Tumoral calcinosis
Tumoral calcinosis of the temporomandibular joint: CT and MR findings
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Tumoral calcinosis in the cervical spine: a case report and review of the literature
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Benet-Pagès, Anna (2006): Characterization of native FGF23 protein and mutant forms causing autosomal dominant hypophosphatemic rickets and familial tumoral calcinosis. Dissertation, LMU München: Fakultät für Biologie
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Juxta-articular tumoral calcinosis associated with the temporomandibular joint: a case report and concise review
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A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis
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Autoimmune hyperphosphatemic tumoral calcinosis in a patient with FGF23 autoantibodies
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Effects of parathyroidectomy on tumoral calcinosis in uremic patients with secondary hyperparathyroidism
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Hyperostosis With Hyperphosphatemia: Evidence of Familial Occurrence and Association With Tumoral Calcinosis
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Abstract Background: Calcinosis cutis is a very rare condition where in calcium deposits form in the skin. It occurs in
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Vitamin D endocrine system
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Efficacy of thalidomide in a girl with inflammatory calcinosis, a severe complication of juvenile dermatomyositis
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Tumoral response and tumoral phenotypic changes in a rat model of diethylnitrosamine-induced hepatocellular carcinoma after salirasib and sorafenib administration
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Idiopathic scrotal calcinosis: report of 2 cases, and review of pathogenesis and factors that determine patients’ acceptance of surgical treatment
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Iatrogenic calcinosis cutis in a child affected by Acute Lymphoblastic Leukemia
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Vol 29, No 4 (2019)
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Scl 86, a marker antigen for diffuse scleroderma
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Effectiveness of Rituximab Therapy on Severe Calcinosis in 4 Children with Juvenile Dermatomyositis
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Addressing intra-tumoral heterogeneity and therapy resistance
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Clinical phenotypes and biologic treatment use in juvenile dermatomyositis-associated calcinosis
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Fahr’s syndrome with seizure presentation
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