Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Amy Marzolf"'
Autor:
Nosheen Reza, Alejandro de Feria, Jessica L. Chowns, Lily Hoffman-Andrews, Laura Vann, Jessica Kim, Amy Marzolf, Anjali Tiku Owens
Publikováno v:
Cardiogenetics, Vol 12, Iss 1, Pp 24-36 (2022)
Background: Variants in the desmoplakin (DSP) gene have been recognized in association with the pathogenesis of arrhythmogenic right ventricular cardiomyopathy (ARVC) for nearly 20 years. More recently, genetic variation in DSP has also been associat
Externí odkaz:
https://doaj.org/article/104626092b524d00a0d0bdb5b23ac303
Autor:
Nosheen Reza, MD, Alejandro De Feria, MD, Teresa Wang, MD, Jessica L. Chowns, CGC, Lily Hoffman-Andrews, CGC, Jessica Kim, BS, Nicole Hornsby, CRNP, Amy Marzolf, CRNP, Pavan Atluri, MD, Howard C. Herrmann, MD, Anjali Tiku Owens, MD
Publikováno v:
Transplantation Direct, Vol 8, Iss 1, p e1279 (2022)
Background. Hypertrophic cardiomyopathy (HCM) in pediatric solid organ transplant recipients has been reported in association with use of calcineurin inhibitors. However, data on the incidence and prevalence of HCM in adult posttransplant patients ar
Externí odkaz:
https://doaj.org/article/7bd983f034324074b31ed17e405b965d
Autor:
Nosheen Reza, Jessica L. Chowns, Amy Marzolf, Jessica Kim, Lisa D. Levine, Gregory Supple, Anjali Tiku Owens
Publikováno v:
Case Reports in Cardiology, Vol 2019 (2019)
Lamin A/C cardiac disease is a genetic cardiomyopathy and arrhythmia syndrome caused by alterations in the function of the nuclear lamin A and C proteins. It is inherited in an autosomal dominant manner and usually presents in mid- to late adulthood
Externí odkaz:
https://doaj.org/article/8dbdd10fb8604425bef37b4323af6f44
Autor:
Alyssa Ritter, Jacqueline Leonard, Christopher Gray, Kosuke Izumi, Katharine Levinson, Divya R. Nair, Matthew O'Connor, Joseph Rossano, Venkat Shankar, Jessica Chowns, Amy Marzolf, Anjali Owens, Rebecca C. Ahrens‐Nicklas
Publikováno v:
American Journal of Medical Genetics Part A. 188:2772-2776
Publikováno v:
Med Clin North Am
Many cardiovascular disorders have underlying genetic causes. Clinical genetic testing for cardiovascular disease has become widely available and can be useful for diagnosis, management, and cascade screening in selected conditions and circumstances.
Publikováno v:
Medical Clinics of North America. 106:313-324
Autor:
Nosheen Reza, Alejandro De Feria, Teresa Wang, Jessica Chowns, Lily Hoffman-Andrews, Jessica Kim, Nicole Hornsby, Amy Marzolf, Pavan Atluri, Howard C Herrmann, Anjali T Owens
Publikováno v:
Circulation. 144
Introduction: Data on the incidence and prevalence of HCM in adult post-transplant patients are limited. We describe the characteristics of adult solid organ transplant recipients diagnosed with HCM at a single center. Methods: Solid organ transplant
Autor:
Nosheen Reza, Alejandro De Feria, Teresa Wang, Jessica L. Chowns, Lily Hoffman-Andrews, Jessica Kim, Nicole Hornsby, Amy Marzolf, Pavan Atluri, Howard C. Herrmann, Anjali Tiku Owens
Publikováno v:
Transplantation Direct
Transplantation Direct, Vol 8, Iss 1, p e1279 (2022)
Transplantation Direct, Vol 8, Iss 1, p e1279 (2022)
Background. Hypertrophic cardiomyopathy (HCM) in pediatric solid organ transplant recipients has been reported in association with use of calcineurin inhibitors. However, data on the incidence and prevalence of HCM in adult posttransplant patients ar
Autor:
Bridget E. Shields, Jessica L. Chowns, Nosheen Reza, Anjali T. Owens, Amy Marzolf, Lily Hoffman-Andrews
Publikováno v:
Circ Genom Precis Med
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acdd0dbe2fdf354612bd436cb113d92e
https://europepmc.org/articles/PMC7583655/
https://europepmc.org/articles/PMC7583655/
Autor:
Jessica L. Chowns, Anjali T. Owens, Nosheen Reza, Lisa D. Levine, Jessica Kim, Amy Marzolf, Gregory E. Supple
Publikováno v:
Case Reports in Cardiology
Case Reports in Cardiology, Vol 2019 (2019)
Case Reports in Cardiology, Vol 2019 (2019)
Lamin A/C cardiac disease is a genetic cardiomyopathy and arrhythmia syndrome caused by alterations in the function of the nuclear lamin A and C proteins. It is inherited in an autosomal dominant manner and usually presents in mid- to late adulthood