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Publikováno v:
Rheumatology International. 7:23-27
In order to assess whether distal esophageal hypomotility in scleroderma is unique to this disease or not, we studied 25 normal volunteers and 109 patients with autoimmune rheumatic diseases (27 with primary Sjogren's syndrome, 25 with idiopathic Ray
Oesophageal motility was studied in 22 patients with primary Sjogren's syndrome and 20 normal volunteers. Oesophageal dysfunction was detected in eight of the 22 patients (36.4%) with primary Sjogren's syndrome. No abnormalities were detected in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2051d9a1ed2c254772dd59ce01506a83
https://europepmc.org/articles/PMC1001719/
https://europepmc.org/articles/PMC1001719/