D
Duncan T. Wilcox
Researcher at Boston Children's Hospital
Publications - 189
Citations - 4058
Duncan T. Wilcox is an academic researcher from Boston Children's Hospital. The author has contributed to research in topics: Congenital diaphragmatic hernia & Lung. The author has an hindex of 34, co-authored 174 publications receiving 3614 citations. Previous affiliations of Duncan T. Wilcox include University of Colorado Boulder & Anschutz Medical Campus.
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Journal ArticleDOI
Prenatal diagnosis of cloacal anomalies.
TL;DR: Prenatal diagnosis in facilitating prenatal counselling and planning optimal perinatal care for persistent cloaca, a complex malformation with variable presentation and a difficult reconstructive challenge for the paediatric urologist and surgeon is evaluated.
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The Yang–Monti ileovesicostomy: a problematic channel?
TL;DR: Compared the differences in the quality of Mitrofanoff channels created using appendix and re‐tubularized small bowel (the Yang–Monti ileovesicostomy) are compared.
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Perfluorocarbon-associated gas exchange improves pulmonary mechanics, oxygenation, ventilation, and allows nitric oxide delivery in the hypoplastic lung congenital diaphragmatic hernia lamb model
Duncan T. Wilcox,Philip L. Glick,Hratch L. Karamanoukian,Corinne L. Leach,Frederick C. Morin,Bradley P. Fuhrman +5 more
TL;DR: Perfluorocarbon-associated gas exchange significantly improved gas exchange, dynamic compliance, and tidal volumes, and inhaled nitric oxide can be effectively delivered during perfluoroc Argon gas exchange to reduce pulmonary hypertension and enhance oxygenation.
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Regarding the consensus statement on 21-hydroxylase deficiency from the Lawson Wilkins Pediatric Endocrine Society and the European Society for Paediatric Endocrinology.
Sarah M. Creighton,P.G. Ransley,Patrick G. Duffy,Duncan T. Wilcox,Imran Mushtaq,Peter Cuckow,Christopher Woodhouse,Catherine L Minto,Naomi S. Crouch,Richard Stanhope,Ieuan Hughes,Mehul T. Dattani,Peter C. Hindmarsh,Caroline Brain,John Achermann,Gerard S. Conway,L.-M. Liao,Angela Barnicoat,Les Perry +18 more
TL;DR: Despite over 50 yr of experience with steroid replacement therapy, the management of congenital adrenal hyperplasia (CAH) remains difficult and clinical practice varies substantially throughout the world.
Journal ArticleDOI
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome
Stefanie Weber,Holger Thiele,Sevgi Mir,Mohammad R. Toliat,Betül Sözeri,Heiko Reutter,Heiko Reutter,Markus Draaken,Michael Ludwig,Janine Altmüller,Peter Frommolt,Helen M. Stuart,Parisa Ranjzad,Neil A. Hanley,Rachel E. Jennings,William G. Newman,Duncan T. Wilcox,Uwe Thiel,Karl P. Schlingmann,Rolf Beetz,Peter F. Hoyer,Martin Konrad,Franz Schaefer,Peter Nürnberg,Adrian S. Woolf +24 more
TL;DR: A muscarinic acetylcholine receptor M3 (CHRM3) (1q41-q44) homozygous frameshift mutation in familial congenital bladder malformation associated with a prune-belly-like syndrome is described, defining an isolated gene defect underlying this sometimes devastating disease.