Romano–Ward syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Romano–Ward syndrome" in English language version.

refsWebsite

Global rank English rank

23nih.gov

4^th place

11doi.org

2^nd place

7web.archive.org

1^st place

1orpha.net

3,537^th place

7,177^th place

1harvard.edu

18^th place

17^th place

1semanticscholar.org

11^th place

8^th place

doi.org

Tester DJ, Schwartz PJ, Ackerman MJ (2013). "Congenital Long QT Syndrome". In Gussak I, Antzelevitch C (eds.). Electrical Diseases of the Heart. Springer London. pp. 439–468. doi:10.1007/978-1-4471-4881-4_27. ISBN 9781447148814. {{cite book}}: |work= ignored (help)
Mizusawa Y, Horie M, Wilde AA (2014-01-01). "Genetic and clinical advances in congenital long QT syndrome". Circulation Journal. 78 (12): 2827–2833. doi:10.1253/circj.CJ-14-0905. PMID 25274057.
Bohnen MS, Peng G, Robey SH, Terrenoire C, Iyer V, Sampson KJ, Kass RS (January 2017). "Molecular Pathophysiology of Congenital Long QT Syndrome". Physiological Reviews. 97 (1): 89–134. doi:10.1152/physrev.00008.2016. PMC 5539372. PMID 27807201.
Priori SG, Blomström-Lundqvist C, Mazzanti A, Blom N, Borggrefe M, Camm J, et al. (Task Force for the Management of Patients with Ventricular Arrhythmias the Prevention of Sudden Cardiac Death of the European Society of Cardiology (ESC)) (November 2015). "2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: The Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of the European Society of Cardiology (ESC)Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC)". Europace. 17 (11): 1601–1687. doi:10.1093/europace/euv319. PMID 26318695.
Nakajima T, Kaneko Y, Kurabayashi M (2015). "Unveiling specific triggers and precipitating factors for fatal cardiac events in inherited arrhythmia syndromes". Circulation Journal. 79 (6): 1185–1192. doi:10.1253/circj.CJ-15-0322. PMID 25925977.
Giudicessi JR, Wilde AA, Ackerman MJ (October 2018). "The genetic architecture of long QT syndrome: A critical reappraisal". Trends in Cardiovascular Medicine. 28 (7): 453–464. doi:10.1016/j.tcm.2018.03.003. PMC 6590899. PMID 29661707.
Huang H, Kuenze G, Smith JA, Taylor KC, Duran AM, Hadziselimovic A, et al. (March 2018). "Mechanisms of KCNQ1 channel dysfunction in long QT syndrome involving voltage sensor domain mutations". Science Advances. 4 (3): eaar2631. Bibcode:2018SciA....4.2631H. doi:10.1126/sciadv.aar2631. PMC 5842040. PMID 29532034.
Demirbilek H, Galcheva S, Vuralli D, Al-Khawaga S, Hussain K (May 2019). "Ion Transporters, Channelopathies, and Glucose Disorders". International Journal of Molecular Sciences. 20 (10): 2590. doi:10.3390/ijms20102590. PMC 6566632. PMID 31137773.
Giudicessi JR, Ackerman MJ (October 2013). "Genotype- and phenotype-guided management of congenital long QT syndrome". Current Problems in Cardiology. 38 (10): 417–455. doi:10.1016/j.cpcardiol.2013.08.001. PMC 3940076. PMID 24093767.
Giudicessi JR, Wilde AA, Ackerman MJ (October 2018). "The genetic architecture of long QT syndrome: A critical reappraisal". Trends in Cardiovascular Medicine. 28 (7): 453–464. doi:10.1016/j.tcm.2018.03.003. PMC 6590899. PMID 29661707.
Li G, Zhang L (November 2018). "The role of mexiletine in the management of long QT syndrome". Journal of Electrocardiology. 51 (6): 1061–1065. doi:10.1016/j.jelectrocard.2018.08.035. PMID 30497731. S2CID 54167081.

harvard.edu

ui.adsabs.harvard.edu

Huang H, Kuenze G, Smith JA, Taylor KC, Duran AM, Hadziselimovic A, et al. (March 2018). "Mechanisms of KCNQ1 channel dysfunction in long QT syndrome involving voltage sensor domain mutations". Science Advances. 4 (3): eaar2631. Bibcode:2018SciA....4.2631H. doi:10.1126/sciadv.aar2631. PMC 5842040. PMID 29532034.

nih.gov

pubmed.ncbi.nlm.nih.gov

Mizusawa Y, Horie M, Wilde AA (2014-01-01). "Genetic and clinical advances in congenital long QT syndrome". Circulation Journal. 78 (12): 2827–2833. doi:10.1253/circj.CJ-14-0905. PMID 25274057.
Bohnen MS, Peng G, Robey SH, Terrenoire C, Iyer V, Sampson KJ, Kass RS (January 2017). "Molecular Pathophysiology of Congenital Long QT Syndrome". Physiological Reviews. 97 (1): 89–134. doi:10.1152/physrev.00008.2016. PMC 5539372. PMID 27807201.
Alders M, Christiaans I (1993-01-01). "Long QT Syndrome". In Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJ, Bird TD, Ledbetter N, Mefford HC (eds.). GeneReviews. Seattle (WA): University of Washington, Seattle. PMID 20301308. Archived from the original on 2017-01-28. Retrieved 2017-09-11.update 2015
Priori SG, Blomström-Lundqvist C, Mazzanti A, Blom N, Borggrefe M, Camm J, et al. (Task Force for the Management of Patients with Ventricular Arrhythmias the Prevention of Sudden Cardiac Death of the European Society of Cardiology (ESC)) (November 2015). "2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: The Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of the European Society of Cardiology (ESC)Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC)". Europace. 17 (11): 1601–1687. doi:10.1093/europace/euv319. PMID 26318695.
Nakajima T, Kaneko Y, Kurabayashi M (2015). "Unveiling specific triggers and precipitating factors for fatal cardiac events in inherited arrhythmia syndromes". Circulation Journal. 79 (6): 1185–1192. doi:10.1253/circj.CJ-15-0322. PMID 25925977.
Giudicessi JR, Wilde AA, Ackerman MJ (October 2018). "The genetic architecture of long QT syndrome: A critical reappraisal". Trends in Cardiovascular Medicine. 28 (7): 453–464. doi:10.1016/j.tcm.2018.03.003. PMC 6590899. PMID 29661707.
Huang H, Kuenze G, Smith JA, Taylor KC, Duran AM, Hadziselimovic A, et al. (March 2018). "Mechanisms of KCNQ1 channel dysfunction in long QT syndrome involving voltage sensor domain mutations". Science Advances. 4 (3): eaar2631. Bibcode:2018SciA....4.2631H. doi:10.1126/sciadv.aar2631. PMC 5842040. PMID 29532034.
Demirbilek H, Galcheva S, Vuralli D, Al-Khawaga S, Hussain K (May 2019). "Ion Transporters, Channelopathies, and Glucose Disorders". International Journal of Molecular Sciences. 20 (10): 2590. doi:10.3390/ijms20102590. PMC 6566632. PMID 31137773.
Giudicessi JR, Ackerman MJ (October 2013). "Genotype- and phenotype-guided management of congenital long QT syndrome". Current Problems in Cardiology. 38 (10): 417–455. doi:10.1016/j.cpcardiol.2013.08.001. PMC 3940076. PMID 24093767.
Giudicessi JR, Wilde AA, Ackerman MJ (October 2018). "The genetic architecture of long QT syndrome: A critical reappraisal". Trends in Cardiovascular Medicine. 28 (7): 453–464. doi:10.1016/j.tcm.2018.03.003. PMC 6590899. PMID 29661707.
Li G, Zhang L (November 2018). "The role of mexiletine in the management of long QT syndrome". Journal of Electrocardiology. 51 (6): 1061–1065. doi:10.1016/j.jelectrocard.2018.08.035. PMID 30497731. S2CID 54167081.

ncbi.nlm.nih.gov

Bohnen MS, Peng G, Robey SH, Terrenoire C, Iyer V, Sampson KJ, Kass RS (January 2017). "Molecular Pathophysiology of Congenital Long QT Syndrome". Physiological Reviews. 97 (1): 89–134. doi:10.1152/physrev.00008.2016. PMC 5539372. PMID 27807201.
Alders M, Christiaans I (1993-01-01). "Long QT Syndrome". In Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJ, Bird TD, Ledbetter N, Mefford HC (eds.). GeneReviews. Seattle (WA): University of Washington, Seattle. PMID 20301308. Archived from the original on 2017-01-28. Retrieved 2017-09-11.update 2015
Giudicessi JR, Wilde AA, Ackerman MJ (October 2018). "The genetic architecture of long QT syndrome: A critical reappraisal". Trends in Cardiovascular Medicine. 28 (7): 453–464. doi:10.1016/j.tcm.2018.03.003. PMC 6590899. PMID 29661707.
Huang H, Kuenze G, Smith JA, Taylor KC, Duran AM, Hadziselimovic A, et al. (March 2018). "Mechanisms of KCNQ1 channel dysfunction in long QT syndrome involving voltage sensor domain mutations". Science Advances. 4 (3): eaar2631. Bibcode:2018SciA....4.2631H. doi:10.1126/sciadv.aar2631. PMC 5842040. PMID 29532034.
Demirbilek H, Galcheva S, Vuralli D, Al-Khawaga S, Hussain K (May 2019). "Ion Transporters, Channelopathies, and Glucose Disorders". International Journal of Molecular Sciences. 20 (10): 2590. doi:10.3390/ijms20102590. PMC 6566632. PMID 31137773.
Giudicessi JR, Ackerman MJ (October 2013). "Genotype- and phenotype-guided management of congenital long QT syndrome". Current Problems in Cardiology. 38 (10): 417–455. doi:10.1016/j.cpcardiol.2013.08.001. PMC 3940076. PMID 24093767.
Giudicessi JR, Wilde AA, Ackerman MJ (October 2018). "The genetic architecture of long QT syndrome: A critical reappraisal". Trends in Cardiovascular Medicine. 28 (7): 453–464. doi:10.1016/j.tcm.2018.03.003. PMC 6590899. PMID 29661707.
"ANK2 ankyrin 2 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Archived from the original on 2018-09-07. Retrieved 2017-04-06.
"KCNE1 potassium voltage-gated channel subfamily E regulatory subunit 1 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Archived from the original on 2018-09-07. Retrieved 2017-04-06.
"KCNE2 potassium voltage-gated channel subfamily E regulatory subunit 2 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Archived from the original on 2016-10-11. Retrieved 2017-04-06.

ghr.nlm.nih.gov

"Romano-Ward syndrome". Genetics Home Reference. Archived from the original on 2017-04-01. Retrieved 2017-04-01.

rarediseases.info.nih.gov

"Long QT syndrome 1 | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Archived from the original on 2018-04-18. Retrieved 2018-04-17.

orpha.net

"Orphanet: Romano Ward syndrome". www.orpha.net. Archived from the original on 2017-04-02. Retrieved 2017-04-01.

semanticscholar.org

api.semanticscholar.org

Li G, Zhang L (November 2018). "The role of mexiletine in the management of long QT syndrome". Journal of Electrocardiology. 51 (6): 1061–1065. doi:10.1016/j.jelectrocard.2018.08.035. PMID 30497731. S2CID 54167081.

web.archive.org

"Romano-Ward syndrome". Genetics Home Reference. Archived from the original on 2017-04-01. Retrieved 2017-04-01.
"Orphanet: Romano Ward syndrome". www.orpha.net. Archived from the original on 2017-04-02. Retrieved 2017-04-01.
"Long QT syndrome 1 | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Archived from the original on 2018-04-18. Retrieved 2018-04-17.
Alders M, Christiaans I (1993-01-01). "Long QT Syndrome". In Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJ, Bird TD, Ledbetter N, Mefford HC (eds.). GeneReviews. Seattle (WA): University of Washington, Seattle. PMID 20301308. Archived from the original on 2017-01-28. Retrieved 2017-09-11.update 2015
"ANK2 ankyrin 2 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Archived from the original on 2018-09-07. Retrieved 2017-04-06.
"KCNE1 potassium voltage-gated channel subfamily E regulatory subunit 1 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Archived from the original on 2018-09-07. Retrieved 2017-04-06.
"KCNE2 potassium voltage-gated channel subfamily E regulatory subunit 2 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Archived from the original on 2016-10-11. Retrieved 2017-04-06.