Literature DB >> 11986566

The molecular basis of cardiac arrhythmias.

Kalyanam Shivkumar1, Narayana S Murali, Subramaniam C Krishnan.   

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Year:  2002        PMID： 11986566     DOI： 10.1067/mnc.2002.122763

Source DB:  PubMed          Journal:  J Nucl Cardiol        ISSN： 1071-3581            Impact factor:   5.952


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  29 in total

1.  Increased vulnerability of the subendocardium to ischaemic injury: an electrophysiological explanation.

Authors:  S C Krishnan; K Shivkumar; H Garan; J N Ruskin
Journal:  Lancet       Date:  1995-12-16       Impact factor: 79.321

2.  Actin mutations in dilated cardiomyopathy, a heritable form of heart failure.

Authors:  T M Olson; V V Michels; S N Thibodeau; Y S Tai; M T Keating
Journal:  Science       Date:  1998-05-01       Impact factor: 47.728

3.  Identification of a gene responsible for familial Wolff-Parkinson-White syndrome.

Authors:  M H Gollob; M S Green; A S Tang; T Gollob; A Karibe; A S Ali Hassan ; F Ahmad; R Lozado; G Shah; L Fananapazir; L L Bachinski; R Roberts; A S Hassan
Journal:  N Engl J Med       Date:  2001-06-14       Impact factor: 91.245

4.  Arrhythmogenic marker for the sudden unexplained death syndrome in Thai men.

Authors:  K Nademanee; G Veerakul; S Nimmannit; V Chaowakul; K Bhuripanyo; K Likittanasombat; K Tunsanga; S Kuasirikul; P Malasit; S Tansupasawadikul; P Tatsanavivat
Journal:  Circulation       Date:  1997-10-21       Impact factor: 29.690

Review 5.  Molecular biology and the prolonged QT syndromes.

Authors:  J A Towbin; M Vatta
Journal:  Am J Med       Date:  2001-04-01       Impact factor: 4.965

Review 6.  Calcium-induced release of calcium from the cardiac sarcoplasmic reticulum.

Authors:  A Fabiato
Journal:  Am J Physiol       Date:  1983-07

7.  Genetically defined therapy of inherited long-QT syndrome. Correction of abnormal repolarization by potassium.

Authors:  S J Compton; R L Lux; M R Ramsey; K R Strelich; M C Sanguinetti; L S Green; M T Keating; J W Mason
Journal:  Circulation       Date:  1996-09-01       Impact factor: 29.690

8.  Right ventricular outflow tract tachycardia due to a somatic cell mutation in G protein subunitalphai2.

Authors:  B B Lerman; B Dong; K M Stein; S M Markowitz; J Linden; D F Catanzaro
Journal:  J Clin Invest       Date:  1998-06-15       Impact factor: 14.808

9.  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

10.  Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.

Authors:  P J Schwartz; S G Priori; E H Locati; C Napolitano; F Cantù; J A Towbin; M T Keating; H Hammoude; A M Brown; L S Chen; T J Colatsky
Journal:  Circulation       Date:  1995-12-15       Impact factor: 29.690
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  1 in total

1.  Gene-specific paradoxical QT responses during rapid eye movement sleep in women with congenital long QT syndrome.

Authors:  Paola A Lanfranchi; Michael J Ackerman; Tomas Kara; Abu S M Shamsuzzaman; Robert Wolk; Pavel Jurak; Raouf Amin; Virend K Somers
Journal:  Heart Rhythm       Date:  2010-05-12       Impact factor: 6.343
  1 in total

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