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
8 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene.
Eur J Hum Genet. 1999 Sep;7(6):724-8. doi: 10.1038/sj.ejhg.5200323.
Eur J Hum Genet. 1999.
PMID: 10482963
Mutations in the HERG K+-ion channel: a novel link between long QT syndrome and sudden infant death syndrome.
Christiansen M, Tønder N, Larsen LA, Andersen PS, Simonsen H, Oyen N, Kanters JK, Jacobsen JR, Fosdal I, Wettrell G, Kjeldsen K.
Christiansen M, et al. Among authors: fosdal i.
Am J Cardiol. 2005 Feb 1;95(3):433-4. doi: 10.1016/j.amjcard.2004.09.054.
Am J Cardiol. 2005.
PMID: 15670565
Item in Clipboard
Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death.
Nyegaard M, Overgaard MT, Søndergaard MT, Vranas M, Behr ER, Hildebrandt LL, Lund J, Hedley PL, Camm AJ, Wettrell G, Fosdal I, Christiansen M, Børglum AD.
Nyegaard M, et al. Among authors: fosdal i.
Am J Hum Genet. 2012 Oct 5;91(4):703-12. doi: 10.1016/j.ajhg.2012.08.015.
Am J Hum Genet. 2012.
PMID: 23040497
Free PMC article.
Item in Clipboard
[Molecular genetics of the long QT syndrome. Genes causing syncope and sudden death].
Fosdal I, Wettrell G, Christiansen M, Kanters JK, Larsen LA.
Fosdal I, et al.
Lakartidningen. 2001 Feb 21;98(8):810-5.
Lakartidningen. 2001.
PMID: 11265565
Review.
Swedish.
Item in Clipboard
Third trimester fetal heart rate predicts phenotype and mutation burden in the type 1 long QT syndrome.
Winbo A, Fosdal I, Lindh M, Diamant UB, Persson J, Wettrell G, Rydberg A.
Winbo A, et al. Among authors: fosdal i.
Circ Arrhythm Electrophysiol. 2015 Aug;8(4):806-14. doi: 10.1161/CIRCEP.114.002552. Epub 2015 May 27.
Circ Arrhythm Electrophysiol. 2015.
PMID: 26019114
Item in Clipboard
Analysis of short stature homeobox-containing gene ( SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity.
Grigelioniene G, Schoumans J, Neumeyer L, Ivarsson A, Eklöf O, Enkvist O, Tordai P, Fosdal I, Myhre AG, Westphal O, Nilsson NO, Elfving M, Ellis I, Anderlid BM, Fransson I, Tapia-Paez I, Nordenskjöld M, Hagenäs L, Dumanski JP.
Grigelioniene G, et al. Among authors: fosdal i.
Hum Genet. 2001 Nov;109(5):551-8. doi: 10.1007/s00439-001-0609-y. Epub 2001 Oct 19.
Hum Genet. 2001.
PMID: 11735031
Item in Clipboard
Overnight testing of renal concentrating capacity in children using desmopressin tablets: sensitivity, repeatability and non-inferiority versus intranasal spray.
Asa Rembratt, Jens-Kristian Jensen, Kjell Tullus, Staffan Mårild; Renal Concentrating Capacity Test (RCCT) study group.
Asa Rembratt, et al.
Scand J Urol Nephrol. 2008;42(3):274-7. doi: 10.1080/00365590701685736.
Scand J Urol Nephrol. 2008.
PMID: 17943639
Clinical Trial.
Item in Clipboard
Efficacy and safety during long-term treatment of primary monosymptomatic nocturnal enuresis with desmopressin. Swedish Enuresis Trial Group.
Tullus K, Bergström R, Fosdal I, Winnergård I, Hjälmås K.
Tullus K, et al. Among authors: fosdal i.
Acta Paediatr. 1999 Nov;88(11):1274-8. doi: 10.1080/080352599750030428.
Acta Paediatr. 1999.
PMID: 10591433
Clinical Trial.
Item in Clipboard
Cite
Cite