R. Iwanaga

发表

The mitochondrial DNA C3303T mutation can cause cardiomyopathy and/or skeletal myopathy.

S. Dimauro, M. Zeviani, C. Bruno, 1999, The Journal of pediatrics.

Fatal hypertrophic cardiomyopathy associated with an A8296G mutation in the mitochondrial tRNALys gene

Y. Nakamura, Y. Koga, N. Wada, 2000, Human mutation.

Decreased cerebrospinal fluid levels of β-endorphin and ACTH in children with infantile spasms

T. Matsuishi, Y. Yamashita, H. Kato, 2001, Journal of Neural Transmission.

Mutation analysis of the methyl-CpG-binding protein 2 gene (MECP2) in Rett patients with preserved speech

T. Matsuishi, I. Kondo, Y. Yamashita, 2001, Brain and Development.

Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome

T. Matsuishi, I. Kondo, Y. Yamashita, 2000, Journal of medical genetics.

Congenital Cytomegalovirus Infection Associated with Fetal Ascites and Intrahepatic Calcifications

Shinya Kaneko, Y. Yamashita, R. Iwanaga, 1989, Acta paediatrica Scandinavica.

Single-fiber analysis of mitochondrial A3243G mutation in four different phenotypes

T. Matsuishi, Y. Koga, H. Kato, 2000, Acta Neuropathologica.

Serial magnetic resonance images in a patient with congenital sensory neuropathy with anhidrosis and complications resembling heat stroke

T. Matsuishi, A. Ohnishi, H. Kato, 1996, Journal of the Neurological Sciences.

Inter- and/or Intra-organ distribution of mitochondrial C3303T or A3243G mutation in mitochondrial cytopathy

S. Kato, Y. Koga, H. Kato, 2001, Acta Neuropathologica.

Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome

T. Matsuishi, I. Kondo, Y. Yamashita, 2000, Journal of medical genetics.