Results 41 to 50 of about 137,186 (203)
Concurrent validity and agreement of Bayley‐4, AIMS, and HINE assessments in 1‐year‐old children
In this cross‐sectional study of children around 1‐year‐old, the Bayley‐4 showed concurrent validity and moderate to substantial agreement with the AIMS and the HINE in both clinical and home settings. Abstract Aim To examine concurrent validity between the Bayley Scales of Infant and Toddler Development, Fourth Edition (Bayley‐4) gross motor subtest ...
Weiyang Deng +14 more
wiley +1 more source
Atresia do Esôfago: Análise de casos em seis anos. [PDF]
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina.
Machado, Thais Kroeff
core
Vocal rehabilitation with implantation of voice prosthesis has been recognized as one of the most popular intervention for patients after total laryngectomy.
Jakub Spałek +6 more
doaj +1 more source
Co‐Occurring Non‐Cardiac Congenital Anomalies Among Cases With Congenital Heart Defects
ABSTRACT Cases with congenital heart defects (CHD) often have other associated anomalies. The aim of this investigation was to assess the prevalence and the types of co‐occurring anomalies in CHD in a well‐defined population. The anomalies co‐occurring with CHD were ascertained in all live births, stillbirths and terminations of pregnancy for fetal ...
Claude Stoll +2 more
wiley +1 more source
Double balloon esophageal catheter for diagnosis of tracheo-esophageal fistula
Congenital H-type and recurrent tracheo-esophageal fistulas (TEF) are always difficult to diagnose. For a more accurate diagnosis we designed a new double balloon catheter, which is a modification of esophageal dilatation balloon.
KIYAN, GÜRSU
core +1 more source
Utility of 64-row MDCT in assessment of neonates with congenital EA and distal TEF
Introduction: Esophageal atresia (EA), with or without trachea-esophageal fistula (TEF), is one of the most challenging congenital anomalies in neonates, due to its high morbidity and mortality.
Hosam El-Deen Galal Mohamed El-Malah +3 more
doaj +1 more source
Genetic factors in esophageal atresia, tracheo-esophageal fistula and the VACTERL association: Roles for FOXF1 and the 16q24.1 FOX transcription factor gene cluster, and review of the literature [PDF]
Esophageal atresia with/without tracheo-esophageal fistula is a relatively common malformation, occurring in around 1 in 3500 births. In around half of cases, additional malformations are present, forming either a syndrome of known genetic aetiology, or ...
Shaw-Smith, Charles
core +1 more source
Congenital esophageal stenosis in 3 children: A case series
Congenital esophageal stenosis (CES) is rare condition found in 1 per 25,000 to 50,000 live births. It is characterized by intrinsic narrowing of the esophagus secondary to congenital malformation of the esophageal wall architecture.
Mackenzie C. Lees, Bryan J. Dicken
doaj +1 more source
ABSTRACT Port catheters provide a reliable, long‐term venous access option in children for repeated administration of medications or parenteral nutrition. A cardiac catheterization procedure was performed in a 7‐year‐old girl in whom lateral chest radiography revealed posterior deviation suggestive of azygos vein malposition.
Axel Rentzsch +3 more
wiley +1 more source
Weaning difficulty in a near hanging patient: An unusual cause
Suicidal hanging causes damage to the airways, neck blood vessels as well as soft tissue injuries. We report the development of tracheo-esophageal fistula in such a patient. Recurrent soiling of the airways and the resultant lung infection led to weaning
Animesh Ray +3 more
doaj +1 more source

