Results 61 to 70 of about 252,175 (379)
Frontiers in Pediatrics, 2022 BackgroundSkeletal muscle deficits are associated with worse exercise performance in adults with pulmonary hypertension (PH) but the impact is poorly understood in pediatric PH.ObjectiveTo study muscle deficits, physical inactivity, and performance on ...
Catherine M. Avitabile +12 more
doaj +1 more source
Dual energy X-ray absorptiometry diagnostic discordance between Z scores and T scores in a young Iranian population [PDF]
, 2014 Background: Dual-energy X-ray Absorptiometry (DXA) is considered the gold standard for non-invasive measurement of bone mass. T-scores and Z-scores are used to present the results of bone mass. The present study was designed to evaluate the discordance
Heidari, Benham +5 more
core +1 more source
The nature of medical evidence and its inherent uncertainty for the clinical consultation : qualitative study [PDF]
, 2005 Objective To describe how clinicians deal with the uncertainty inherent in medical evidence in clinical consultations. Design Qualitative study. Setting Clinical consultations related to hormone replacement therapy, bone densitometry, and breast ...
Green, Eillen +2 more
core +2 more sources
European Journal of Radiology, 1992 In response to our publication (Gluer et al, 1990a), Wilson and colleagues (1990) proposed the adoption of a uniform terminology and corresponding abbreviation for Dual X-ray Absorptiometry (DXA). We supported this suggestion (Gluer et al, 1990b). Since then, the number of papers on DXA has increased considerably.
Genant, H. K. +6 more
openaire +12 more sources
FEBS Open Bio, EarlyView.NF90–NF45 functions as a negative regulator of methyltransferase‐like 3/14 (METTL3/14)‐mediated N6‐methyladenosine (m6A) modification on primary microRNAs (pri‐miRNAs). NF90–NF45 binds to anti‐oncogenic pri‐miRNAs and inhibits their m6A modification, thereby suppressing the biogenesis of anti‐oncogenic miRNAs.
Takuma Higuchi +6 more
wiley +1 more source
Molecular Genetics and Metabolism ReportsObjectives: Phenylketonuria is a hereditary condition caused by the deficiency of the enzyme phenylalanine hydroxylase, leading to abnormal phenylalanine metabolism.
Akram Ehsasat Vatan, M.D. +3 more
doaj +1 more source
CLINICAL CASE OF RARE TYPE V OSTEOGENESIS IMPERFECTA
Педиатрическая фармакология, 2015 Osteogenesis imperfecta, also known as the brittle bone disease, is a clinically heterogenic hereditary connective tissue disease characterized by brittle bones and high risk of skeletal bone fractures.
G. T. Yakhyayeva +8 more
doaj +1 more source
Measuring of Mandible Bone Density in Dogs Using /Digital Radiography/ Radiovisigraphy
Acta Veterinaria, 2020 Radiological diagnostics serves as one of the basic monitoring techniques in veterinary dental practice. The recent up-to-date literature data based on the findings of digital radiology/radiovisiography (RVG) in general dentistry inspired the authors to ...
Ilić Dragan +5 more
doaj +1 more source
Cutaneous Melanoma Drives Metabolic Changes in the Aged Bone Marrow Immune Microenvironment
Aging and Cancer, EarlyView.Melanoma, the deadliest form of skin cancer, increasingly affects older adults. Our study reveals that melanoma induces changes in iron and lipid levels in the bone marrow, impacting immune cell populations and increasing susceptibility to ferroptosis.
Alexis E. Carey +12 more
wiley +1 more source
Visual Recovery Reflects Cortical MeCP2 Sensitivity in Rett Syndrome
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Rett syndrome (RTT) is a devastating neurodevelopmental disorder with developmental regression affecting motor, sensory, and cognitive functions. Sensory disruptions contribute to the complex behavioral and cognitive difficulties and represent an important target for therapeutic interventions.
Alex Joseph Simon +12 more
wiley +1 more source