Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Kouichi Utsumi"'
Publikováno v:
International heart journal. 57(5)
Fabry disease, an X-linked lysosomal storage disorder due to α-galactosidase A deficiency, is associated with dysfunction of various cell types and results in a systemic vasculopathy. We describe a 29-year-old woman with Fabry disease presenting wit
Publikováno v:
Journal of Nippon Medical School. 79:111-114
Chronic kidney disease (CKD) is defined as either kidney damage or an estimated glomerular filtration rate (eGFR) of less than 60 mL/min/1.73 msup2/supfor more than 3 months. Kidney damage is defined as pathological abnormalities or markers of damage
Autor:
Tomohiro Kaneko, Hiroki Yamaguchi, Kenji Tajika, Yuh Fukuda, Akiko Mii, Shin-ichi Tsuchiya, Kouichi Utsumi, Yasuo Katayama, Emiko Fujita, Teppei Fujino, Megumi Fukui, Yasuhiko Iino, Akira Shimizu
Publikováno v:
Pathology International. 61:518-527
Thrombotic microangiopathy (TMA) is a major complication after hematopoietic stem cell transplantation (HSCT). In this study, we examined the clinical and pathologic features of 2 patients and 5 autopsy cases with HSCT-associated renal TMA to clarify
Autor:
Akira Shimizu, Yukinari Masuda, Arimi Ishikawa, T. Arai, Yasuhiko Iino, Kyoko Wakamatsu, Kouichi Utsumi, Akiko Mii, Tomohiro Kaneko, Yuh Fukuda, Kenji Tajika, Yasuo Katayama, Teppei Fujino
Publikováno v:
Pathology International. 61:34-41
Thrombotic microangiopathy (TMA) is a known complication of hematopoietic stem cell transplantation (HSCT). The pathogenesis of TMA is controversial but considered to involve various factors such as total body irradiation, use of calcineurin inhibito
Autor:
Akio Hirama, Kae Ueda, Akiko Mii, Yasuo Katayama, Yasuhiko Iino, Tomohiro Kaneko, Kouichi Utsumi
Publikováno v:
Nihon Ika Daigaku Igakkai Zasshi. 6:17-22
Chronic kidney disease (CKD) is defined by two criteria. One criterion is abnormal renal function or morphology, especially proteinuria. A second criterion is an estimated glomerular filtration rate (eGFR) less than 60 mL/min/1.73m2 calculated with t
Autor:
Hiroshi Nagayama, Ken-ichiro Katsura, Yasuo Katayama, Toshihiko Araki, Takehiro Seta, Kouichi Utsumi, Makoto Hamamoto, Masayuki Yokochi
Publikováno v:
Clinical Neurology and Neurosurgery. 107:491-496
Objective: This study was performed to evaluate which factors influence the outcome of Guillain–Barre Syndrome (GBS), focusing on the choice of treatments. Methods: Sixty-three GBS patients were retrospectively studied and the following factors wer
Autor:
Toshiya Katsumata, Genki Mizukoshi, Daisuke Takada, Yasuhiko Iino, Tomohiro Kaneko, Chisako Kamano, Yuko Fujita, Ken-ichiro Katsura, Yasuo Katayama, Syoichiro Kijima, Kouichi Utsumi, Kae Ueda
Publikováno v:
Nihon Ika Daigaku Igakkai Zasshi. 1:21-25
A 32-year-old man with a history of adult-onset asthma and a high level of P-ANCA and eosinophilia was referred to our hospital because of renal insufficiency. Renal and skin biopsy specimens confirmed a diagnosis of Churg-Strauss Syndrome (CSS). Tre
Publikováno v:
Journal of Nippon Medical School. 72:254-261
Fabry disease is an inherited lysosomal storage disorder characterized by a pathological intracellular glycosphingolipid deposition. The disease is caused by a deficit in the lysosomal enzyme alpha-galatosidase A, the gene for which is located in the
Publikováno v:
Stroke. 35:472-476
Background and Purpose— Crossed cerebellar diaschisis (CCD) refers to reduced metabolism and blood flow in the cerebellar hemisphere contralateral to a cerebral lesion. Many cortical areas have been reported to cause CCD without consideration of co
Publikováno v:
Clinical and Experimental Nephrology. 7:63-66
Reversible posterior leukoencephalopathy syndrome is one of the most serious complications of immunosuppressive therapy. The clinical features include headache, altered mental functioning, seizures, cortical blindness and other visual disturbances, w