3 results match your criteria: "and Rheumatology) Nippon Medical School[Affiliation]"

Article Synopsis
  • - Pulmonary arterial hypertension (PAH) is a serious condition that typically requires treatments like pulmonary vasodilators, but new drug developments are exploring different mechanisms, particularly targeting specific patient needs.
  • - A connection has been found between interleukin-6 (IL-6) levels and PAH, leading researchers to investigate this cytokine as a potential target for treatment in patients showing elevated IL-6.
  • - A clinical study is currently being conducted to see if an antibody called satralizumab can effectively treat PAH in patients identified through biomarker profiles, focusing on those with increased IL-6 levels.
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Thrombosis in Japanese patients with Fabry disease.

J Neurol Sci

August 2009

Department of Internal Medicine (Divisions of Neurology, Nephrology, and Rheumatology) Nippon Medical School, Tokyo, Japan.

Fabry disease is an X-linked lysosomal storage disease resulting from deficient activity of the enzyme alpha-galactosidase (alpha-Gal) A. It has been postulated that the accumulation of globotriaosylceramide in the endothelial cells of blood vessels may lead to thrombosis of the brain and other tissues. Recently, enzyme replacement therapy (ERT) for Fabry disease is available.

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Background: Arteriosclerosis obliterans (ASO) is a serious complication in patients with end-stage renal disease (ESRD) caused by diabetic nephropathy. Adsorption of low-density lipoprotein (LDL) has been performed to treat ASO. While efficacy of this treatment has been reported in limb ischemia, the mechanism underlying the benefit remains unclear.

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