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Scleroderma-related interstitial lung disease

Overview of attention for article published in Respiratory Medicine Case Reports, July 2017
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Title
Scleroderma-related interstitial lung disease
Published in
Respiratory Medicine Case Reports, July 2017
DOI 10.1016/j.rmcr.2017.07.007
Pubmed ID
Authors

Sally Suliman, Abdalhamid Al Harash, William Neil Roberts, Rafael L. Perez, Jesse Roman

Abstract

Scleroderma-related interstitial lung disease (SSc-ILD) is a pulmonary fibrosing disorder characterized by systemic inflammation and progressive scarring of the lungs that leads to respiratory failure. Although certain immunosuppressive therapies may slow disease progression, current treatment strategies are not curative; consequently, SSc-ILD continues to be a major cause of morbidity and mortality. We present four cases of SSc-ILD that emphasize the importance of early screening and detection, close follow-up, and aggressive management. We also highlight the need for well-conducted clinical trials designed to identify new and effective treatments.

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The data shown below were collected from the profiles of 5 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 67 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 67 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 11 16%
Other 10 15%
Researcher 8 12%
Student > Postgraduate 7 10%
Student > Master 6 9%
Other 5 7%
Unknown 20 30%
Readers by discipline Count As %
Medicine and Dentistry 24 36%
Biochemistry, Genetics and Molecular Biology 4 6%
Agricultural and Biological Sciences 4 6%
Nursing and Health Professions 4 6%
Pharmacology, Toxicology and Pharmaceutical Science 3 4%
Other 3 4%
Unknown 25 37%