Results 161 to 170 of about 3,250,107 (354)
Magnetic soft robots offer promise in biomedicine due to their wireless actuation and rapid response, but current fabrication methods are complex and have limited cellular compatibility. A new, contactless bioassembly strategy using hydrodynamic instabilities is introduced, enabling customizable, centimeter‐scale robots.
Wei Gao +5 more
wiley +1 more source
Abdulaziz Ahmed Abdulaziz,1 Osama Mohammed Qasim,2 Abdullah Hesham Alsawaf,3 Abdulraheem A Almokhtar,4 Khalid Jubran Idris,4 Atif Ahmed Labban,5 Khalid Ibrahim Najjar5 1Orthopedic Surgery, King Faisal Medical Complex, Taif, Saudi Arabia; 2College of ...
Abdulaziz AA +6 more
doaj
Essentials of Orthopedic Surgery [electronic resource] /
Wiesel and Delahay’s Essentials of Orthopedic Surgery, now in its fourth edition, is an ideal reference for students of the musculoskeletal system. Through its many photographs and illustrations, concise text, consistent format and breadth of scope, this
Wiesel, Sam W.editor.edthttp://id.loc.gov/vocabulary/relators/edt +2 more
core +1 more source
Association between outpatient orthopedic surgery costs and healthcare facility characteristics
Purpose The purpose of this paper is to examine the association between outpatient orthopedic surgery costs and Japan’s healthcare facilities using a large-scale Japanese medical claims database.
Yuichi Watanabe, Yoshinori Nakata
core +1 more source
35 Individuals With HUWE1‐Related Neurodevelopmental Disorder and Suggested Clinical Evaluations
ABSTRACT HUWE1 (HECT, UBA, and WWE Domain Containing E3 Ubiquitin Protein Ligase1, OMIM 300697), located at Xp11.22, encodes a ubiquitin ligase that is highly conserved across species. Genetic variants in HUWE1 described in multiple independent studies cause X‐linked intellectual disability, including in the patients identified by Juberg, Marsidi, and ...
Mindy H. Li +25 more
wiley +1 more source
ABSTRACT Heterozygous variants in the AHDC1 gene are associated with Xia Gibbs Syndrome (XGS), a genetic disorder with a highly variable phenotype. Cognitive impairment, motor delay, language delay, neonatal hypotonia, and sleep apnea are considered “cardinal” signs of the disease.
Giulia Cinelli +18 more
wiley +1 more source
ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli +11 more
wiley +1 more source
The vascularised fibular graft for limb salvage after bone tumour surgery A MULTICENTRE STUDY
Vascularised fibular grafts (VFGs) are a valuable surgical technique in limb salvage after resection of a tumour. The primary objective of this multicentre study was to assess the risk factors for failure and complications for using a VFG after resection
Hilven, P.H. +23 more
core +1 more source
ABSTRACT Evidence on developmental milestones in children with arthrogryposis multiplex congenita (AMC) under the age of five is scarce. This multisite cross‐sectional study described developmental status and examined factors associated with milestone attainment in 143 children aged 0–66 months from a pediatric AMC Registry.
Ahlam Zidan +13 more
wiley +1 more source
Prolonged treatment with bisphosphonates has commonly been associated with atypical femur fractures. Localized periosteal thickening of the femoral lateral cortex is considered one of the minor features of these fractures and is caused by distribution of
Shuichi Miyamoto +6 more
doaj +1 more source

