Literature DB >> 18823823

Sudden infant death syndrome: do ion channels play a role?

David W Van Norstrand1, Michael J Ackerman.   

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Year:  2008        PMID： 18823823      PMCID： PMC3940066          DOI： 10.1016/j.hrthm.2008.07.028

Source DB:  PubMed          Journal:  Heart Rhythm        ISSN： 1547-5271            Impact factor:   6.343


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  58 in total

Review 1.  Cardiac sympathetic innervation and the sudden infant death syndrome. A possible pathogenetic link.

Authors:  P J Schwartz
Journal:  Am J Med       Date:  1976-02       Impact factor: 4.965

2.  Potential role of QT interval prolongation in sudden infant death syndrome.

Authors:  B J Maron; C E Clark; R E Goldstein; S E Epstein
Journal:  Circulation       Date:  1976-09       Impact factor: 29.690

Review 3.  Defining the sudden infant death syndrome.

Authors:  J Bruce Beckwith
Journal:  Arch Pediatr Adolesc Med       Date:  2003-03

4.  Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia.

Authors:  S G Priori; C Napolitano; N Tiso; M Memmi; G Vignati; R Bloise; V Sorrentino; G A Danieli
Journal:  Circulation       Date:  2001-01-16       Impact factor: 29.690

Review 5.  The long QT syndrome: ion channel diseases of the heart.

Authors:  M J Ackerman
Journal:  Mayo Clin Proc       Date:  1998-03       Impact factor: 7.616

6.  Mutations in the hminK gene cause long QT syndrome and suppress IKs function.

Authors:  I Splawski; M Tristani-Firouzi; M H Lehmann; M C Sanguinetti; M T Keating
Journal:  Nat Genet       Date:  1997-11       Impact factor: 38.330

7.  Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.

Authors:  Q Wang; M E Curran; I Splawski; T C Burn; J M Millholland; T J VanRaay; J Shen; K W Timothy; G M Vincent; T de Jager; P J Schwartz; J A Toubin; A J Moss; D L Atkinson; G M Landes; T D Connors; M T Keating
Journal:  Nat Genet       Date:  1996-01       Impact factor: 38.330

8.  Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report.

Authors:  P Brugada; J Brugada
Journal:  J Am Coll Cardiol       Date:  1992-11-15       Impact factor: 24.094

9.  SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome.

Authors:  Q Wang; J Shen; I Splawski; D Atkinson; Z Li; J L Robinson; A J Moss; J A Towbin; M T Keating
Journal:  Cell       Date:  1995-03-10       Impact factor: 41.582

10.  A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome.

Authors:  M E Curran; I Splawski; K W Timothy; G M Vincent; E D Green; M T Keating
Journal:  Cell       Date:  1995-03-10       Impact factor: 41.582
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  13 in total

Review 1.  Sodium channel β subunits: emerging targets in channelopathies.

Authors:  Heather A O'Malley; Lori L Isom
Journal:  Annu Rev Physiol       Date:  2015       Impact factor: 19.318

2.  Comparative proteome analysis for identification of differentially abundant proteins in SIDS.

Authors:  Noha El-Kashef; Iva Gomes; Katja Mercer-Chalmers-Bender; Peter M Schneider; Markus A Rothschild; Martin Juebner
Journal:  Int J Legal Med       Date:  2017-07-17       Impact factor: 2.686

3.  Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts.

Authors:  Christian Paludan-Müller; Jonas Ghouse; Oliver B Vad; Cecilie B Herfelt; Pia Lundegaard; Gustav Ahlberg; Nicole Schmitt; Jesper H Svendsen; Stig Haunsø; Henning Bundgaard; Torben Hansen; Jørgen K Kanters; Morten S Olesen
Journal:  Eur J Hum Genet       Date:  2019-05-01       Impact factor: 4.246

Review 4.  Sudden infant death syndrome caused by cardiac arrhythmias: only a matter of genes encoding ion channels?

Authors:  Georgia Sarquella-Brugada; Oscar Campuzano; Sergi Cesar; Anna Iglesias; Anna Fernandez; Josep Brugada; Ramon Brugada
Journal:  Int J Legal Med       Date:  2016-02-12       Impact factor: 2.686

Review 5.  Role of congenital long-QT syndrome in unexplained sudden infant death: proposal for an electrocardiographic screening in relatives.

Authors:  Alban-Elouen Baruteau; Julien Baruteau; Ryad Joomye; Raphael Martins; Frédéric Treguer; Remi Baruteau; Jean-Claude Daubert; Philippe Mabo; Michel Roussey
Journal:  Eur J Pediatr       Date:  2009-03-06       Impact factor: 3.183

6.  Long QT syndrome-associated mutations in intrauterine fetal death.

Authors:  Lia Crotti; David J Tester; Wendy M White; Daniel C Bartos; Roberto Insolia; Alessandra Besana; Jennifer D Kunic; Melissa L Will; Ellyn J Velasco; Jennifer J Bair; Alice Ghidoni; Irene Cetin; Daniel L Van Dyke; Myra J Wick; Brian Brost; Brian P Delisle; Fabio Facchinetti; Alfred L George; Peter J Schwartz; Michael J Ackerman
Journal:  JAMA       Date:  2013-04-10       Impact factor: 56.272

Review 7.  Voltage-Gated Sodium Channel β Subunits and Their Related Diseases.

Authors:  Alexandra A Bouza; Lori L Isom
Journal:  Handb Exp Pharmacol       Date:  2018

8.  Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome.

Authors:  David J Tester; Leonie C H Wong; Pritha Chanana; Belinda Gray; Amie Jaye; Jared M Evans; Margaret Evans; Peter Fleming; Iona Jeffrey; Marta Cohen; Jacob Tfelt-Hansen; Michael A Simpson; Elijah R Behr; Michael J Ackerman
Journal:  J Pediatr       Date:  2018-09-26       Impact factor: 4.406

9.  Sudden infant death syndrome in Korea: a retrospective analysis of autopsy-diagnosed cases.

Authors:  Seong Ho Yoo; Angela Julie Kim; Shin-Mong Kang; Han Young Lee; Joong-Seok Seo; Tae Jung Kwon; Kyung-Moo Yang
Journal:  J Korean Med Sci       Date:  2013-03-04       Impact factor: 2.153

10.  Cardiac ion channelopathies and the sudden infant death syndrome.

Authors:  Ronald Wilders
Journal:  ISRN Cardiol       Date:  2012-12-05
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