Results 11 to 20 of about 280,125 (195)

Markers of Type 2 Inflammation and Immunosenescence Are Upregulated in Localized Scleroderma. [PDF]

open access: goldInt J Mol Sci
Khoury L   +8 more
europepmc   +2 more sources

Unique and shared transcriptomic signatures underlying localized scleroderma pathogenesis identified using interpretable machine learning. [PDF]

open access: goldJCI Insight
Rosen AB   +9 more
europepmc   +2 more sources

Clinical periodontal diagnosis

open access: yesPeriodontology 2000, EarlyView., 2023
Abstract Periodontal diseases include pathological conditions elicited by the presence of bacterial biofilms leading to a host response. In the diagnostic process, clinical signs such as bleeding on probing, development of periodontal pockets and gingival recessions, furcation involvement and presence of radiographic bone loss should be assessed prior ...
Giovanni E. Salvi   +5 more
wiley   +1 more source

Antinuclear Antibodies in Localized Scleroderma [PDF]

open access: yesArthritis & Rheumatism, 1983
AbstractWhen HeLa cells were used as the substrate for detection by the indirect immunofluorescence method, antinuclear antibodies were demonstrated in 16 of 22 (72.7%) sera from patients with localized scleroderma. When mouse kidney sections were used, the positive rate for antinuclear antibodies was 50% (11 of 22).
Yasuharu Nakabayashi   +3 more
openaire   +4 more sources

Surgical Management of Localized Scleroderma [PDF]

open access: yesArchives of Craniofacial Surgery, 2017
Localized scleroderma is characterized by a thickening of the skin from excessive collagen deposits. It is not a fatal disease, but quality of life can be adversely affected due to changes in skin appearance, joint contractures, and, rarely, serious deformities of the face and extremities.
Jae Hyun Lee   +3 more
openaire   +3 more sources

Synchrotron-based near-field photothermal microspectroscopy: Development of a quantitative nanohistology set-up with expansion of the infrared capability 2 [PDF]

open access: yesarXiv, 2022
The purpose was two-fold: To explore the capability of the Diamond Synchrotron infra-red so as to include near-field photothermal microspectroscopy (PTMS); and Toward a quantitative nanohistology - investigation of scleroderma using synchrotron radiation (mu- FTIR). With recent advances in AFM, the integration of an IR temperature-based system on an IR
arxiv  

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