Results 101 to 110 of about 15,405 (218)
Parry-Romberg Syndrome Associated with Localized Scleroderma
Case Reports in Neurology, 2010 Parry-Romberg syndrome is a rare neurocutaneous disorder of unknown origin. It is characterized by progressive facial hemiatrophy and frequently overlaps with a condition known as linear scleroderma ‘en coup de sabre’.
Jelena Maletic +4 more
doaj +1 more source
Juvenile localized scleroderma
Sri Lanka Journal of Child Health, 2019 No abstract available Sri Lanka Journal of Child Health, 2019; 48(4): 364 ...
Luis Zavaleta-Medina +4 more
openaire +2 more sources
A case of localized bullous scleroderma
Vestnik Dermatologii i Venerologii, 2017 Bullous scleroderma is a rare type of the focal form of the disease mainly affecting the skin and characterized by induration and sclerosis foci as well as subepidermal blisters containing a transparent matter.
A. L. Bakulev +3 more
doaj +1 more source
Topical application of a peptide inhibitor of transforming growth factor-beta1 ameliorates bleomycin-induced skin fibrosis [PDF]
, 2005 Transforming growth factor-beta (TGF-beta) plays a crucial role in the pathogenesis of skin fibrotic diseases. Systemic TGF-beta inhibitors effectively inhibit fibrosis in different animal models; however, systemic inhibition of TGF-beta raises important
Borras-Cuesta, F. (Francisco) +8 more
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Experience with Lipofilling in Children with Localized Scleroderma: Case Study
Вопросы современной педиатрииBackground. Localized scleroderma (LS) is an inflammatory sclerosing disease of unknown etiology. It is characterized by progressive lesion of connective tissue leading to sclerosis and/or atrophy of the skin and underlying tissues.
Alina R. Misbakhova +4 more
doaj +1 more source
Treatment of systemic sclerosis: potential role for stem cell transplantation. [PDF]
, 2009 Hematopoietic stem cell transplantation may reset the immune reconstitution and induce self tolerance of autoreactive lymphocytes, and has been explored in the treatments for systemic sclerosis.
Derk, Chris T, Xiong, Wen
core +2 more sources
, 2011 The classification of rheumatic diseases is still challenging due to several reasons. First, those diseases have several differential clinical features, which giving overlap symptoms.
D, H. P. (H) +4 more
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Synthetic Nucleic Acid Antigens in Localized Scleroderma. [PDF]
Int J Mol Sci, 2023 Khatri S +5 more
europepmc +1 more source
Патогенетичні взаємовідношення між бляшковою склеродермією, атрофодермією Пазіні–П’єріні та склероатрофічним ліхеном [PDF]
, 2015 У 130 хворих на бляшкову склеродермію, склероатрофічний ліхен, атрофодермію констатовані подібні показники порушень імунної системи (CD3, CD4, CD8, CD16, CD22, CD25, CD38, CD95, IgA, IgG, IgM, ЦІК, TNFα, IL-2, IL-4, IL-6, IL-10), адсорбційно-реологічних ...
Горбунцов, В.В. +2 more
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