Results 111 to 120 of about 2,247 (190)

Hereditary Multiple Exostoses-A Review of the Molecular Background, Diagnostics, and Potential Therapeutic Strategies. [PDF]

Front Genet, 2021
Bukowska-Olech E, Trzebiatowska W, Czech W, Drzymała O, Frąk P, Klarowski F, Kłusek P, Szwajkowska A, Jamsheer A.   +8 more
europepmc   +1 more source

Chest wall osteochondroma resection with biologic acellular bovine dermal mesh reconstruction in pediatric hereditary multiple exostoses: A case report and review of literature. [PDF]

World J Clin Cases, 2023
Alshehri A.
europepmc   +1 more source

Clinical survey of a pedigree with hereditary multiple exostoses and identification of EXT‑2 gene deletion mutation. [PDF]

Mol Med Rep, 2022
Wang W, Yang M, Shen Y, Chen K, Wu D, Yang C, Bai J, He D, Gao J.   +8 more
europepmc   +1 more source

Osteochondroma formation is independent of heparanase expression as revealed in a mouse model of hereditary multiple exostoses. [PDF]

J Orthop Res, 2022
Mundy C, Chung J, Koyama E, Bunting S, Mahimkar R, Pacifici M.   +5 more
europepmc   +1 more source

Total Knee Arthroplasty With Patient-Specific Instrumentation to Correct Severe Valgus Deformity in a Patient With Hereditary Multiple Exostoses. [PDF]

Arthroplast Today, 2022
Sasaki U, Tamaki M, Tomita T, Okada S.
europepmc   +1 more source

Thoracic solitary pedunculated osteochondroma in a child: a case report

Orthopedic Research and Reviews, 2013
Zubair Wali,1 Khalid I Khoshhal21Department of Orthopedic Surgery, King Fahd Hospital, Almadinah Almunawwarah, Saudi Arabia; 2Department of Orthopedic Surgery, College of Medicine, Taibah University, Almadinah Almunawwarah, Saudi ArabiaObjective: This ...
Wali Z, Khoshhal KI
doaj  

Identification of a novel EXT2 frameshift mutation in a family with hereditary multiple exostoses by whole-exome sequencing. [PDF]

J Clin Lab Anal, 2021
Yang M, Xie H, Xu B, Xiang Q, Wang H, Hu T, Liu S.   +6 more
europepmc   +1 more source

C1 C2 spinal cord compression in hereditary multiple exostoses: case report and review of the literature. [PDF]

Int J Surg Case Rep, 2021
Jemel N, Gader G, Bedioui A, Zammel I, Badri M.   +4 more
europepmc   +1 more source

Mutation spectrum of EXT1 and EXT2 in the Saudi patients with hereditary multiple exostoses. [PDF]

Orphanet J Rare Dis, 2021
Al-Zayed Z, Al-Rijjal RA, Al-Ghofaili L, BinEssa HA, Pant R, Alrabiah A, Al-Hussainan T, Zou M, Meyer BF, Shi Y.   +9 more
europepmc   +1 more source

Perturbed body fluid distribution and osmoregulation in response to high salt intake in patients with hereditary multiple exostoses. [PDF]

Mol Genet Metab Rep, 2021
Oppelaar JJ, Rorije NMG, Olde Engberink RHG, Chahid Y, van Vlies N, Verberne HJ, van den Born BH, Vogt L.   +7 more
europepmc   +1 more source