Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Yvonne Paris"'
Autor:
Yvonne Paris, Olga H. Toro‐Salazar, Naomi S. Gauthier, Kathleen M. Rotondo, Lucy Arnold, Rose Hamershock, David E. Saudek, David R. Fulton, Ashley Renaud, Mark E. Alexander
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 5, Iss 2 (2016)
BackgroundPediatric syncope is common. Cardiac causes are rarely found. We describe and assess a pragmatic approach to these patients first seen by a pediatric cardiologist in the New England region, using Standardized Clinical Assessment and Managem
Externí odkaz:
https://doaj.org/article/b2fd7e6635b24854960cec4c20b354c9
Publikováno v:
Journal of Perinatology
Objective Evaluate predictors of successful PDA closure following acetaminophen treatment. Study design Retrospective cohort study of ≤30 weeks GA infants born from 1 January 2013–30 September 2019, and treated with single course acetaminophen by
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 33:2723-2729
Purpose: Patent ductus arteriosus (PDA) continues to be one of the most common complications associated with preterm birth. Up to 70% of infants born before 28 weeks gestational age may require som...
Publikováno v:
Pediatrics In Review. 30:39-46
Publikováno v:
Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography. 16(2)
Alstrom Syndrome is an extremely rare, autosomal recessive genetic disorder characterized by a group of signs and symptoms including infantile onset dilated cardiomyopathy, blindness, hearing impairment/loss, and obesity; with diabetes, and hepatic a
Autor:
Donna M. McDonald-McGinn, Deborah A. Driscoll, Lynn Bason, Katherine Christensen, David Lynch, Kathleen Sullivan, Douglas Canning, William Zavod, Norman Quinn, Jonathan Rome, Yvonne Paris, Paul Weinberg, Bernard J. Clark, Beverly S. Emanuel, Elaine H. Zackai
Publikováno v:
American journal of medical genetics. 59(1)
We report on a family with autosomal dominant paternally inherited "Opitz" GBBB syndrome and an additional case with findings which have been reported in that syndrome. In each case the propositus presented with a vascular ring. Since a vascular ring