Michinori Ito

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Adrenocorticotropic hormone therapy for infantile spasms alters pyruvate metabolism in the central nervous system

T. Hashimoto, M. Miyazaki, Y. Kuroda, 1998, Brain and Development.

Sisters with α-mannosidosis and systemic lupus erythematosus

S. Kagami, M. Urushihara, K. Yasutomo, 2004, European Journal of Pediatrics.

Dynamic Changes in Serum Leptin Concentrations during the Fetal and Neonatal Periods

T. Murakami, I. Yokota, J. Matsuda, 1999, Pediatric Research.

THE ENZYMATIC BASIS FOR THE METABOLISM AND INHIBITORY ACTION OF VALPROATE (VP): DEHYDROGENATION OF VP-CoA BY 2-METHYL-BRANCHED CHAIN ACYL-CoA DEHYDROGENASE (2-me BCAD)

G. Finocchiaro, Kay Tanaka, Y. Ikeda, 1987, Pediatric Research.

Authors’ Response: N-Octanoylated Ghrelin Levels in Cord and Neonatal Blood

K. Kangawa, I. Yokota, J. Matsuda, 2004 .

Demonstration of an Unstable Variant of Pyruvate Dehydrogenase Protein (E1) in Cultured Fibroblasts from a Patient with Congenital Lactic Acidemia

T. Saijo, E. Naito, Y. Kuroda, 1991, Pediatric Research.

Transforming growth factor-β in renal disease with glycogen storage disease I

S. Kagami, M. Urushihara, K. Yasutomo, 2004, Pediatric Nephrology.

Ghrelin concentration in cord and neonatal blood: relation to fetal growth and energy balance.

K. Kangawa, I. Yokota, J. Matsuda, 2003, The Journal of clinical endocrinology and metabolism.

Effects of Dichloroacetate on Pyruvate Metabolism in Rat Brain in Vivo

Y. Kuroda, M. Miyao, Toshiyuki Watanabe, 1984, Pediatric Research.

Effect of sodium dichloroacetate on human pyruvate metabolism

I. Yokota, T. Saijo, E. Naito, 1989, Brain and Development.

Molecular Analysis of Abnormal Pyruvate Dehydrogenase in a Patient with Thiamine-Responsive Congenital Lactic Acidemia

I. Yokota, E. Naito, Y. Kuroda, 1994, Pediatric Research.

Activation of branched-chain α-ketoacid dehydrogenase complex by α-chloroisocaproate in normal and enzyme-deficient fibroblasts

I. Yokota, E. Naito, Y. Kuroda, 1985 .

A Survey of the Newborn Populations in Belgium, Germany, Poland, Czech Republic, Hungary, Bulgaria, Spain, Turkey, and Japan for the G985 Variant Allele with Haplotype Analysis at the Medium Chain Acyl-CoA

H. Eiberg, A. Ribes, S. Kmoch, 1997, Pediatric Research.

Cytidine 5'-Diphosphate Reductase and Thymidine Kinase Activities in Phytohemagglutinin-stimulated Lymphocytes of Normal Subjects of Various Ages and Patients with Immunodeficiency

E. Naito, Y. Kuroda, M. Miyao, 1984, Pediatric Research.

Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case report

T. Taketani, S. Fukuda, Y. Hasegawa, 2019, Brain and Development.

The Cost of Self-Monitoring of Blood Glucose Is an Important Factor Limiting Glycemic Control in Diabetic Patients

I. Yokota, E. Naito, Y. Kuroda, 2002 .

Mutations in the X‐linked pyruvate dehydrogenase (E1) α subunit gene (PDHA1) in patients with a pyruvate dehydrogenase complex deficiency

S. Seneca, L. de Meirleir, E. Naito, 2000, Human mutation.

Diagnosis of Atlantoaxial Subluxation in Morquio's Syndrome and Spondyloepiphyseal Dysplasia Congenita

T. Saijo, E. Naito, Y. Kuroda, 1991, Acta paediatrica Japonica : Overseas edition.

Presumed hypoplastic intrahepatic portal system due to patent ductus venosus: Importance of direct occlusion test of ductus venosus under open laparotomy

H. Takehara, K. Mori, Michinori Ito, 2004, Pediatrics international : official journal of the Japan Pediatric Society.

Genetic heterogeneity of histidinemia detected by screening newborn infants in Japan

Y. Kuroda, M. Miyao, Toshiyuki Watanabe, 1985, Japanese Journal of Human Genetics.

A survey of the newborn populations in Belgium, Germany, Poland, Czech Republic, Hungary, Bulgaria, Spain, Turkey, and Japan for the G985 variant allele with haplotype analysis at the medium chain Acyl-CoA dehydrogenase gene locus: clinical and evolutionary consideration.

H. Eiberg, A. Ribes, S. Kmoch, 1997 .

Thiamine-responsive pyruvate dehydrogenase deficiency in two patients caused by a point mutation (F205L and L216F) within the thiamine pyrophosphate binding region.

I. Yokota, J. Matsuda, T. Saijo, 2002, Biochimica et biophysica acta.

Diagnosis and molecular analysis of three male patients with thiamine-responsive pyruvate dehydrogenase complex deficiency

I. Yokota, T. Saijo, E. Naito, 2002, Journal of the Neurological Sciences.

Concomitant administration of sodium dichloroacetate and thiamine in West syndrome caused by thiamine-responsive pyruvate dehydrogenase complex deficiency

I. Yokota, T. Saijo, E. Naito, 1999, Journal of the Neurological Sciences.

Enzymologic Studies and Therapy of Leigh's Disease Associated with Pyruvate Decarboxylase Deficiency

Y. Kuroda, T. Hashimoto, Kunio, 1982, Pediatric Research.

[Case of methylmalonic acidemia presenting clinically Leigh encephalopathy].

I. Yokota, E. Naito, Y. Kuroda, 2004, No to hattatsu = Brain and development.

Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene

I. Yokota, J. Matsuda, T. Saijo, 1992 .

Molecular analysis of thiamine-responsive pyruvate dehydrogenase complex deficiency

I. Yokota, J. Matsuda, E. Naito, 1995 .

Management of acute metabolic decompensation in maple syrup urine disease: A multi‐center study

Y. Kuroda, Kazuko Hashimoto, Y. Koga, 1999, Pediatrics international : official journal of the Japan Pediatric Society.

Effect of Long‐Term Treatment with Massive Doses of 1α‐Hydroxyvitamin D3 on Calcium‐Phosphate Balance in Patients with Vitamin D‐Dependent Rickets Type II

I. Yokota, T. Saijo, M. Ito, 1990, Acta paediatrica Japonica : Overseas edition.

Association between vitamin D receptor genotype and age of onset in juvenile Japanese patients with type 1 diabetes.

I. Yokota, E. Naito, Y. Kuroda, 2002, Diabetes care.

Effects of long-term zinc treatment in Japanese patients with Wilson disease: efficacy, stability, and copper metabolism.

S. Ida, H. Kodama, N. Horiike, 2010, Translational research : the journal of laboratory and clinical medicine.

Three novel SURF-1 mutations in Japanese patients with Leigh syndrome.

I. Yokota, T. Saijo, E. Naito, 2002, Pediatric neurology.

Evaluation of a Cytokine Combination Including Thrombopoietin for Improved Transduction of a Retroviral Gene into G‐CSF‐Mobilized CD34+ Human Blood Cells

T. Shimada, Hyeoung-Joon Kim, Y. Kawano, 1997, Stem cells.

Treatment of chronic congenital lactic acidosis by oral administration of dichloroacetate

E. Naito, M. Ito, Y. Kuroda, 1986, Journal of Inherited Metabolic Disease.

Paradoxical weight loss with extra energy expenditure at brown adipose tissue in adolescent patients with Duchenne muscular dystrophy.

I. Yokota, E. Naito, M. Ito, 2001, Metabolism: clinical and experimental.

Comparison of GAD and ICA512/IA-2 Antibodies at and After the Onset of IDDM

I. Yokota, J. Matsuda, E. Naito, 1998, Diabetes Care.

Molecular genetic analysis of a female patient with pyruvate dehydrogenase deficiency: detection of a new mutation and differential expression of mutant gene product in cultured cells

M. Hirose, I. Yokota, J. Matsuda, 1995, Journal of Inherited Metabolic Disease.

DNA diagnosis of pyruvate dehydrogenase deficiency in female patients with congenital lactic acidaemia

I. Yokota, J. Matsuda, E. Naito, 1995, Journal of Inherited Metabolic Disease.

Disorders of Histidine Metabolism

Y. Kuroda, Michinori Ito, 2003 .

Serum leptin concentration in cord blood: relationship to birth weight and gender.

I. Yokota, J. Matsuda, E. Naito, 1997, The Journal of clinical endocrinology and metabolism.

Sisters with alpha-mannosidosis and systemic lupus erythematosus.

S. Kagami, M. Urushihara, K. Yasutomo, 2004, European journal of pediatrics.