Results 51 to 60 of about 13,213 (233)

Mutations in the EXT1 and EXT2 genes in Spanish patients with multiple osteochondromas [PDF]

open access: yes, 2013
Multiple osteochondromas is an autosomal dominant skeletal disorder characterized by the formation of multiple cartilage-capped tumours. Two causal genes have been identified, EXT1 and EXT2, which account for 65% and 30% of cases, respectively.
Anton, J.   +14 more
core   +1 more source

Surgical treatment of rare case of scapula osteochondroma in a resource limited setting: A case report

open access: yesInternational journal of surgery case reports, 2019
Highlights • Osteochondroma is a frequent benign tumor in the growing adolescent and involves mostly the growth plate of long bones and seldomly the scapula.• Solitary osteochondroma of the scapula is a rare and usually incidental finding and usually ...
F. O. Ngongang   +6 more
semanticscholar   +1 more source

Examining the Role of Artificial Intelligence in Assessment: A Comparative Study of ChatGPT and Educator‐Generated Multiple‐Choice Questions in a Dental Exam

open access: yesEuropean Journal of Dental Education, EarlyView.
ABSTRACT Aim To compare the item difficulty and discriminative index of multiple‐choice questions (MCQs) generated by ChatGPT with those created by dental educators, based on the performance of dental students in a real exam setting. Materials and Methods A total of 40 MCQs—20 generated by ChatGPT 4.0 and 20 by dental educators—were developed based on ...
Nezaket Ezgi Özer   +4 more
wiley   +1 more source

Parosteal Lipoma Associated with a Growing Osteochondroma of the Right Ilium

open access: yes대한영상의학회지, 2021
Parosteal lipoma is a rare type of lipoma, the incidence being approximately 0.3% of all lipomas. Moreover, parosteal lipoma coexisting with osteochondroma is extremely rare. A few cases with coexistence of osteochondroma and parosteal lipoma have been
Min Jae Myung   +5 more
doaj   +1 more source

An Unusual Location of Osteochondroma: Dorsal Scapula

open access: yesCureus, 2019
Osteochondromas commonly affect the proximal humerus, pelvis, and knee but are rarely seen on flat bones. Herein, we present the case of a 15-year-old female patient with osteochondroma located at the dorsal aspect of the scapula.
Y. Bektaş, Ramadan Ozmanevra
semanticscholar   +1 more source

Successful repair of a carpal sheath synovial hernia using a polypropylene mesh

open access: yesEquine Veterinary Education, EarlyView.
Summary A cob‐cross mare presented with a carpal sheath synovial hernia on the distolateral antebrachium following carpal sheath tenoscopy to treat a radial physeal exostosis and deep digital flexor tendon injury. The presumed source of pain was the weakened skin over the hernia as the intrathecal pathology identified at the initial tenoscopy had ...
S. R. L. Neild   +3 more
wiley   +1 more source

Scapular osteochondroma with winging: A case report

open access: yesInternational journal of surgery case reports, 2018
Highlights • Osteochondroma is a benign cartilaginous tumour that rarely affects the scapula.• We present a rare case of osteochondroma with winging of scapula, present in his fourth decade of life.• This symptomatic scapular osteochondroma exhibited ...
Raheef Alatassi   +3 more
semanticscholar   +1 more source

Physiotherapist's Management of Suspected Cauda Equina Syndrome in the United Kingdom: A National Survey

open access: yesPhysiotherapy Research International, Volume 31, Issue 2, April 2026.
ABSTRACT Background and Purpose Cauda Equina Syndrome (CES) is a rare but serious spinal condition requiring urgent diagnosis and management. Physiotherapists in UK musculoskeletal (MSK) services increasingly encounter suspected CES cases, but little is known about their clinical decision‐making and referral practices.
Rob Tyer, Nick Livadas, Robert Hogg
wiley   +1 more source

Towards the production of radiotherapy treatment shells on 3D printers using data derived from DICOM CT and MRI: preclinical feasibility studies [PDF]

open access: yes, 2015
Background: Immobilisation for patients undergoing brain or head and neck radiotherapy is achieved using perspex or thermoplastic devices that require direct moulding to patient anatomy. The mould room visit can be distressing for patients and the shells
C. D. Scrase   +11 more
core   +1 more source

Pathogenesis and potential therapeutic targets of trichorhinophalangeal syndrome; lessons obtained from animal studies

open access: yesDevelopmental Dynamics, Volume 255, Issue 3, Page 228-245, March 2026.
Abstract Trichorhinophalangeal syndrome (TRPS) is a rare genetic disease inherited in an autosomal dominant manner. It occurs in 1 in 100,000 people globally and is caused by several types of mutations of the TRPS1 gene. Since the first human patient was reported in 1966, typical and atypical pathologies, disease courses, and treatment case ...
Naoya Saeki   +6 more
wiley   +1 more source

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