Results 61 to 70 of about 4,863,546 (170)

Subtypes of Enteric Neurons in Hirschsprung Disease: A Comparison of Fully Ganglionic and Transitional Zone

Neurogastroenterology &Motility, Volume 38, Issue 9, September 2026.
Neuronal subtype composition is comparable between transitional and fully ganglionic zones in children with Hirschsprung disease. Thus, our study did not support a major contribution of shifts in neuronal subtype composition to persistent postoperative bowel dysfunction. ABSTRACT Background Hirschsprung disease (HD) is characterized by aganglionosis of
C. Nebeling, M. Lee‐Theilen, E. Gradhand, F. Friedmacher, U. Rolle, Y. Braun   +5 more
wiley   +1 more source

Anorectal manometry and Hirschsprung’s disease

The recent report on anorectal manometry in following up post-operative Hirschsprung’s disease is very ...
Viroj Wiwanitkit, Somsri Wiwanitkit
core   +1 more source

Anorectal manometry under adequate sedation or anesthesia as a highly reliable diagnostic tool for Hirschsprung's disease in neonates and young infants: A multicenter retrospective study

Global Pediatrics
Background: Hirschsprung's disease is a congenital disorder characterized by the absence of enteric ganglion cells. The diagnostic gold standard for Hirschsprung's disease is a rectal mucosal biopsy; however, its accuracy in neonates and young infants ...
Yohei Sanmoto, Atsuki Naoe, Yudai Goto, Mikihiro Inoue, Kouji Masumoto   +4 more
doaj   +1 more source

Percutaneous Deployment of the Sinus‐SuperFlex‐DS Stent for Hybrid Stage I Palliation in Neonates Weighing ≤ 2.5 kg: A Multicenter Study

Catheterization and Cardiovascular Interventions, Volume 108, Issue 2, Page 644-652, August 1, 2026.
ABSTRACT Background Hybrid stage I palliation (HS1P) has developed as an alternative to the Norwood stage I palliation for neonates with hypoplastic left heart and related left‐sided obstructive lesions. HS1P is currently used in various clinical settings, such as single ventricle palliation, bridge to decision, bridge to biventricular repair, or ...
Johanna Hummel, Jochen Grohmann, Katarzyna Gendera, Götz Müller, Harald Bertram, Matthias Sigler, Dietmar Schranz, Christian Jux, Markus Khalil   +8 more
wiley   +1 more source

Hirschsprung’s Disease and Rehbein’s Procedure – Our Results in the Last 30 Years [PDF]

, 2006
Hirschsprung’s disease is congenital anomaly of the intestine and Harald Hirschsprung gave the first description of this disease1. The aim of this follow-up study was to evaluate the results of Rehbein’s procedure in the treatment of Hirschsprung’s ...
Višnjić, Stjepan, Cigit, Irenej, Butković, Diana, Žganjer, Mirko, Car, Andrija   +4 more
core   +1 more source

Oral and dental status in children with intestinal failure: A descriptive cross‐sectional study

Journal of Parenteral and Enteral Nutrition, Volume 50, Issue 6, Page 873-880, August 2026.
Abstract Background Children with intestinal failure often experience feeding difficulties and complex daily care needs, yet their oral and dental health remains underexplored. We aimed to describe oral and dental health characteristics in pediatric intestinal failure.
Anat Guz‐Mark, Dror S. Shouval, Raanan Shamir, Esti Davidovich   +3 more
wiley   +1 more source

Hirschsprung’s disease: genetic mutations in mice and men

, 1997
Hirschsprung’s disease is a neuronal dysplasia of the hindgut, characterised by a loss of neurones, which affects about 1 in 5000 live births.1 Genetic factors have been implicated in the aetiology of this disease in about 20% of cases and a dominant ...
K ROBERTSON, S HALL, I MASON
core   +1 more source

Transition of Care From Pediatric to Adult Services for Patients With Anorectal Malformations: A Qualitative Study

World Journal of Surgery, Volume 50, Issue 8, Page 2372-2379, August 2026.
Little is known about how patients with anorectal malformations (ARMs), their caregivers and healthcare providers perceive and experience transition from pediatric to adult care (transition of care) in low‐ and middle‐income countries. This study aimed to explore the perceptions and experiences of young adults, adolescents, their caregivers, and ...
Leila Hartford, Niveshni Maistry, Giulia Brisighelli, Juan Scribante   +3 more
wiley   +1 more source

Retrospective study of Hirschsprung's disease in Erbil city/Iraq during 2004–2016

Medical Journal of Babylon, 2020
Background: Hirschsprung's disease is caused by the failure of ganglion cells to migrate cephalocaudal through the neural crest during 4–12 weeks of gestation, causing an absence of ganglion cells in all or part of the colon.
Suhel Mawlud Alnajjar, Jawhar Tahir Omer, Salah Abubakir Ali   +2 more
doaj   +1 more source

The Swedish National Pediatric Cataract Register (PECARE): Coexisting systemic disorders 2007–2023

Acta Ophthalmologica, Volume 104, Issue 5, Page 510-516, August 2026.
Abstract Purpose To analyse the frequency and type of coexisting systemic disorders in children operated on for cataract in Sweden. Methods Data were retrieved from the Swedish National Pediatric Cataract Register (PECARE) for children operated between January 1, 2007, and December 31, 2023 (n = 975), including follow‐ups at age 1, 2, 5 and 10 ...
David Wackerberg, Jenny Gyllén, Birgitte Haargaard, Alf Nyström, Arzu Karatepe Hashas, Anna Linnarsson Wiklund, Eric Trocmé, Ulrika Kjellström, Kristina Tornqvist, Gunilla Magnusson   +9 more
wiley   +1 more source