Results 21 to 30 of about 9,336,073 (253)

Distribution of carbon monoxide-producing neurons in human colon and in Hirschsprung's disease patients [PDF]

open access: yes, 2002
Hirschsprung's disease (HSCR) is characterized by the absence of ganglion cells and impaired relaxation of the gut. Nitric oxide (NO) and, more recently, carbon monoxide (CO) have been identified as inhibitory neurotransmitters causing relaxation.
Chen, Y, Lui, VCH, Sham, MH, Tam, PKH
core   +1 more source

Predictability of 48-h delayed retention of contrast in barium enema in cases of chronic constipation

open access: yesAfrican Journal of Paediatric Surgery, 2020
Introduction: Diagnosis of Hirschsprung's disease depends on rectal biopsy. This study was designed to find an alternate diagnostic modality to exclude Hirschsprung's disease.
Nitin Sharma   +5 more
doaj   +1 more source

Validity of Barium Enema as Hirschsprung’s Disease Diagnostic Tools for Infant in Sanglah Hospital Denpasar

open access: yesJBN (Jurnal Bedah Nasional), 2021
Aim: To determine the validity (sensitivity, specificity, likelihood ratio) of barium enema as Hirschsprung's disease diagnostic tool in infants. Methods: This study was a diagnostic test of barium enema compared with postoperative histopathology ...
I Made Darmajaya, I Ketut Subhawa
doaj   +1 more source

Reduced RET expression in gut tissue of individuals carrying risk alleles of Hirschsprung's disease [PDF]

open access: yes, 2010
Receptor tyrosine kinase (RET) single nucleotide polymorphisms (SNPs) are associated with the Hirschsprung's disease (HSCR). We investigated whether the amount of RET expressed in the ganglionic gut of human was dependent on the genotype of three ...
Chen, Y   +9 more
core   +1 more source

Long‐term functional outcomes and quality of life in patients with Hirschsprung's disease

open access: yesBritish Journal of Surgery, 2019
It is unclear whether functional outcomes improve or deteriorate with age following surgery for Hirschsprung's disease. The aim of this cross‐sectional study was to determine the long‐term functional outcomes and quality of life (QoL) in patients with ...
Rob J Meinds   +8 more
semanticscholar   +1 more source

Hirschsprung’s Disease Complicated by Sigmoid Volvulus: A Systematic Review

open access: yesBalkan Medical Journal, 2020
Background Hirschsprung’s disease and sigmoid volvulus can sometimes be seen in the same patient. Aims To investigate the presence of Hirschsprung’s disease in patients with sigmoid volvulus and to discuss the diagnosis and treatment methods.
U. Uylaş, O. Gunes, C. Kayaalp
semanticscholar   +1 more source

A case of Hirschsprung's disease underwent surgery in adulthood

open access: yesJournal of Pediatric Surgery Case Reports, 2016
Adult Hirschsprung's disease is a rare motor disorder of the gut that is frequently misdiagnosed as refractory constipation. We describe a 30-year-old patient with adult Hirschsprung's disease with a history of chronic constipation requiring daily enema.
Richi Nakatake   +7 more
doaj   +1 more source

Surgical Correction of Hirschsprung's Disease in Children Using the Soave-Boley Technique with Manual Colorectal Anastomosis

open access: yesGalician Medical Journal, 2020
Introduction. Current trends in surgical treatment of Hirschsprung's disease are aimed at minimally invasive interventions. However, the experience of using Soave-Boley procedure in surgical treatment of Hirschsprung's disease in children of different ...
Oleh Kurtash
doaj   +1 more source

Intestinal transplantation under tacrolimus monotherapy after perioperative lymphoid depletion with rabbit anti-thymocyte globulin (thymoglobulin®) [PDF]

open access: yes, 2005
Modifications in the timing and dosage of immunosuppression can ameliorate the morbidity and mortality that has prevented widespread use of intestinal transplantation (ITx) in children.
Abu-Elmagd, K   +8 more
core   +1 more source

Congenital intestinal hypoganglionosis: A radiologic mimic of Hirschsprung's disease

open access: yesRadiology Case Reports, 2019
Intestinal hypoganglionosis or isolated hypoganglionosis is a rare entity with a clinical and radiologic presentation that can mimic Hirschsprung's disease in the neonatal period.
Gayathri Sreedher, MD   +4 more
doaj   +1 more source

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