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Author

Nobuyuki Ishige

Observed institution: Tokyo Health Service Association
ORCID: 0000-0002-1386-2705
Observed ORCID: 0000-0002-1386-2705
OpenAlex ID: A5078798216
Plasma globotriaosylsphingosine as a biomarker of Fabry disease
2010 · Tadayasu Togawa, Takashi Kodama, et al. · Molecular Genetics and Metabolism · 150
Non-invasive screening method for Fabry disease by measuring globotriaosylceramide in whole urine samples using tandem mass spectrometry
2005 · Teruo Kitagawa, Nobuyuki Ishige, et al. · Molecular Genetics and Metabolism · 61
Influence of antibody formation on reduction of globotriaosylceramide (GL-3) in urine from Fabry patients during agalsidase beta therapy
2007 · Toya Ohashi, Mio Sakuma, et al. · Molecular Genetics and Metabolism · 53
Prevalence of Fabry disease in dialysis patients: Japan Fabry disease screening study (J-FAST)
2015 · Osamu Saito, Eiji Kusano, et al. · Clinical and Experimental Nephrology · 42
Newborn screening for carnitine palmitoyltransferase II deficiency using (C16 + C18:1)/C2: Evaluation of additional indices for adequate sensitivity and lower false-positivity
2017 · Go Tajima, Keiichi Hara, et al. · Molecular Genetics and Metabolism · 31
Development of Second-Tier Liquid Chromatography-Tandem Mass Spectrometry Analysis for Expanded Newborn Screening in Japan
2021 · Yosuke Shigematsu, Miori Yuasa, et al. · International Journal of Neonatal Screening · 27
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Non-invasive high-risk screening for Fabry disease hemizygotes and heterozygotes
2008 · Teruo Kitagawa, Ken Suzuki, et al. · Pediatric Nephrology · 19
Elevation of pivaloylcarnitine by sivelestat sodium in two children
2015 · Kenji Yamada, Hironori Kobayashi, et al. · Molecular Genetics and Metabolism · 16
The High Relevance of 21-Deoxycortisol, (Androstenedione + 17α-Hydroxyprogesterone)/Cortisol, and 11-Deoxycortisol/17α-Hydroxyprogesterone for Newborn Screening of 21-Hydroxylase Deficiency
2022 · Kazuhiro Watanabe, Atsumi Tsuji-Hosokawa, et al. · The Journal of Clinical Endocrinology & Metabolism · 15
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Minimum requirement of donor cells to reduce the glycolipid storage following bone marrow transplantation in a murine model of Fabry disease
2011 · Takayuki Yokoi, Hiroshi Kobayashi, et al. · The Journal of Gene Medicine · 11
Hypocarnitinemia Observed in an Infant Treated with Short-Term Administration of Antibiotic Containing Pivalic Acid
2018 · Kimitaka Nakazaki, Erika Ogawa, et al. · The Tohoku Journal of Experimental Medicine · 9
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Primary carnitine deficiency with severe acute hepatitis following rotavirus gastroenteritis
2019 · Mika Ishige, Tatsuo Fuchigami, et al. · Journal of Infection and Chemotherapy · 6
Enhancing Accuracy of Newborn Screening for 21OHD: Strategic Use of 21-Deoxycortisol in a Large-Scale Tokyo Cohort
2025 · Haruki Yamano, Kazuhiro Watanabe, et al. · The Journal of Clinical Endocrinology & Metabolism · 2
Clinical Application of Liquid Chromatography Tandem Mass Spectrometry Using Dried Blood Spot as a More Rapid Method for Determination of Methylmalonic Acid, Propionylcarnitine, and Total Homocysteine
2020 · Hiroyuki Iijima, Nobuyuki Ishige, et al. · Journal of Inborn Errors of Metabolism and Screening · 2
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Nationwide TREC/KREC-based newborn screening and clinical outcomes in Japan
2026 · Tsubasa Nishinosono, Hideki Muramatsu, et al. · Journal of Human Immunity · 1
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Comparison of Four Screening Markers [(C16 + C18:1)/C2, C14/C3, C12/C0, and C12/C2] for Carnitine Palmitoyltransferase II Deficiency in the Nationwide Newborn Screening Program in Japan
2026 · Go Tajima, Nobuyuki Ishige, et al. · International Journal of Neonatal Screening · 1
Role of the Gut–Liver–Kidney Axis in Disease Manifestation and Biomarker Alterations
2026 · Ryuichi Mashima, Nobuyuki Ishige · International Journal of Molecular Sciences
Analytical Study Showing a False-Negative Limitation of Deletion-Based Newborn Screening for Spinal Muscular Atrophy Using a Compound Heterozygous SMN1 Control
2026 · Yuichi Abe, Sato Suzuki-Muromoto, et al. · International Journal of Neonatal Screening
A Two-Step LC-MS/MS method to differentiate 21OHD and PORD in Screen-Positive newborns
2026 · Hisae Nakatani, Kazuhiro Watanabe, et al. · Endocrine
Genetic studies of Japanese cases with high C5-OH level in newborn screening
2020 · Kobayashi Masahisa, Matsuda Junko, et al.
透析患者におけるファブリー病有病率:日本ファブリー病スクリーニング研究(j‐fast)
2016 · Osamu Saitô, Eiji Kusano, et al. · Clinical and Experimental Nephrology
ろ紙血液中アシルカルニチンの保存期間と保存温度による安定性の検討-有機酸・脂肪酸代謝異常症患者の検体を用いた検討-
2011 · Nobuyuki Ishige, Fujikawa Kento, et al.
Works count: 22
Citation count: 446
H-index: 10
I10-index: 10
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