Hasil Pencarian - Hiroyuki Akagawa

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  1. 1
    Whole-exome sequencing in a Japanese multiplex family identifies new susceptibility genes for intracranial aneurysms.

    Whole-exome sequencing in a Japanese multiplex family identifies new susceptibility genes for intracranial aneurysms. oleh Tatsuya Maegawa, Hiroyuki Akagawa, Hideaki Onda, Hidetoshi Kasuya

    Diterbitkan 2022-01-01
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  2. 2
    Whole-exome sequencing in a Japanese multiplex family identifies new susceptibility genes for intracranial aneurysms

    Whole-exome sequencing in a Japanese multiplex family identifies new susceptibility genes for intracranial aneurysms oleh Tatsuya Maegawa, Hiroyuki Akagawa, Hideaki Onda, Hidetoshi Kasuya

    Diterbitkan 2022-01-01
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  3. 3
    Radiofrequency ablation for DYT‐28 dystonia: short term follow‐up of three adult cases

    Radiofrequency ablation for DYT‐28 dystonia: short term follow‐up of three adult cases oleh Shiro Horisawa, Kenkou Azuma, Hiroyuki Akagawa, Taku Nonaka, Takakazu Kawamata, Takaomi Taira

    Diterbitkan 2020-10-01
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  4. 4
    Deep intronic deletion in intron 3 of PLP1 is associated with a severe phenotype of Pelizaeus-Merzbacher disease

    Deep intronic deletion in intron 3 of PLP1 is associated with a severe phenotype of Pelizaeus-Merzbacher disease oleh Keiko Yamamoto-Shimojima, Hiroyuki Akagawa, Kumiko Yanagi, Tadashi Kaname, Nobuhiko Okamoto, Toshiyuki Yamamoto

    Diterbitkan 2021-04-01
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  5. 5
    Synergistic Interaction of Thyroid Autoantibodies and Ring Finger Protein 213 Variant in Moyamoya Disease

    Synergistic Interaction of Thyroid Autoantibodies and Ring Finger Protein 213 Variant in Moyamoya Disease oleh Thiparpa THAMAMONGOOD, Shoko HARA, Hiroyuki AKAGAWA, Motoki INAJI, Yoji TANAKA, Tadashi NARIAI, Taketoshi MAEHARA

    Diterbitkan 2024-01-01
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  6. 6
    Case Report: Long-Term Suppression of Paroxysmal Kinesigenic Dyskinesia After Bilateral Thalamotomy

    Case Report: Long-Term Suppression of Paroxysmal Kinesigenic Dyskinesia After Bilateral Thalamotomy oleh Masato Murakami, Shiro Horisawa, Kenko Azuma, Hiroyuki Akagawa, Taku Nonaka, Takakazu Kawamata, Takaomi Taira

    Diterbitkan 2021-12-01
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  7. 7
    Systematic Validation of RNF213 Coding Variants in Japanese Patients With Moyamoya Disease

    Systematic Validation of RNF213 Coding Variants in Japanese Patients With Moyamoya Disease oleh Yosuke Moteki, Hideaki Onda, Hidetoshi Kasuya, Taku Yoneyama, Yoshikazu Okada, Kengo Hirota, Maki Mukawa, Tadashi Nariai, Shohei Mitani, Hiroyuki Akagawa

    Diterbitkan 2015-05-01
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  8. 8
    Role of BRCA1-associated protein (BRAP) variant in childhood pulmonary arterial hypertension.

    Role of BRCA1-associated protein (BRAP) variant in childhood pulmonary arterial hypertension. oleh Ayako Chida-Nagai, Masaki Shintani, Hiroki Sato, Tomotaka Nakayama, Masaki Nii, Hiroyuki Akagawa, Toru Furukawa, Amer Rana, Yoshiyuki Furutani, Kei Inai, Shigeaki Nonoyama, Toshio Nakanishi

    Diterbitkan 2019-01-01
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  9. 9
    Mutation Type and Intracranial Aneurysm Formation in Autosomal Dominant Polycystic Kidney Disease

    Mutation Type and Intracranial Aneurysm Formation in Autosomal Dominant Polycystic Kidney Disease oleh Hiroshi Kataoka, Hiroyuki Akagawa, Yusuke Ushio, Masayo Sato, Shun Manabe, Shiho Makabe, Keiko Kawachi, Taro Akihisa, Naomi Iwasa, Rie Yoshida, Ken Tsuchiya, Kosaku Nitta, Toshio Mochizuki

    Diterbitkan 2022-09-01
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  10. 10
    Impact of kidney function and kidney volume on intracranial aneurysms in patients with autosomal dominant polycystic kidney disease

    Impact of kidney function and kidney volume on intracranial aneurysms in patients with autosomal dominant polycystic kidney disease oleh Hiroshi Kataoka, Hiroyuki Akagawa, Rie Yoshida, Naomi Iwasa, Yusuke Ushio, Taro Akihisa, Masayo Sato, Shun Manabe, Shiho Makabe, Keiko Kawachi, Junichi Hoshino, Ken Tsuchiya, Kosaku Nitta, Toshio Mochizuki

    Diterbitkan 2022-10-01
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  11. 11
    Whole-exome sequencing reveals the genetic causes and modifiers of moyamoya syndrome

    Whole-exome sequencing reveals the genetic causes and modifiers of moyamoya syndrome oleh Akikazu Nakamura, Shunsuke Nomura, Shoko Hara, Thiparpa Thamamongood, Taketoshi Maehara, Tadashi Nariai, Shasha Khairullah, Kay Sin Tan, Kenko Azuma, Ayako Chida‐Nagai, Yoshiyuki Furutani, Takahiro Hori, Koji Yamaguchi, Takakazu Kawamata, Constantin Roder, Hiroyuki Akagawa

    Diterbitkan 2024-10-01
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  12. 12
    Identification of Prostaglandin I2 Synthase Rare Variants in Patients With Williams Syndrome and Severe Peripheral Pulmonary Stenosis

    Identification of Prostaglandin I2 Synthase Rare Variants in Patients With Williams Syndrome and Severe Peripheral Pulmonary Stenosis oleh Ayako Chida‐Nagai, Hiroyuki Akagawa, Saori Sawai, Yue‐Jiao Ma, Satoshi Yakuwa, Jun Muneuchi, Kazushi Yasuda, Hirokuni Yamazawa, Toshiyuki Yamamoto, Emi Takakuwa, Utano Tomaru, Yoshiyuki Furutani, Tatsuya Kato, Gen Harada, Kei Inai, Toshio Nakanishi, Atsushi Manabe, Atsuhito Takeda, Zhi‐Cheng Jing

    Diterbitkan 2024-05-01
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  13. 13
    Variant spectrum of PIEZO1 and KCNN4 in Japanese patients with dehydrated hereditary stomatocytosis

    Variant spectrum of PIEZO1 and KCNN4 in Japanese patients with dehydrated hereditary stomatocytosis oleh Erina Nakahara, Keiko Shimojima Yamamoto, Hiromi Ogura, Takako Aoki, Taiju Utsugisawa, Kenko Azuma, Hiroyuki Akagawa, Kenichiro Watanabe, Michiko Muraoka, Fumihiko Nakamura, Michi Kamei, Koji Tatebayashi, Jun Shinozuka, Takahisa Yamane, Makoto Hibino, Yoshiya Katsura, Sonoko Nakano-Akamatsu, Norimitsu Kadowaki, Yoshiro Maru, Etsuro Ito, Shouichi Ohga, Hiroshi Yagasaki, Ichiro Morioka, Toshiyuki Yamamoto, Hitoshi Kanno

    Diterbitkan 2023-03-01
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