Nozu Kandai
Kobe University
H-index: 46
Asia-Japan
Top articles of Nozu Kandai
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
A case of pseudo-Bartter/Gitelman syndrome caused by long-term laxative abuse, leading to end-stage kidney disease | CEN Case Reports | Atsushi Kondo Kunihiko Yoshiya Nana Sakakibara China Nagano Tomoko Horinouchi | 2024/2/2 |
In steroid-resistant nephrotic syndrome that meets the strict definition, monogenic variants less common than previously reported | Yuta Ichikawa Nana Sakakibara Yuta Inoki Yu Tanaka Chika Ueda | 2024/3/5 | |
Rituximab in combination with cyclosporine and steroid pulse therapy for childhood-onset multidrug-resistant nephrotic syndrome: a multicenter single-arm clinical trial … | Clinical and Experimental Nephrology | Kandai Nozu Mayumi Sako Seiji Tanaka Yuji Kano Yoko Ohwada | 2023/11/27 |
Longitudinal data of serum creatine kinase levels and motor, pulmonary, and cardiac functions in 337 patients with Duchenne muscular dystrophy | Muscle & Nerve | Hiroyuki Awano Yoshinori Nambu Chieko Itoh Akihiro Kida Tetsushi Yamamoto | 2024/5/1 |
Range of protein induced by vitamin K absence or antagonist-II levels in neonates at birth | Scientific Reports | Tomohiro Sameshima Mariko Ashina Takuya Fukuda Takumi Kido Shinya Abe | 2024/1/9 |
Factors related to recurrence of proteinuria in childhood IgA nephropathy | Pediatric Nephrology | Yuko Shima Hironobu Mukaiyama Yu Tanaka Wataru Shimabukuro Kandai Nozu | 2024/2 |
Recurrent transient severe hypocalcaemia in two siblings with type 1 Bartter syndrome | Nephrology | Juri Kanda Shoichiro Kanda Yoshiki Hayashi Kandai Nozu Shohei Ariji | 2023/12/7 |
End-stage ADPKD with a low-frequency PKD1 mosaic variant accelerated by chemoradiotherapy | Human Genome Variation | Hiroaki Hanafusa Hiroshi Yamaguchi Naoya Morisada Ming Juan Ye Riki Matsumoto | 2024/3/28 |
Novel Digenic Variants in COL4A4 and COL4A5 Causing X-Linked Alport Syndrome: A Case Report | Case Reports in Nephrology and Dialysis | Hideki Uedono Katsuhito Mori Shinya Nakatani Kohei Watanabe Rino Nakaya | 2024/1/3 |
Clinical characteristics and outcomes of immune-complex membranoproliferative glomerulonephritis and C3 glomerulopathy in Japanese children | Pediatric Nephrology | Chika Ueda Tomoko Horinouchi Yuta Inoki Yuta Ichikawa Yu Tanaka | 2024/4/25 |
IgA nephropathy in a boy with frequently relapsing nephrotic syndrome | CEN Case Reports | Yuta Ichikawa Tomoko Horinouchi Yu Tanaka Chika Ueda Hideaki Kitakado | 2023/4/24 |
A child with TSC2/PKD1 contiguous gene deletion syndrome successfully treated with tolvaptan for rapidly enlarging renal cysts | CEN Case Reports | Chika Muroga Hiroki Yokoyama Ryo Kinoshita Daisuke Fujimori Yuko Yamada | 2024/2/27 |
A novel NFKB1 variant in a Japanese pedigree with common variable immunodeficiency | Human Genome Variation | Naoko Nakatani Akihiro Tamura Hiroaki Hanafusa Nanako Nino Nobuyuki Yamamoto | 2024/3/22 |
Amyloid deposition through endocytosis in vascular endothelial cells | Experimental Hematology | Seiji Nishikage Akira Fujisawa Hiromi Endoh Hirotaka Sakamoto Tomohide Suzuki | 2024/1/1 |
Trimerization profile of type IV collagen COL4A5 exon deletion in X-linked Alport syndrome | Clinical and Experimental Nephrology | Yuimi Koyama Mary Ann Suico Aimi Owaki Ryoichi Sato Jun Kuwazuru | 2024/4/24 |
Clinical characteristics and long-term outcomes of immune-complex membranoproliferative glomerulonephritis and C3 glomerulopathy in Japanese children | Neurology | Elena F Mouresan Eleni Mentesidou Anders Berglund Kyla A Mckay Jan Hillert | 2024/3/26 |
Immunohistological analysis reveals IgG1-dominant immunophenotype of tubulointerstitial nephritis unassociated with IgG4-related diseases | International Urology and Nephrology | Toshiki Hyodo Shigeo Hara Shunsuke Goto Hideki Fujii Shinichi Nishi | 2024/2/21 |
Nail-patella syndrome with nephropathy in a de novo LMX1B mutation: triangular lunula of the thumb and lack of finger creases as clues | Yoshinori Banno Masako Ikemiyagi Riku Hamada Kandai Nozu Kentaro Matsuoka | 2023/12/6 | |
Brothers with Becker muscular dystrophy show discordance in skeletal muscle computed tomography findings: A case report | SAGE Open Medical Case Reports | Yoshinori Nambu Taku Shirakawa Kayo Osawa Hisahide Nishio Kandai Nozu | 2024/1 |
Prolonged Hypokalemia Long After Causative Factor Elimination in Pseudo-Bartter/Gitelman Syndrome | Atsushi Kondo Tomoko Horinouchi Yuta Inoki Yuta Ichikawa Yu Tanaka | 2024/4/22 |
