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Results: 1 to 20 of 119

1.

Cardiac channelopathies and sudden infant death syndrome.

Tfelt-Hansen J, Winkel BG, Grunnet M, Jespersen T.

Cardiology. 2011;119(1):21-33. Epub 2011 Jul 16. Review.

PMID:: 21778721; [PubMed - indexed for MEDLINE]

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2.

Sudden cardiac death in children and adolescents (excluding Sudden Infant Death Syndrome).

Gajewski KK, Saul JP.

Ann Pediatr Cardiol. 2010 Jul;3(2):107-12.

PMID:: 21234187; [PubMed]

Free PMC Article

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3.

Cardiac ion channel mutations in the sudden infant death syndrome.

Klaver EC, Versluijs GM, Wilders R.

Int J Cardiol. 2011 Oct 20;152(2):162-70. Epub 2011 Jan 6. Review.

PMID:: 21215473; [PubMed - indexed for MEDLINE]

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4.

Genetics of the sudden infant death syndrome.

Courts C, Madea B.

Forensic Sci Int. 2010 Dec 15;203(1-3):25-33. Epub 2010 Aug 2.

PMID:: 20674198; [PubMed - indexed for MEDLINE]

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5.

Gene variants predisposing to SIDS: current knowledge.

Opdal SH, Rognum TO.

Forensic Sci Med Pathol. 2011 Mar;7(1):26-36. Epub 2010 Jul 11. Review.

PMID:: 20623341; [PubMed - indexed for MEDLINE]

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6.

Repolarization abnormalities in the newborn.

Schwartz PJ, Stramba-Badiale M.

J Cardiovasc Pharmacol. 2010 Jun;55(6):539-43. Review.

PMID:: 20555231; [PubMed - indexed for MEDLINE]

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7.

Sudden infant death syndrome-associated mutations in the sodium channel beta subunits.

Tan BH, Pundi KN, Van Norstrand DW, Valdivia CR, Tester DJ, Medeiros-Domingo A, Makielski JC, Ackerman MJ.

Heart Rhythm. 2010 Jun;7(6):771-8. Epub 2010 Feb 1.

PMID:: 20226894; [PubMed - indexed for MEDLINE]

Free PMC Article

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8.

A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death.

Nof E, Cordeiro JM, Pérez GJ, Scornik FS, Calloe K, Love B, Burashnikov E, Caceres G, Gunsburg M, Antzelevitch C.

Circ Cardiovasc Genet. 2010 Apr;3(2):199-206. Epub 2010 Feb 24.

PMID:: 20181576; [PubMed - indexed for MEDLINE]

Free PMC Article

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9.

Cardiac sodium channelopathies.

Amin AS, Asghari-Roodsari A, Tan HL.

Pflugers Arch. 2010 Jul;460(2):223-37. Epub 2009 Nov 29. Review.

PMID:: 20091048; [PubMed - indexed for MEDLINE]

Free PMC Article

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10.

Human voltage-gated sodium channel mutations that cause inherited neuronal and muscle channelopathies increase resurgent sodium currents.

Jarecki BW, Piekarz AD, Jackson JO 2nd, Cummins TR.

J Clin Invest. 2010 Jan;120(1):369-78. doi: 10.1172/JCI40801. Epub 2009 Dec 28.

PMID:: 20038812; [PubMed - indexed for MEDLINE]

Free PMC Article

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11.

Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current.

Cheng J, Van Norstrand DW, Medeiros-Domingo A, Valdivia C, Tan BH, Ye B, Kroboth S, Vatta M, Tester DJ, January CT, Makielski JC, Ackerman MJ.

Circ Arrhythm Electrophysiol. 2009 Dec;2(6):667-76. Epub .

PMID:: 20009079; [PubMed - indexed for MEDLINE]

Free PMC Article

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12.

Cardiomyopathies--misdiagnosed as Sudden Infant Death Syndrome (SIDS).

Dettmeyer RB, Kandolf R.

Forensic Sci Int. 2010 Jan 30;194(1-3):e21-4.

PMID:: 19931342; [PubMed - indexed for MEDLINE]

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13.

The role of genetic testing in paediatric syndromes of sudden death: state of the art and future considerations.

McCormack J.

Cardiol Young. 2009 Nov;19 Suppl 2:54-65. Review. No abstract available.

PMID:: 19857351; [PubMed - indexed for MEDLINE]

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14.

GPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5A.

Valdivia CR, Ueda K, Ackerman MJ, Makielski JC.

Am J Physiol Heart Circ Physiol. 2009 Oct;297(4):H1446-52. Epub 2009 Aug 7.

PMID:: 19666841; [PubMed - indexed for MEDLINE]

Free PMC Article

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15.

Electrocardiogram screening of infants for long QT syndrome: survey of pediatric cardiologists in North America.

Chang RK, Rodriguez S, Gurvitz MZ.

J Electrocardiol. 2010 Jan-Feb;43(1):4-7. Epub .

PMID:: 19665725; [PubMed - indexed for MEDLINE]

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16.

State of postmortem genetic testing known as the cardiac channel molecular autopsy in the forensic evaluation of unexplained sudden cardiac death in the young.

Ackerman MJ.

Pacing Clin Electrophysiol. 2009 Jul;32 Suppl 2:S86-9. Review.

PMID:: 19602172; [PubMed - indexed for MEDLINE]

Free PMC Article

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17.

Protein-protein interactions involving voltage-gated sodium channels: Post-translational regulation, intracellular trafficking and functional expression.

Shao D, Okuse K, Djamgoz MB.

Int J Biochem Cell Biol. 2009 Jul;41(7):1471-81. Epub 2009 Feb 2. Review.

PMID:: 19401147; [PubMed - indexed for MEDLINE]

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18.

Contribution of long-QT syndrome genetic variants in sudden infant death syndrome.

Millat G, Kugener B, Chevalier P, Chahine M, Huang H, Malicier D, Rodriguez-Lafrasse C, Rousson R.

Pediatr Cardiol. 2009 May;30(4):502-9. Epub 2009 Mar 26.

PMID:: 19322600; [PubMed - indexed for MEDLINE]

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19.

Biophysical characterization of a new SCN5A mutation S1333Y in a SIDS infant linked to long QT syndrome.

Huang H, Millat G, Rodriguez-Lafrasse C, Rousson R, Kugener B, Chevalier P, Chahine M.

FEBS Lett. 2009 Mar 4;583(5):890-6. Epub 2009 Feb 10.

PMID:: 19302788; [PubMed - indexed for MEDLINE]

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20.

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

Baruteau AE, Baruteau J, Joomye R, Martins R, Treguer F, Baruteau R, Daubert JC, Mabo P, Roussey M.

Eur J Pediatr. 2009 Jul;168(7):771-7. Epub 2009 Mar 6. Review.

PMID:: 19266217; [PubMed - indexed for MEDLINE]

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20 free full-text articles in PubMed Central

Sudden cardiac death in children and adolescents (excluding Sudden Infant Death Syndrome). [Ann Pediatr Cardiol. 2010]
Sudden cardiac death in children and adolescents (excluding Sudden Infant Death Syndrome).
Gajewski KK, Saul JP. Ann Pediatr Cardiol. 2010 Jul; 3(2):107-12.
Sudden infant death syndrome-associated mutations in the sodium channel beta subunits. [Heart Rhythm. 2010]
Sudden infant death syndrome-associated mutations in the sodium channel beta subunits.
Tan BH, Pundi KN, Van Norstrand DW, Valdivia CR, Tester DJ, Medeiros-Domingo A, Makielski JC, Ackerman MJ. Heart Rhythm. 2010 Jun; 7(6):771-8. Epub 2010 Feb 1.
A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death. [Circ Cardiovasc Genet. 2010]
A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death.
Nof E, Cordeiro JM, Pérez GJ, Scornik FS, Calloe K, Love B, Burashnikov E, Caceres G, Gunsburg M, Antzelevitch C. Circ Cardiovasc Genet. 2010 Apr; 3(2):199-206. Epub 2010 Feb 24.

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