Results 71 to 80 of about 5,141 (253)

Sonographic Assessments to Consider in Future Studies about Crystal-related Arthritis

Journal of Medical Ultrasound
Background: Ultrasonography has shown a high sensitivity and specificity in the diagnosis of gout and chondrocalcinosis. Methods: The author considers it appropriate to discuss a new ultrasound technique and previous sonographic findings in crystal ...
Angel Checa
doaj   +1 more source

CPPD crystal deposition disease in patients with rheumatoid arthritis [PDF]

, 2018
The aim of this study was to assess the frequency and the outcome of patients suffering from rheumatoid arthritis in which calcium pyrophosphate dihydrate (CPPD) crystal deposits were found to coexist in synovial fluid analysis. Such association was more
Dudler, J., Gerster, J., Kern, J., So, A., Varisco, P.   +4 more
core  

Gitelman syndrome [PDF]

, 2013
Hypokalaemia is a common clinical disorder, the cause of which can usually be determined by the patient's clinical history. Gitelman syndrome is an inherited tubulopathy that must be considered in some settings of hypokalaemia.
Costa, F, Cotovio, P, Oliveira, N, Silva, C   +3 more
core   +1 more source

An Organ‐on‐Chip Platform for Strain‐Controlled, Tissue‐Specific Compression of Cartilage and Mineralized Osteochondral Interface to Study Mechanical Overloading in Osteoarthritis

Advanced Healthcare Materials, Volume 14, Issue 23, September 8, 2025.
A mechanically active OsteoChondral Unit (OCU)‐on‐Chip platform mimicking the OCU's functional anatomy and the strain gradient across the osteochondral interface is presented. Upon compartment‐specific hyperphysiological compression, the model replicates mechanisms observed in osteoarthritis (OA) progression, such as calcium crystal accumulation ...
Andrea Mainardi, Anastasiya Börsch, Paola Occhetta, Robert Ivanek, Martin Ehrbar, Lisa Krattiger, Philipp Oertle, Marko Loparic, Ivan Martin, Marco Rasponi, Andrea Barbero   +10 more
wiley   +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]

, 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, Fuentes, Paola, Herrera, Michelle, Matus, Carla, Vega S., Jorge, Vergara, Cristián, Webar, Javier   +6 more
core  

An effective encoding of human medical conditions in disease space provides a versatile framework for deciphering disease associations

Quantitative Biology, Volume 13, Issue 3, September 2025.
Abstract It is challenging to identify comorbidity patterns and mechanistically investigate disease associations based on health‐related data that are often sparse, large‐scale, and multimodal. Adopting a systems biology approach, embedding‐based algorithms provide a new perspective to examine diseases under a unified framework by mapping diseases into
Tianxin Xu, Yu Li, Xin Gao, Andrey Rzhetsky, Gengjie Jia   +4 more
wiley   +1 more source

Association of 4-basepair G-to-A transition in the 5′-untranslated region of ANKH gene with selected patients of primary knee osteoarthritis: A cross sectional study

Journal of Family Medicine and Primary Care, 2019
Method: A cohort study was carried out for a year to evaluate the presence of G-to-A transition in 5′-untranslated region of ankylosis human (ANKH) gene in Indian Khatri patients (closely resembling Europeans of primary knee osteoarthritis (OA), residing
Puneet Kumar, Aarti Sharma, Siddharth Das, Ragini Srivastava, Nikhil Gupta   +4 more
doaj   +1 more source

Comparison of outcomes after UKA in patients with and without chondrocalcinosis: a matched cohort study [PDF]

, 2017
Purpose: Chondrocalcinosis can be associated with an inflammatory arthritis and aggressive joint destruction. There is uncertainty as to whether chondrocalcinosis represents a contraindication to unicompartmental knee arthroplasty (UKA).
Athanasou, N, Borror, W, Dodd, CAF, Hamilton, TW, Jenkins, C, Kumar, V, Liddle, AD, Mellon, SJ, Murray, DW, Pandit, HG   +9 more
core  

Cri du Chat syndrome [PDF]

, 2006
The Cri du Chat syndrome (CdCS) is a genetic disease resulting from a deletion of variable size occurring on the short arm of chromosome 5 (5p-). The incidence ranges from 1:15,000 to 1:50,000 live-born infants.
Paola Cerruti Mainardi
core   +2 more sources

Novel Pathogenic Genotype in SLC12A3 Associated to Gitelman Syndrome: A Case Report

Nephrology, Volume 30, Issue 9, September 2025.
ABSTRACT Gitelman syndrome (GS) is considered one of the most common hereditary renal tubular disorders, characterised by hypokalemia, hypomagnesemia, hypocalciuria, and metabolic alkalosis. The primary cause of this disorder resides in the SLC12A3 gene, which encodes the NaCl cotransporter in the distal convoluted tubule, and for which more than 500 ...
Patricia Tomás‐Simó, Antonio Sierra‐Rivera, Ana Checa‐Ros, Raquel Rodríguez‐López, Antonio Galán‐Serrano, Luis D'Marco   +5 more
wiley   +1 more source