Results 41 to 50 of about 28,064 (260)

Regulating Cells Fate and Function to Facilitate Bone Regeneration via Designing Programmable Bio‐Interactive Materials

open access: yesAdvanced Science, EarlyView.
This article aims to elucidate the biological mechanisms of bone repair and the evolution of material design, highlighting key cellular and molecular processes. It further proposes strategies and prospects for programmable bio‐interactive materials, which enable precisely guided bone tissue regeneration by dynamically regulating cell behavior and the ...
Qingrui Fan   +6 more
wiley   +1 more source

Machine Learning for Opportunistic Screening for Osteoporosis from CT Scans of the Wrist and Forearm

open access: yesDiagnostics, 2022
Background: We investigated whether opportunistic screening for osteoporosis can be done from computed tomography (CT) scans of the wrist/forearm using machine learning.
Ronnie Sebro, Cynthia De la Garza-Ramos
doaj   +1 more source

Toward Fully Soft and Multifunctional Shape Sensing via Optical Waveguide Arrays

open access: yesAdvanced Intelligent Systems, EarlyView.
This work develops a sheet made with arrays of soft optical fibers that can reconstruct its 3D surface shape. Synergy of the waveguides’ responses to bending and pressing force allows shape reconstruction with resilience to damage. Applied onto surfaces of robotic or living systems, our design can be implemented in virtual reality, teleoperation ...
Qifan Yu, Nina Cao, Kaitlyn Becker
wiley   +1 more source

THE METHOD OF BONE DEFECTS PLASTY IN PATIENTS WITH FOREARM OSTEOMYELITIS BY MUSCLE FLAP FORMING FROM MUSCULUS PRONATOR QVADRATUS

open access: yesTravmatologiâ i Ortopediâ Rossii, 2011
The authors presented new method of plasty of postoperative bone defects in patients with chronic forearm osteomyelitis using muscle flap, which is formed of musculus pronator qvadratus. This method was used in 58 patients. Good or excellent results were
S. A. Linnik   +4 more
doaj   +1 more source

PUS7 Deficiency: Phenotypical Expansion of PUS7‐Related Neurodevelopmental Disorders

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Pathogenic variants in PUS7, encoding pseudouridine synthase 7, cause a rare neurodevelopmental disorder marked by intellectual disability, microcephaly, short stature, and behavioral disturbances. Since the first report in 2018, only 16 patients have been described.
Alice Muda   +5 more
wiley   +1 more source

Lateral Ulnar Collateral Ligament Reconstruction Through a Mini-Invasive Approach. [PDF]

open access: yesArthrosc Tech
Abstract Posterolateral rotatory instability is the most common form of elbow instability, secondary to valgus, supination, and axial loading in elbow extension. The lateral ulnar collateral ligament (LUCL) is the primary restraint to posterolateral rotatory instability and multiple techniques of repair and reconstruction of the LUCL have been reported
Vismara V   +5 more
europepmc   +2 more sources

Investigation of the Relationship Between Wrist Ganglion Cysts and the Ulnar Variance Using 3-Tesla Magnetic Resonance Imaging

open access: yesHaseki Tıp Bülteni, 2022
Aim:A ganglion cyst is the most common soft tissue mass in the wrist and although the etiology of ganglion cysts remains unclear, the commonly accepted theory is that they are due to acute or chronic stress in the joint, which may be also caused by ulnar
Murat Bayav
doaj   +1 more source

Severe Phenotype in an Indian Family With Progressive Pseudorheumatoid Arthropathy of Childhood

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Progressive pseudorheumatoid arthropathy of childhood (PPAC) is a rare autosomal recessive progressive condition that affects the cartilage of joints and bones. The symptoms of PPAC include stiffness of the joints, bony swelling of the toes and fingers, short stature, kyphosis, and muscle weakness.
Narinder Singh   +5 more
wiley   +1 more source

Fracturedislocations of the proximal ulna

open access: yesActa Orthopaedica et Traumatologica Turcica, 2020
Abstract Objective: To investigate the relationship between injury patterns, complications, and the functional outcomes of patients with proximal-ulna fracture-dislocations. Methods: Retrospective analysis of 15 patients (10 men, 5 women; mean age, 49.1 years; mean follow-up 49 months) with 6 anterior and 9 posterior fracture-dislocations of the ...
Gereli, Arel   +4 more
openaire   +2 more sources

A Rare Form of Microcephalic Primordial Dwarfism due to NSMCE2 Deficiency (Seckel Syndrome Type 10): A Report of Macular Involvement

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Biallelic variants in NSMCE2 (MMS21), which encodes the SUMO E3 ligase subunit of the SMC5/6 chromatin‐maintenance complex, have recently been implicated in microcephalic primordial dwarfism (MPD), corresponding to Seckel syndrome type 10 (OMIM #617246).
Cristina Peduto   +5 more
wiley   +1 more source

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