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Mitochondrial involvement in Alzheimer's disease.
Bonilla E, Tanji K, Hirano M, Vu TH, DiMauro S, Schon EA. Bonilla E, et al. Among authors: tanji k. Biochim Biophys Acta. 1999 Feb 9;1410(2):171-82. doi: 10.1016/s0005-2728(98)00165-0. Biochim Biophys Acta. 1999. PMID: 10076025 Free article. Review.
Mitochondrial genes for generalized epilepsies.
DiMauro S, Kulikova R, Tanji K, Bonilla E, Hirano M. DiMauro S, et al. Among authors: tanji k. Adv Neurol. 1999;79:411-9. Adv Neurol. 1999. PMID: 10514830 Review. No abstract available.
Analysis of mtDNA deletions in muscle by in situ hybridization.
Vu TH, Tanji K, Pallotti F, Golzi V, Hirano M, DiMauro S, Bonilla E. Vu TH, et al. Among authors: tanji k. Muscle Nerve. 2000 Jan;23(1):80-5. doi: 10.1002/(sici)1097-4598(200001)23:1<80::aid-mus10>3.0.co;2-v. Muscle Nerve. 2000. PMID: 10590409 Clinical Trial.
Navajo neurohepatopathy is caused by a mutation in the MPV17 gene.
Karadimas CL, Vu TH, Holve SA, Chronopoulou P, Quinzii C, Johnsen SD, Kurth J, Eggers E, Palenzuela L, Tanji K, Bonilla E, De Vivo DC, DiMauro S, Hirano M. Karadimas CL, et al. Among authors: tanji k. Am J Hum Genet. 2006 Sep;79(3):544-8. doi: 10.1086/506913. Epub 2006 Jun 28. Am J Hum Genet. 2006. PMID: 16909392 Free PMC article.
LAMP-2 deficiency (Danon disease).
Di Mauro S, Tanji K, Hirano M. Di Mauro S, et al. Among authors: tanji k. Acta Myol. 2007 Jul;26(1):79-82. Acta Myol. 2007. PMID: 17915578 Free PMC article. No abstract available.
336 results