Hasil Pencarian - Rini Rossanti

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  1. 1
    Short term memory, physical fitness, and serum brain-derived neurotrophic factor in obese adolescents

    Short term memory, physical fitness, and serum brain-derived neurotrophic factor in obese adolescents oleh Rini Rossanti, Dida Akhmad Gurnida, Eddy Fadlyana

    Diterbitkan 2015-10-01
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  2. 2
    2,8-Dihydroxyadenine nephrolithiasis with chronic kidney disease in children: A case report and review of literature

    2,8-Dihydroxyadenine nephrolithiasis with chronic kidney disease in children: A case report and review of literature oleh Rizky Ramdhani, Akhmad Mustafa, Safendra Siregar, Jupiter Sibarani, Tjahjodjati Tjahjodjati, Ahmedz Widiasta, Rini Rossanti

    Diterbitkan 2023-11-01
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  3. 3
    Pathogenic evaluation of synonymous COL4A5 variants in X‐linked Alport syndrome using a minigene assay

    Pathogenic evaluation of synonymous COL4A5 variants in X‐linked Alport syndrome using a minigene assay oleh Tomoko Horinouchi, Tomohiko Yamamura, Shogo Minamikawa, China Nagano, Nana Sakakibara, Koichi Nakanishi, Yuko Shima, Naoya Morisada, Shinya Ishiko, Yuya Aoto, Hiroaki Nagase, Hiroki Takeda, Rini Rossanti, Shingo Ishimori, Hiroshi Kaito, Masafumi Matsuo, Kazumoto Iijima, Kandai Nozu

    Diterbitkan 2020-08-01
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  4. 4
    Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome

    Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome oleh Tomohiko Yamamura, Kandai Nozu, Shogo Minamikawa, Tomoko Horinouchi, Nana Sakakibara, China Nagano, Yuya Aoto, Shinya Ishiko, Koichi Nakanishi, Yuko Shima, Hiroaki Nagase, Rini Rossanti, Ming J. Ye, Yoshimi Nozu, Shingo Ishimori, Naoya Morisada, Hiroshi Kaito, Kazumoto Iijima

    Diterbitkan 2019-09-01
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  5. 5
    Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases

    Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases oleh Atsushi Kondo, China Nagano, Shinya Ishiko, Takashi Omori, Yuya Aoto, Rini Rossanti, Nana Sakakibara, Tomoko Horinouchi, Tomohiko Yamamura, Sadayuki Nagai, Eri Okada, Yuko Shima, Koichi Nakanishi, Takeshi Ninchoji, Hiroshi Kaito, Hiroki Takeda, Hiroaki Nagase, Naoya Morisada, Kazumoto Iijima, Kandai Nozu

    Diterbitkan 2021-08-01
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  6. 6
    Corrigendum to “Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease”Kidney International Reports, Volume 7, Issue 4, April 2022, Pages 857-866.

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

    Diterbitkan 2023-05-01
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  7. 7
    Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5

    Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5 oleh Tomohiko Yamamura, Tomoko Horinouchi, Tomomi Adachi, Maki Terakawa, Yutaka Takaoka, Kohei Omachi, Minoru Takasato, Kiyosumi Takaishi, Takao Shoji, Yoshiyuki Onishi, Yoshito Kanazawa, Makoto Koizumi, Yasuko Tomono, Aki Sugano, Akemi Shono, Shogo Minamikawa, China Nagano, Nana Sakakibara, Shinya Ishiko, Yuya Aoto, Misato Kamura, Yutaka Harita, Kenichiro Miura, Shoichiro Kanda, Naoya Morisada, Rini Rossanti, Ming Juan Ye, Yoshimi Nozu, Masafumi Matsuo, Hirofumi Kai, Kazumoto Iijima, Kandai Nozu

    Diterbitkan 2020-06-01
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