Results 51 to 60 of about 4,293 (240)

Resolution of uremic tumoral calcinosis in a patient on peritoneal dialysis with long-term low-calcium dialysate treatment

open access: yesKidney Research and Clinical Practice, 2014
Tumoral calcinosis is a rare complication in uremic patients. An in-depth review of published literature suggests that most patients with uremic tumoral calcinosis do not respond to medical treatment.
Yaerim Kim, Eunah Hwang, Sungbae Park
doaj   +1 more source

A case report of scrotal tumoral calcinosis in a patient on maintenance hemodialysis

open access: yesUrology Case Reports, 2020
Giant tumoral calcinosis is frequently seen around the joints in patients on maintenance hemodialysis (MHD), while it is rarely seen in the scrotum alone.
Hong Li   +4 more
doaj   +1 more source

Tumoral calcinosis [PDF]

open access: yesCleveland Clinic Journal of Medicine, 2021
Hiroyuki, Yano, Mitsuyo, Kinjo
openaire   +3 more sources

Multimodal imaging in the differential diagnosis of soft tissue calcinosis

open access: yesReumatismo, 2011
Soft tissue calcinosis is a common radiographic finding, which may be related to different types of pathological processes. Multimodality imaging, combined with analysis of clinical and laboratory data, plays an important role for the differential ...
G. Garlaschi   +6 more
doaj   +1 more source

Calcinosis of the internal jugular vein: Interesting presentation of tertiary hyperparathyroidism

open access: yesClinical Case Reports, 2022
Tumoral calcinosis is a severe complication of hemodialysis. A 49‐year‐old male on dialysis for end‐stage renal disease developed a large calcified retropharyngeal mass. This caused stridor and dyspnea, necessitating an emergency awake tracheostomy. This
Courtney B. Shires, Mona Shete
doaj   +1 more source

Hyperphosphatemic Tumoral Calcinosis

open access: yesPlastic and Reconstructive Surgery, 2000
Tumoral calcinosis is a rare syndrome characterized by progressively growing and painless masses of calcium phosphate deposits within periarticular areas. Biochemical findings are normal except for an association with hyperphosphatemia. This report describes hyperphosphatemic tumoral calcinosis in a 22-year-old man who had been operated on five times ...
Savaci, N   +3 more
openaire   +3 more sources

Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans [PDF]

open access: yes, 2017
It is well established that somatic genomic changes can influence phenotypes in cancer, but the role of adaptive changes in developmental disorders is less well understood.
Angela F. Brady   +30 more
core   +4 more sources

Increased uptake on 99mTc bone scintigraphy in a case of tumoral calcinosis in a child

open access: yesBJR|case reports, 2015
Tumoral calcinosis is an idiopathic condition resulting in the periarticular deposition of calcium crystals and salts in soft tissues. It is rare in children, and even rarer in idiopathic form.
N Jawad, M Dumba, P Brock, K McHugh
doaj   +1 more source

Establishment of sandwich ELISA for soluble alpha-Klotho measurement: Age-dependent change of soluble alpha-Klotho levels in healthy subjects [PDF]

open access: yes, 2010
Background α-Klotho (αKl) regulates mineral metabolism such as calcium ion (Ca2+) and inorganic phosphate (Pi) in circulation. Defects in mice result in clinical features resembling disorders found in human aging.
Aono, Yukiko   +20 more
core   +1 more source

FGF23 Deficiency Leads to Mixed Hearing Loss and Middle Ear Malformation in Mice [PDF]

open access: yes, 2014
Fibroblast growth factor 23 (FGF23) is a circulating hormone important in phosphate homeostasis. Abnormal serum levels of FGF23 result in systemic pathologies in humans and mice, including renal phosphate wasting diseases and hyperphosphatemia. We sought
Caruso, Paul   +7 more
core   +7 more sources

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