Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Sharon Edman"'
Autor:
Thanh T. Hoang, Paulo Henrique Manso, Sharon Edman, Laura Mercer-Rosa, Laura E. Mitchell, Anshuman Sewda, Michael D. Swartz, Mark A. Fogel, A. J. Agopian, Elizabeth Goldmuntz
Publikováno v:
Journal of Cardiovascular Magnetic Resonance, Vol 21, Iss 1, Pp 1-10 (2019)
Abstract Background Studies suggest that right ventricular (RV) fibrosis is associated with RV remodeling and long-term outcomes in patients with tetralogy of Fallot (TOF). Pre-operative hypoxia may increase expression of hypoxia inducible factor-1-a
Externí odkaz:
https://doaj.org/article/332f7a2ac8004734b36b89f90eb6cda8
Autor:
Thanh T Hoang, Elizabeth Goldmuntz, Amy E Roberts, Wendy K Chung, Jennie K Kline, John E Deanfield, Alessandro Giardini, Adolfo Aleman, Bruce D Gelb, Meghan Mac Neal, George A Porter, Richard Kim, Martina Brueckner, Richard P Lifton, Sharon Edman, Stacy Woyciechowski, Laura E Mitchell, A J Agopian
Publikováno v:
PLoS ONE, Vol 13, Iss 1, p e0191319 (2018)
The Pediatric Cardiac Genomics Consortium (PCGC) designed the Congenital Heart Disease Genetic Network Study to provide phenotype and genotype data for a large congenital heart defects (CHDs) cohort. This article describes the PCGC cohort, overall an
Externí odkaz:
https://doaj.org/article/5c89952bd9834bd483cf3a56b9537a9f
Autor:
Sharon Edman, Daniel E. McGinn, Donna M. McDonald-McGinn, Chiara Pandolfi de Rinaldis, Alice Bailey, Shrey Patel, Elizabeth Goldmuntz, Adam Butensky, T. Blaine Crowley, Jungwon Min, Elaine H. Zackai, Melissa Wasserman
Publikováno v:
Pediatric Cardiology. 42:1594-1600
Aortic root dilation (ARD) has been reported in patients with 22q11.2 deletion syndrome (22q11.2DS) with and without congenital heart defects (CHDs). However, the long-term implications of isolated ARD in 22q11.2DS remain undefined. In this study, we
Autor:
Cgc, T. Blaine Crowley, Elizabeth Goldmuntz, Jungwon Min, Elaine H. Zackai, Donna M. McDonald-McGinn, Shrey Patel, Sharon Edman, Daniel E. McGinn, Adam M. Butensky, Alice Bailey, Chiara Pandolfi de Rinaldis
Publikováno v:
Section on Cardiology and Cardiac Surgery Program.
Background: The 22q11.2 duplication syndrome (22q11.2DupS) has been diagnosed more frequently with the advent of microarray technology. Given that it disrupts the same region as the more familiar 22q11.2 deletion syndrome (22q11.2DS), patients with t
Autor:
Chiara Pandolfi, de Rinaldis, Adam, Butensky, Shrey, Patel, Sharon, Edman, Melissa, Wasserman, Daniel E, McGinn, Alice, Bailey, Elaine H, Zackai, T Blaine, Crowley, Donna M, McDonald-McGinn, Jungwon, Min, Elizabeth, Goldmuntz
Publikováno v:
Pediatric cardiology. 42(7)
Aortic root dilation (ARD) has been reported in patients with 22q11.2 deletion syndrome (22q11.2DS) with and without congenital heart defects (CHDs). However, the long-term implications of isolated ARD in 22q11.2DS remain undefined. In this study, we
Autor:
Shrey Patel, Donna M. McDonald-McGinn, T. Blaine Crowley, Daniel E. McGinn, Alice Bailey, Sharon Edman, Jungwon Min, Adam Butensky, Chiara Pandolfi de Rinaldis, Elizabeth Goldmuntz, Elaine H. Zackai
Publikováno v:
American journal of medical genetics. Part AREFERENCES. 185(3)
The 22q11.2 duplication syndrome (22q11.2DupS) is characterized by phenotypic heterogeneity, from seemingly asymptomatic to severely affected patients. Our study sought to detail the cardiac phenotype associated with 22q11.2DupS, the prevalence of ao
Autor:
Cgc, Alice Bailey, T. Blaine Crowley, Donna M. McDonald-McGinn, Chiara Pandolfi de Rinaldis, Elizabeth Goldmuntz, Jungwon Min, Elaine H. Zackai, Adam M. Butensky, Sharon Edman, Melissa Wasserman, Shrey Patel, Daniel E. McGinn
Publikováno v:
Pediatrics. 147:378-379
Background: Aortic root dilation (ARD) has been reported in patients with 22q11.2 deletion syndrome (22q11.2DS) with and without congenital heart defects (CHDs). The long-term implications of ARD in 22q11.2DS are unknown and thus the timing and neces
Autor:
Mark A. Fogel, A. J. Agopian, Elizabeth Goldmuntz, Sharon Edman, Thanh T. Hoang, Laura Mercer-Rosa, Michael D. Swartz, Paulo Henrique Manso, Laura E. Mitchell, Anshuman Sewda
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Journal of Cardiovascular Magnetic Resonance
Journal of Cardiovascular Magnetic Resonance, Vol 21, Iss 1, Pp 1-10 (2019)
Universidade de São Paulo (USP)
instacron:USP
Journal of Cardiovascular Magnetic Resonance
Journal of Cardiovascular Magnetic Resonance, Vol 21, Iss 1, Pp 1-10 (2019)
Background Studies suggest that right ventricular (RV) fibrosis is associated with RV remodeling and long-term outcomes in patients with tetralogy of Fallot (TOF). Pre-operative hypoxia may increase expression of hypoxia inducible factor-1-alpha (HIF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c94699109cfbc069a617bbfd65e8c8fe
Autor:
Philip J. Lupo, Elizabeth Goldmuntz, Stacy Woyciechowski, Jennifer Garbarini, Laura E. Mitchell, Sharon Edman, Shabnam Peyvandi, Beverly S. Emanuel
Publikováno v:
Pediatric cardiology, vol 34, iss 7
The 22q11.2 deletion syndrome is characterized by multiple congenital anomalies including conotruncal cardiac defects. Identifying the patient with a 22q11.2 deletion (22q11del) can be challenging because many extracardiac features become apparent la
Autor:
Adolfo Aleman, Bruce D. Gelb, Jennie Kline, Richard P. Lifton, John E. Deanfield, Alessandro Giardini, Thanh T. Hoang, Wendy K. Chung, Elizabeth Goldmuntz, Martina Brueckner, Stacy Woyciechowski, Sharon Edman, George A. Porter, Richard B. Kim, Meghan K Mac Neal, A. J. Agopian, Laura E. Mitchell, Amy E. Roberts
Publikováno v:
PLoS ONE, Vol 13, Iss 1, p e0191319 (2018)
PLoS ONE
PLoS ONE
The Pediatric Cardiac Genomics Consortium (PCGC) designed the Congenital Heart Disease Genetic Network Study to provide phenotype and genotype data for a large congenital heart defects (CHDs) cohort. This article describes the PCGC cohort, overall an