Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Mayumi Yahata"'
Autor:
Eriko Nishi, Takuma Iwaki, Toru Igarashi, Naoya Morisada, Shuichi Ito, Shunsuke Goto, Nobuya Takahashi, Shoichiro Kanda, Tomoaki Ishikawa, Yasufumi Ohtsuka, Koji Nagatani, Takayuki Okamoto, Ming Juan Ye, Nobuhiko Okamoto, Yuji Inaba, Shihomi Ina, Naoko Ito, Kazumoto Iijima, Ken Ito, Mayumi Yahata, Kenji Ishikura, Kandai Nozu, Kazuyuki Ueno, Ai Unzaki, Tatsuo Matsunaga, Kohei Omune
Publikováno v:
Journal of Human Genetics. 63:647-656
Branchio-oto-renal (BOR) syndrome is a rare autosomal dominant disorder characterized by branchiogenic anomalies, hearing loss, and renal anomalies. The aim of this study was to reveal the clinical phenotypes and their causative genes in Japanese BOR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5db57333aa05cf8406328a7c3ee7778
https://doi.org/10.1038/s10038-018-0429-8
https://doi.org/10.1038/s10038-018-0429-8
Publikováno v:
Nephrology.
Aim Advanced glycation end products and their precursors cause vascular damage through oxidative stress. We investigated the hypothesis that methylglyoxal (MG), 3-deoxyglucosone (3-DG) and pentosidine influence outcomes of chronic kidney disease (CKD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d0350167279009d3447ce62a508d0ea
https://doi.org/10.1111/nep.13526
https://doi.org/10.1111/nep.13526
Autor:
Izaya Nakaya, Tsutomu Sakuma, Mayumi Yahata, Jun Soma, Yugo Shibagaki, Tomomi Sasajima, Satoko Takahashi
Publikováno v:
Internal Medicine. 52:2503-2509
Objective The aim of this study was to elucidate the efficacy of cyclophosphamide (CY) in Japanese patients with antineutrophil cystoplasmic antibody (ANCA)-associated microscopic polyangiitis (MPA). Methods Sixty-four patients, newly diagnosed with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::685119abe2640cbe8a887316bde55ffb
https://doi.org/10.2169/internalmedicine.52.0199
https://doi.org/10.2169/internalmedicine.52.0199
Publikováno v:
Clinical Nephrology. 74:315-318
Rapidly progressive renal insufficiency is rare in patients with classic polyarteritis nodosa (cPAN). We describe two cases of cPAN who presented with rapid and progressive deterioration of renal function. Renal biopsies showed severe necrotizing vas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::652d0017eda82813514da0ccfab0ff2b
https://doi.org/10.5414/cnp74315
https://doi.org/10.5414/cnp74315
Publikováno v:
Internal Medicine. 49:1411-1415
Heavy chain deposition disease (HCDD) is characterized by glomerular and tubular deposition of non-amyloidotic monoclonal heavy chains without associated light chains. We describe a case of gamma1-HCDD who presented with nephrotic syndrome, microhema
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9641b0226aa093eb1bad17f530414bf9
https://doi.org/10.2169/internalmedicine.49.3499
https://doi.org/10.2169/internalmedicine.49.3499
Publikováno v:
Nihon Toseki Igakkai Zasshi. 43:601-608
症例は47歳，男性．2008年8月頃より全身浮腫と呼吸苦が出現したため前医受診，Cr 3.33 mg/dLと腎機能障害がみられ9月当院紹介入院となった．高度蛋白尿と血尿がみられ，さらに腎機能の悪
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e0706ce2ec3e29f33ddaa8a3c5c145a
https://doi.org/10.4009/jsdt.43.601
https://doi.org/10.4009/jsdt.43.601
Autor:
Yoichiro Chikamatsu, Tsutomu Sakuma, Hiroyo Sasaki, Jun Soma, Izaya Nakaya, Kazuhiro Yoshikawa, Mayumi Yahata
Publikováno v:
Journal of Nephrology & Therapeutics.
Background: Sarcoidosis is a multi-system disorder characterized by noncaseating epitheloid granuloma in multiple organs. However, granulomatous interstitial nephritis in the absence of extrarenal renal lesions is very rare. Case presentation: A 64-y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13360d0dec54c2c8a0304f4450652a31
https://doi.org/10.4172/2161-0959.s1-008
https://doi.org/10.4172/2161-0959.s1-008
Autor:
Tasuku Yoshie, Yasuhito Yamamoto, Tsuyoshi Onoe, Mitsuaki Isobe, Toshikazu Saito, Makoto Noda, Mayumi Yahata, Kenichiro Ichikawa, Michio Usui
Publikováno v:
Nihon Naika Gakkai Zasshi. 95:2547-2549
症例は42歳, 女性. 進行する浮腫, 全身倦怠感にて来院. 心エコー上右心負荷所見が強く当初原発性肺高血圧症を疑った. 入院後急性増悪しショック, 急性腎不全となったが右心カテーテル
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a99ef97240f68441f373e889980f8f27
https://doi.org/10.2169/naika.95.2547
https://doi.org/10.2169/naika.95.2547
Publikováno v:
BMC Research Notes
Background Bevacizumab, a recombinant humanized monoclonal antibody for vascular endothelial growth factor, has been widely used in various cancers offering substantial clinical benefit. It is reportedly associated with development of high-grade prot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29fe9fae900729418b92547902b2c3d6
https://doi.org/10.1186/1756-0500-6-450
https://doi.org/10.1186/1756-0500-6-450
Publikováno v:
Internal medicine (Tokyo, Japan). 51(13)
A 25-year-old woman presented with fever, arthralgia and proteinuria exhibiting leukopenia, hypocomplementemia, increased serum IgG and IgG4, and positive antinuclear and anti-double-stranded DNA antibodies. Renal biopsy revealed membranous nephropat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e98b7d2e8fbfd8556cf6e72d9b060f77
https://pubmed.ncbi.nlm.nih.gov/22790135
https://pubmed.ncbi.nlm.nih.gov/22790135