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https://olympias.lib.uoi.gr/jspui/handle/123456789/23931Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Pavlidis, N. A. | en |
| dc.contributor.author | Drosos, A. A. | en |
| dc.contributor.author | Galanopoulos, V. | en |
| dc.contributor.author | Siamopoulos, C. | en |
| dc.contributor.author | Tsianos, E. B. | en |
| dc.date.accessioned | 2015-11-24T19:36:44Z | - |
| dc.date.available | 2015-11-24T19:36:44Z | - |
| dc.identifier.issn | 0040-3660 | - |
| dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/23931 | - |
| dc.rights | Default Licence | - |
| dc.subject | Adult | en |
| dc.subject | Female | en |
| dc.subject | Greece | en |
| dc.subject | Humans | en |
| dc.subject | Hypertrophy | en |
| dc.subject | Lymphoma/etiology | en |
| dc.subject | Middle Aged | en |
| dc.subject | Parotid Gland/pathology | en |
| dc.subject | Raynaud Disease/diagnosis | en |
| dc.subject | Sjogren's Syndrome/complications/diagnosis/*ethnology | en |
| dc.subject | United States | en |
| dc.subject | Xerophthalmia/diagnosis/ethnology | en |
| dc.subject | Xerostomia/diagnosis/ethnology | en |
| dc.title | The natural course of primary Sjogren's syndrome (a clinical study) | en |
| heal.type | journalArticle | - |
| heal.type.en | Journal article | en |
| heal.type.el | Άρθρο Περιοδικού | el |
| heal.identifier.secondary | http://www.ncbi.nlm.nih.gov/pubmed/3394101 | - |
| heal.language | ru | - |
| heal.access | campus | - |
| heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικής | el |
| heal.publicationDate | 1988 | - |
| heal.abstract | In this work the authors analyzed the clinical course and diagnostic procedures of 104 patients with primary Sjogren's syndrome (pSS): 57 patients diagnosed and followed-up at Ioannina University and 47 similar patients treated at the National Institute of Health (USA). Both studies have shown that pSS is predominantly a female disease with a latent period of 6-8 yrs from the time of the first symptom to the time of final diagnosis. Although the syndrome begins almost exclusively with glandular manifestations (xerostomia, xerophthalmia or parotid gland enlargement), in a respectable percentage of patients it eventually progresses to extraglandular involvement. pSS can be potentially complicated by benign (pseudolymphoma) or malignant (lymphoma) lymphoproliferative disorders. | en |
| heal.journalName | Ter Arkh | en |
| heal.journalType | peer-reviewed | - |
| heal.fullTextAvailability | TRUE | - |
| Appears in Collections: | Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ | |
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