Xue Jun Fu

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

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

Natural history of genetically proven autosomal recessive Alport syndrome

Masafumi Oka, Kandai Nozu, Hiroshi Kaito et al. · Pediatric Nephrology · 2014 · 93 citations

Life Sciences, Genetics, Molecular Genetics +6

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

Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain

Yuya Hashimura, Kandai Nozu, Hiroshi Kaito et al. · Kidney International · 2013 · 92 citations

Medicine, Pathology, Human Genetics +9