I. Mitsuyoshi

发表

Juvenile dermatomyositis associated with subclinical hypothyroidism due to auto-immune thyroiditis

T. Go, I. Mitsuyoshi, 2002, European Journal of Pediatrics.

Phosphorus Deficiency Syndrome in Two Very Low Birthweight Infants

H. Tsukahara, K. Nakamura, H. Fukuhara, 1988, Acta paediatrica Japonica : Overseas edition.

Complete skipping of exon 66 due to novel mutations of the dystrophin gene was identified in two Japanese families of Duchenne muscular dystrophy with severe mental retardation

Y. Takeshima, M. Matsuo, A. Surono, 2000, Brain and Development.

Assessment of tubular function in neonates using urinary β2-microglobulin

H. Tsukahara, K. Kikuchi, M. Sudo, 1990, Pediatric Nephrology.

A case of epileptic negative myoclonus: therapeutic considerations

Y. Shirasaka, I. Mitsuyoshi, 1999, Brain and Development.

Congenital fiber type disproportion: severe form with marked improvement.

M. Tsuji, H. Hattori, Y. Higuchi, 1999, Pediatric neurology.

Brain atrophy in congenital neuromuscular disease with uniform type 1 fibers.

T. Kanda, H. Hattori, Y. Higuchi, 1997, Pediatric neurology.

Benzodiazepine receptor binding in the spontaneously epileptic rat and its parent strains

T. Serikawa, H. Mikawa, Y. Shirasaka, 1991, Experimental Neurology.

Assessment of tubular function in neonates using urinary beta 2-microglobulin.

H. Tsukahara, K. Nakamura, K. Kikuchi, 1990, Pediatric nephrology.

Phenotypic differences between T-->C and T-->G mutations at nt 8993 of mitochondrial DNA in Leigh syndrome.

M. Tsuji, H. Hattori, Y. Higuchi, 1998, Pediatric neurology.

Changes of NMDA receptor binding in spontaneously epileptic rat and parent strains

T. Serikawa, H. Mikawa, Y. Shirasaka, 1993, Neurochemical Research.