Results 41 to 50 of about 5,141 (253)

Consistency of the sonographic image (double contour sign) in patients with gout after ambulation

Journal of Medical Ultrasound, 2019
The aim of this study was to know whether or not any crystal shedding occurs after ambulation in patients with gout and how it affects the consistency of the sonographic image of crystal deposition on hyaline cartilage. A total of 18 consecutive patients
Angel Checa
doaj   +1 more source

Articular cartilage mineralization in osteoarthritis of the hip [PDF]

, 2009
Background The aim of this study was to examine the frequency of articular cartilage calcification in patients with end-stage hip OA. Further, its impact on the clinical situation and the OA severity are analyzed.
Martin Fuerst, Oliver Niggemeyer, Lydia Lammers, Fritz Schäfer, Christoph Lohmann, Wolfgang Rüther, LM Ryan, BA Derfus, PB Halverson, L Sokoloff, M Abreu, DR Mitrovic, K Ishikawa, T Ohira, H Mitsuyama, M Fuerst, R Altman, WH Harris, JH Kellgren, HJ Mankin, F Echtermeyer, T Neogi, MP Morgan, GM McCarthy, HK Ea, KP Pritzker, A Yavorskyy, HS Cheung, RG Russell   +28 more
core   +1 more source

Epidemiology of gout and chondrocalcinosis

Reumatismo, 2012
Gout is the most common cause of inflammatory arthritis affecting at least 1% of the population in industrialized countries. It is closely associated with hyperuricemia and is characterized by formation and reversible deposition of monosodium urate ...
M. Govoni, A. Bortoluzzi, G. Ciancio
doaj   +1 more source

Orthostatic hypotension as an unusual presentation of spinal calcium pyrophosphate deposition disease: case report and review of literature

Romanian Journal of Internal Medicine, 2023
Calcium pyrophosphate crystal deposition disease (CPPD), also known as pseudogout, with spinal involvement, is associated with clinical manifestations of acute nerve compression or chronic spinal stenosis.
De Azevedo Sofia Moura, Pichel Rita Carrilho, Freitas Egídio, Campar Ana, Marinho António, Mendonça Teresa   +5 more
doaj   +1 more source

Heritability of crystal related arthropathies [PDF]

Romanian Journal of Rheumatology, 2022
The most common types of crystal arthropathies are gout and calcium pyrophosphate deposition (CPPD) disease. Serum urate levels are influenced by a combination of genetic factors and the environment. There are studies estimating the heritability of urate
Claudiu Avram, Razvan Gabriel Dragoi, Mihai Bojinca, Horatiu Popoviciu, Cristiana Adina Avram   +4 more
doaj   +1 more source

Condrocalcinose articular familiar Familial articular chondrocalcinosis

Revista 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, Liliana Galrão, Isabella Lima, Lucas Prado, Melba Moura   +4 more
doaj   +1 more source

Calcium Pyrophosphate Dihydrate Crystal Deposition Disease Involving the Ligamentum Flavum of the Cervical Spine with Intense Enhancement on MRI: A Case Report

대한영상의학회지, 2020
Calcium pyrophosphate dihydrate (CPPD) crystal deposition disease is characterized by chondrocalcinosis, which mainly affects the knees, wrists, pelvis, and rarely, the spine.
Junyoung Lee, Seunghun Lee, Jiyoon Bae
doaj   +1 more source

Gitelman syndrome associated with chondrocalcinosis: description of two cases

Reumatismo, 2011
Gitelman syndrome is a rare inherited tubulopathy, characterized by hypomagnesemia, hypokalemia, metabolic alkalosis, hypocalciuria and hyperreninemic hyperaldosteronism.
E. Filippucci, L. Di Geso, M. Tardella, G. Giacchetti, C. Bertolazzi, F. Silveri, M. Gutierrez, W. Grassi   +7 more
doaj   +1 more source

Calcium pyrophosphate crystal deposition disease as a risk factor for cardiovascular diseases

Научно-практическая ревматология, 2020
Calcium pyrophosphate crystal deposition disease (CPPD) is an inflammatory joint disease associated with abnormal accumulation of inorganic pyrophosphate.
A. M. Novikova
doaj   +1 more source

Hypophosphatasia [PDF]

, 2007
Hypophosphatasia is a rare inherited disorder characterized by defective bone and teeth mineralization, and deficiency of serum and bone alkaline phosphatase activity. The prevalence of severe forms of the disease has been estimated at 1/100 000.
Etienne Mornet, D Fraser, MP Whyte, M Shohat, RM Pauli, CA Moore, D Wenkert, MP Whyte, D Cole, MD Fallon, K Kozlowski, HJ Girschick, HJ Girschick, MP Whyte, MP Whyte, J Beumer 3rd, R Jemmerson, L Hessle, MF Hoylaerts, E Mornet, CR Greenberg, MJRK Weiss, E Mornet, E Mornet, N Sugimoto, M Fukushi, H Shibata, L Zurutuza, G Cai, M Fukushi-Irie, A Taillandier, H Watanabe, M Ito, Y Ishida, H Watanabe, K Komaru, KN Fedde, S Di Mauro, H Orimo, M Nasu, I Brun-Heath, EE Kim, MH Le Du, MP Whyte, JR Eastman, FHS Eberic, PS Henthorn, HL Muller, JC Hu, AS Lia-Baldini, M Herasse, M Robinow, X Lepe, J Millan, H Rasmussen, H Orimo, H Orimo, E Mornet, M Goseki-Sone, S Mumm, H Watanabe, H Watanabe, MP Whyte, CR Greenberg, A Taillandier, M Spentchian, I Brun-Heath, M Spentchian, A Watanabe, PS Henthorn, H Orimo, E Mornet, SJ Iqbal, D Wenkert, HJ Girschick, MP Whyte, RA Cahill, MJ Weiss, SE Antonarakis   +78 more
core   +2 more sources