A case of renal hypouricemia due to T217M mutation in SLC22A12 incidentally associated with IgA nephropathy.

Autor: Sakurabu, Yoshimasa¹ (AUTHOR), Uchida, Haruhito A.^1,2 (AUTHOR) hauchida@okayama‐u.ac.jp, Tahara, Toshihisa¹ (AUTHOR), Asakawa, Tomohiko¹ (AUTHOR), Yamasaki, Haruka^1,3 (AUTHOR), Katayama, Katsuyoshi¹ (AUTHOR), Okamoto, Shugo¹ (AUTHOR), Onishi, Yasuhiro¹ (AUTHOR), Matsuoka‐Uchiyama, Natsumi¹ (AUTHOR), Tanaka, Keiko¹ (AUTHOR), Takeuchi, Hidemi¹ (AUTHOR), Tsuji, Kenji¹ (AUTHOR), Umebayashi, Ryoko¹ (AUTHOR), Ohashi, Yuki^4,5 (AUTHOR), Ichida, Kimiyoshi⁴ (AUTHOR), Wada, Jun¹ (AUTHOR)

Publikováno v: Clinical Case Reports. Sep2024, Vol. 12 Issue 9, p1-7. 7p.

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Circulating GPIHBP1 levels and microvascular complications in patients with type 2 diabetes: A cross-sectional study

Autor: Kurooka, Naoko, Eguchi, Jun, Murakami, Kazutoshi, Kamei, Shinji, Kikutsuji, Toru, Sasaki, Sakiko, Seki, Akiho, Yamaguchi, Satoshi, Nojima, Ichiro, Watanabe, Mayu, Higuchi, Chigusa, Katayama, Akihiro, Uchida, Haruhito A., Nakatsuka, Atsuko, Shikata, Kenichi, Wada, Jun

Publikováno v: In Journal of Clinical Lipidology March-April 2022 16(2):237-245

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Late-onset renal variant Fabry disease with R112H mutation and mild increase in plasma globotriaosylsphingosine: a case report.

Autor: Keiko Tanaka, Hitoshi Sugiyama, Hiroshi Morinaga, Akifumi Onishi, Katsuyuki Tanabe, Uchida, Haruhito A., Hiroki Maruyama, Jun Wada

Publikováno v: Frontiers in Medicine; 2024, p1-5, 5p