Results 1 to 10 of about 22,842 (259)
Some of the next articles are maybe not open access.
Heterotopic Ossification in Burns
Journal of Burn Care & Rehabilitation, 1984Walter Peters +3 more
openaire +2 more sources
[Heterotopic endobulbar ossification].
Bollettino d'oculistica, 1998G, SCASSELLATI SFORZOLINI, R, FRIGNANI
openaire +2 more sources
Use of Acellular Dermal Matrix to Prevent Recurrence of Radioulnar Heterotopic Ossification [PDF]
Summary:. Radioulnar heterotopic ossification is a rare occurrence found in approximately 2% of all forearm injuries. Treatment is complicated by relatively high recurrence rates.
Daniel J. Gould, MD, PhD +3 more
doaj +3 more sources
Heterotopic ossification in the middle finger: a case report [PDF]
A case of heterotopic ossification developed after traumatic laceration of the middle finger. It is extremely rare for heterotopic ossification to locate in the finger.
Barlaan, PIG, Ip, WY
core +4 more sources
Early surgery in rare knee heterotopic ossification leads to successful functional outcome: a case report [PDF]
Background: Heterotopic ossification is a common complication after joint replacement surgery, such as hip or knee arthroplasty. In the intensive care unit, it is most commonly associated with traumatic brain injury or spinal cord injury.
Stijn Pierreux +3 more
doaj +2 more sources
Sudden death of a swimmer in water caused by heterotopic intracranial ossification and anomaly of the skull base [PDF]
Background. Expression of immersion syndrome implies sudden and unexpected death of swimmer in water. A drowned swimmer is still a riddle for the forensic and clinical doctors.
Budakov Branislav +4 more
core +3 more sources
Tendinous heterotopic ossification can cause pain and restricted joint mobility in affected areas, and it is a common and severe complication following tendon injuries.
Hang Liu +9 more
doaj +2 more sources
Cell Senescence in Heterotopic Ossification. [PDF]
The formation of bone outside the normal skeleton, or heterotopic ossification (HO), occurs through genetic and acquired mechanisms. Fibrodysplasia ossificans progressiva (FOP), the most devastating genetic condition of HO, is due to mutations in the ACVR1/ALK2 gene and is relentlessly progressive.
Pignolo RJ, Kaplan FS, Wang H.
europepmc +4 more sources

