Results 121 to 130 of about 43,856 (265)

Morgagni hernia repair in children over two decades: Institutional experience, systematic review, and meta-analysis of 296 patients [PDF]

, 2018
BACKGROUND/PURPOSE: Morgagni diaphragmatic hernia (MH) is rare. We report our experience based on routine patch use in MH repair to curb recurrence. A systematic review and meta-analysis were performed to study the recurrence and complications associated
Banerjee, D, Blackburn, SC, Cross, KM, Curry, JI, De Coppi, P, Eaton, S, Giuliani, S, GOSH team, Rees, CM, Tan, Y-W   +9 more
core   +1 more source

DIAPHRAGMATIC HERNIA

Journal of Thoracic Surgery, 1950
R, DANIEL, F T, BILLINGS
openaire   +5 more sources

Area of Focus in 3D Volumetry and Botulinum Toxin A Injection for Giant Diaphragmatic Hernia with Loss of Domain: A Case Report with Video Illustration

Journal of Abdominal Wall Surgery
BackgroundChronic giant diaphragmatic hernia is a severe disease with challenging diagnosis and treatment. Given the risk of loss of domain, the use of botulinum toxin A is an option but has been minimally studied in diaphragmatic hernia surgery.Case ...
Sylvie Nachtergaele, Haitham Khalil, Paul Martre, Jean-Marc Baste, Edouard Roussel   +4 more
doaj   +1 more source

Late presentation of congenital diaphragmatic hernia: A diagnostic dilemma

Bangabandhu Sheikh Mujib Medical University Journal, 2016
Congenital diaphragmatic hernias are commonly symptomatic within 24 hours after birth, but late presentation is not uncommon. Late presentation of congenital diaphragmatic hernia poses diagnostic difficulties as clinical picture are vague, and more ...
Dinesh Gurung, Shanker Bhandari, Md. Aftabuddin, Asit Baran Adhikary   +3 more
doaj   +1 more source

Genotype–Phenotype Correlations, Treatment, and Prognosis of Children With Early‐Onset (Neonatal) Marfan Syndrome

Clinical Genetics, Volume 108, Issue 2, Page 134-145, August 2025.
Early‐onset Marfan syndrome (eoMFS) is a rare disorder with atrioventricular valve insufficiency being the most severe symptom. We propose to regard eoMFS as a spectrum, ranging from a severe disorder life‐threatening already before or immediately after birth, to a disorder with a better survival rate, creating a window for atrioventricular valve ...
Eva C. van der Leest, Annelies E. van der Hulst, Gerard Pals, Lidiia Zhytnik, Lillian Lai, Caroline Jacquemart, Lindsay Mills, Michiel Houben, Petr Jira, Bert L. Lunshof, Jessica Warnink‐Kavelaars, Vivian de Waard, Leonie A. Menke   +12 more
wiley   +1 more source

Congenital diaphragmatic hernia: current status and review of the literature [PDF]

, 2018
Treatment of congenital diaphragmatic hernia (CDH) challenges obstetricians, pediatric surgeons, and neonatologists. Persistent pulmonary hypertension (PPHT) associated with lung hypoplasia in CDH leads to a high mortality rate at birth.
de Buys Roessingh, Anthony, Dinh-Xuan, Anh   +1 more
core  

Thoracoscopic operations in children [PDF]

, 2014
published_or_final_versio
CT Lau, Jessie Leung, Kenneth KY Wong, null null, Theresa WC Hui   +4 more
core   +1 more source

REPORT OF A CASE OF DIAPHRAGMATIC HERNIA [PDF]

, 1917
George F. Koehler
openalex   +1 more source

CONGENITAL DIAPHRAGMATIC HERNIA AND ESOPHAGEAL ATRESIA: THE IMPORTANCE OF RESPIRATORY FOLLOW-UP IN CONGENITAL THORACIC MALFORMATION [PDF]

, 2013
Esophageal atresia, congenital diaphragmatic hernia, pulmonary function test, respiratory morbidity, Long-term follow ...
CORSELLO, Giovanni, GIUFFRE, Mario, Matina, F, PICCIONE, Maria, PIRO, Ettore, Zicari, C   +5 more
core  

A CASE OF DIAPHRAGMATIC HERNIA [PDF]

Archives of Pediatrics & Adolescent Medicine, 1917
History. —Baby G., 3% months old, came under my care Oct. 6, 1916, with a history of recurrent attacks characterized by extreme cyanosis, dyspnea, and, judging from his hard crying, severe pain, the condition being relieved by a movement of the bowels or by the expulsion of gas, sometimes in large quantities. His birth history was unimportant, and for
openaire   +3 more sources