FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Kandai Nozu

Research Profile

Disorders

Physiology

Mutation

Anatomy

Kidneys

Procedures

Chemicals & Drugs

Living Beings

Infants

Concepts & Ideas

Geographic Areas

Japan

Co-author Network

Publications

TOP 3
Taketsugu Hama; Kazumoto Iijima; Hironobu Mukaiyama; Koichi Nakanishi; Kandai Nozu; Mayumi Sako; Yuko Shima; Hiroko Togawa; Norishige Yoshikawa
Endoplasmic reticulum stress with low-dose cyclosporine in frequently relapsing nephrotic syndrome.
Yuko Shima; Ryojiro Tanaka; Hiroko Togawa; Taketsugu Hama; Kazumoto Iijima; Hiroshi Kaito; Hironobu Mukaiyama; Koichi Nakanishi; Kandai Nozu; Mayumi Sako; Norishige Yoshikawa
Spontaneous remission in children with IgA nephropathy.
Michelle Kwon; Alexandra Lerch-Gaggl; Lauren M North; Kandai Nozu; Ellis D Avner; Joe B Blumer; Daria V Ilatovskaya; Hyunho Kim; Tengis S Pavlov; Feng Qian; Shauna A Rasmussen; Alexander Staruschenko; William E Sweeney; Frank Park
G-protein signaling modulator 1 deficiency accelerates cystic disease in an orthologous mouse model of autosomal dominant polycystic kidney disease.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Kandai Nozu (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Taketsugu Hama; Kazumoto Iijima; Hironobu Mukaiyama; Koichi Nakanishi; Kandai Nozu; Mayumi Sako; Yuko Shima; Hiroko Togawa; Norishige Yoshikawa
Endoplasmic reticulum stress with low-dose cyclosporine in frequently relapsing nephrotic syndrome.
Pediatric nephrology (Berlin, Germany) 2013;28(6):903-9.
2013: Yuko Shima; Ryojiro Tanaka; Hiroko Togawa; Taketsugu Hama; Kazumoto Iijima; Hiroshi Kaito; Hironobu Mukaiyama; Koichi Nakanishi; Kandai Nozu; Mayumi Sako; Norishige Yoshikawa
Spontaneous remission in children with IgA nephropathy.
Pediatric nephrology (Berlin, Germany) 2013;28(1):71-6.
2012: Michelle Kwon; Alexandra Lerch-Gaggl; Lauren M North; Kandai Nozu; Ellis D Avner; Joe B Blumer; Daria V Ilatovskaya; Hyunho Kim; Tengis S Pavlov; Feng Qian; Shauna A Rasmussen; Alexander Staruschenko; William E Sweeney; Frank Park
G-protein signaling modulator 1 deficiency accelerates cystic disease in an orthologous mouse model of autosomal dominant polycystic kidney disease.
Proceedings of the National Academy of Sciences of the United States of America 2012;109(52):21462-7.
2012: Hiroko Chikamoto; Hiroshi Fujii; Motoshi Hattori; Masataka Hisano; Kiyonobu Ishizuka; Hiroshi Kaito; Yuko Kajiho; Nao Kuroda; Hideki Matsumura; Kandai Nozu; Yuko Akioka; Maki Shimizu
Pretransplantation combined therapy with plasmapheresis and rituximab in a second living-related kidney transplant pediatric recipient with a very high risk for focal segmental glomerulosclerosis recurrence.
Pediatric transplantation 2012;16(7):E286-90.
2012: Kazumoto Iijima; Shuichi Ito; Koichi Kamei; Kentaro Matsuoka; Michio Nagata; Koichi Nakanishi; Kandai Nozu; Hirofumi Ohashi; Tomonosuke Someya; Satoshi Sasaki
Focal segmental glomerulosclerosis in patients with complete deletion of one WT1 allele.
Pediatrics 2012;129(6):e1621-5.
2012: Naoto Nishizaki; Kandai Nozu; Yoshiyuki Ohtomo; Toshiaki Shimizu; Shuichiro Fujinaga; Daishi Hirano; Hiroaki Kanai; Hitoshi Kaya; Kazunari Kaneko
Hereditary renal hypouricemia: a cause of calcium oxalate urolithiasis in a young female.
Clinical nephrology 2012;77(2):161-3.
2011: Keisuke Otsubo; Yoji Sasahara; Kiyoshi Takatsu; Ikuya Tsuge; Hisashi Mori; Yoshinori Nagai; Kandai Nozu; Hans D Ochs; Akira Hayakawa; Reiko Horikawa; Kazumoto Iijima; Masue Imaizumi; Shuichi Ito; Yoshiro Kamachi; Hirokazu Kanegane; Ichiro Kobayashi; Toshio Miyawaki
Identification of FOXP3-negative regulatory T-like (CD4(+)CD25(+)CD127(low)) cells in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
Clinical immunology (Orlando, Fla.) 2011;141(1):111-20.
2011: Kazumichi Fujioka; Shigeru Honda; Kazumoto Iijima; Ichiro Morioka; Masashi Nishimoto; Kandai Nozu; Mizuki Tagami; Hideto Yamada; Naoki Yokoyama; Mariko Amano; Masafumi Matsuo
A surviving case of papillorenal syndrome with the phenotype of Potter sequence.
Pediatrics international : official journal of the Japan Pediatric Society 2011;53(3):406-8.
2011: Yuko Shima; Kandai Nozu; Yoshimi Nozu; Hiroko Togawa; Hiroshi Kaito; Masafumi Matsuo; Kazumoto Iijima; Koichi Nakanishi; Norishige Yoshikawa
Recurrent EIARF and PRES with severe renal hypouricemia by compound heterozygous SLC2A9 mutation.
Pediatrics 2011;127(6):e1621-5.
2011: Kevin R Regner; Kandai Nozu; Stephen M Lanier; Joe B Blumer; Ellis D Avner; William E Sweeney; Frank Park
Loss of activator of G-protein signaling 3 impairs renal tubular regeneration following acute kidney injury in rodents.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2011;25(6):1844-55.
2011: Takeshi Ninchoji; Hiroshi Kaito; Kandai Nozu; Yuya Hashimura; Kyoko Kanda; Ichiro Kamioka; Yuko Shima; Kiyoshi Hamahira; Koichi Nakanishi; Ryojiro Tanaka; Norishige Yoshikawa; Kazumoto Iijima; Masafumi Matsuo
Treatment strategies for Henoch-Schönlein purpura nephritis by histological and clinical severity.
Pediatric nephrology (Berlin, Germany) 2011;26(4):563-9.
2011: Yi-Fen Lo; Kandai Nozu; Kazumoto Iijima; Takahiro Morishita; Che-Chung Huang; Sung-Sen Yang; Huey-Kang Sytwu; Yu-Wei Fang; Min-Hua Tseng; Shih-Hua Lin
Recurrent deep intronic mutations in the SLC12A3 gene responsible for Gitelman's syndrome.
Clinical journal of the American Society of Nephrology : CJASN 2011;6(3):630-9.
2011: Hiroko Togawa; Koichi Nakanishi; Hironobu Mukaiyama; Taketsugu Hama; Yuko Shima; Mayumi Sako; Masayasu Miyajima; Kandai Nozu; Kazuhiro Nishii; Shizuko Nagao; Hisahide Takahashi; Kazumoto Iijima; Norishige Yoshikawa
Epithelial-to-mesenchymal transition in cyst lining epithelial cells in an orthologous PCK rat model of autosomal-recessive polycystic kidney disease.
American journal of physiology. Renal physiology 2011;300(2):F511-20.
2011: Yorihiro Iwasaki; Sadayuki Matsumoto; Kandai Nozu; Makio Takahashi; Hiroyuki Koshiyama
Two adjacent mutations on chromosome 16 discovered in a patient presenting with generalized convulsions after influenza A virus infection.
Internal medicine (Tokyo, Japan) 2011;50(19):2179-83.
2011: Kandai Nozu
[Bartter's syndrome].
Nihon Jinzo Gakkai shi 2011;53(2):163-8.
2011: Kyoko Kanda; Kandai Nozu; Hiroshi Kaito; Kazumoto Iijima; Koichi Nakanishi; Norishige Yoshikawa; Takeshi Ninchoji; Yuya Hashimura; Masafumi Matsuo; Michael L Moritz
The relationship between arginine vasopressin levels and hyponatremia following a percutaneous renal biopsy in children receiving hypotonic or isotonic intravenous fluids.
Pediatric nephrology (Berlin, Germany) 2011;26(1):99-104.
2011: Yuko Shima; Koichi Nakanishi; Koichi Kamei; Hiroko Togawa; Kandai Nozu; Ryojiro Tanaka; Satoshi Sasaki; Kazumoto Iijima; Norishige Yoshikawa
Disappearance of glomerular IgA deposits in childhood IgA nephropathy showing diffuse mesangial proliferation after 2 years of combination/prednisolone therapy.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2011;26(1):163-9.
2010: Kandai Nozu; Kazumoto Iijima; Kyoko Kanda; Koichi Nakanishi; Norishige Yoshikawa; Kenichi Satomura; Hiroshi Kaito; Yuya Hashimura; Takeshi Ninchoji; Hiroshi Komatsu; Koichi Kamei; Ritsuko Miyashita; Masaaki Kugo; Hiroshi Ohashi; Hajime Yamazaki; Hiroyo Mabe; Asa Otsubo; Takashi Igarashi; Masafumi Matsuo
The pharmacological characteristics of molecular-based inherited salt-losing tubulopathies.
The Journal of clinical endocrinology and metabolism 2010;95(12):E511-8.
2010: Kazumoto Iijima; Kandai Nozu; Koichi Kamei; Makiko Nakayama; Shuichi Ito; Kentaro Matsuoka; Tsutomu Ogata; Hiroshi Kaito; Koichi Nakanishi; Masafumi Matsuo
Severe Alport syndrome in a young woman caused by a t(X;1)(q22.3;p36.32) balanced translocation.
Pediatric nephrology (Berlin, Germany) 2010;25(10):2165-70.
2010: Naoya Morisada; Nanna Dahl Rendtorff; Kandai Nozu; Takahiro Morishita; Takayuki Miyakawa; Tohru Matsumoto; Satoshi Hisano; Kazumoto Iijima; Lisbeth Tranebjaerg; Akira Shirahata; Masafumi Matsuo; Koichi Kusuhara
Branchio-oto-renal syndrome caused by partial EYA1 deletion due to LINE-1 insertion.
Pediatric nephrology (Berlin, Germany) 2010;25(7):1343-8.
2010: Hideki Kumagai; Shizuko Matsumoto; Kandai Nozu
Hypokalemic rhabdomyolysis in a child with Gitelman's syndrome.
Pediatric nephrology (Berlin, Germany) 2010;25(5):953-5.
2010: Kazunari Kaneko; Masafumi Hasui; Atsuko Hata; Daisuke Hata; Kandai Nozu
Focal segmental glomerulosclerosis in a boy with Dent-2 disease.
Pediatric nephrology (Berlin, Germany) 2010;25(4):781-2.
2010: Kazunari Kaneko; Sachiyo Tanaka; Masafumi Hasui; Kandai Nozu; Rafal Przybyslaw Krol; Kazumoto Iijima; Keisuke Sugimoto; Tsukasa Takemura
A family with X-linked benign familial hematuria.
Pediatric nephrology (Berlin, Germany) 2010;25(3):545-8.
2009: Teruo Fujita; Takeshi Shimooka; Yoshie Teraoka; Yoshifumi Sugita; Hiroshi Kaito; Kazumoto Iijima; Masafumi Matsuo; Kandai Nozu; Ryojiro Tanaka
Acute renal failure due to obstructive uric acid stones associated with acute gastroenteritis.
Pediatric nephrology (Berlin, Germany) 2009;24(12):2467-9.
2009: Kandai Nozu; Kazumoto Iijima; Yoshimi Nozu; Ei Ikegami; Takehide Imai; Xue Jun Fu; Hiroshi Kaito; Koichi Nakanishi; Norishige Yoshikawa; Masafumi Matsuo
A deep intronic mutation in the SLC12A3 gene leads to Gitelman syndrome.
Pediatric research 2009;66(5):590-3.
2009: Kandai Nozu; Kazumoto Iijima; Kazuo Kawai; Yoshimi Nozu; Atsushi Nishida; Yasuhiro Takeshima; Xue Jun Fu; Yuya Hashimura; Hiroshi Kaito; Koichi Nakanishi; Norishige Yoshikawa; Masafumi Matsuo
In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation.
Human genetics 2009;126(4):533-8.
2009: Kandai Nozu; Rafal Przybyslaw Krol; Koichi Nakanishi; Norishige Yoshikawa; Yoshimi Nozu; Yasufumi Ohtsuka; Kazumoto Iijima; Masafumi Matsuo
Detection by multiplex ligation-dependent probe amplification of large deletion mutations in the COL4A5 gene in female patients with Alport syndrome.
Pediatric nephrology (Berlin, Germany) 2009;24(9):1773-4.
2009: Koichi Kamei; Shuichi Ito; Kandai Nozu; Shuichiro Fujinaga; Makiko Nakayama; Mayumi Sako; Mari Saito; Maki Yoneko; Kazumoto Iijima
Single dose of rituximab for refractory steroid-dependent nephrotic syndrome in children.
Pediatric nephrology (Berlin, Germany) 2009;24(7):1321-8.
2009: Yuya Hashimura; Kandai Nozu; Hirokazu Kanegane; Toshio Miyawaki; Akira Hayakawa; Norishige Yoshikawa; Koichi Nakanishi; Minoru Takemoto; Kazumoto Iijima; Masafumi Matsuo
Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
Pediatric nephrology (Berlin, Germany) 2009;24(6):1181-6.
2009: Hiroko Togawa; Koichi Nakanishi; Yuko Shima; Mina Obana; Mayumi Sako; Kandai Nozu; Ryojiro Tanaka; Kazumoto Iijima; Norishige Yoshikawa
Increased chymase-positive mast cells in children with crescentic glomerulonephritis.
Pediatric nephrology (Berlin, Germany) 2009;24(5):1071-5.
2009: Kazunari Kaneko; Naho Taniguchi; Yuko Tanabe; Takahide Nakano; Masafumi Hasui; Kandai Nozu
Oxidative imbalance in idiopathic renal hypouricemia.
Pediatric nephrology (Berlin, Germany) 2009;24(4):869-71.
2009: Yuko Shima; Koichi Nakanishi; Hiroko Togawa; Mina Obana; Mayumi Sako; Masakazu Miyawaki; Kandai Nozu; Kazumoto Iijima; Norishige Yoshikawa
Membranous nephropathy associated with thyroid-peroxidase antigen.
Pediatric nephrology (Berlin, Germany) 2009;24(3):605-8.
2009: Kyoko Kanda; Kandai Nozu; Naoki Yokoyama; Ichiro Morioka; Akihiro Miwa; Yuya Hashimura; Hiroshi Kaito; Kazumoto Iijima; Masafumi Matsuo
Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene.
BMC nephrology 2009;10():37.
2008: Kandai Nozu; Rafal Przybyslaw Krol; Yasufumi Ohtsuka; Koichi Nakanishi; Norishige Yoshikawa; Yoshimi Nozu; Hiroshi Kaito; Kyoko Kanda; Yuya Hashimura; Yuhei Hamasaki; Kazumoto Iijima; Masafumi Matsuo
Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients.
Pediatric nephrology (Berlin, Germany) 2008;23(11):2085-90.
2008: Ichiro Kamioka; Kunihiko Yoshiya; Kenichi Satomura; Hiroshi Kaito; Teruo Fujita; Kazumoto Iijima; Koichi Nakanishi; Norishige Yoshikawa; Kandai Nozu; Masafumi Matsuo
Risk factors for developing severe clinical course in HUS patients: a national survey in Japan.
Pediatrics international : official journal of the Japan Pediatric Society 2008;50(4):441-6.
2008: Rafal Przybyslaw Krol; Kandai Nozu; Koichi Nakanishi; Kazumoto Iijima; Yasuhiro Takeshima; Xue Jun Fu; Yoshimi Nozu; Hiroshi Kaito; Kyoko Kanda; Masafumi Matsuo; Norishige Yoshikawa
Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2008;23(8):2525-30.
2008: Keiji Iida; Kandai Nozu; Yutaka Takahashi; Yasuhiko Okimura; Hidesuke Kaji; Masafumi Matsuo; Kazuo Chihara
Characterization of a splicing abnormality in Gitelman syndrome.
American journal of kidney diseases : the official journal of the National Kidney Foundation 2008;51(6):1077-8.
2008: Nahoko Yata; Koichi Nakanishi; Yuko Shima; Hiroko Togawa; Mina Obana; Mayumi Sako; Kandai Nozu; Ryojiro Tanaka; Kazumoto Iijima; Norishige Yoshikawa
Improved renal survival in Japanese children with IgA nephropathy.
Pediatric nephrology (Berlin, Germany) 2008;23(6):905-12.
2008: Kandai Nozu; T Inagaki; Xue Jun Fu; Y Nozu; Hiroshi Kaito; Kyoko Kanda; Takashi Sekine; Takashi Igarashi; Koichi Nakanishi; Norishige Yoshikawa; Kazumoto Iijima; Masafumi Matsuo
Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness.
Journal of medical genetics 2008;45(3):182-6.
2008: Makiko Nakayama; Koichi Kamei; Kandai Nozu; Kentaro Matsuoka; Atsuko Nakagawa; Mayumi Sako; Kazumoto Iijima
Rituximab for refractory focal segmental glomerulosclerosis.
Pediatric nephrology (Berlin, Germany) 2008;23(3):481-5.
2008: Kazumoto Iijima; Ichiro Kamioka; Kandai Nozu
Management of diarrhea-associated hemolytic uremic syndrome in children.
Clinical and experimental nephrology 2008;12(1):16-9.
2007: Tsutomu Nakamura; Kandai Nozu; Kazumoto Iijima; Norishige Yoshikawa; Yuka Moriya; Motohiro Yamamori; Asae Kako; Masafumi Matsuo; Aki Sakurai; Noboru Okamura; Toshihisa Ishikawa; Katsuhiko Okumura; Toshiyuki Sakaeda
Association of cumulative cyclosporine dose with its irreversible nephrotoxicity in Japanese patients with pediatric-onset autoimmune diseases.
Biological & pharmaceutical bulletin 2007;30(12):2371-5.
2007: Teruo Fujita; Kandai Nozu; Kazumoto Iijima; Ichiro Kamioka; Hiroshi Kaito; Ryojiro Tanaka; Koichi Nakanishi; Masafumi Matsuo; Norishige Yoshikawa
Long-term follow-up of juvenile acute nonproliferative glomerulitis (JANG).
Pediatric nephrology (Berlin, Germany) 2007;22(11):1957-61.
2007: Kandai Nozu; Xue Jun Fu; Koichi Nakanishi; Norishige Yoshikawa; Hiroshi Kaito; Kyoko Kanda; Rafal Przybyslaw Krol; Ritsuko Miyashita; Hidekazu Kamitsuji; Shoichiro Kanda; Yoshiki Hayashi; Kenichi Satomura; Nobuhiko Shimizu; Kazumoto Iijima; Masafumi Matsuo
Molecular analysis of patients with type III Bartter syndrome: picking up large heterozygous deletions with semiquantitative PCR.
Pediatric research 2007;62(3):364-9.
2007: Kandai Nozu; Xue Jun Fu; Hiroshi Kaito; Kyoko Kanda; Naoki Yokoyama; Rafal Przybyslaw Krol; Toshihiro Nakajima; Mizutaka Kajiyama; Kazumoto Iijima; Masafumi Matsuo
A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism.
Pediatric nephrology (Berlin, Germany) 2007;22(8):1219-23.
2007: Takashi Sekine; Kandai Nozu; Rashmi Iyengar; Xue Jun Fu; Masafumi Matsuo; Ryojiro Tanaka; Kazumoto Iijima; Emiko Matsui; Yutaka Harita; Jun Inatomi; Takashi Igarashi
OCRL1 mutations in patients with Dent disease phenotype in Japan.
Pediatric nephrology (Berlin, Germany) 2007;22(7):975-80.
2007: Ichiro Kamioka; Kandai Nozu; Teruo Fujita; Hiroshi Kaito; Ryojiro Tanaka; Kunihiko Yoshiya; Kazumoto Iijima; Koichi Nakanishi; Norishige Yoshikawa; Masafumi Matsuo
Prognosis and pathological characteristics of five children with non-Shiga toxin-mediated hemolytic uremic syndrome.
Pediatrics international : official journal of the Japan Pediatric Society 2007;49(2):196-201.
2007: Hiroshi Kaito; Kandai Nozu; Xue Jun Fu; Ichiro Kamioka; Teruo Fujita; Kyoko Kanda; Rafal P Krol; Ryo Suminaga; Akihito Ishida; Kazumoto Iijima; Masafumi Matsuo
Detection of a transcript abnormality in mRNA of the SLC12A3 gene extracted from urinary sediment cells of a patient with Gitelman's syndrome.
Pediatric research 2007;61(4):502-5.
2006: Hiroshi Kaito; Kandai Nozu; Kazumoto Iijima; Koichi Nakanishi; Kunihiko Yoshiya; Kyoko Kanda; Rafal Przybyslaw Krol; Norishige Yoshikawa; Masafumi Matsuo
The effect of aldosterone blockade in patients with Alport syndrome.
Pediatric nephrology (Berlin, Germany) 2006;21(12):1824-9.
2006: Akiko Kitamura; Hiroyasu Tsukaguchi; Kazumoto Iijima; Jungo Araki; Motoshi Hattori; Masahiro Ikeda; Masataka Honda; Kandai Nozu; Hitoshi Nakazato; Norishige Yoshikawa; Shoji Kagami; Masaaki Muramatsu; Yong Choi; Hae Il Cheong; Toshio Doi
Genetics and clinical features of 15 Asian families with steroid-resistant nephrotic syndrome.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2006;21(11):3133-8.
2006: Xue Jun Fu; Kandai Nozu; Katsumi Goji; Kazushige Ikeda; Ichiro Kamioka; Teruo Fujita; Hiroshi Kaito; Hisahide Nishio; Kazumoto Iijima; Masafumi Matsuo
Enamel-renal syndrome associated with hypokalaemic metabolic alkalosis and impaired renal concentration: a novel syndrome?
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2006;21(10):2959-62.
2006: Mina Obana; Koichi Nakanishi; Mayumi Sako; Nahoko Yata; Kandai Nozu; Ryojiro Tanaka; Kazumoto Iijima; Norishige Yoshikawa
Segmental membranous glomerulonephritis in children: comparison with global membranous glomerulonephritis.
Clinical journal of the American Society of Nephrology : CJASN 2006;1(4):723-9.
2006: Kandai Nozu; Kazumoto Iijima; Ichiro Kamioka; Teruo Fujita; Kunihiko Yoshiya; Ryojiro Tanaka; Koichi Nakanishi; Norishige Yoshikawa; Masafumi Matsuo
High-dose mizoribine treatment for adolescents with systemic lupus erythematosus.
Pediatrics international : official journal of the Japan Pediatric Society 2006;48(2):152-7.
2006: Michiyo Okada; Rika Fujimaru; Noriko Morimoto; Kenichi Satomura; Yoshikazu Kaku; Kazuo Tsuzuki; Kandai Nozu; Torayuki Okuyama; Kazumoto Iijima
EYA1 and SIX1 gene mutations in Japanese patients with branchio-oto-renal (BOR) syndrome and related conditions.
Pediatric nephrology (Berlin, Germany) 2006;21(4):475-81.
2006: Teruo Fujita; Kandai Nozu; Kazumoto Iijima; Ichiro Kamioka; Kunihiko Yoshiya; Ryojiro Tanaka; Kiyoshi Hamahira; Koichi Nakanishi; Norishige Yoshikawa; Masafumi Matsuo
Long-term follow-up of atypical membranoproliferative glomerulonephritis: are steroids indicated?
Pediatric nephrology (Berlin, Germany) 2006;21(2):194-200.
2006: Toshiyuki Sakaeda; Kazumoto Iijima; Kandai Nozu; Tsutomu Nakamura; Yuka Moriya; Mika Nishikawa; Atsushi Wada; Noboru Okamura; Masafumi Matsuo; Katsuhiko Okumura
Prediction of systemic exposure to cyclosporine in Japanese pediatric patients.
Journal of human genetics 2006;51(11):969-76.
2005: Kandai Nozu; Kazumoto Iijima; Masato Fujisawa; Atsuko Nakagawa; Norishige Yoshikawa; Masafumi Matsuo
Rituximab treatment for posttransplant lymphoproliferative disorder (PTLD) induces complete remission of recurrent nephrotic syndrome.
Pediatric nephrology (Berlin, Germany) 2005;20(11):1660-3.
2005: Kandai Nozu; Kazumoto Iijima; Toshiyuki Sakaeda; Katsuhiko Okumura; Koichi Nakanishi; Norishige Yoshikawa; Masataka Honda; Masahiro Ikeda; Masafumi Matsuo
Cyclosporin A absorption profiles in children with nephrotic syndrome.
Pediatric nephrology (Berlin, Germany) 2005;20(7):910-3.
2005: Teguh Haryo Sasongko; Ahmad Hamim Sadewa; Pungky Ardani Kusuma; Martua Parlindungan Damanik; Myeong Jin Lee; Hitoshi Ayaki; Kandai Nozu; Akinobu Goto; Masafumi Matsuo; Hisahide Nishio
ACE gene polymorphism in children with nephrotic syndrome in the Indonesian population.
The Kobe journal of medical sciences 2005;51(3-4):41-7.
2004: Xue Jun Fu; Kazumoto Iijima; Kandai Nozu; Kiyoshi Hamahira; Ryojiro Tanaka; Tatsuya Oda; Norishige Yoshikawa; Masafumi Matsuo
Role of p38 MAP kinase pathway in a toxin-induced model of hemolytic uremic syndrome.
Pediatric nephrology (Berlin, Germany) 2004;19(8):844-52.
2004: Koichi Nakanishi; Mayumi Sako; Nahoko Yata; Noriyuki Aoyagi; Kandai Nozu; Ryojiro Tanaka; Kazumoto Iijima; Norishige Yoshikawa
A-20C angiotensinogen gene polymorphism and proteinuria in childhood IgA nephropathy.
Pediatric nephrology (Berlin, Germany) 2004;19(2):144-7.
2002: Kazumoto Iijima; Kiyoshi Hamahira; Ryojiro Tanaka; Akiko Kobayashi; Kandai Nozu; Hajime Nakamura; Norishige Yoshikawa
Risk factors for cyclosporine-induced tubulointerstitial lesions in children with minimal change nephrotic syndrome.
Kidney international 2002;61(5):1801-5.