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Results: 1-13 |
Results: 13
Molecular autopsy of sudden unexplained death in the young
Authors: Ackerman, MJ Tester, DJ Driscoll, DJ
Citation: Mj. Ackerman et al., Molecular autopsy of sudden unexplained death in the young, AM J FOREN, 22(2), 2001, pp. 105-111
Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome
Authors: Ackerman, MJ Siu, BL Sturner, WQ Tester, DJ Valdivia, CR Makielski, JC Towbin, JA
Citation: Mj. Ackerman et al., Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome, J AM MED A, 286(18), 2001, pp. 2264-2269
Diagnostic accuracy of screening electrocardiograms in long QT syndrome I
Authors: Miller, MD Porter, CJ Ackerman, MJ
Citation: Md. Miller et al., Diagnostic accuracy of screening electrocardiograms in long QT syndrome I, PEDIATRICS, 108(1), 2001, pp. NIL_120-NIL_124
Pulmonary atresia with ventricular septal defect and persistent airway hyperresponsiveness
Authors: Ackerman, MJ Wylam, ME Feldt, RH Porter, CJ Dewald, G Scanlon, PD Driscoll, DJ
Citation: Mj. Ackerman et al., Pulmonary atresia with ventricular septal defect and persistent airway hyperresponsiveness, J THOR SURG, 122(1), 2001, pp. 169-177
Cardiac sodium channel gene mutations and sudden infant death syndrome - Confirmation of proof of concept?
Authors: Towbin, JA Ackerman, MJ
Citation: Ja. Towbin et Mj. Ackerman, Cardiac sodium channel gene mutations and sudden infant death syndrome - Confirmation of proof of concept?, CIRCULATION, 104(10), 2001, pp. 1092-1093
Imaging outcomes from the National Library of Medicine's Visible Human Project (R)
Authors: Ackerman, MJ Banvard, RA
Citation: Mj. Ackerman et Ra. Banvard, Imaging outcomes from the National Library of Medicine's Visible Human Project (R), COMP MED IM, 24(3), 2000, pp. 125-126
The long-QT syndrome. Reply
Authors: Ackerman, MJ Porter, CJ
Citation: Mj. Ackerman et Cj. Porter, The long-QT syndrome. Reply, N ENG J MED, 342(7), 2000, pp. 515-515
Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy
Authors: Olson, TM Doan, TP Kishimoto, NY Whitby, FG Ackerman, MJ Fananapazir, L
Citation: Tm. Olson et al., Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy, J MOL CEL C, 32(9), 2000, pp. 1687-1694
Electronics and health care revisited: Thirty-eight years later
Authors: Ackerman, MJ
Citation: Mj. Ackerman, Electronics and health care revisited: Thirty-eight years later, P IEEE, 88(5), 2000, pp. 706-707
The Visible Human Project (R): A resource for education
Authors: Ackerman, MJ
Citation: Mj. Ackerman, The Visible Human Project (R): A resource for education, ACAD MED, 74(6), 1999, pp. 667-670
Molecular diagnosis of the inherited long-QT syndrome in a woman who died after near-drowning
Authors: Ackerman, MJ Tester, DJ Porter, CJ Edwards, WD
Citation: Mj. Ackerman et al., Molecular diagnosis of the inherited long-QT syndrome in a woman who died after near-drowning, N ENG J MED, 341(15), 1999, pp. 1121-1125
Swimming, a gene-specific arrhythmogenic trigger for inherited long QT syndrome
Authors: Ackerman, MJ Tester, DJ Porter, CJ
Citation: Mj. Ackerman et al., Swimming, a gene-specific arrhythmogenic trigger for inherited long QT syndrome, MAYO CLIN P, 74(11), 1999, pp. 1088-1094
Custody evaluation practices: A survey of experienced professionals (revisited) (vol 28, pg 137, 1997)
Authors: Ackerman, MJ Ackerman, MC
Citation: Mj. Ackerman et Mc. Ackerman, Custody evaluation practices: A survey of experienced professionals (revisited) (vol 28, pg 137, 1997), FAM LAW Q, 33(3), 1999, pp. VII-VII
Risultati: 1-13 |