Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Noboru Tsuru"'
Autor:
Noboru Tsuru, Kentaro Kamezaki, Tomohiro Kamoda, Kenji Ihara, Satoshi Akamine, Toshiro Hara, Ryo Sumazaki, Naoko Ito
Publikováno v:
CEN Case Reports. 4:218-222
Autosomal dominant distal renal tubular acidosis (dRTA) is a rare disorder caused by a mutation in the AE1 gene encoding the chloride–bicarbonate (Cl−/HCO3 −) anion exchanger 1 (AE1). Most patients with this disorder present with clinical sympt
Autor:
Thomas J. Jentsch, Noboru Tsuru, Junzou Suzuki, Willy Günther, Toshio Yanagihara, Mitsunobu Shimazu, Takashi Sekine, Jun Inatomi, Takashi Igarashi, Hiroshi Shiraga, Shouri Takahashi, Rajesh V. Thakker
Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent's Japan disease. Background The annual urinary screening of Japanese children above three years of age has identified a progressive renal tubular disorder ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55c16c86313dd6893425c2da2f58206f
https://ora.ox.ac.uk/objects/uuid:4583e597-9bae-4714-886d-65c278faa545
https://ora.ox.ac.uk/objects/uuid:4583e597-9bae-4714-886d-65c278faa545
Autor:
Makoto Ninomiya, Yuhei Ito, Shinzaburo Hattori, Zyunichi Miyata, Shigehiro Anan, Fumihiro Akashi, Hisataka Awata, Hisashi Kawanami, Isamu Kinoshita, Noboru Tsuru, Hironori Tominaga, Kunio Tomimasu, Toshiaki Toyota, Tamotsu Fujimoto
Publikováno v:
Nihon Shoni Jinzobyo Gakkai Zasshi. 21:146-156
Publikováno v:
Pediatric Nephrology. 17:363-366
Familial non-immune-mediated glomerulopathy has recently been recognized as a distinct clinical entity. The presentation includes proteinuria, often in the nephrotic range, microscopic hematuria, and hypertension. Renal function may remain intact lon
Autor:
Noboru Tsuru, Kazuhiko Niimi
Publikováno v:
Nihon Shoni Jinzobyo Gakkai Zasshi. 12:45-54
Autor:
Kasumi Kuramitsu Abe, Toshiki Hiratsuka, Keiko Tokieda, Kikuo Arakawa, Setsuya Naito, Noboru Tsuru, Isao Michinaga, Satoru Ogahara
Publikováno v:
Nephron. 70:28-34
We identified human leukocyte alloantigens (HLA) class II alleles in 24 Japanese children with steroid-sensitive nephrotic syndrome (SSNS) by deoxyribonucleic acid (DNA) typing. The DQA1 and DQB1 alleles were identified using sequence-specific oligon
Publikováno v:
Pediatric Nephrology. 8:423-426
We evaluated the clinicopathological features and the outcome of 33 children with primary glomerulonephritis (GN) as the cause of renal failure; 17 had asymptomatic (ASP) haematuria and/or proteinuria and the remaining 16 had symptoms suggestive of G
Autor:
Kumiko Mukuno, Makoto Ninomiya, Minoru Hohjoh, Minoru Yamagishi, Makoto Uchiyama, Shinzaburo Hattori, Satoshi Hisano, Yuhei Itoh, Norikazu Kuriya, Koichiroh Tamanaha, Kanehide Hashiguchi, Fumio Yamashita, Akio Furuse, Noboru Tsuru, Keizo Ohbu, Kiyoaki Nagano, Tetsuro Yanase
Publikováno v:
Pediatrics International. 32:343-348
We performed an epidemiologic study on the basis of a questionnaire survey of 162 children with end-stage renal disease (ESRD). Sixty-nine (43%) of our 162 children, including 25 detected at mass screening of urine, were found by chance hematuria and
Autor:
Akihisa Mitsudome, Noboru Tsuru, Kazuhiko Niimi, Yoshitsugu Kaku, Yuko Fukuma, Ken Hatae, Yasuhiro Kiyoshi, Satoshi Hisano, Hiroshi Iwasaki, Yoshie Segawa
Publikováno v:
American journal of kidney diseases : the official journal of the National Kidney Foundation. 47(3)
Background: Clinicopathologic correlation of C1q nephropathy is clarified poorly. The aim of our study is to clarify clinicopathologic correlation in childhood C1q nephropathy. Methods: Thirty children aged 3 to 15 years who met criteria proposed by
Autor:
Noboru Tsuru, Kazuyoshi Kuwano, Akihiko Nomura, Yusuke Saito, Shinichi Aishima, Nobutaka Nakashima, Shouichi Ohga, Hidetoshi Takada, Toshiro Hara
Publikováno v:
Pediatric pulmonology. 40(3)
Bronchiolitis obliterans organizing pneumonia (BOOP) is a rare complication of adult systemic lupus erythematosus (SLE). This is the first report of a pediatric patient with BOOP as an initial presentation of SLE. She had dyspnea, cough, arthralgia,