Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Jean Murdoch"'
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 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
Publikováno v:
Journal of Medical Imaging and Radiation Oncology. 65:293-300
INTRODUCTION Early diagnosis and treatment of intestinal volvulus are important to reduce morbidity. A fluoroscopic upper GI study is the gold standard for diagnosis and may be performed in a secondary or tertiary care centre prior to surgery. It is
Autor:
Mark D. Stringer, Katherine Hall, M. Jean Murdoch, Katherine Neas, Timothy A. Little, Kathryn E. Compson, Diane Kenwright
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
Autor:
Sonja T. Bastin, David Davies-Payne, Jean Murdoch, Andrew C. Mclaughlin, Susan Craw, Rita L. Teele, Francessa Wilson, Karin L. Phillips, Glen D. Thomson, Helen L. Bird, Iona Thomas, David Duncan, Russell Metcalfe, Sally Vogel, Kirsten Pearce, Philippa Depree, Diana Browne, David Perry, Alina Leigh
Publikováno v:
Journal of Medical Imaging and Radiation Oncology. 59:54-65
Introduction Clinically occult fractures from non-accidental injury (NAI) are best detected on radiographic skeletal survey. However, there are regional variations regarding the views included in such surveys. We undertook a systematic review of the
Autor:
Alexa Kidd, Lisa Fox, Kevin P. Pringle, Esko Wiltshire, David E. C. Cole, Joel L. Sadowsky, Jean Murdoch
Publikováno v:
Pediatrics. 120(5)
We describe the use of pamidronate to control marked hypercalcemia in an extremely premature infant with neonatal hyperparathyroidism that resulted from an inactivating mutation (R220W) of the calcium-sensing receptor. Despite improvement in bone min
Autor:
Jean Murdoch
Publikováno v:
Interlending & Document Supply. 25:25-26
Sets out to examine the extent to which electronic document supply poses a threat to scientific subscriptions. Describes a survey undertaken at the British Library’s Document Supply Service comparing the use of the document supply service with a li
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