Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Raymond Morales"'
Autor:
Yolandee Bell-Cheddar, William A. Devine, Carlos-Eduardo Diaz-Castrillon, Laura Seese, Mario Castro-Medina, Raymond Morales, Christopher W. Follansbee, Tarek Alsaied, Jiuann-Huey I. Lin
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
This review article addresses the history, morphology, anatomy, medical management, and different surgical options for patients with double outlet right ventricle.
Externí odkaz:
https://doaj.org/article/5f85f091e0bc4c1893833141badc3982
Publikováno v:
Annals of Pediatric Cardiology, Vol 13, Iss 3, Pp 241-243 (2020)
Holt–Oram syndrome (HOS) (OMIM#142900) is a rare condition with upper extremity malformations as well as structural and conduction cardiac anomalies. There are sparse reports in the literature documenting malignancy in association with HOS. We repo
Externí odkaz:
https://doaj.org/article/f9c69c7a4236460bb1547fedb3a598c6
Publikováno v:
Cardiogenetics, Vol 10, Iss 1 (2020)
We report the first case of a 294 kb loss, notable for including the entirety of GPD1L, on chromosome 3p22.3—p24 in a 3-year-old girl with multiple congenital anomalies including absent left foot, single umbilical artery, bilateral vesico-ureteral
Externí odkaz:
https://doaj.org/article/14d3ef2af3984df8a0dd200ba06098a7
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e26903 (2011)
Topoisomerases play a fundamental role in genome stability, DNA replication and repair. As a result, topoisomerases have served as therapeutic targets of interest in Eukarya and Bacteria, two of the three domains of life. Since members of Archaea, th
Externí odkaz:
https://doaj.org/article/effa5ef5dcca4660b0710d6ae1961cf2
Autor:
Lamya Mubayed, Osama Eltayeb, Raymond Morales, John Bokowski, Hoang H. Nguyen, Marium Iqbal, Krishna Kishore Umapathi
Publikováno v:
Tex Heart Inst J
Congenital complete heart block is a potentially fatal complication that can occur in neonates whose mothers have autoimmune disorders; it has rarely been reported in the presence of Sjögren syndrome. Pacemaker implantation is recommended to treat r
Publikováno v:
Pediatric Cardiology. 41:1529-1531
Chiari network is an embryonic remnant of the right sinus venosus. It appears as a thin, fenestrated membrane attached to two or more regions within the right atrium. Usually, a Chiari network has a benign course; however, rare complications associat
Publikováno v:
Cardiogenetics, Vol 10, Iss 1 (2020)
Cardiogenetics
Volume 10
Issue 1
Cardiogenetics
Volume 10
Issue 1
We report the first case of a 294 kb loss, notable for including the entirety of GPD1L, on chromosome 3p22.3—p24 in a 3-year-old girl with multiple congenital anomalies including absent left foot, single umbilical artery, bilateral vesico-ureteral
Publikováno v:
Pediatric cardiology. 41(6)
Congenital coronary artery anomalies are estimated to affect about 1% of the general population. Hypoplastic coronary artery disease is an uncommon subset associated with significant mortality regardless whether another major cardiac anomaly is prese
Publikováno v:
Pediatric cardiology. 40(1)
An atrial septal aneurysm (ASA) is an increasingly recognized entity that involves septal tissue significantly bulging into either atria instead of remaining in a relatively neutral position. ASAs may be described based on the length of the segment o
Autor:
Lauren Rodriguez, Angad P. Singh, Lydia P Mendoza, Erin Stratta, Monica B. Vela, Raymond Morales, Melissa A. Valerio
Patients with limited English proficiency (LEP) may be at risk for medical errors and worse health outcomes. Language concordance between patient and provider has been shown to improve health outcomes for Spanish-speaking patients. Nearly 40 % of His
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b3a635362b0a8bc22464a4b8cf99eb6
https://europepmc.org/articles/PMC4579233/
https://europepmc.org/articles/PMC4579233/