126 Tc-99mMIBIシンチマンモグラフィの3次元表示の評価 von 大津, 菜々, 鹿嶋, 勝, 鈴木, 伊三郎, 依田, 昌樹, 井上, 優介

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P-040 川崎市乳がん検診二次読影における取り組み(2) von 小川衣美, 大津菜々, 鈴木信子, 前原善昭, 小泉美都枝

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In steroid-resistant nephrotic syndrome that meets the strict definition, monogenic variants are less common than expected von Ichikawa, Yuta, Sakakibara, Nana, Nagano, China, Inoki, Yuta, Tanaka, Yu, Ueda, Chika, Kitakado, Hideaki, Kondo, Atsushi, Ishimori, Shingo, Horinouchi, Tomoko, Iijima, Kazumoto, Nozu, Kandai

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Saline versus balanced crystalloids for hydration post-kidney biopsy von Tanaka, Yu, Horinouchi, Tomoko, Inoki, Yuta, Ichikawa, Yuta, Ueda, Chika, Kitakado, Hideaki, Kondo, Atsushi, Sakakibara, Nana, Ishimori, Shingo, Yamamura, Tomohiko, Nagano, China, Nozu, Kandai

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Clinical characteristics and outcomes of immune-complex membranoproliferative glomerulonephritis and C3 glomerulopathy in Japanese children von Ueda, Chika, Horinouchi, Tomoko, Inoki, Yuta, Ichikawa, Yuta, Tanaka, Yu, Kitakado, Hideaki, Kondo, Atsushi, Sakakibara, Nana, Nagano, China, Yamamura, Tomohiko, Fujimura, Junya, Kamiyoshi, Naohiro, Ishimori, Shingo, Ninchoji, Takeshi, Kaito, Hiroshi, Shima, Yuko, Iijima, Kazumoto, Nozu, Kandai, Yoshikawa, Norishige

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Evaluation of pathogenicity of WT1 intron variants by in vitro splicing analysis von Inoue, Seiya, Kondo, Atsushi, Inoki, Yuta, Ichikawa, Yuta, Tanaka, Yu, Ueda, Chika, Kitakado, Hideaki, Suzuki, Ryota, Okada, Eri, Sakakibara, Nana, Horinouchi, Tomoko, Nozu, Kandai

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Comprehensive genetic analysis using next-generation sequencing for the diagnosis of nephronophthisis-related ciliopathies in the Japanese population von Sakakibara, Nana, Nozu, Kandai, Yamamura, Tomohiko, Horinouchi, Tomoko, Nagano, China, Ye, Ming Juan, Ishiko, Shinya, Aoto, Yuya, Rossanti, Rini, Hamada, Riku, Okamoto, Nobuhiko, Shima, Yuko, Nakanishi, Koichi, Matsuo, Masafumi, Iijima, Kazumoto, Morisada, Naoya

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All reported non-canonical splice site variants in GLA cause aberrant splicing von Okada, Eri, Horinouchi, Tomoko, Yamamura, Tomohiko, Aoto, Yuya, Suzuki, Ryota, Ichikawa, Yuta, Tanaka, Yu, Masuda, Chika, Kitakado, Hideaki, Kondo, Atsushi, Sakakibara, Nana, Ishiko, Shinya, Nagano, China, Ishimori, Shingo, Usui, Joichi, Yamagata, Kunihiro, Matsuo, Masafumi, Nozu, Kandai

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BCS1L mutations produce Fanconi syndrome with developmental disability von Kanako, Kojima-Ishii, Sakakibara, Nana, Murayama, Kei, Nagatani, Koji, Murata, Satoshi, Otake, Akira, Koga, Yasutoshi, Suzuki, Hisato, Uehara, Tomoko, Kosaki, Kenjiro, Yoshiura, Koh-Ichiro, Mishima, Hiroyuki, Ichimiya, Yuko, Mushimoto, Yuichi, Horinouchi, Tomoko, Nagano, China, Yamamura, Tomohiko, Iijima, Kazumoto, Nozu, Kandai

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Comparison of clinical and genetic characteristics between Dent disease 1 and Dent disease 2 von Sakakibara, Nana, Nagano, China, Ishiko, Shinya, Horinouchi, Tomoko, Yamamura, Tomohiko, Minamikawa, Shogo, Shima, Yuko, Nakanishi, Koichi, Ishimori, Shingo, Morisada, Naoya, Iijima, Kazumoto, Nozu, Kandai

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Distinct Expression Profiles of Neuroblastoma-Associated mRNAs in Peripheral Blood and Bone Marrow of Non-High-Risk and High-Risk Neuroblastoma Patients von Nakatani, Naoko, Win, Kaung Htet Nay, Mon, Cho Yee, Fujikawa, Tomoko, Uemura, Suguru, Saito, Atsuro, Ishida, Toshiaki, Mori, Takeshi, Hasegawa, Daiichiro, Kosaka, Yoshiyuki, Inoue, Shotaro, Nishimura, Akihiro, Nino, Nanako, Tamura, Akihiro, Yamamoto, Nobuyuki, Nozu, Kandai, Nishimura, Noriyuki

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Aberrant splicing caused by exonic single nucleotide variants positioned 2nd or 3rd to the last nucleotide in the COL4A5 gene von Okada, Eri, Aoto, Yuya, Horinouchi, Tomoko, Yamamura, Tomohiko, Ichikawa, Yuta, Tanaka, Yu, Ueda, Chika, Kitakado, Hideaki, Kondo, Atsushi, Sakakibara, Nana, Suzuki, Ryota, Usui, Joichi, Yamagata, Kunihiro, Iijima, Kazumoto, Nozu, Kandai

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Clinical, Pathological, and Genetic Characteristics of Patients with Digenic Alport Syndrome von Inoki, Yuta, Horinouchi, Tomoko, Yamamura, Tomohiko, Ishimori, Shingo, Ichikawa, Yuta, Tanaka, Yu, Ueda, Chika, Kitakado, Hideaki, Kondo, Atsushi, Sakakibara, Nana, Nagano, China, Nozu, Kandai

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IgA nephropathy in a boy with frequently relapsing nephrotic syndrome von Ichikawa, Yuta, Horinouchi, Tomoko, Tanaka, Yu, Ueda, Chika, Kitakado, Hideaki, Kondo, Atsushi, Sakakibara, Nana, Yoshikawa, Norishige, Nozu, Kandai

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Last Nucleotide Substitutions of COL4A5 Exons Cause Aberrant Splicing von Aoto, Yuya, Horinouchi, Tomoko, Yamamura, Tomohiko, Kondo, Atsushi, Nagai, Sadayuki, Ishiko, Shinya, Okada, Eri, Rossanti, Rini, Sakakibara, Nana, Nagano, China, Awano, Hiroyuki, Nagase, Hiroaki, Shima, Yuko, Nakanishi, Koichi, Matsuo, Masafumi, Iijima, Kazumoto, Nozu, Kandai

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Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease von Suzuki, Ryota, Sakakibara, Nana, Ichikawa, Yuta, Kitakado, Hideaki, Ueda, Chika, Tanaka, Yu, Okada, Eri, Kondo, Atsushi, Ishiko, Shinya, Ishimori, Shingo, Nagano, China, Yamamura, Tomohiko, Horinouchi, Tomoko, Okamoto, Takayuki, Nozu, Kandai

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Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease von Okada, Eri, Morisada, Naoya, Horinouchi, Tomoko, Fujii, Hideki, Tsuji, Takayuki, Miura, Masayoshi, Katori, Hideyuki, Kitagawa, Masashi, Morozumi, Kunio, Toriyama, Takanobu, Nakamura, Yuki, Nishikomori, Ryuta, Nagai, Sadayuki, Kondo, Atsushi, Aoto, Yuya, Ishiko, Shinya, Rossanti, Rini, Sakakibara, Nana, Nagano, China, Yamamura, Tomohiko, Ishimori, Shingo, Usui, Joichi, Yamagata, Kunihiro, Iijima, Kazumoto, Imasawa, Toshiyuki, Nozu, Kandai

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Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes von Ishiko, Shinya, Morisada, Naoya, Kondo, Atsushi, Nagai, Sadayuki, Aoto, Yuya, Okada, Eri, Rossanti, Rini, Sakakibara, Nana, Nagano, China, Horinouchi, Tomoko, Yamamura, Tomohiko, Ninchoji, Takeshi, Kaito, Hiroshi, Hamada, Riku, Shima, Yuko, Nakanishi, Koichi, Matsuo, Masafumi, Iijima, Kazumoto, Nozu, Kandai

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A novel NFKB1 variant in a Japanese pedigree with common variable immunodeficiency von Nakatani, Naoko, Tamura, Akihiro, Hanafusa, Hiroaki, Nino, Nanako, Yamamoto, Nobuyuki, Awano, Hiroyuki, Tanaka, Yasuhiro, Morisada, Naoya, Uemura, Suguru, Saito, Atsuro, Hasegawa, Daiichiro, Nozu, Kandai, Kosaka, Yoshiyuki

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Efficacy of combination therapy for childhood complicated focal IgA nephropathy von Aoto, Yuya, Ninchoji, Takeshi, Kaito, Hiroshi, Shima, Yuko, Fujimura, Junya, Kamiyoshi, Naohiro, Ishimori, Shingo, Nakanishi, Koichi, Minamikawa, Shogo, Ishiko, Shinya, Sakakibara, Nana, Nagano, China, Horinouchi, Tomoko, Yamamura, Tomohiko, Nagai, Sadayuki, Kondo, Atsushi, Inaguma, Yosuke, Tanaka, Ryojiro, Yoshikawa, Norishige, Iijima, Kazumoto, Nozu, Kandai

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