Results 41 to 50 of about 59,583 (277)

Diffusion‐Weighted Imaging for the Evaluation of the Sacroiliac Joint in Pediatric Patients

open access: yesArthritis Care &Research, EarlyView.
Objective Maturational signal in the sacroiliac joint (SIJ) of skeletally immature youth is often misinterpreted as inflammation. Diagnostic tools that improve specificity are greatly needed. Apparent diffusion coefficient (ADC) values from diffusion‐weighted imaging (DWI), when used with standard imaging, may enhance diagnostic accuracy.
Michael L. Francavilla   +6 more
wiley   +1 more source

ASUHAN KEPERAWATAN LANSIA YANG MENGALAMI GANGGUAN MOBILITAS FISIK DENGAN REUMTOID ARTRITIS DI UPTD GRIYA WERDHA SURABAYA [PDF]

open access: yes, 2016
Pada lansia sering kali dijumpai gangguan pada sistem muskulo skeletal salah satu penyebab paling besar adalah reumathoid artritis, data dari UPTD Griya Werdaha Surabaya sekitar 20% lansia mengalami Reumatoid Artritis.
SUTOWO, EFAN WIRATNO
core  

Synergistic Osteogenesis After Co‐Administration of cmRNAs Encoding BMP‐2 and BMP‐7 Utilizing a Transcript‐Activated Matrix

open access: yesAdvanced Functional Materials, EarlyView.
This study demonstrates that the dual delivery of BMP‐2/‐7 coding cmRNAs for bone healing is demonstrated as feasible, safe, and highly osteogenic. Compared to single BMP‐2 or BMP‐7 cmRNAs, the combination enhances the production of both mineral and organic components of the extracellular matrix when delivered using a collagen‐HA scaffold, supporting ...
Claudia Del Toro Runzer   +7 more
wiley   +1 more source

GATA3 Deletion Associated With Juvenile Idiopathic Arthritis: Expanding the Phenotypic Spectrum of Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia (HDR) Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Hypoparathyroidism, sensorineural deafness, and renal dysplasia (HDR) syndrome is caused by pathogenic variants in the GATA3 gene located on chromosome 10p14. Here we present a 10‐year‐old girl with HDR syndrome who also has oligoarticular juvenile idiopathic arthritis (JIA).
Lauren N. Meiss   +8 more
wiley   +1 more source

Desarrollo de psoriasis durante el tratamiento con Abatacept en artritis reumatoidea

open access: yesRevista Argentina de Reumatología, 2019
Abatacept es el primer agente biológico aprobado para el tratamiento de la Artritis Reumatoidea (AR) que actúa inhibiendo la co-estimulación de linfocitos T.
J.A. Riera   +4 more
doaj   +1 more source

Infección por VPH en mujeres con artritis reumatoide [PDF]

open access: yes, 2008
Antecedentes: el virus del papiloma humano (VPH) es el principal factor de riesgo de cáncer de cuello uterino, que sigue siendo la neoplasia más frecuente en nuestro país. Existen datos que muestran que los pacientes con inmunosupresión son más propensos
Flores Alvarado, Diana Elsa   +5 more
core  

Psychiatric Comorbidities and Treatment Modalities in Children With Osteogenesis Imperfecta: A Systematic Review of Mental Health

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT To evaluate the prevalence of psychiatric signs and symptoms and describe psychotherapeutic and psychopharmacological interventions among children with osteogenesis imperfecta (OI). PRISMA guidelines were followed, and the study was registered in PROSPERO (CRD42024588284). Studies (n = 1419) were identified across five databases.
Julia M. Morales   +13 more
wiley   +1 more source

Ateroesclerosis carotídea en pacientes con artritis reumatoide y nódulos reumatoides [PDF]

open access: yes, 2008
Objetivo: Determinar la asociación entre la presencia de nódulos reumatoides y el engrosamiento íntima media y placa de las arterias carótidas como marcador de ateroesclerosis.
Esquivel Valerio, Jorge Antonio   +2 more
core  

Alu Overexpression Leads to an Increased Double‐Stranded RNA Signature in Dermatomyositis

open access: yesArthritis &Rheumatology, EarlyView.
Objective Dermatomyositis is an autoimmune condition characterized by a high interferon signature of unknown etiology. Because coding sequences constitute <1.2% of our genomes, there is a need to explore the role of the noncoding genome in disease pathogenesis.
Rayan Najjar   +2 more
wiley   +1 more source

Prevalencia de hiperlaxitud ligamentaria y su asociación con dolor articular crónico

open access: yesRevista Reumatología al Día, 2016
El Síndrome de Hiperlaxitud Ligamentaria (SHL) es una entidad que asocia un rango de movilidad articular mayor al normal junto con alteraciones musculoesqueléticas.
Natalia Argüello Santillán   +2 more
doaj  

Home - About - Disclaimer - Privacy