Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Chiara Pandolfi de Rinaldis"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a717dd9ed0d0696c7edb13cabab226e
https://doi.org/10.1007/s00246-021-02645-7
https://doi.org/10.1007/s00246-021-02645-7
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2236f8ed80e7c329da387d6d3562100
https://doi.org/10.1542/peds.147.3_meetingabstract.405
https://doi.org/10.1542/peds.147.3_meetingabstract.405
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1689dca90c1ed4254524832eaebec131
https://pubmed.ncbi.nlm.nih.gov/34128123
https://pubmed.ncbi.nlm.nih.gov/34128123
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31bedde5c4682f1b473572f48e63b40b
https://pubmed.ncbi.nlm.nih.gov/33369133
https://pubmed.ncbi.nlm.nih.gov/33369133
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fbad29dd2c6ce2e72b1558acba59ea8
https://doi.org/10.1542/peds.147.3ma4.378
https://doi.org/10.1542/peds.147.3ma4.378