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pro vyhledávání: '"David C. Tapscott"'
Autor:
John V. Horberg, MD, David C. Tapscott, MD, Brian P. Kurcz, MD, Ryan J. O’Rourke, MD, Timothy A. Mikesell, MD, Trevor M. Owen, MD, D. Gordon Allan, MD
Publikováno v:
Arthroplasty Today, Vol 6, Iss 4, Pp 644-649 (2020)
Background: Varus malposition is a risk of early failure in total hip arthroplasty. The degree to which the tip of the greater trochanter (GT) overhangs the canal can increase this risk. Although we know proximal femoral anatomy is variable, no study
Externí odkaz:
https://doaj.org/article/216f4cf8c26a4de1b8e3dabce7809dd6
Autor:
James W. Connelly, Jourdan H. Meltzer, David C. Tapscott, Janine Molino, Andrew Green, E. Scott Paxton
Publikováno v:
Injury.
The optimal surgical treatment of displaced proximal humerus fractures (PHFs) remains controversial. There are advocates for both open reduction and internal fixation with plate and screws (ORIF) and intramedullary nailing (IMN). The purpose this stu
Autor:
James Ross, Bailey, David C, Tapscott, Norman Y, Otsuka, Kyle T, Boden, Robert M, Becker, Tom E, Kwasigroch, Brian D, Johnston
Publikováno v:
Journal of surgical orthopaedic advances. 30(2)
Physical examination education begins early for medical learners. A hindrance to physical exam competency is lack of exposure to pathology in standardized patient settings. This research focuses on improving medical education through the utilization
Autor:
Brian P. Kurcz, Timothy A. Mikesell, Trevor M. Owen, John V. Horberg, David C. Tapscott, Ryan J. O’Rourke, D. Gordon Allan
Publikováno v:
Arthroplasty Today
Arthroplasty Today, Vol 6, Iss 4, Pp 644-649 (2020)
Arthroplasty Today, Vol 6, Iss 4, Pp 644-649 (2020)
Background: Varus malposition is a risk of early failure in total hip arthroplasty. The degree to which the tip of the greater trochanter (GT) overhangs the canal can increase this risk. Although we know proximal femoral anatomy is variable, no study
Autor:
Anjali Patwardhan, David C. Tapscott
Publikováno v:
Annals of Paediatric Rheumatology. 3:35
Monosomy 1p36 is a congenital genetic disorder characterized by moderate to severe global developmental and growth delay, hearing and vision impairment, hypotonia, seizures, and distinct facial features. We present the first published description of