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
Search Results
3 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
FHF1 (FGF12) epileptic encephalopathy.
Neurol Genet. 2016 Oct 28;2(6):e115. doi: 10.1212/NXG.0000000000000115. eCollection 2016 Dec.
Neurol Genet. 2016.
PMID: 27830185
Free PMC article.
Arginine:glycine amidinotransferase (AGAT) deficiency: Clinical features and long term outcomes in 16 patients diagnosed worldwide.
Stockler-Ipsiroglu S, Apatean D, Battini R, DeBrosse S, Dessoffy K, Edvardson S, Eichler F, Johnston K, Koeller DM, Nouioua S, Tazir M, Verma A, Dowling MD, Wierenga KJ, Wierenga AM, Zhang V, Wong LJ.
Stockler-Ipsiroglu S, et al. Among authors: dessoffy k.
Mol Genet Metab. 2015 Dec;116(4):252-9. doi: 10.1016/j.ymgme.2015.10.003. Epub 2015 Oct 17.
Mol Genet Metab. 2015.
PMID: 26490222
Free article.
Item in Clipboard
Airway malacia in children with achondroplasia.
Dessoffy KE, Modaff P, Pauli RM.
Dessoffy KE, et al.
Am J Med Genet A. 2014 Feb;164A(2):407-14. doi: 10.1002/ajmg.a.36303. Epub 2013 Dec 5.
Am J Med Genet A. 2014.
PMID: 24311312
Item in Clipboard
Cite
Cite