Results 91 to 100 of about 43,523 (230)
Ibuprofen for Ductus Arteriosus Months after Birth
Ibuprofen is a well-known agent used to treat patent ductus arteriosus in preterm neonates in the first days of life. In the current case report we illustrate the potential use of ibuprofen in two preterm neonates 60 and 88 days after birth, respectively.
Odile Frauenfelder +3 more
doaj +1 more source
Ethnical variations in the incidence of congenital heart defects in Gorgan, Northern Iran: A single-center study [PDF]
Background: Congenital heart disease (CHD) is the most common congenital anomaly in newborns. This study was performed to determine the live birth incidence of CHD by ethnicity and sex in Gorgan, Northern Iran.
Golalipour, M.J. +4 more
core
Genetic Diagnoses Among Congenital Anomaly Cases in Europe: Data From the EUROCAT Network
ABSTRACT Background Surveillance of congenital anomaly prevalence over time can identify new teratogens. Anomalies with a genetic cause are excluded from the monitoring. Objectives We examined temporal changes in the proportion of genetic diagnoses among cases with a congenital anomaly.
Jorieke E. H. Bergman +23 more
wiley +1 more source
Tratamiento del ductus arterioso persistente en prematuros con ibuprofeno oral: metanalisis de la literatura [PDF]
Introducción El ductus arterioso persistente (DAP) es una de las complicaciones más frecuente en recién nacidos pretérmino (RNPT). Desde 1976 el uso de Indometacina para su cierre farmacológico ha cambiado el pronóstico en cuanto a morbimortalidad; sin ...
Coca Cifuentes, Isabel +3 more
core +1 more source
ABSTRACT A 12‐year‐old female spayed Border Collie dog was presented for evaluation of 6 months of intermittent hematuria and weight loss. A highly vascularized right renal mass deforming the renal architecture and paraneoplastic hypertrophic osteopathy were found. Cytologic evaluation of the mass obtained by fine‐needle aspiration guided by ultrasound
Félix Romero‐Vélez +7 more
wiley +1 more source
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim +9 more
wiley +1 more source
Heart Murmur in Neonates: How Often Is It Caused by Congenital Heart Disease [PDF]
Objective: Congenital heart disease (CHD) is the most common form of cardiovascular diseases in children. This study was performed from September 2006 to August 2007 in Ardebil, Westnorthern Iran.
انتشاری مقدم, افسانه +5 more
core
ABSTRACT The FGFR2 gene, encoding the FGFR2 protein, plays a crucial role in embryonic cell development, particularly in bone tissue. Bent Bone Dysplasia (BBD), FGFR2‐related (MIM# 614592), is a rare severe skeletal dysplasia characterized by craniofacial differences, reduced bone mineral density, and bowed long bones.
Cheyenne Bates +6 more
wiley +1 more source
Hemodynamic prediction in patent ductus arteriosus morphologies [PDF]
Patent ductus arteriosus (PDA) is a condition in which the ductus arteriosus remain opened after birth, causing the blood to shunt through from the aorta to the pulmonary artery.
Kori, M. I., Osman, K., Taib, I.
core
ABSTRACT The detailed anatomical situation of male stillborn cephalo‐thoracopagus twins in a wild ranging northern bat (Eptesicus nilssonii) is described by means of full body micro‐CT scans in high resolution with three‐dimensional computational reconstruction.
J. Meyer +5 more
wiley +1 more source

