jervell lange nielsen syndrome OR romano ward syndrome OR ((long ...
jervell lange nielsen syn...jervell lange nielsen syndrome OR romano ward syndrome OR ((long qt syndrome) genetic diseases, inborn)(460) ...
http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&Cmd=Detai...
|
BioPortfolio - Jervell-Lange Nielsen Syndrome - InDepth
Romano-Ward forms of long QT syndrome in a Chinese family. ... Departamento de Electrocardiologia, Instituto Nacional de Cardiologia- Arch Cardiol Mex. 2006 ...
http://www.bioportfolio.com/indepth/Jervell-Lange_Nielsen_Sy...
|
The Long QT Syndrome
Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneous. ... [PubMed]; Vetter DE, Mann JR, Wangemann P, et al. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=15...
|
BioMed Central | Full text | Long QT Syndrome: A Preventable Cause ...
Homozygous mutations of KVLQT1 appear to cause the Jervell-Lange-Nielsen syndrome, ..... reentrant mechanism of torsade de pointes in the long-QT syndrome. ...
http://www.biomedcentral.com/1534-5874/3/126...
|
Congenital and drug-induced long-QT syndrome: an update
Atrioventricular pacemaker placement in Romano-Ward syndrome and recurrent torsades de pointes. Am J Cardiol. 1987 Jan 1;59(1):171–172. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=24...
|
Long QT Syndrome: A Preventable Cause of Sudden Death in Women
mechanism of torsade de pointes in the long-QT syndrome. Circulation 2002, 105: 1247–1253. 7. Roden DM, Lazzara R, Rosen M, et al.: Multiple mechanisms ...
http://www.biomedcentral.com/content/pdf/cr-wr3215.pdf...
|
Mutations in a dominant-negative isoform correlate with phenotype ...
Laboratoire de Physiopathologie et de Pharmacologie Cellulaires et Moléculaires .... syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneous. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=13...
|
1750-1172-3-18 1750-1172 Review Congenital long QT syndrome Crotti ...
Clinical description Romano-Ward syndrome The two cardinal manifestations of ... (From C. Pernot: Le syndrome cardio-auditif de Jervell et Lange-Nielsen. ...
http://www.biomedcentral.com/content/download/xml/1750-1172-...
|
Long QT syndrome - Glossary Entry - Genetics Home Reference
... and congenital deafness is called the JERVELL-LANGE NIELSEN SYNDROME. An autosomal dominant form without deafness is called the ROMANO-WARD SYNDROME. ...
http://ghr.nlm.nih.gov/glossary=longqtsyndrome...
|
[Clinical aspects and molecular genetics of the Jervell- and Lange ...
In contrast to the Romano-Ward (R-W) syndrome, the Jervell and Lange-Nielsen ... DNA Mutational Analysis; Humans; Jervell-Lange Nielsen Syndrome/diagnosis ...
http://www.ncbi.nlm.nih.gov/pubmed/12132284...
|