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Koji Nagatani

Showing results (1-10 of 11) with videos related to

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BMJ Case Reports|January 27, 2026
Elevated salivary amylase levels in paediatric acute recurrent pancreatitis: possible involvement of <i>CFTR</i> mutationsHaruka Honda, Koji Nagatani, Erina Ozaki, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 16, 2013
Involvement of CD5+CD19+Cell in steroid-dependent nephrotic syndrome treated with B-cell targeting therapyKoji Nagatani, Rie Yamaoka, Yuko Tezuka, et al.
Modern Rheumatology Case Reports|June 26, 2026
A Case of Neonatal Lupus Presenting with Fever and Rash in Early Infancy with Anti-dsDNA Antibodies, Born to an Asymptomatic Mother Negative for Anti-dsDNA AntibodiesMei Takemoto, Koji Nagatani, Sawa Tomomatsu, et al.
Pediatric Nephrology (Berlin, Germany)|February 22, 2012
Alport-like glomerular basement membrane changes with renal-coloboma syndromeHiromi Ohtsubo, Naoya Morisada, Hiroshi Kaito, et al.
Muscle & Nerve|November 15, 2019
Renal dysfunction can occur in advanced-stage Duchenne muscular dystrophyTakahiro Motoki, Yuko Shimizu-Motohashi, Isao Saito, et al.
Journal of Human Genetics|November 8, 2018
Clinical spectrum of male patients with OFD1 mutationsNana Sakakibara, Naoya Morisada, Kandai Nozu, et al.
Journal of Human Genetics|October 15, 2021
BCS1L mutations produce Fanconi syndrome with developmental disabilityKojima-Ishii Kanako, Nana Sakakibara, Kei Murayama, et al.
Kidney International Reports|June 12, 2026
Genetic Screening of Patients With Inherited Fanconi SyndromeYuta Inoki, Nana Sakakibara, Asahi Yamamoto, et al.
Journal of Human Genetics|March 4, 2018
Clinically diverse phenotypes and genotypes of patients with branchio-oto-renal syndromeAi Unzaki, Naoya Morisada, Kandai Nozu, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 29, 2021
Identification of novel OCRL isoforms associated with phenotypic differences between Dent disease-2 and Lowe syndromeNana Sakakibara, Takeshi Ijuin, Tomoko Horinouchi, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
BMJ Case Reports|January 27, 2026
Elevated salivary amylase levels in paediatric acute recurrent pancreatitis: possible involvement of <i>CFTR</i> mutationsHaruka Honda, Koji Nagatani, Erina Ozaki, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 16, 2013
Involvement of CD5+CD19+Cell in steroid-dependent nephrotic syndrome treated with B-cell targeting therapyKoji Nagatani, Rie Yamaoka, Yuko Tezuka, et al.
Modern Rheumatology Case Reports|June 26, 2026
A Case of Neonatal Lupus Presenting with Fever and Rash in Early Infancy with Anti-dsDNA Antibodies, Born to an Asymptomatic Mother Negative for Anti-dsDNA AntibodiesMei Takemoto, Koji Nagatani, Sawa Tomomatsu, et al.
Pediatric Nephrology (Berlin, Germany)|February 22, 2012
Alport-like glomerular basement membrane changes with renal-coloboma syndromeHiromi Ohtsubo, Naoya Morisada, Hiroshi Kaito, et al.
Muscle & Nerve|November 15, 2019
Renal dysfunction can occur in advanced-stage Duchenne muscular dystrophyTakahiro Motoki, Yuko Shimizu-Motohashi, Isao Saito, et al.
Journal of Human Genetics|November 8, 2018
Clinical spectrum of male patients with OFD1 mutationsNana Sakakibara, Naoya Morisada, Kandai Nozu, et al.
Journal of Human Genetics|October 15, 2021
BCS1L mutations produce Fanconi syndrome with developmental disabilityKojima-Ishii Kanako, Nana Sakakibara, Kei Murayama, et al.
Kidney International Reports|June 12, 2026
Genetic Screening of Patients With Inherited Fanconi SyndromeYuta Inoki, Nana Sakakibara, Asahi Yamamoto, et al.
Journal of Human Genetics|March 4, 2018
Clinically diverse phenotypes and genotypes of patients with branchio-oto-renal syndromeAi Unzaki, Naoya Morisada, Kandai Nozu, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 29, 2021
Identification of novel OCRL isoforms associated with phenotypic differences between Dent disease-2 and Lowe syndromeNana Sakakibara, Takeshi Ijuin, Tomoko Horinouchi, et al.
Pageof 2