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Takashi Miyajima

ORCID: 0000-0002-2125-8401
Observed ORCID: 0000-0002-2125-8401
OpenAlex ID: A5048071002
Future clinical and biochemical predictions of Fabry disease in females by methylation studies of the GLA gene
2019 · Mohammad Arif Hossain, Chen Wu, et al. · Molecular Genetics and Metabolism Reports · 22
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A combination of 7-ketocholesterol, lysosphingomyelin and bile acid-408 to diagnose Niemann-Pick disease type C using LC-MS/MS
2020 · Chen Wu, Takeo Iwamoto, et al. · PLoS ONE · 19
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Dysregulated DNA methylation of GLA gene was associated with dysfunction of autophagy
2019 · Hiroko Yanagisawa, Mohammad Arif Hossain, et al. · Molecular Genetics and Metabolism · 19
The severe clinical phenotype for a heterozygous Fabry female patient correlates to the methylation of non-mutated allele associated with chromosome 10q26 deletion syndrome
2017 · Mohammad Arif Hossain, Hiroko Yanagisawa, et al. · Molecular Genetics and Metabolism · 18
Application of a diagnostic methodology by quantification of 26:0 lysophosphatidylcholine in dried blood spots for Japanese newborn screening of X-linked adrenoleukodystrophy
2017 · Chen Wu, Takeo Iwamoto, et al. · Molecular Genetics and Metabolism Reports · 17
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A neuropathological cell model derived from Niemann−Pick disease type C patient-specific iPSCs shows disruption of the p62/SQSTM1−KEAP1−NRF2 Axis and impaired formation of neuronal networks
2021 · Ryo Saito, Takashi Miyajima, et al. · Molecular Genetics and Metabolism Reports · 12
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A Case of Adult-onset Pompe Disease with Cerebral Stroke and Left Ventricular Hypertrophy
2018 · Mohammad Arif Hossain, Takashi Miyajima, et al. · Journal of Stroke and Cerebrovascular Diseases · 12
Characteristics of PPT1 and TPP1 enzymes in neuronal ceroid lipofuscinosis (NCL) 1 and 2 by dried blood spots (DBS) and leukocytes and their application to newborn screening
2018 · Rina Itagaki, Masahiro Endo, et al. · Molecular Genetics and Metabolism · 12
Characterization of cellular phenotypes in neurons derived from induced pluripotent stem cells of male patients with Fabry disease
2022 · Takashi Miyajima, Ryo Saito, et al. · Journal of Inherited Metabolic Disease · 8
Ten-year-long enzyme replacement therapy shows a poor effect in alleviating giant leg ulcers in a male with Fabry disease
2017 · Jun Okada, Mohammad Arif Hossain, et al. · Molecular Genetics and Metabolism Reports · 6
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Neurogenin 2-induced central neurons generated from NPC patient-derived iPSC display attenuated neurite outgrowth while accumulating cholesterol
2025 · Miki Igarashi, Takashi Miyajima, et al. · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · 1
The effect of arimoclomol treatment of fibroblasts on the activity of causal enzymes of Fabry disease and neuronal ceroid lipofuscinosis
2025 · MIYO MUNAKATA, Mohammad Arif Hossain, et al. · Research Square
Neuropathological analysis of Niemann-Pick disease type C using patient-derived iPSCs
2021 · Ryo Saito, Takashi Miyajima, et al. · Proceedings for Annual Meeting of The Japanese Pharmacological Society
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An update on biomarkers of 7-ketocholesterol, lysosphingomyelin, bile acid-408 and glucosylsphingosine for Niemann-Pick disease type C
2020 · Chen Wu, Takeo Iwamoto, et al. · Molecular Genetics and Metabolism
Development of neuropathological model using Niemann-Pick type C patients derived iPSCs
2020 · Ryo Saito, Takashi Miyajima, et al. · Molecular Genetics and Metabolism
DNA methylation study of GLA gene and its association with autophagy and clinical severity of heterozygous Fabry disease females
2020 · Mohammad A. Hossain, Chen Wu, et al. · Molecular Genetics and Metabolism
Evaluation of long-term effects by ERT for Fabry disease biochemical and EM pictures
2019 · Mohammad A. Hossain, Chen Wu, et al. · Molecular Genetics and Metabolism
Generation of iPS cells derived from skin fibroblasts of patients with Fabry disease using RNA-reprogramming
2019 · Takashi Miyajima, Hiroko Yanagisawa, et al. · Molecular Genetics and Metabolism
The correlation between brain MRI imaging and biochemical and molecular findings in Japanese female patients with Fabry disease
2019 · Kaoru Eto, Arif Hossein, et al. · Molecular Genetics and Metabolism
Neuronal ceroid lipofuscinosis (NCL) types 1 and 2: Enzyme characteristics of PPT1 and TPP1, and their high risk and newborn screenings
2019 · Rina Itagaki, Masahiro Endo, et al. · Molecular Genetics and Metabolism
Combination of lysosphingomyelin, 7-ketocholesterol and bile acid W for diagnosis of Japanese patients with Niemann Pick disease type C by MS/MS
2018 · Chen Wu, Takeo Iwamoto, et al. · Molecular Genetics and Metabolism
Methylation study of CpG islands in GLA gene: best clinical phenotype predictor for heterozygous Fabry female
2018 · Mohammad A. Hossain, Chen Wu, et al. · Molecular Genetics and Metabolism
Effects of immunosuppressants to two Japanese transplanted patients with Fabry disease
2018 · Kaoru Eto, Takashi Miyajima, et al. · Molecular Genetics and Metabolism
Lysosomal acid lipase deficiency high-risk screening of patients with fatty liver and dyslipidemia using DBS in Japan
2017 · Takashi Miyajima, Keiko Akiyama, et al. · Molecular Genetics and Metabolism
The severity of phenotype for a heterozygous Fabry female patient correlates to the methylation of non-mutated allele
2017 · Mohammad A. Hossain, Hiroko Yanagisawa, et al. · Molecular Genetics and Metabolism
Works count: 27
Citation count: 146
H-index: 8
I10-index: 8
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