Results 131 to 140 of about 16,051 (234)
Introduction. Progressive facial hemiatrophy (Parry-Romberg syndrome)is a relatively rare disease of unclear aetiology. Some authorspostulate its relation with linear scleroderma.Objective.
Ligia Brzezińska-Wcisło +2 more
doaj
Serum SERPINA3 levels were higher in BOS compared to non‐BOS patients. OPG and SERPINA3 positive cells colocalized with tryptase positive mast cells in airways from BOS lung tissue. OPG and SERPINA3 staining positively correlated in partially and completely obstructed airways.
Yanzhe Liu +8 more
wiley +1 more source
Twardzina ograniczona pęcherzowa – przedstawienie dwóch przypadków, trudności terapeutyczne
tissue disease. The main symptoms are atrophy and fibrosis of the connectivetissue stroma, preceded by changes in the small blood vessels.Pathogenesis of morphea is still unknown.
Dorota Krasowska +5 more
doaj
The Therapeutic Effects of Semaglutide in Congenital Linear Scleroderma. [PDF]
Chen H, Elhawi M, Tarbox M.
europepmc +1 more source
Long-term follow-up of linear scleroderma en coup de sabre in children with central nervous system involvement. [PDF]
Chang X +8 more
europepmc +1 more source
Linear Scleroderma of the Head - Updates in management of Parry Romberg Syndrome and En coup de sabre: A rapid scoping review across subspecialties. [PDF]
Glaser DH +4 more
europepmc +1 more source
Recurrent Seizures in a Case of Linear Scleroderma En Coup de Sabre. [PDF]
Ahn SH, Lee HS, Yeom S, Park KI.
europepmc +1 more source
Advanced Neuroimaging and Clinical Findings in a Case of Linear Scleroderma En Coup De Sabre Presenting With Seizures. [PDF]
Kimura Y +2 more
europepmc +1 more source

