikopensius T, Kals M, Annilo T, Nelis M, Ounap K, Reimand T, Talvik I, Ilves P, Piirsoo A, Seppet E, Metspalu A, Talvik T. Vaher U, et al. Among authors: piirsoo a. J Child Neurol. 2014 Dec;29(12):NP202-6. doi: 10.1177/0883073813511300. Epub 2013 Dec 18. J Child Neurol. 2014. PMID: 24352161
A Diagnostic Algorithm for Mitochondrial Disorders in Estonian Children.
Joost K, Rodenburg RJ, Piirsoo A, van den Heuvel L, Zordania R, Põder H, Talvik I, Kilk K, Soomets U, Ounap K. Joost K, et al. Among authors: piirsoo a. Mol Syndromol. 2012 Sep;3(3):113-119. doi: 10.1159/000341375. Epub 2012 Jul 25. Mol Syndromol. 2012. PMID: 23112753 Free PMC article.
De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportion.
Pajusalu S, Talvik I, Noormets K, Talvik T, Põder H, Joost K, Puusepp S, Piirsoo A, Stenzel W, Goebel HH, Nikopensius T, Annilo T, Nõukas M, Metspalu A, Õunap K, Reimand T. Pajusalu S, et al. Among authors: piirsoo a. Neuromuscul Disord. 2016 Mar;26(3):236-9. doi: 10.1016/j.nmd.2015.11.011. Epub 2015 Dec 3. Neuromuscul Disord. 2016. PMID: 26782017
56 results