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CLINICAL-LABORATORY, IMMUNOLOGICAL, PATHOGENETIC MANIFESTATIONS OF ANTIPHOSPHOLIPID SYNDROME AND IDENTIFICATION OF EFFECTIVE TREATMENT REGIMENS (REVIEWS)

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dc.contributor.author Musakov Mirzokhid Sabitdjanovich, Samatova Lobar Dilmurodovna, Turaxojaeva Sabokhat Sultanshikovna, Salaeva Muborak Saidabdullayevna, Tursunova Minavvar Ulug’bekovna
dc.date.accessioned 2024-01-13T19:31:35Z
dc.date.available 2024-01-13T19:31:35Z
dc.date.issued 2023-05
dc.identifier.issn 2751-1731
dc.identifier.uri http://repository.tma.uz/xmlui/handle/1/9944
dc.description.abstract Antiphospholipid syndrome (APS) is one of the leading causes of thrombosis. According to some estimates, the incidence of APS is about 5 new cases per 100,000 people per year and the prevalence is about 40-50 cases per 100,000 people [1], thus the problem of APS remains one of the most important in medicine. en_US
dc.language.iso en en_US
dc.publisher Spectrum Journal of Innovation, Reforms and Development en_US
dc.subject antiphospholipid syndrome (APS), antiphospholipid antibodies, lupus anticoagulant. en_US
dc.title CLINICAL-LABORATORY, IMMUNOLOGICAL, PATHOGENETIC MANIFESTATIONS OF ANTIPHOSPHOLIPID SYNDROME AND IDENTIFICATION OF EFFECTIVE TREATMENT REGIMENS (REVIEWS) en_US
dc.type Article en_US


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