Results 21 to 30 of about 9,596 (176)

Screening of adolescent idiopathic scoliosis using generative adversarial network (GAN) inversion method in chest radiographs.

open access: yesPLoS ONE, 2023
ObjectiveConventional computer-aided diagnosis using convolutional neural networks (CNN) has limitations in detecting sensitive changes and determining accurate decision boundaries in spectral and structural diseases such as scoliosis.
Jun Soo Lee   +8 more
doaj   +1 more source

Research progress on the etiology and pathogenesis of adolescent idiopathic scoliosis

open access: yesChinese Medical Journal, 2020
. Etiology of adolescent idiopathic scoliosis (AIS), a complicated three-dimensional spinal deformity with early-onset, receives continuous attention but remains unclear.
Yue Peng   +5 more
doaj   +1 more source

Brace-Related Stress and Quality-of-Life Parameters in Adolescents with Idiopathic Scoliosis

open access: yesSpine Surgery and Related Research, 2022
Introduction: This study investigated brace-related stress, trunk appearance perception, and quality of life in adolescent girls with idiopathic scoliosis who wear the Milwaukee brace for treatment.
Vahideh Moradi   +4 more
doaj   +1 more source

BODY IMAGE AND SOCIAL ANXIETY IN ADOLESCENT FEMALES WITH IDIOPATHIC SCOLIOSIS: EXPLORING SELF-ESTEEM AS MEDIATOR

open access: yesJurnal Ilmu Keluarga dan Konsumen
Adolescent females diagnosed with idiopathic scoliosis frequently encounter body image-related psychological difficulties that induce social anxiety, a condition significantly influenced by their level of self-esteem.
Siti Fatimah Nurhajah   +2 more
doaj   +1 more source

Prevalence of low back pain in adolescents with idiopathic scoliosis: a systematic review

open access: yesChiropractic & Manual Therapies, 2017
Background Adolescent idiopathic scoliosis is the most common spinal deformity occurring in adolescents and its established prevalence varies from 2 to 3%. Adolescent idiopathic scoliosis has been identified as a potential risk factor for the development
Jean Théroux   +6 more
doaj   +1 more source

Whole‐Genome Sequencing Pilot of the Central Asian Genomic Diversity Project Reveals Distinct Histories, Adaptation, and Introgression

open access: yesAdvanced Science, EarlyView.
As a pilot phase of the Central Asian Genomic Diversity Project, whole‐genome sequencing of 166 individuals from 20 Central Asian and Afghan Hazara populations reveals fine‐scale substructure shaped by repeated trans‐Eurasian migration and admixture. Integrated analyses uncover post‐admixture adaptation, archaic introgression, and medically relevant ...
Mengge Wang   +11 more
wiley   +1 more source

Scoliosis in an identical twin: a case report with literature review

open access: yesPAMJ Clinical Medicine, 2020
Scoliosis is called the lateral angulation of the vertebra more than 10 degrees. Scoliosis is divided into two groups that is congenital and idiopathic scoliosis. Congenital scoliosis was presented in one of the two 14-year-old sisters who were identical
Serdar Toy, Sinan Yilar
doaj   +1 more source

The Impact of Aging on the Anatomical Course of the Azygos Vein: A Retrospective, Computed Tomography Study

open access: yesClinical Anatomy, EarlyView.
ABSTRACT The azygos vein (AV) is typically described as ascending vertically to the right of the vertebral column before arching anteriorly to drain into the superior vena cava. However, a small number of studies suggest that it is found leftward in older adults.
Lauren R. Hector   +4 more
wiley   +1 more source

Zebrafish inversin mutants develop scoliosis in the absence of laterality defects

open access: yesDevelopmental Dynamics, EarlyView.
Abstract Background Human mutations in INVERSIN are associated with nephronophthisis, variable penetrance of situs inversus and congenital heart disease. Inversin has been shown to localize to cilia and many of the patient phenotypes are attributed to disrupted cilia function.
Christopher J. Derrick   +3 more
wiley   +1 more source

KBG syndrome: A scoping review of electroclinical features of patients with epilepsy

open access: yesEpileptic Disorders, EarlyView.
Abstract Background and Objectives KBG syndrome is a rare autosomal developmental disorder caused by pathogenic variants of the ANKRD11 gene. This scoping review aimed to explore all current literature data regarding clinical and electroencephalographic features of patients with KBG syndrome and epilepsy. Materials and Methods We conducted a literature
Stefania Kalampokini   +6 more
wiley   +1 more source

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