K Iinuma

Comparative Appraisal of CT Scan and MRI in the Diagnosis of Leigh Encephalomyelopathy in Two Siblings

Kenji Yamada, T. Matsuzawa, K Yamada, 1987, Journal of child neurology.

Mutation detection by TaqMan‐allele specific amplification: Application to molecular diagnosis of glycogen storage disease type Ia and medium‐chain acyl‐CoA dehydrogenase deficiency

Y. Matsubara, P. Rinaldo, Y. Suzuki, 2000, Human mutation.