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 · 129 citations · Full text

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 · 106 citations

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 · 89 citations · Full text

Differential Diagnosis, Diagnosis, Pseudo–bartter/gitelman Syndrome +3

Natural history of genetically proven autosomal recessive Alport syndrome

Masafumi Oka, Kandai Nozu, Hiroshi Kaito et al. · Pediatric Nephrology · 2014 · 88 citations

Mendelian Disorder, Genetic Disorder, Genetics +5

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 · 88 citations

X-linked Alport Syndrome, Pathology, Milder Clinical Aspects +4