Mitsuhiro Kato
Yamagata, Japan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
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.
Journal: Journal of human genetics
Published: January 14, 2011
Topics of brain malformation and epilepsy--age-dependent epileptic encephalopathies and interneuronopathies
Journal: No to hattatsu = Brain and development
Published: September 18, 2010
Frameshift mutations of the ARX gene in familial Ohtahara syndrome.
Journal: Epilepsia
Published: April 14, 2010
A longer polyalanine expansion mutation in the ARX gene causes early infantile epileptic encephalopathy with suppression-burst pattern (Ohtahara syndrome).
Journal: American journal of human genetics
Published: February 26, 2007
A new paradigm for West syndrome based on molecular and cell biology.
Journal: Epilepsy research
Published: December 28, 2005
X-linked lissencephaly with abnormal genitalia as a tangential migration disorder causing intractable epilepsy: proposal for a new term, "interneuronopathy".
Journal: Journal of child neurology
Published: June 01, 2005
Mutation of the doublecortin gene in male patients with double cortex syndrome: somatic mosaicism detected by hair root analysis.
Journal: Annals of neurology
Published: October 17, 2001
Showing 1-8 of 8
Last Updated: 09/26/2026