Therapeutic Advances in Chronic Disease
SCIE-ISI SCOPUS (2010-2023)
2040-6231
2040-6223
Mỹ
Cơ quản chủ quản: SAGE Publications Ltd , SAGE Publications Inc.
Lĩnh vực:
Medicine (miscellaneous)
Các bài báo tiêu biểu
Management of arthropathy in inflammatory bowel diseases The most common extra-intestinal manifestation in patients with inflammatory bowel disease (IBD) is articular involvement, with a prevalence ranging between 17% and 39%. It is frequently characterized by an involvement of the axial joints but may also be associated with peripheral arthritis. The target of therapy in the management of arthritis associated with IBD is to reduce the inflamma... ... hiện toàn bộ
Tập 6 Số 2 - Trang 65-77 - 2015
Interstitial lung disease is a major characteristic of anti-KS associated ant-synthetase syndromeBackground: Anti-KS autoantibodies are rare myositis-specific autoantibodies that have been described to target asparaginyl-transfer RNA synthetase. Methods: Here, we review the published literature on critical issues concerning the detection of anti-KS antibodies and the clinical features ass...
Tập 11 - 2020
Plasma ST6GAL1 regulates IgG sialylation to control IgA nephropathy progressionBackground: Our previous study revealed that plasma levels of a-2,6-sialyltransferase 1 (ST6GAL1) were increased in patients with IgA nephropathy (IgAN). ST6GAL1 catalyzes terminal sialylation of IgG to shift the antibody effector function to the anti-inflammatory pattern. However, the role of plasma ST6GAL1 in the progression of IgAN and underlying mecha...
Tập 12 - Trang 204062232110486 - 2021
Prescribing in care homes: the role of the geriatrician Large numbers of frail elderly people spend some time of their lives in care homes. Increasing age is associated with altered physiology, multiple diagnoses and complex comorbidity, and polypharmacy. Those living in care homes often take larger numbers of medications than those who live in the community and the risk of morbidity as a direct or indirect result of medications is high. Many ... ... hiện toàn bộ
Tập 2 Số 6 - Trang 353-358 - 2011
Novel homozygous mutation of PNLIP gene in congenital pancreatic lipase deficiency: an extended family studyIntroduction: Congenital pancreatic lipase deficiency (MIM 614338) is a rare genetic disorder caused by homozygous mutation in the PNLIP gene. Few cases have been reported worldwide and among them, few cases were genetically confirmed. Patients and methods: A 3-year-old girl presented with abu...
Tập 13 - 2022