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Journal of Clinical Medicine|June 10, 2023
Acute Encephalopathy Caused by Inherited Metabolic DiseasesYohei Sugiyama, Kei MurayamaThe Journal of Toxicological Sciences|July 3, 2009
Children's toxicology from bench to bed--Liver Injury (4): Mitochondrial respiratory chain disorder and liver disease in childrenKei Murayama, Akira OhtakeNihon Rinsho. Japanese Journal of Clinical Medicine|March 16, 2011
[Acute encephalopathy in inherited metabolic diseases]Ayako Fujinami, Kei Murayama, Masaki TakayanagiEuropean Heart Journal. Case Reports|March 1, 2021
A case report of Leigh syndrome diagnosed by endomyocardial biopsyYuji Maruo, Yuki Ueda, Kei Murayama, et al.Clinical and Experimental Nephrology|December 3, 2024
Comprehensive review of mitochondrial nephropathy-a renal phenotype in mitochondrial disease: causative genes, clinical and pathological features, diagnosis, prognosis, and treatmentToshiyuki Imasawa, Kei Murayama, Daishi Hirano, et al.Journal of Human Genetics|November 22, 2018
Recent topics: the diagnosis, molecular genesis, and treatment of mitochondrial diseasesKei Murayama, Masaru Shimura, Zhimei Liu, et al.CEN Case Reports|November 11, 2024
Presence of mitochondrial dysfunction in a case of Fanconi syndrome with normoglycemic MODY1Yuko Fujii, Hideki Matsumura, Kei Murayama, et al.Cureus|October 29, 2025
Adult-Onset Neurological Deterioration in Dravet Syndrome Associated With a Novel SCN1A Missense Variant (p.Gly1371Asp): A Case ReportKoji Yokoyama, Sayaka Miyazaki, Kei Murayama, et al.Cureus|March 2, 2026
New Neuroimaging Findings in Enoyl-CoA Hydratase Short-Chain 1 (ECHS1) DeficiencyHiroko Tada, Keiko Ichimoto, Kei Murayama, et al.Heliyon|April 21, 2023
Changes in histopathology and heteroplasmy rates over 8 years and effectiveness of taurine supplementation in a patient with mitochondrial nephropathy caused by <i>MT-TL1</i> mutation: A case reportToshiyuki Imasawa, Hiroshi Kitamura, Takehiko Kawaguchi, et al.Pageof 21