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Cell and Tissue Research|February 29, 2012
Human first-trimester chorionic villi have a myogenic potentialReiko Arakawa, Ryoko Aoki, Masayuki Arakawa, et al.
Brain & Development|November 18, 2019
Analysis of spinal muscular atrophy-like patients by targeted resequencingShinichi Hosokawa, Yuji Kubo, Reiko Arakawa, et al.
Brain & Development|June 12, 2017
Relationships between long-term observations of motor milestones and genotype analysis results in childhood-onset Japanese spinal muscular atrophy patientsKaori Kaneko, Reiko Arakawa, Mari Urano, et al.
Internal Medicine (Tokyo, Japan)|July 31, 2022
Hereditary Hemorrhagic Telangiectasia Presenting with Asymptomatic Liver Lesions and a History of Early-onset Myocardial Infarction and Multiple Intracranial AneurysmsMaki Sakuma, Takeshi Inagaki, Reiko Arakawa, et al.
Plos One|August 14, 2018
A new biomarker candidate for spinal muscular atrophy: Identification of a peripheral blood cell population capable of monitoring the level of survival motor neuron proteinNoriko Otsuki, Reiko Arakawa, Kaori Kaneko, et al.
Biochemical and Biophysical Research Communications|September 30, 2014
A novel evaluation method of survival motor neuron protein as a biomarker of spinal muscular atrophy by imaging flow cytometryMasayuki Arakawa, Reiko Arakawa, Shinichi Tatsumi, et al.
Pediatric Neurology|June 30, 2016
Imaging Flow Cytometry Analysis to Identify Differences of Survival Motor Neuron Protein Expression in Patients With Spinal Muscular AtrophyReiko Arakawa, Masayuki Arakawa, Kaori Kaneko, et al.
Clinical Journal of Gastroenterology|May 21, 2021
Seventeen primary malignant neoplasms involving the skin, ovary, esophagus, colon, oral cavity, and ear canal: a case report and review of the literatureRyusuke Sumiya, Kyoji Ito, Nobuyuki Takemura, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 14, 2025
Evaluation of cardiac function in patients with SMA after treatment with onasemnogene abeparvovecAkihisa Horigome, Satoshi Takasago, Reiko Arakawa, et al.
Human Genome Variation|April 1, 2021
Venous thromboembolism is caused by prothrombin p.Arg541Trp mutation in Japanese individualsJumpei Yamamoto, Masaya Yamamoto, Kozue Takano, et al.
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