Mitsuhiro Kato
Department of Pediatrics
Yamagata University Faculty of Medicine
Yamagata
Japan
[email]@med.id.yamagata-u.ac.jp
Name/email consistency: high
- Going BAC or oligo microarray to the well: a commentary on Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies. Kato, M. J. Hum. Genet. (2011)
- Frameshift mutations of the ARX gene in familial Ohtahara syndrome. Kato, M., Koyama, N., Ohta, M., Miura, K., Hayasaka, K. Epilepsia (2010)
- A longer polyalanine expansion mutation in the ARX gene causes early infantile epileptic encephalopathy with suppression-burst pattern (Ohtahara syndrome). Kato, M., Saitoh, S., Kamei, A., Shiraishi, H., Ueda, Y., Akasaka, M., Tohyama, J., Akasaka, N., Hayasaka, K. Am. J. Hum. Genet. (2007)
- A new paradigm for West syndrome based on molecular and cell biology. Kato, M. Epilepsy Res. (2006)
- X-linked lissencephaly with abnormal genitalia as a tangential migration disorder causing intractable epilepsy: proposal for a new term, "interneuronopathy". Kato, M., Dobyns, W.B. J. Child Neurol. (2005)
- Mutation of the doublecortin gene in male patients with double cortex syndrome: somatic mosaicism detected by hair root analysis. Kato, M., Kanai, M., Soma, O., Takusa, Y., Kimura, T., Numakura, C., Matsuki, T., Nakamura, S., Hayasaka, K. Ann. Neurol. (2001)
- A novel mutation of the doublecortin gene in Japanese patients with X-linked lissencephaly and subcortical band heterotopia. Kato, M., Kimura, T., Lin, C., Ito, A., Kodama, S., Morikawa, T., Soga, T., Hayasaka, K. Hum. Genet. (1999)
