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Takao Konomoto

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Pediatric Nephrology (Berlin, Germany)|January 11, 2014
Nephrotic syndrome complicated by idiopathic central diabetes insipidusTakao Konomoto, Etsuko Tanaka, Hideaki Imamura, et al.
Pediatric Nephrology (Berlin, Germany)|November 16, 2025
Re-evaluating the MYH9 p.I1816V variant in a patient with atypical clinical presentationTakao Konomoto, Fumito Wakamatsu, Hiromi Sakaguchi, et al.
Case Reports in Nephrology|June 15, 2026
A Novel NPHS1-Associated Phenotype Characterized by Recurrent Transient ProteinuriaEtsuko Tanaka, Takao Konomoto, Hiromi Sakaguchi, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 12, 2015
Familial C3 glomerulonephritis associated with mutations in the gene for complement factor BHideaki Imamura, Takao Konomoto, Etsuko Tanaka, et al.
European Journal of Pediatrics|August 19, 2015
Sporadic paraganglioma caused by de novo SDHB mutations in a 6-year-old girlHideaki Imamura, Koji Muroya, Etsuko Tanaka, et al.
Cancer Medicine|November 7, 2019
TAE226, a dual inhibitor of focal adhesion kinase and insulin-like growth factor-I receptor, is effective for Ewing sarcomaHiroshi Moritake, Yusuke Saito, Daisuke Sawa, et al.
Nephrology (Carlton, Vic.)|November 13, 2015
Clinical and histological findings of autosomal dominant renal-limited disease with LMX1B mutationTakao Konomoto, Hideaki Imamura, Mayuko Orita, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 19, 2022
Eculizumab for paediatric patients with atypical haemolytic uraemic syndrome: full dataset analysis of post-marketing surveillance in JapanShuichi Ito, Hiroshi Hataya, Akira Ashida, et al.
Pediatric Nephrology (Berlin, Germany)|May 15, 2025
Kidney pathological findings of MYH9-related disease: a cross-sectional nationwide survey in JapanRyo Nakatani, Kenichiro Miura, Yoko Shirai, et al.
Journal of Human Genetics|October 28, 2016
Cryptic exon activation in SLC12A3 in Gitelman syndromeKandai Nozu, Yoshimi Nozu, Keita Nakanishi, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Pediatric Nephrology (Berlin, Germany)|January 11, 2014
Nephrotic syndrome complicated by idiopathic central diabetes insipidusTakao Konomoto, Etsuko Tanaka, Hideaki Imamura, et al.
Pediatric Nephrology (Berlin, Germany)|November 16, 2025
Re-evaluating the MYH9 p.I1816V variant in a patient with atypical clinical presentationTakao Konomoto, Fumito Wakamatsu, Hiromi Sakaguchi, et al.
Case Reports in Nephrology|June 15, 2026
A Novel NPHS1-Associated Phenotype Characterized by Recurrent Transient ProteinuriaEtsuko Tanaka, Takao Konomoto, Hiromi Sakaguchi, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 12, 2015
Familial C3 glomerulonephritis associated with mutations in the gene for complement factor BHideaki Imamura, Takao Konomoto, Etsuko Tanaka, et al.
European Journal of Pediatrics|August 19, 2015
Sporadic paraganglioma caused by de novo SDHB mutations in a 6-year-old girlHideaki Imamura, Koji Muroya, Etsuko Tanaka, et al.
Cancer Medicine|November 7, 2019
TAE226, a dual inhibitor of focal adhesion kinase and insulin-like growth factor-I receptor, is effective for Ewing sarcomaHiroshi Moritake, Yusuke Saito, Daisuke Sawa, et al.
Nephrology (Carlton, Vic.)|November 13, 2015
Clinical and histological findings of autosomal dominant renal-limited disease with LMX1B mutationTakao Konomoto, Hideaki Imamura, Mayuko Orita, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 19, 2022
Eculizumab for paediatric patients with atypical haemolytic uraemic syndrome: full dataset analysis of post-marketing surveillance in JapanShuichi Ito, Hiroshi Hataya, Akira Ashida, et al.
Pediatric Nephrology (Berlin, Germany)|May 15, 2025
Kidney pathological findings of MYH9-related disease: a cross-sectional nationwide survey in JapanRyo Nakatani, Kenichiro Miura, Yoko Shirai, et al.
Journal of Human Genetics|October 28, 2016
Cryptic exon activation in SLC12A3 in Gitelman syndromeKandai Nozu, Yoshimi Nozu, Keita Nakanishi, et al.
Pageof 2