Deletion of entire LMNA gene as a cause of cardiomyopathy

por Cirino, Allison L., Cuddy, Sarah, Lakdawala, Neal K.
Publicado 2020

Assessment of the Diagnostic Yield of Combined Cardiomyopathy and Arrhythmia Genetic Testing

por Dellefave-Castillo, Lisa M., Cirino, Allison L., Callis, Thomas E., Esplin, Edward D., Garcia, John, Hatchell, Kathryn E., Johnson, Britt, Morales, Ana, Regalado, Ellen, Rojahn, Susan, Vatta, Matteo, Nussbaum, Robert L., McNally, Elizabeth M.
Publicado 2022

The uptake of family screening in hypertrophic cardiomyopathy and an online video intervention to facilitate family communication

por Harris, Stephanie, Cirino, Allison L., Carr, Christina W., Tafessu, Hiwot M., Parmar, Siddharth, Greenberg, Jeffrey O., Szent‐Gyorgyi, Lara E., Ghazinouri, Roya, Glowny, Michelle G., McNeil, Kara, Kaynor, Efthalia F., Neumann, Catherine, Seidman, Christine E., MacRae, Calum A., Ho, Carolyn Y., Lakdawala, Neal K.
Publicado 2019

Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights From the Sarcomeric Human Cardiomyopathy Registry (SHaRe)

por Ho, Carolyn Y., Day, Sharlene M., Ashley, Euan A., Michels, Michelle, Pereira, Alexandre C., Jacoby, Daniel, Cirino, Allison L., Fox, Jonathan C., Lakdawala, Neal K., Ware, James S., Caleshu, Colleen A., Helms, Adam S., Colan, Steven D., Girolami, Francesca, Cecchi, Franco, Seidman, Christine E., Sajeev, Gautam, Signorovitch, James, Green, Eric M., Olivotto, Iacopo
Publicado 2018

Biomarkers of cardiovascular stress and fibrosis in preclinical hypertrophic cardiomyopathy

por Ho, Jennifer E, Shi, Ling, Day, Sharlene M, Colan, Steven D, Russell, Mark W, Towbin, Jeffrey A, Sherrid, Mark V, Canter, Charles E, Jefferies, John Lynn, Murphy, Anne, Taylor, Matthew, Mestroni, Luisa, Cirino, Allison L, Sleeper, Lynn A, Jarolim, Peter, Lopez, Begoña, Gonzalez, Arantxa, Diez, Javier, Orav, E John, Ho, Carolyn Y
Publicado 2017