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Nana Sakakibara

Showing results (1-10 of 87) with videos related to

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Pediatric Nephrology (Berlin, Germany)|March 31, 2025
Tubular proteinuria due to hereditary endocytic receptor disorder of the proximal tubule: Dent disease and chronic benign proteinuriaNana Sakakibara, Kandai Nozu
Pediatrics International : Official Journal of the Japan Pediatric Society|April 22, 2016
High-mobility group box-1 release into fetal circulation from umbilical cord tissue and amniotic epithelium in fetal ischemiaToshihiko Nakamura, Toshirou Yoshioka, Shingo Yamada, et al.
CEN Case Reports|February 2, 2024
A case of pseudo-Bartter/Gitelman syndrome caused by long-term laxative abuse, leading to end-stage kidney diseaseAtsushi Kondo, Kunihiko Yoshiya, Nana Sakakibara, et al.
Pediatric Nephrology (Berlin, Germany)|April 29, 2025
Clinical differences between female monozygotic twins with X-linked Alport syndrome with somatic mosaicismNaoaki Mikami, Hideaki Kitakado, Naoki Kimura, 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.
CEN Case Reports|April 23, 2023
IgA nephropathy in a boy with frequently relapsing nephrotic syndromeYuta Ichikawa, Tomoko Horinouchi, Yu Tanaka, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|December 13, 2019
Inherited salt-losing tubulopathy: An old condition but a new category of tubulopathyKandai Nozu, Tomohiko Yamamura, Tomoko Horinouchi, et al.
CEN Case Reports|January 3, 2026
Whole-genome sequencing identified a deep intronic COL4A5 variant causing aberrant splicing in a female patient with X-linked Alport syndromeChina Nagano, Shuhei Aoyama, Yuka Kimura, et al.
CEN Case Reports|June 28, 2020
Poststreptococcal acute glomerulonephritis can be a risk factor for accelerating kidney dysfunction in Alport syndrome: a case experienceYoshinori Araki, Azusa Kawaguchi, Nana Sakakibara, et al.
Clinical and Experimental Nephrology|July 16, 2020
Onset mechanism of a female patient with Dent disease 2Takayuki Okamoto, Nana Sakakibara, Kandai Nozu, et al.
Pageof 9

Showing results (1-10 of 87) with videos related to

Sort By:
Pageof 9
Pediatric Nephrology (Berlin, Germany)|March 31, 2025
Tubular proteinuria due to hereditary endocytic receptor disorder of the proximal tubule: Dent disease and chronic benign proteinuriaNana Sakakibara, Kandai Nozu
Pediatrics International : Official Journal of the Japan Pediatric Society|April 22, 2016
High-mobility group box-1 release into fetal circulation from umbilical cord tissue and amniotic epithelium in fetal ischemiaToshihiko Nakamura, Toshirou Yoshioka, Shingo Yamada, et al.
CEN Case Reports|February 2, 2024
A case of pseudo-Bartter/Gitelman syndrome caused by long-term laxative abuse, leading to end-stage kidney diseaseAtsushi Kondo, Kunihiko Yoshiya, Nana Sakakibara, et al.
Pediatric Nephrology (Berlin, Germany)|April 29, 2025
Clinical differences between female monozygotic twins with X-linked Alport syndrome with somatic mosaicismNaoaki Mikami, Hideaki Kitakado, Naoki Kimura, 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.
CEN Case Reports|April 23, 2023
IgA nephropathy in a boy with frequently relapsing nephrotic syndromeYuta Ichikawa, Tomoko Horinouchi, Yu Tanaka, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|December 13, 2019
Inherited salt-losing tubulopathy: An old condition but a new category of tubulopathyKandai Nozu, Tomohiko Yamamura, Tomoko Horinouchi, et al.
CEN Case Reports|January 3, 2026
Whole-genome sequencing identified a deep intronic COL4A5 variant causing aberrant splicing in a female patient with X-linked Alport syndromeChina Nagano, Shuhei Aoyama, Yuka Kimura, et al.
CEN Case Reports|June 28, 2020
Poststreptococcal acute glomerulonephritis can be a risk factor for accelerating kidney dysfunction in Alport syndrome: a case experienceYoshinori Araki, Azusa Kawaguchi, Nana Sakakibara, et al.
Clinical and Experimental Nephrology|July 16, 2020
Onset mechanism of a female patient with Dent disease 2Takayuki Okamoto, Nana Sakakibara, Kandai Nozu, et al.
Pageof 9