Genomic risk factors in sudden infant death syndrome

Por Van Norstrand, David W, Ackerman, Michael J
Publicado em 2010

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

Por Van Norstrand, David W., Ackerman, Michael J.
Publicado em 2008

Over-Representation of the Pro-Arrhythmic, Sudden Death Predisposing Sodium Channel Polymorphism, S1103Y, in a Population-Based Cohort of African American Sudden Infant Death Syndr...

Por Van Norstrand, David W., Tester, David J., Ackerman, Michael J.
Publicado em 2008

Molecular and Functional Characterization of Novel Glycerol-3-Phosphate Dehydrogenase 1–Like Gene (GPD1-L) Mutations in Sudden Infant Death Syndrome

Por Van Norstrand, David W., Valdivia, Carmen R., Tester, David J., Ueda, Kazuo, London, Barry, Makielski, Jonathan C., Ackerman, Michael J.
Publicado em 2007

Connexin43 Mutation Causes Heterogeneous Gap Junction Loss and Sudden Infant Death

Por Van Norstrand, David W., Asimaki, Angeliki, Rubinos, Clio, Dolmatova, Elena, Srinivas, Miduturu, Tester, David J., Saffitz, Jeffrey E., Duffy, Heather S., Ackerman, Michael J.
Publicado em 2011

Sudden Infant Death Syndrome-Associated Mutations in the Sodium Channel Beta Subunits

Por Tan, Bi-Hua, Pundi, Kavitha N, Van Norstrand, David W, Valdivia, Carmen R, Tester, David J, Medeiros-Domingo, Argelia, Makielski, Jonathan C., Ackerman, Michael J.
Publicado em 2010

α1-Syntrophin Mutations Identified in Sudden Infant Death Syndrome Cause an Increase in Late Cardiac Sodium Current

Por Cheng, Jianding, Van Norstrand, David W., Medeiros-Domingo, Argelia, Valdivia, Carmen, Tan, Bi-hua, Ye, Bin, Kroboth, Stacie, Vatta, Matteo, Tester, David J., January, Craig T., Makielski, Jonathan C., Ackerman, Michael J.
Publicado em 2009