T
Takeshi Ninchoji
Researcher at Kobe University
Publications - 61
Citations - 827
Takeshi Ninchoji is an academic researcher from Kobe University. The author has contributed to research in topics: Alport syndrome & Medicine. The author has an hindex of 13, co-authored 56 publications receiving 546 citations.
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Journal ArticleDOI
Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome
Naohiro Kamiyoshi,Kandai Nozu,Xue Jun Fu,Naoya Morisada,Yoshimi Nozu,Ming Juan Ye,Aya Imafuku,Kenichiro Miura,Tomohiko Yamamura,Shogo Minamikawa,Akemi Shono,Takeshi Ninchoji,Ichiro Morioka,Koichi Nakanishi,Norishige Yoshikawa,Hiroshi Kaito,Kazumoto Iijima +16 more
TL;DR: It may be difficult to make an accurate diagnosis of autosomal dominant Alport syndrome on the basis of clinical or pathologic findings, and no modifier genes were identified among the known podocyte-related genes.
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Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain.
Yuya Hashimura,Kandai Nozu,Hiroshi Kaito,Koichi Nakanishi,Xue Jun Fu,Hiromi Ohtsubo,Fusako Hashimoto,Masafumi Oka,Takeshi Ninchoji,Shingo Ishimori,Naoya Morisada,Natsuki Matsunoshita,Naohiro Kamiyoshi,Norishige Yoshikawa,Kazumoto Iijima +14 more
TL;DR: The results help to clarify the milder clinical manifestations and molecular characteristics of male X-linked Alport syndrome patients expressing the α5(IV) chain.
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Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo-Bartter/Gitelman syndrome based on clinical characteristics.
Natsuki Matsunoshita,Kandai Nozu,Akemi Shono,Yoshimi Nozu,Xue Jun Fu,Naoya Morisada,Naohiro Kamiyoshi,Hiromi Ohtsubo,Takeshi Ninchoji,Shogo Minamikawa,Tomohiko Yamamura,Koichi Nakanishi,Norishige Yoshikawa,Yuko Shima,Hiroshi Kaito,Kazumoto Iijima +15 more
TL;DR: This study clarified the clinical differences between BS, GS, and p-BS/GS for the first time, which will help clinicians establish differential diagnoses for these three conditions.
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Natural History and Genotype-Phenotype Correlation in Female X-Linked Alport Syndrome.
Tomohiko Yamamura,Kandai Nozu,Xue Jun Fu,Yoshimi Nozu,Ming Juan Ye,Akemi Shono,Satoko Yamanouchi,Shogo Minamikawa,Naoya Morisada,Koichi Nakanishi,Yuko Shima,Norishige Yoshikawa,Takeshi Ninchoji,Ichiro Morioka,Hiroshi Kaito,Kazumoto Iijima +15 more
TL;DR: Clinicians must pay careful attention to the clinical course and appropriate treatment in females with XLAS, as phenotypes in female XLAS patients may be severe, but genotype does not help to predict the disease severity.
Journal ArticleDOI
The Pharmacological Characteristics of Molecular-Based Inherited Salt-Losing Tubulopathies
Kandai Nozu,Kazumoto Iijima,Kyoko Kanda,Koichi Nakanishi,Norishige Yoshikawa,Kenichi Satomura,Hiroshi Kaito,Yuya Hashimura,Takeshi Ninchoji,Hiroshi Komatsu,Koichi Kamei,Ritsuko Miyashita,Masaaki Kugo,Hiroshi Ohashi,Hajime Yamazaki,Hiroyo Mabe,Asa Otsubo,Takashi Igarashi,Masafumi Matsuo +18 more
TL;DR: This study revealed the following characteristics of these disorders: subjects with CLCNKB mutations showed one or more biochemical features of Gitelman syndrome, and subjects with KCNJ1 mutations appeared to show normal fractional chloride excretion sensitivity to furosemide and thiazide administration.