Current Position, Affiliation
- Professor, Department of Pediatrics, Kobe University Graduate School of Medicine
Professional and Research Experience
- 2003, ,
Awards & Honors
- 2017, Japanese Society of Nephrology Clinical Scientist Award
Selected Publications
- Yamamura T, Horinouchi T, Nagano C, Omori T, Sakakibara N, Aoto Y, Ishiko S, Nakanishi K, Shima Y, Nagase H, Takeda H, Rossanti R, Ye MJ, Nozu Y, Ishimori S, Ninchoji T, Kaito H, Morisada N, Iijima K, ＊Nozu K: Genotype-phenotype correlations influence the response to angiotensin-targeting drugs in Japanese patients with male X-linked Alport syndrome. Kidney Int, 98, 1605-1614, 2020
- Yamamura T, Horinouchi T, Adachi T, Terakawa M, Takaoka Y, Omachi K, Takasato M, Takaishi K, Shoji T, Onishi Y, Kanazawa Y, Koizumi M, Tomono Y, Sugano A, Shono A, Minamikawa S, Nagano C, Sakakibara N, Ishiko S, Aoto Y, Kamura M, Harita Y, Miura K, Kanda S, Morisada N, Rossanti R, Ye MJ, Nozu Y, Matsuo M, Kai H, Iijima K, ＊Nozu K: Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5. Nat Commun, 11: 2777, 2020
- Iijima K, Sako M, Nozu K, Mori R, Tuchida N, Kamei K, Miura K, Aya K, Nakanishi K, Ohtomo Y, Takahashi S, Tanaka R, Kaito H, Nakamura H, Ishikura K, Ito S, Ohashi Y, Rituximab for Childhood-onset Refractory Nephrotic Syndrome Study G: Rituximab for childhood-onset, complicated, frequently relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: a multicentre, double-blind, randomised, placebo-controlled trial. Lancet, 2014, 384: 1273-1281
- Hashimura Y, ＊Nozu K, Kaito H, Nakanishi K, Fu XJ, Ohtsubo H, Hashimoto F, Oka M, Ninchoji T, Ishimori S, Morisada N, Matsunoshita N, Kamiyoshi N, Yoshikawa N, Iijima K: Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV alpha5 chain. Kidney Int, 2014, 85: 1208-1213
- Nozu K, Vorechovsky I, Kaito H, Fu XJ, Nakanishi K, Hashimura Y, Hashimoto F, Kamei K, Ito S, Kaku Y, Imasawa T, Ushijima K, Shimizu J, Makita Y, Konomoto T, Yoshikawa N, Iijima K: X-Linked Alport Syndrome Caused by Splicing Mutations in COL4A5. Clin J Am Soc Nephrol, 2014, 9: 1958-1964
APSN-TSN CME (1): Update on Rare and Inherited Kidney Disease
Role
Speaker
Date & Time
12/05 09:30 - 09:55
Place
Room 7 ( 703 )
Lecture Title
Comprehensive Approach to Alport Syndrome
Hereditary Kidney Diseases
Role
Speaker
Date & Time
12/06 17:35 - 17:50
Place
Room 7 ( 703 )
Lecture Title
Overview of Tubulopathies