Results 251 to 260 of about 114,602 (311)

Hepatic blood flow velocity before and 3 months after Kasai portoenterostomy is a prognostic indicator for native liver survival in biliary atresia. [PDF]

Eur J Pediatr
Sabo J, Kolorz J, Schipper L, Selvamoorthy T, Gudayol IM, Hühne T, Hüsing A, Siaj R, Lainka E, Kampmann K, Prusinskas B, Franke D, Uecker M, Baumann U, Petersen C, Dingemann J, Berger M, Madadi-Sanjani O.   +17 more
europepmc   +1 more source

Giant Pulmonary Hamartoma in a Child: A Case Report

Journal of Paediatrics and Child Health, Volume 62, Issue 5, Page 869-873, May 2026.
Jurgen Schleef, Marianna Carbi, Valentina Kiren, Marco Rabusin, Sergio Ghirardo, Massimo Maschio, Egidio Barbi, Rossana Bussani, Claudio Granata, Anita Spezzacatene   +9 more
wiley   +1 more source

Management of Proximal Jejunal Atresia by Enterostomy with a Modified T-tube: A Comparative Clinical Study.

J Indian Assoc Pediatr Surg
Manohar DM, Anusiri I, Sharif MN, Rajesh M, Srinivas S, Rao CB.   +5 more
europepmc   +1 more source

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Intestinal Atresias

Pediatrics In Review, 2022
Intestinal atresia is a form of congenital bowel obstruction that requires operative repair in the early neonatal period. Duodenal atresia and jejunoileal (JI) atresia are appropriately seen as distinct entities. Both can be suspected with fetal imaging, which can assist with prenatal counseling of families. Duodenal atresia is more commonly associated
Barrie S, Rich, Eran, Bornstein, Stephen E, Dolgin   +2 more
openaire   +2 more sources

Esophageal atresia, choanal atresia, and dysautonomia

Journal of Pediatric Surgery, 1991
Patients with esophageal atresia (EA) or choanal atresia (CA) manifest similar clinical and pathophysiological features. To determine the significance of this observation, the clinical records of 80 patients with EA and 57 with CA were reviewed. This survey showed that similarities between the two conditions included inspiratory and expiratory dyspnea,
F, Cozzi, N A, Myers, L, Madonna, S, Drago, G, Fiocca, S, Piacenti, A, Pierro   +6 more
openaire   +2 more sources

Oesophageal atresia associated with pyloric atresia

The British Journal of Radiology, 1980
Pyloroduodenal atresia is a rare and usually isolated anomaly. Crowe and Sumner (1978) recently reported a newborn with pyloroduodenal atresia, isolated oesophageal atresia (Gross Type 1) and cardiac and skeletal malformations. We wish to report a similar case and review the diagnostic techniques that can lead to the correct diagnosis of a second ...
A P, Friedman, F T, Velcek, M A, Ergin, J O, Haller   +3 more
openaire   +2 more sources