Internal Med Medical News about Calcinosis

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Familial Tumoral Calcinosis: From Characterization of a Rare Phenotype to the Pathogenesis of Ectopic Calcification
Journal of Investigative Dermatology, 10/30/09

Sprecher E et al. – The data gathered through the study of these rare disorders have recently led to the discovery of novel aspects of the pathogenesis of common disorders in humans, underscoring the potential concealed within the study of rare diseases.

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Tumoral calcinosis in children, a challenging and possibly underdiagnosed condition
Acta Orthopaedica Belgica, 11/17/09 Relevance Score: 88%

Tumoral Calcinosis Mimicking Recurrent Osteosarcoma
Radiology Case Reports, 10/23/09 Relevance Score: 87%

Familial tumoral calcinosis and hyperostosis–hyperphosphataemia syndrome are different manifestations of the same disease: novel missense mutations in GALNT3
Skeletal Radiology, 10/21/09 Relevance Score: 84%

Defective O-Glycosylation due to a Novel Homozygous S129P Mutation Is Associated with Lack of Fibroblast Growth Factor 23 Secretion and Tumoral Calcinosis
Journal of Clinical Endocrinology and Metabolism, 10/29/09 Relevance Score: 83%

Microstructure and mineral composition of dystrophic calcification associated with the idiopathic inflammatory myopathies
Arthritis Research & Therapy, 10/27/09 Relevance Score: 83%