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Yoko Aoki

Showing results (11-20 of 255) with videos related to

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Congenital Anomalies|February 7, 2017
Patient with a novel purine-rich element binding protein A mutationNobuhiko Okamoto, Hideto Nakao, Tetsuya Niihori, et al.
Journal of Human Genetics|October 9, 2015
Recent advances in RASopathiesYoko Aoki, Tetsuya Niihori, Shin-ichi Inoue, et al.
American Journal of Medical Genetics. Part A|June 27, 2017
Craniosynostosis in patients with RASopathies: Accumulating clinical evidence for expanding the phenotypeKimiko Ueda, Masako Yaoita, Tetsuya Niihori, et al.
Case Reports in Neurology|April 1, 2021
A Patient with Noonan Syndrome with a <i>KRAS</i> Mutation Who Presented Severe Nerve Root HypertrophyYoshihito Ando, Mikio Sawada, Tadataka Kawakami, et al.
Human Mutation|September 1, 2005
Mutations in the holocarboxylase synthetase gene HLCSYoichi Suzuki, Xue Yang, Yoko Aoki, et al.
Human Mutation|May 13, 2008
The RAS/MAPK syndromes: novel roles of the RAS pathway in human genetic disordersYoko Aoki, Tetsuya Niihori, Yoko Narumi, et al.
International Journal of Rheumatic Diseases|March 13, 2014
Invasive sphenoid sinus aspergillosis mimicking giant cell arteritisTakamasa Murosaki, Takao Nagashima, Kyoko Honne, et al.
Journal of Multidisciplinary Healthcare|June 9, 2022
Multidisciplinary Management of Costello Syndrome: Current PerspectivesChiara Leoni, Germana Viscogliosi, Marco Tartaglia, et al.
Japanese Journal of Infectious Diseases|October 1, 2020
Isolation of Coxsackievirus A21 from Patients with Acute Respiratory Infection in Yamagata, Japan in 2019Tatsuya Ikeda, Yoko Aoki, Kenichi Komabayashi, et al.
Toxicon : Official Journal of the International Society on Toxinology|June 10, 2026
Species Identification and Tetrodotoxin Distribution in Natural Hybrid Pufferfish Collected from Japanese Coastal WatersKosuke Ota, Takuo Sanada, Hiroshi Takahashi, et al.
Pageof 26

Showing results (11-20 of 255) with videos related to

Sort By:
Pageof 26
Congenital Anomalies|February 7, 2017
Patient with a novel purine-rich element binding protein A mutationNobuhiko Okamoto, Hideto Nakao, Tetsuya Niihori, et al.
Journal of Human Genetics|October 9, 2015
Recent advances in RASopathiesYoko Aoki, Tetsuya Niihori, Shin-ichi Inoue, et al.
American Journal of Medical Genetics. Part A|June 27, 2017
Craniosynostosis in patients with RASopathies: Accumulating clinical evidence for expanding the phenotypeKimiko Ueda, Masako Yaoita, Tetsuya Niihori, et al.
Case Reports in Neurology|April 1, 2021
A Patient with Noonan Syndrome with a <i>KRAS</i> Mutation Who Presented Severe Nerve Root HypertrophyYoshihito Ando, Mikio Sawada, Tadataka Kawakami, et al.
Human Mutation|September 1, 2005
Mutations in the holocarboxylase synthetase gene HLCSYoichi Suzuki, Xue Yang, Yoko Aoki, et al.
Human Mutation|May 13, 2008
The RAS/MAPK syndromes: novel roles of the RAS pathway in human genetic disordersYoko Aoki, Tetsuya Niihori, Yoko Narumi, et al.
International Journal of Rheumatic Diseases|March 13, 2014
Invasive sphenoid sinus aspergillosis mimicking giant cell arteritisTakamasa Murosaki, Takao Nagashima, Kyoko Honne, et al.
Journal of Multidisciplinary Healthcare|June 9, 2022
Multidisciplinary Management of Costello Syndrome: Current PerspectivesChiara Leoni, Germana Viscogliosi, Marco Tartaglia, et al.
Japanese Journal of Infectious Diseases|October 1, 2020
Isolation of Coxsackievirus A21 from Patients with Acute Respiratory Infection in Yamagata, Japan in 2019Tatsuya Ikeda, Yoko Aoki, Kenichi Komabayashi, et al.
Toxicon : Official Journal of the International Society on Toxinology|June 10, 2026
Species Identification and Tetrodotoxin Distribution in Natural Hybrid Pufferfish Collected from Japanese Coastal WatersKosuke Ota, Takuo Sanada, Hiroshi Takahashi, et al.
Pageof 26