Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Paula M, Kelly"'
Autor:
Evelyn P. Murphy, Catherine Howells, Olga Gallagher, Paula M. Kelly, Patrick O’Kelly, Jacques Noel, David Moore, Patrick J. O’Toole, Jim Kennedy
Publikováno v:
Journal of Pediatric Orthopaedics. 42:552-557
Publikováno v:
Journal of Children's Orthopaedics
Purpose In this article we report the results of a pilot study analysing the implications of performing pelvic osteotomies for developmental dysplasia of the hip (DDH) as a day case. We assess the advantages of performing paediatric pelvic osteotomie
Autor:
Gerard A. Sheridan, Maria Noonan, David P. Moore, John Tristan Cassidy, Aaron Donnelly, Paula M. Kelly
Publikováno v:
Strategies in Trauma and Limb Reconstruction
Aim and objective Fibular autograft is a known technique for the reconstruction of traumatic and non-traumatic bone defects in both adult and paediatric populations. We aim to describe our outcomes using various stabilisation methods for non-vascular
Autor:
David P. Moore, Patrick O’Toole, Christopher Fenelon, Jim Kennedy, Michael D. O’Sullivan, Evelyn P. Murphy, Paula M. Kelly, Jacques Noel
Publikováno v:
Journal of pediatric orthopedics. 41(4)
Background The aim was to describe the introduction and operation of a virtual developmental dysplasia of the hip (DDH) clinic. Our secondary objectives were to provide an overview of DDH referral reasons, treatment outcomes, and adverse events assoc
Autor:
Gregory J Nason, Joseph F Baker, Patrick O'Toole, Anna Walsh, Darren F Lui, Francis O'Neill, Maureen O'Sullivan, Paula M Kelly
Publikováno v:
Journal of Orthopaedic Surgery, Vol 21 (2013)
Tendon sheath fibromas are rare, benign soft-tissue tumours and usually involve tendons of the upper extremities, particularly the fingers. The most common presentation is a painless, slow-growing swelling. Tendon sheath fibromas are composed of dens
Externí odkaz:
https://doaj.org/article/8d31324278fd42e7986b5565c4764638
Autor:
Pat O'Toole, David P. Moore, Paula M. Kelly, Dave M. Moore, Jim Kennedy, Pat Kiely, Michael O'Sullivan, Jacques Noel
Publikováno v:
The surgeon : journal of the Royal Colleges of Surgeons of Edinburgh and Ireland. 20(2)
Twenty-five-hydroxy-vitamin D3 (25-OH-vit D) is a prohormone that is essential for normal calcium homeostasis and bone metabolism. Understanding its role is an important component of the proper care of the pediatric orthopaedic patient. The aim of th
Autor:
Gerard A. Sheridan, David P. Moore, Patrick O’Toole, Olga Gallagher, Catherine Howells, Matthew Nagle, Patrick Kiely, Paula M. Kelly
Publikováno v:
Irish journal of medical science. 189(1)
We describe the first radiographic clinic in the literature for DDH and how this novel clinic can significantly improve the efficiency and cost-effectiveness of service in a tertiary referral centre. A radiographic clinic for the management of develo
Publikováno v:
Journal of Children's Orthopaedics
In this article we report the results of a pilot study analysing the implications of performing pelvic osteotomies for developmental dysplasia of the hip (DDH) as a day case. We assess the advantages of performing paediatric pelvic osteotomies as day
Autor:
Kevin J. Mulhall, E E Fogarty, Jacques Noel, Ellen Crushell, Anne O'Meara, Paula M. Kelly, Jim Kennedy
Publikováno v:
Journal of Pediatric Orthopaedics. 36:25-28
BACKGROUND After successful hematopoietic stem cell transplantation, maintaining function and mobility have become key goals in the management of patients with Hurler syndrome, (mucopolysaccharoidosis type 1H). The aim of this study was to establish
Autor:
Paula M. Kelly, Paul J. Orchard, Catherine Breen, Tyler G. Ketterl, Klane K. White, Weston P. Miller, Jim Kennedy, Ralph J. B. Sakkers, Troy C. Lund, Anne O'Meara, Olga C. Knaven, Simon Jones, Jean Mercer, Rick R. van Rijn, Matthijs M. den Os, Eveline J. Langereis, Frits A. Wijburg
Publikováno v:
Journal of bone and joint surgery. American volume, 98A(5), 386-395. Journal of Bone and Joint Surgery Inc.
Background: Dysostosis multiplex contributes substantially to morbidity in patients with Hurler syndrome (mucopolysaccharidosis type I Hurler phenotype [MPS I-H]), even after successful hematopoietic stem cell transplantation (HSCT). One of the hallm