T. Sano

Mitochondrial leucine tRNA mutation in a mitochondrial encephalomyopathy

K. Ohno, T. Ozawa, Masashi Tanaka, 1991, The Lancet.

An autopsy case of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with a point mutation of mitochondrial DNA

Y. Morimatsu, A. Terauchi, Masanori Kobayashi, 1996, Brain and Development.

Interstitial deletion of the long arm of chromosome 2: A dose study on isocitrate dehydrogenase 1

S. Sumi, N. Ogasawara, H. Oishi, 1988, Japanese Journal of Human Genetics.

Molecular and Genetic Analyses of Two Patients with Pearson's Marrow-Pancreas Syndrome

K. Ohno, T. Ozawa, Masashi Tanaka, 1993, Pediatric Research.

Multiple enzyme defects in mitochondria of a case with congenital lactic acidosis and hyperammonaemia

H. Togari, Y. Wada, E. Naito, 1992, Journal of Inherited Metabolic Disease.

Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease.

K. Ohno, T. Ozawa, H. Ino, 1991, Biochemical and biophysical research communications.

Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

K. Ohno, T. Ozawa, H. Ino, 1991, Biochemical and biophysical research communications.

Dopamine penetrates to the central nervous system in developing rats

S. Fujimoto, H. Togari, I. Kato, 1999, Pediatrics international : official journal of the Japan Pediatric Society.