M. Ito

发表

Application of 1H-NMR spectroscopy for qualitative measurement of muscle carnitine levels.

H. Sugie, S. Tsurui, H. Nakajima, 1994, Clinica chimica acta; international journal of clinical chemistry.

Novel exon 11 skipping mutation in a patient with glycogen storage disease type IIId

I. Nonaka, T. Fukuda, Y. Sugie, 2001, Journal of Inherited Metabolic Disease.

Novel mutations in two Japanese cases of glycogen storage disease type IIIa and a review of the literature of the molecular basis of glycogen storage disease type III

T. Fukuda, H. Sugie, M. Ito, 2000, Journal of Inherited Metabolic Disease.

A Novel Missense Mutation (837T→C) in the Phosphoglycerate Kinase Gene of a Patient With a Myopathic Form of Phosphoglycerate Kinase Deficiency

T. Fukuda, M. Ito, Hideo Sugie, 1998, Journal of child neurology.

Recurrent Myoglobinuria in a Child With Mental Retardation: Phosphoglycerate Kinase Deficiency

Y. Sugie, H. Sugie, Y. Igarashi, 1989, Journal of child neurology.

A case of Costello syndrome and glycogen storage disease type III

T. Fukuda, H. Sugie, M. Kaji, 2002, Journal of medical genetics.

Genetic analysis of Japanese patients with myophosphorylase deficiency (McArdle's disease): single-codon deletion in exon 17 is the predominant mutation.

I. Nonaka, T. Fukuda, Y. Sugie, 1995, Clinica chimica acta; international journal of clinical chemistry.

Bilateral facial palsy caused by bilateral masked mastoiditis.

T. Fukuda, H. Sugie, M. Ito, 1998, Pediatric neurology.

[Clinical evaluation of treatment with fluvoxamine, a selective serotonin reuptake inhibitor in children with autistic disorder].

T. Fukuda, Y. Sugie, H. Sugie, 2001, No to hattatsu = Brain and development.

[Clinical and biochemical analysis of 27 patients with myoglobinuria of unknown causes].

H. Sugie, Y. Igarashi, S. Tsurui, 1995, Rinshō shinkeigaku Clinical neurology.

High‐dose iv human immunoglobulin in a case with infantile opsoclonus polymyoclonia syndrome

Y. Sugie, H. Sugie, M. Ito, 1992, Acta paediatrica.

Opsoclonus polymyoclonia syndrome

Y. Sugie, H. Sugie, F. Vassella, 1993, Acta paediatrica.

[Evaluation of the 2nd to 4th digit ratio in the patients with autism].

T. Fukuda, T. Ohzeki, Y. Sugie, 2005, No to hattatsu = Brain and development.

A case of Costello syndrome and glycogen storage disease type III

M. Kaji, T. Fukuda, H. Sugie, 2002, Journal of medical genetics.