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Nephron
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November 14, 2017
Detection of a Splice Site Variant in a Patient with Glomerulopathy and Fibronectin Deposits
Yurika Tsuji, Kandai Nozu, Tadashi Sofue, et al.
Kidney International Reports
|
January 1, 2019
Clinical and Genetic Characteristics in Patients With Gitelman Syndrome
Junya Fujimura, Kandai Nozu, Tomohiko Yamamura, et al.
Kidney International Reports
|
December 23, 2017
Natural History and Genotype-Phenotype Correlation in Female X-Linked Alport Syndrome
Tomohiko Yamamura, Kandai Nozu, Xue Jun Fu, et al.
Journal of Human Genetics
|
October 28, 2016
Cryptic exon activation in SLC12A3 in Gitelman syndrome
Kandai Nozu, Yoshimi Nozu, Keita Nakanishi, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
June 10, 2016
Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome
Naohiro Kamiyoshi, Kandai Nozu, Xue Jun Fu, et al.
Journal of Human Genetics
|
November 8, 2018
Clinical spectrum of male patients with OFD1 mutations
Nana Sakakibara, Naoya Morisada, Kandai Nozu, et al.
Molecular Genetics & Genomic Medicine
|
August 1, 2019
Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome
Tomohiko Yamamura, Kandai Nozu, Shogo Minamikawa, et al.
Clinical and Experimental Nephrology
|
November 1, 2016
Female X-linked Alport syndrome with somatic mosaicism
Kana Yokota, Kandai Nozu, Shogo Minamikawa, et al.
Journal of Human Genetics
|
February 21, 2018
Development of ultra-deep targeted RNA sequencing for analyzing X-chromosome inactivation in female Dent disease
Shogo Minamikawa, Kandai Nozu, Yoshimi Nozu, et al.
Kidney International
|
July 27, 2020
Genotype-phenotype correlations influence the response to angiotensin-targeting drugs in Japanese patients with male X-linked Alport syndrome
Tomohiko Yamamura, Tomoko Horinouchi, China Nagano, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
Nephron
|
November 14, 2017
Detection of a Splice Site Variant in a Patient with Glomerulopathy and Fibronectin Deposits
Yurika Tsuji, Kandai Nozu, Tadashi Sofue, et al.
Kidney International Reports
|
January 1, 2019
Clinical and Genetic Characteristics in Patients With Gitelman Syndrome
Junya Fujimura, Kandai Nozu, Tomohiko Yamamura, et al.
Kidney International Reports
|
December 23, 2017
Natural History and Genotype-Phenotype Correlation in Female X-Linked Alport Syndrome
Tomohiko Yamamura, Kandai Nozu, Xue Jun Fu, et al.
Journal of Human Genetics
|
October 28, 2016
Cryptic exon activation in SLC12A3 in Gitelman syndrome
Kandai Nozu, Yoshimi Nozu, Keita Nakanishi, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
June 10, 2016
Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome
Naohiro Kamiyoshi, Kandai Nozu, Xue Jun Fu, et al.
Journal of Human Genetics
|
November 8, 2018
Clinical spectrum of male patients with OFD1 mutations
Nana Sakakibara, Naoya Morisada, Kandai Nozu, et al.
Molecular Genetics & Genomic Medicine
|
August 1, 2019
Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome
Tomohiko Yamamura, Kandai Nozu, Shogo Minamikawa, et al.
Clinical and Experimental Nephrology
|
November 1, 2016
Female X-linked Alport syndrome with somatic mosaicism
Kana Yokota, Kandai Nozu, Shogo Minamikawa, et al.
Journal of Human Genetics
|
February 21, 2018
Development of ultra-deep targeted RNA sequencing for analyzing X-chromosome inactivation in female Dent disease
Shogo Minamikawa, Kandai Nozu, Yoshimi Nozu, et al.
Kidney International
|
July 27, 2020
Genotype-phenotype correlations influence the response to angiotensin-targeting drugs in Japanese patients with male X-linked Alport syndrome
Tomohiko Yamamura, Tomoko Horinouchi, China Nagano, et al.
Page
of 3