Results 71 to 80 of about 3,931 (219)

Condrocalcinose articular familiar Familial articular chondrocalcinosis

open access: yesRevista Brasileira de Reumatologia, 2004
Condrocalcinose articular familiar é uma condição clínica caracterizada pela deposição de cristais de pirofosfato de cálcio no líquido sinovial e cartilagens articulares levando à artrite.
Mittermayer Barreto Santiago   +4 more
doaj   +1 more source

Enfermedad por depósito de cristales de pirofosfato de calcio como ejemplo de forma de manifestación de la enfermedad en el adulto mayor [PDF]

open access: yes, 2015
Indexación: Web of Science; Scielo.Illness presentation in the elderly may be entirely non-specific, with fatigue, loss of function or the presence of geriatric syndromes.
Barthel M, Elizabeth   +6 more
core  

Elemental bio-imaging of calcium phosphate crystal deposits in knee samples from arthritic patients [PDF]

open access: yes, 2009
Laser ablation inductively coupled plasma mass spectrometry (LA ICP-MS) was employed to image deposits of calcium phosphate based crystals in knee cartilage and synovial fluid from arthritic patients.
Andrew L. Rozelle   +39 more
core   +1 more source

Crowned Dens Syndrome Triggered by Dental Treatment

open access: yesClinical Case Reports, Volume 13, Issue 2, February 2025.
ABSTRACT Crowned dens syndrome (CDS) is an important yet often overlooked cause of fever and neck pain, frequently leading to unnecessary examinations and treatments and misdiagnosis as infectious diseases or rheumatic diseases. The mechanism of an acute attack of CDS is not clarified completely, while it is considered that severe systemic stress can ...
Satoru Morita   +4 more
wiley   +1 more source

Adverse events from diagnostic and therapeutic joint injections: a literature review [PDF]

open access: yes, 2018
This review article classifies the various adverse reactions arising from intra-articular injections by severity, diagnostic category, and whether they are due to corticosteroid, local anesthetic or viscosupplementation injections.
Hodler, Juerg, Peterson, Cynthia
core  

Gout in a 15-year-old boy with juvenile idiopathic arthritis: A case study [PDF]

open access: yes, 2014
Joint pain is a common complaint in pediatrics and is most often attributed to overuse or injury. In the face of persistent, severe, or recurrent symptoms, the differential typically expands to include bony or structural causes versus rheumatologic ...
Grant, Kristen   +3 more
core   +2 more sources

Experience With Vaughan‐Jackson Syndrome at Eastern Regional Referral Hospital, Bhutan: Diagnosis and Its Treatment

open access: yesClinical Case Reports, Volume 13, Issue 2, February 2025.
ABSTRACT Vaughan‐Jackson syndrome is a clinical diagnosis that does not require advanced investigations. Timely intervention with tendon suturing or reconstruction, along with addressing the offending structures, can result in a successful functional outcome.
Kinzang Dorji
wiley   +1 more source

Recent Advances in Synovial Fluid Analysis [PDF]

open access: yes, 1974
Synovial fluid analysis is a frequently ignored examination except in suspected cases of septic conditions. It has been shown that it is an extremely valuable procedure in making rapid and accurate diagnoses in many types of joint ...
Owen, Duncan S., Jr.
core   +1 more source

The pathogenesis of tendinopathy. A molecular perspective [PDF]

open access: yes, 2004
There are many publications that discuss the aetiology, diagnosis and treatment of the various forms of tendinopathy, but few are based on conclusive scientific evidence.
Riley, GP
core   +1 more source

PDGFRA::USP8 Fusion in a Cutaneous Inflammatory Myofibroblastic Tumor, Highlighting Genetic Pleiotropy of Kinase Gene Fusions in Soft Tissue Neoplasms

open access: yesGenes, Chromosomes and Cancer, Volume 64, Issue 2, February 2025.
ABSTRACT PDGFRA::USP8 fusions have recently been described in neoplasms in the provisional category of calcified chondroid mesenchymal neoplasm (CCMN). Here, we describe a cutaneous inflammatory myofibroblastic tumor (IMT) on the upper leg of a 24‐year‐old male harboring the same fusion product. The tumor showed a morphology typical of IMT, including a
Astrid I. P. Vernemmen   +6 more
wiley   +1 more source

Home - About - Disclaimer - Privacy