Yoshimi Nozu

Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome

Naohiro Kamiyoshi, Kandai Nozu, Xue Jun Fu et al. · Clinical Journal of the American Society of Nephrology · 2016 · 134 citations

Life Sciences, Genetics, Molecular Genetics +15

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. · Kidney International · 2020 · 111 citations · Full text

Medicine, Genetics, Nephrology +16

Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness

Kandai Nozu, Tetsuji Inagaki, Xue Jun Fu et al. · Journal of Medical Genetics · 2008 · 107 citations

Life Sciences, Genetics, Molecular Genetics +16

Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo–Bartter/Gitelman syndrome based on clinical characteristics

Natsuki Matsunoshita, Kandai Nozu, Akemi Shono et al. · Genetics in Medicine · 2015 · 92 citations · Full text

Medicine, Pathology, Temporomandibular Disorder Clinical Examination +7

Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5

Tomohiko Yamamura, Tomoko Horinouchi, Tomomi Adachi et al. · Nature Communications · 2020 · 91 citations · Full text

Medicine, Genetics, Molecular Genetics +16