Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ilias Kosmidis"'
Publikováno v:
SICOT-J, Vol 6, p 46 (2020)
SICOT-J
SICOT-J
Introduction: The National Institute for Health and Care Excellence (NICE) in 2011 declared standards in the management of fracture neck of femur (NOF) patients suggesting a total hip replacement (THR) if necessary criteria were met. The Best Practic
Publikováno v:
JSES Open Access. 3:245-246
Publikováno v:
Open Journal of Orthopedics. :273-284
Background: Although the original clinical description of fat embolism syndrome (FES) dates from 1873, the condition remains a diagnostic challenge for modern clinicians. The syndrome is described as a serious consequence of fat emboli producing a di
Publikováno v:
Journal of Pediatric Orthopaedics B. 22:70-75
Congenital insensitivity to pain with anhidrosis is a type IV hereditary sensory and autonomic neuropathy, presenting early in life. This disorder results from defective neural crest differentiation with loss of the first-order afferent system, which
Publikováno v:
The Journal of foot and ankle surgery : official publication of the American College of Foot and Ankle Surgeons. 55(5)
Pseudoaneurysm formation around the ankle area is a very rare complication of an anatomic region that is highly exposed to trauma. A review of the published medical data revealed the rarity of the condition. Pseudoaneurysms of the perforating branch
Publikováno v:
The journal of trauma and acute care surgery. 74(2)
Publikováno v:
Acta orthopaedica Belgica. 78(1)
New technology and instrumentation techniques are continually entering the spine field, leaving the scoliosis surgeon with a wide variety of options for the treatment of adolescent idiopathic scoliosis. All-screw constructs are currently the most pop
Publikováno v:
Bone. 48:S145
Publikováno v:
Journal of Orthopaedic Surgery and Research, Vol 5, Iss 1, p 56 (2010)
Journal of Orthopaedic Surgery and Research
Journal of Orthopaedic Surgery and Research
Background and purpose Hemo-lymphangiomas are rare benign tumors that arise from congenital malformation of the vascular system. They are usually diagnosed at birth or early in childhood. The management of hemo-lymphangiomas in children remains chall