Fabry disease is an X‐linked recessive inborn metabolic disorder caused by a deficiency of
the lysosomal enzyme α‐galactosidase A (EC 3.2.1.22). The causative mutations are diverse…

Fabry disease is an X-linked recessive inborn metabolic disorder in which a deficiency in
lysosomal enzyme α-galactosidase A (Gal A) causes the systemic accumulation of …

We describe two cases of Fabry disease in non-blood-related Japanese men, manifesting
recurrent stroke even after the start of enzyme replacement therapy. Both exhibited chronic …

OBJECTIVE: Viral interleukin 10 (vIL-10) has a variety of immunomodulatory properties. We
examined the applicability of vIL-10 gene transfer to the treatment of mice with arthrogen-…

Light and heavy chain deposition disease (LHCDD) is a rare entity with less than two dozen
reported cases [1, 2]. The term LHCDD was proposed in 1984 as a variant of light chain …

Continuous ambulatory peritoneal dialysis (CAPD) peritonitis is a common problem in patients
on peritoneal dialysis, and the bacteriological diagnosis is important for the treatment of …

Recently, we developed a kidney-targeted gene transfer technique, in which naked DNA
was injected into the renal vein while the renal vein and artery were clamped. Kidney-targeted …

This study investigates the circadian blood pressure variation of non-diabetic chronic hemodialysis
(HD) patients on both HD and non-HD days as well as the factors affecting diurnal BP …

Thermal stabilities of four major components (l-menthol, l-menthone, piperitone, and l-menthyl
acetate) of Japanese mint essential oil were evaluated via subcritical water treatment. To …

Anaerobic digestion effluent (ADE) from aquatic macrophytes (Egeria densa, Elodea nuttallii,
Ceratophyllum demersum and Potamogeton maackianus) contains insufficient available …