N. Ishikawa

Neurodevelopmental abnormalities associated with severe congenital neutropenia due to the R86X mutation in the HAX1 gene

M. Ohtsubo, S. Okada, M. Tsumura, 2008, Journal of Medical Genetics.

Severe developmental delay and epilepsy in a Japanese patient with severe congenital neutropenia due to HAX1 deficiency

O. Ohara, T. Kato, S. Okada, 2007, Haematologica.

Increased interleukin-6 and high-sensitivity C-reactive protein levels in pediatric epilepsy patients with frequent, refractory generalized motor seizures

Masao Kobayashi, Y. Fujii, Yoshiyuki Kobayashi, 2015, Seizure.

Ictal Electroencephalography and Electromyography Features in Symptomatic Infantile Epileptic Encephalopathy with Late-Onset Spasms

Masao Kobayashi, Y. Fujii, Yoshiyuki Kobayashi, 2013, Neuropediatrics.

A Case of Neonatal Coxsackie B2 Meningo-Encephalitis in which Serial Magnetic Resonance Imaging Findings Reveal the Development of Lesions

Y. Mizoguchi, K. Nakamura, N. Ishikawa, 2011, Neuropediatrics.