Zobrazeno 1 - 10
of 250
pro vyhledávání: '"Mark D. Stringer"'
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 43, Iss , Pp 58-61 (2019)
An infant born at 35 weeks' gestation with type 2 jejunal atresia underwent resection of the atretic ends of the bowel and primary anastomosis. Histologic examination of the resected distal bowel segment revealed heterotopic gastric mucosa (HGM). The
Externí odkaz:
https://doaj.org/article/c3cff177772745eb8383b394a320f6d9
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 33, Iss , Pp 26-29 (2018)
A congenital perineal hernia develops through a defect in the pelvic floor muscles and presents as a reducible buttock swelling. These hernias are exceptionally rare with only six cases previously documented in the English literature. We report an ex
Externí odkaz:
https://doaj.org/article/978743291fd442dbab33282476ce892f
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 32, Iss , Pp 23-26 (2018)
Heterotopic gastric mucosa (HGM) is occasionally found at endoscopy in the proximal esophagus of adults and children, when it manifests as an asymptomatic small island of reddish pink mucosa just below the upper esophageal sphincter. There are few re
Externí odkaz:
https://doaj.org/article/40e052c1755c4d61be4d4204cebcf547
Autor:
Timothy A. Little, Kathryn E. Compson, Katherine Hall, M. Jean Murdoch, Katherine R. Neas, Diane Kenwright, Mark D. Stringer
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 36, Iss , Pp 16-18 (2018)
Currarino syndrome is rare and consists of an anorectal malformation, a sacrococcygeal bony defect and a presacral mass. Each feature is present to a variable degree in affected individuals. The syndrome develops as a result of a heterozygous mutatio
Externí odkaz:
https://doaj.org/article/747450e80af44726ad134da9faa6be3b
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 47, Iss , Pp - (2019)
We report an infant who developed complete gastric outlet obstruction secondary to gastric antral mucosal hyperplasia and muscular hypertrophy after CDH repair. This condition has been reported only once before when it also occurred in association wi
Externí odkaz:
https://doaj.org/article/6299a3f9a2744870b6a5dd64464afdc4
Publikováno v:
Journal of Paediatrics and Child Health. 58:1420-1424
To investigate the frequency and modality of pre-operative imaging in children with an external angular dermoid cyst and whether this influenced subsequent management.A retrospective study was undertaken to assess the presentation, investigation, tre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66f6347b30ad10afa3c9385e2eb8073d
https://doi.org/10.1111/jpc.16008
https://doi.org/10.1111/jpc.16008
Autor:
Mark D Stringer, Prabal R. Mishra
Publikováno v:
Pediatric Surgery ISBN: 9783030814878
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fb7a28783668740958bfcc836278c2b
https://doi.org/10.1007/978-3-030-81488-5_63
https://doi.org/10.1007/978-3-030-81488-5_63
Autor:
Mark D. Stringer
Publikováno v:
Duodenum and Small Bowel ISBN: 0192862448
The small intestine consists of the duodenum, jejunum, and ileum. The combined length of the jejunum and ileum measured from the duodenojejunal flexure to the ileocaecal junction in vivo varies considerably but is approximately 5 m in adults. The duo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34134941ca94225467e254159edb8e3e
https://doi.org/10.1093/med/9780192862440.003.0001
https://doi.org/10.1093/med/9780192862440.003.0001
Autor:
Mark D. Stringer, Prabal R Mishra
Publikováno v:
Pediatric Surgery International. 37:1607-1612
Intestinal malrotation is life-threatening and often presents during infancy with bilious vomiting. The prevalence and presentation among extremely premature infants are unknown. We retrospectively reviewed all infants born at less than 28 weeks’ g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ecb3b92a3b2ff8ddd578418ba1fbce3
https://doi.org/10.1007/s00383-021-04969-0
https://doi.org/10.1007/s00383-021-04969-0
Autor:
Spencer W. Beasley, Lucy Goddard, Andrew Hobson, Askar Kukkady, Kiarash Taghavi, Stephen Evans, Jonathan Stevenson, Sasikumar Sankaran, Mark D. Stringer
Publikováno v:
ANZ Journal of Surgery. 90:1037-1040
BACKGROUND The aim of this study was to report the contemporary management of Hirschsprung disease (HD) in New Zealand. METHODS We undertook a national multi-centre retrospective review of all newly diagnosed cases of HD during a 16-year period (2000
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::107595b832501589d8f189a9b56f7992
https://doi.org/10.1111/ans.15923
https://doi.org/10.1111/ans.15923