Author:
Sakiyama Yusuke,Okamoto Yuji,Higuchi Itsuro,Inamori Yukie,Sangatsuda Yoko,Michizono Kumiko,Watanabe Osamu,Hatakeyama Hideyuki,Goto Yu-ichi,Arimura Kimiyoshi,Takashima Hiroshi
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Clinical Neurology,Pathology and Forensic Medicine
Reference37 articles.
1. Azher SN, Jankovic J (2005) Camptocormia: pathogenesis, classification, and response to therapy. Neurology 65:355–359
2. Bai RK, Wong LJ (2004) Detection and quantification of heteroplasmic mutant mitochondrial DNA by real-time amplification refractory mutation system quantitative PCR analysis: a single-step approach. Clin Chem 50:996–1001
3. Berio A, Piazzi A (2002) A case of Kearns-Sayre syndrome with autoimmune thyroiditis and possible Hashimoto encephalopathy. Panminerva Med 44:265–269
4. Bernier FP, Boneh A, Dennett X, Chow CW, Cleary MA, Thorburn DR (2002) Diagnostic criteria for respiratory chain disorders in adults and children. Neurology 59:1406–1411
5. Boerkoel CF, Takashima H, Stankiewicz P et al (2001) Periaxin mutations cause recessive Dejerine-Sottas neuropathy. Am J Hum Genet 68:325–333
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