A variant of nephrogenic fibrosing dermopathy with osteoclast-like giant cells: a syndrome of dysregulated matrix remodeling?

Author:

Hershko Klilah,Hull Cheryl,Ettefagh Leila,Nedorost Susan,Dyson Senait,Horn Thomas,Gilliam Anita C.

Publisher

Wiley

Subject

Dermatology,Histology,Pathology and Forensic Medicine

Reference11 articles.

1. Characterization of inflammatory cells and study of TGF beta, type I, and type II collagen synthesis gene expression in affected skin from nephrogenic fibrosing dermopathy, a newly recognized scleroderma-like disease;Jimenez;Arthritis Rheum,2002

2. Molecular aspects of scleroderma;Trojanowska;Front Biosci,2002

3. Scleromyxoedema-like cutaneous diseases in renal-dialysis patients;Cowper;Lancet,2000

4. Nephrogenic fibrosing dermopathy;Cowper;Am J Dermatopathol,2001

5. Histochemistry and biochemistry of tartrate-resistant acid phosphatase (TRAP) and tartrate-resistant acid adenosine triphosphatase (TrATPase) in bone, bone marrow and spleen: implications for osteoclast ontogeny;Lindunger;Bone Miner,1990

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