Zobrazeno 1 - 10
of 531
pro vyhledávání: '"Skeletal disorders"'
Autor:
Manila Boarini, Andrea Romeo, Federico Banchelli, Eleonora Grippa, Silvia Forni, Maria Cecilia la Forgia, Davide Scognamiglio, Paolo Cornaglia Ferraris, Luca Sangiorgi
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-13 (2024)
Abstract Individuals with rare skeletal disorders like Multiple Osteochondromas and Ollier Disease often experience physical and psychological burdens. Adventure therapy, with activities like sailing in outdoor settings, promotes personal growth and
Externí odkaz:
https://doaj.org/article/91af7c3c9aba4a3ba66a799e039fb9a1
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-16 (2024)
Abstract One of the most vital parameters to achieve sustainability in any field is encompassing the Occupational Health and Safety (OHS) of the workers. In mining industry where heavy earth moving machineries are largely employed, ergonomic hazards
Externí odkaz:
https://doaj.org/article/74ce2e20b1834df78ffc1149c975eae2
Autor:
Peng Lin, Yi-Bo Gan, Jian He, Si-En Lin, Jian-Kun Xu, Liang Chang, Li-Ming Zhao, Jun Zhu, Liang Zhang, Sha Huang, Ou Hu, Ying-Bo Wang, Huai-Jian Jin, Yang-Yang Li, Pu-Lin Yan, Lin Chen, Jian-Xin Jiang, Peng Liu
Publikováno v:
Military Medical Research, Vol 11, Iss 1, Pp 1-24 (2024)
Abstract Orthopedic conditions have emerged as global health concerns, impacting approximately 1.7 billion individuals worldwide. However, the limited understanding of the underlying pathological processes at the cellular and molecular level has hind
Externí odkaz:
https://doaj.org/article/0ac6d6f684684c378e0cd477bb235422
Autor:
Maria Gnoli, Marco Gambarotti, Alberto Righi, Eric Lodewijk Staals, Andrea Evangelista, Morena Tremosini, Evelise Brizola, Marina Mordenti, Manila Boarini, Manuela Locatelli, Elena Pedrini, Luca Sangiorgi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-10 (2024)
Abstract Background Multiple osteochondromas is genetic disorder characterized by the formation of multiple benign cartilage-capped bone tumors, named osteochondromas, during skeletal development. The most feared complication is the secondary periphe
Externí odkaz:
https://doaj.org/article/39630631ea254982b0c1ea691e0ae7c2
Publikováno v:
Genes and Diseases, Vol 10, Iss 4, Pp 1291-1317 (2023)
Wnt signaling executes an indispensable performance in osteoblast differentiation, bone development, homeostasis, and remodeling. Wnt signals trigger the intracellular Wnt signaling cascade to initiate regulating the implication of β-catenin in the
Externí odkaz:
https://doaj.org/article/6a792f5bea9846349ae712f836d87be8
Publikováno v:
Bone Reports, Vol 20, Iss , Pp 101747- (2024)
There is a wide spectrum of craniofacial bone disorders and dysplasias because embryological development of the craniofacial region is complex. Classification of craniofacial bone disorders and dysplasias is also complex because they exhibit complex
Externí odkaz:
https://doaj.org/article/c0e900db40634056a967d8a78ff125d8
Autor:
Sophie Feige, Fabian Holzgreve, Laura Fraeulin, Christian Maurer-Grubinger, Werner Betz, Christina Erbe, Albert Nienhaus, David A. Groneberg, Daniela Ohlendorf
Publikováno v:
Bioengineering, Vol 11, Iss 4, p 400 (2024)
Background: Dentists, including endodontists, frequently experience musculoskeletal disorders due to unfavourable working postures. Several measures are known to reduce the ergonomic risk; however, there are still gaps in the research, particularly i
Externí odkaz:
https://doaj.org/article/4863ff1033874efa95aea9b8226be389
Publikováno v:
Veterinary Quarterly, Vol 42, Iss 1, Pp 21-40 (2022)
Lameness or leg weakness is the main cause of poor poultry welfare and serious economic losses in meat-type poultry production worldwide. Disorders related to the legs are often associated with multifactorial aetiology which makes diagnosis and prope
Externí odkaz:
https://doaj.org/article/0beb6c839f48442c8551651726c1925d
Autor:
Pachajoa H, Giraldo-Ocampo S
Publikováno v:
Orthopedic Research and Reviews, Vol Volume 14, Pp 453-458 (2022)
Harry Pachajoa,1,2 Sebastian Giraldo-Ocampo3 1Genetics Division, Fundación Valle del Lili, Cali, Colombia; 2Centro de Investigaciones en Anomalías Congénitas y Enfermedades Raras (CIACER), Universidad Icesi, Cali, Colombia; 3Departamento de Microb
Externí odkaz:
https://doaj.org/article/b1ad9cd9045a40feb83fa45a9165c09c
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