Results 171 to 180 of about 73,086 (343)

Aortic arch malformations [PDF]

open access: yes, 2018
Although anomalies of the aortic arch and its branches are relatively uncommon malformations, they are often associated with congenital heart disease. Isolated lesions may be clinically significant when the airways are compromised by a vascular ring.
Kellenberger, Christian
core  

Association of Placebo, Indomethacin, Ibuprofen, and Acetaminophen With Closure of Hemodynamically Significant Patent Ductus Arteriosus in Preterm Infants: A Systematic Review and Meta-analysis

open access: yesJournal of the American Medical Association (JAMA), 2018
S. Mitra   +9 more
semanticscholar   +1 more source

Skin development in the gray short‐tailed opossum (Monodelphis domestica)—From skin respiration to thermoregulation

open access: yesJournal of Anatomy, Volume 247, Issue 1, Page 108-133, July 2025.
The skin development in the gray short‐tailed opossum (Monodelphis domestica) has been examined using histological, morphometric, and μCT methods. During a long period of postnatal development, the structural differentiation of the skin results in a functional shift from transcutaneous gas exchange to thermoregulation in later life. Abstract Marsupials
Kirsten Ferner
wiley   +1 more source

Patent ductus arteriosus in preterm infant: review of diagnosis and management [PDF]

open access: yes, 2014
A abordagem dos recém-nascidos prematuros (RNPT) constitui uma área de grandes avanços diagnósticos e terapêuticos. Entre as complicações associadas à prematuridade, destaca-se a patência do canal arterial (CA). O CA no RNPT tem sido objeto de inúmeros
Carapuço, C., Mota, C.
core  

De Novo Missense Variant in Bovine WDR33 Associated With a Complex Syndromic Form of Cleft Palate With Pentalogy of Fallot and Internal Hydrocephalus

open access: yesJournal of Veterinary Internal Medicine, Volume 39, Issue 4, July/August 2025.
ABSTRACT Background Cleft palate (CP) is a congenital defect characterized by an opening in the palate. Two crossbred paternal half‐sibs with a complex syndrome including CP were identified. Hypothesis/Objectives Characterize disease phenotype and evaluate the genetic cause of the observed syndrome.
Marilena Bolcato   +5 more
wiley   +1 more source

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