Results 121 to 130 of about 369,634 (311)

Internal Fixation for Unstable Distal Ulnar Fractures by 2.7 mm Semitubular Hook Plate

open access: yesAdvances in Orthopedics
Conclusion: Using the 2.7 mm semitubular hook plate is a successful choice for internal fixation of unstable distal ulnar fractures isolated or associated with distal radius fractures with a favorable union time, functional outcome, and range of motion ...
Mohamed I. Abulsoud   +7 more
doaj   +1 more source

Sound‐Based Assembly of Magnetically Actuated Soft Robots Toward Enhanced Release of Extracellular Vesicles

open access: yesAdvanced Intelligent Systems, Volume 7, Issue 3, March 2025.
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

Construction and validation of a risk prediction model for deep vein thrombosis in orthopedic patients during surgery

open access: yesHuli yanjiu
ObjectiveTo construct a risk prediction model for deep vein thrombosis(DVT) in orthopedic patients during surgery and verify it.MethodsPatients admitted to our hospital who require orthopedic surgery treatment were selected as the research subjects from ...
LYU Mengshuang   +5 more
doaj  

Barnes Hospital Bulletin [PDF]

open access: yes, 1981
https://digitalcommons.wustl.edu/bjc_barnes_bulletin/1186/thumbnail ...

core   +1 more source

Thrust Joint Manipulation Utilization by Us Physical Therapists

open access: yes, 2016
Study Design: Online survey study. Objective: To determine physical therapists’ utilization of thrust joint manipulation (TJM) and their comfort level in using TJM between the cervical, thoracic, and lumbar regions of the spine.
Reilly, Sean   +2 more
core   +1 more source

Challenges for the Female Surgeon in Orthopedic Surgery – A Scoping Review

open access: yesOrthopedic Research and Reviews
Yasmen Alrumaidhi, Norah Alenizi, Nawar Almulla, Zainab Almousa, Danah Alenezi, Ali Lari Department of Orthopedic Surgery, AlRazi National Orthopedic Hospital, Kuwait City, KuwaitCorrespondence: Yasmen Alrumaidhi, Email Alrumaidhi.y@gmail.comBackground ...
Alrumaidhi Y   +5 more
doaj  

Getting Ahead of the Curve: Screening and Early Detection of Scoliosis in Adolescents to Prevent Progression of Spinal Deformity [PDF]

open access: yes, 2018
Scoliosis is a spinal deformity that affects approximately 7 million people in United States. The most common age of onset of idiopathic scoliosis is between 10-15 years old.
Saunders, Patrick
core   +1 more source

35 Individuals With HUWE1‐Related Neurodevelopmental Disorder and Suggested Clinical Evaluations

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
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

Clinical, Behavioral and Neuroradiological Phenotype in an Italian Cohort of Patients With Xia Gibbs Syndrome: A Multicenter Cross‐Sectional Study and Systematic Literature Review

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
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

The Homozygous p.(Arg215Ter) Variant in XRCC2 Is Associated With Atypical Fanconi Anemia Without Major Hematological Abnormalities in Childhood

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
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

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