Results 71 to 80 of about 2,246,673 (121)

Gene mutations in cardiac arrhythmias: a review of recent evidence in ion channelopathies

open access: yesThe Application of Clinical Genetics, 2013
Pi-Yin Hsiao,1 Hui-Chun Tien,2 Chu-Pin Lo,2 Jyh-Ming Jimmy Juang,3 Yi-Hsin Wang,2 Ruey J Sung41Institute of Life Sciences, National Central University, Taoyuan, Taiwan; 2Department of Financial and Computational Mathematics, Providence University ...
Hsiao PY   +5 more
doaj  

Andersen-Tawil syndrome associated with myopathy. [PDF]

open access: yesWorld J Emerg Med, 2020
Wu L, Fang Y, Zhang BR.
europepmc   +1 more source

Andersen-Tawil syndrome with sex-specific phenotype: usefulness of the long exercise test

open access: yesNeurología (English Edition), 2020
S. Parra   +4 more
doaj   +1 more source

Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2‐associated Andersen–Tawil Syndrome

open access: yesJournal of Physiology, 2016
D. Adams   +8 more
semanticscholar   +1 more source

Andersen-Tawil syndrome: deep phenotyping reveals significant cardiac and neuromuscular morbidity.

open access: yesBrain : a journal of neurology, 2021
Vinojini Vivekanandam   +18 more
semanticscholar   +1 more source

Multivariate analysis of TU wave complex on electrocardiogram in Andersen-Tawil syndrome with KCNJ2 mutations. [PDF]

open access: yesAnn Noninvasive Electrocardiol, 2020
Horigome H   +10 more
europepmc   +1 more source

Natural History and Risk Stratification in Andersen-Tawil Syndrome Type 1.

open access: yesJournal of the American College of Cardiology, 2020
A. Mazzanti   +39 more
semanticscholar   +1 more source

024 Andersen-Tawil syndrome: multi-system deep phenotyping of a large UK cohort

open access: yesBMJ Neurology Open, 2021
Michael G Hanna   +2 more
doaj   +1 more source

Coincidence of Andersen-Tawil syndrome and Marfan syndrome: A case report. [PDF]

open access: yesAnn Noninvasive Electrocardiol, 2019
Krych M   +4 more
europepmc   +1 more source

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