Publications by authors named "Ken Hatae"

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Progressive myoclonic epilepsy as an expanding phenotype of NGLY1-associated congenital deglycosylation disorder: A case report and review of the literature.
Yuri Sonoda, Atsushi Fujita, Michiko Torio, Takahiko Mukaino, Ayumi Sakata, Ken Hatae

Eur J Med Genet· February 2024

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Kawasaki Disease and Vaccination: Prospective Case-Control and Case-Crossover Studies among Infants in Japan.
Kenji Murata, Sagano Onoyama, Kenichiro Yamamura, Yumi Mizuno, Kenji Furuno, Ken Hatae

Vaccines (Basel)· July 2021

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Assessment of Pediatric Admissions for Kawasaki Disease or Infectious Disease During the COVID-19 State of Emergency in Japan.
Takuya Hara, Kenji Furuno, Kenichiro Yamamura, Junji Kishimoto, Yumi Mizuno, Ken Hatae

JAMA Netw Open· April 2021

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Clinical Utility of Highly Purified 10% Liquid Intravenous Immunoglobulin in Kawasaki Disease.
Takuya Oda, Hazumu Nagata, Yasutaka Nakashima, Etsuro Nanishi, Yui Takada, Ken Hatae

J Pediatr· November 2019

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Strong Association of the Locus with Childhood Steroid-Sensitive Nephrotic Syndrome in the Japanese Population.
Xiaoyuan Jia, Tomoko Horinouchi, Yuki Hitomi, Akemi Shono, Seik-Soon Khor, Ken Hatae

J Am Soc Nephrol· August 2018

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Clarithromycin Plus Intravenous Immunoglobulin Therapy Can Reduce the Relapse Rate of Kawasaki Disease: A Phase 2, Open-Label, Randomized Control Study.
Etsuro Nanishi, Hisanori Nishio, Hidetoshi Takada, Kenichiro Yamamura, Mitsuharu Fukazawa, Ken Hatae

J Am Heart Assoc· July 2017

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Change in C1q deposition in C1q nephropathy.
Kazunari Kaneko, Masafumi Hasui, Ken Hatae, Hidenori So, Ritsuko Katafuchi

Pediatr Nephrol· September 2009

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Clinicopathologic correlation and outcome of C1q nephropathy.
Satoshi Hisano, Yuko Fukuma, Yoshie Segawa, Kazuhiko Niimi, Yoshitsugu Kaku, Ken Hatae

Clin J Am Soc Nephrol· November 2008

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Clinicopathologic correlation of C1q nephropathy in children.
Yuko Fukuma, Satoshi Hisano, Yoshie Segawa, Kazuhiko Niimi, Noboru Tsuru, Ken Hatae

Am J Kidney Dis· March 2006

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De novo insG619 mutation in PAX2 gene in a Japanese patient with papillorenal syndrome.
Keiko Yoshimura, Shigeo Yoshida, Yoko Yamaji, Aiko Komori, Ayako Yoshida, Ken Hatae

Am J Ophthalmol· April 2005

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