Results 111 to 120 of about 1,382 (156)

Apremilast successfully treats cutaneous polyarteritis nodosa associated with SAPHO syndrome. [PDF]

open access: yesRheumatology (Oxford)
Malochet-Guinamand S   +3 more
europepmc   +1 more source

Quality of Life in Adult Patients With SAPHO Syndrome and Chronic Nonbacterial Osteomyelitis, and Comparison to Chronic Rheumatic and Inflammatory Diseases. [PDF]

open access: yesJ Rheumatol
Lenert A   +15 more
europepmc   +1 more source

Is JAK effective in treating recurrent SAPHO syndrome? TwHF might be a good choice. [PDF]

open access: yesMedicine (Baltimore)
Sun Q   +6 more
europepmc   +1 more source

The challenging diagnosis of synovitis-acne-pustulosis-hyperostosis-osteitis (SAPHO) syndrome: A rare case report. [PDF]

open access: yesSAGE Open Med Case Rep
El Harras Y   +4 more
europepmc   +1 more source
Some of the next articles are maybe not open access.

Related searches:

“SAPHO syndrome and infections”

Autoimmunity Reviews, 2009
The syndrome of synovitis, acne, pustulosis, hyperostosis, osteitis (SAPHO) encompasses a broad spectrum of cutaneous manifestations associated with osteitic and hyperostotic lesions, which typically may involve the anterior chest wall (ACW). The aetiopathogenetic mechanisms as well as the nosographic framing of the disease are still not fully defined ...
Marcello Govoni   +2 more
exaly   +3 more sources

SAPHO-Syndrom

Zeitschrift für Rheumatologie, 2014
The SAPHO syndrome, an acronym for synovitis, acne, pustulosis, hyperostosis and osteitis, is a rare disease which affects bones, joints and the skin. The main osteoarticular features are hyperostosis and osteitis. Osteoarticular symptoms predominantly occur on the anterior chest wall but the spine and the peripheral skeleton can also be involved.
F, Heldmann   +3 more
openaire   +3 more sources

SAPHO Syndrome

Dermatology, 2009
Four women with pustulosis palmoplantaris (PPP) and associated sternocostoclavicular hyperostosis are described. The connection between the two diseases is not coincidental: it is encountered in 9.4% of PPP patients, and was reported in the French literature as part of the SAPHO (synovitis acne pustulosis hyperostosis osteomyelitis) syndrome.
R E, Brandsen   +5 more
openaire   +3 more sources

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