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PP2 EFFECTIVENESS OF SITAGLIPTIN ON IMPROVING VASCULAR INFLAMMATION WITH PRESERVING BETA-CELL FUNCTION IN JAPANESE TYPE 2 DIABETES – PROSPECTIVE AND OBSERVATIONAL STUDY OF SINGLE-Y

Diabetes research and clinical practice, 2014-11, Vol.106, p.S42-S43

2014

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Vitamin D receptor gene polymorphism is associated with Graves' disease in the Japanese population

The journal of clinical endocrinology and metabolism, 2000-12, Vol.85 (12), p.4639-4643

2000

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Laboratory investigation of microelectronics-based stimulators for large-scale suprachoroidal transretinal stimulation (STS)

Journal of neural engineering, 2007-03, Vol.4 (1), p.S85-S91

2007

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Genomic polymorphism in the interferon-induced helicase (IFIH1) gene does not confer susceptibility to autoimmune thyroid disease in the Japanese population

Hormone and metabolic research, 2010-01, Vol.42 (1), p.70

2010

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Vitamin D Receptor Gene Polymorphisms in Hashimoto's Thyroiditis

Thyroid (New York, N.Y.), 2001-06, Vol.11 (6), p.67-608

2001

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Changes in the distribution pattern of gelatin-binding protein of 28 kDa (adiponectin) in myocardial remodelling after ischaemic injury

Histopathology, 2003-01, Vol.42 (1), p.43-52

2003

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Genetic Variation in the Gene Encoding Adiponectin Is Associated With an Increased Risk of Type 2 Diabetes in the Japanese Population

Diabetes (New York, N.Y.), 2002-02, Vol.51 (2), p.536-540

2002

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Correlation between the adiponectin-leptin ratio and parameters of insulin resistance in patients with type 2 diabetes

Metabolism, clinical and experimental, 2005-03, Vol.54 (3), p.281-286

2005

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Correlation of the adipocyte-derived protein adiponectin with insulin resistance index and serum high-density lipoprotein-cholesterol, independent of body mass index, in the Japanese population

Clinical science (1979), 2002-08, Vol.103 (2), p.137

2002

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Lipoma and opthalmoplegia in mitochondrial diabetes associated with small heteroplasmy level of 3243 tRNA(Leu(UUR)) mutation

Diabetes research and clinical practice, 2004-03, Vol.63 (3), p.225

2004

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Association of the mitochondrial DNA 5178A/C polymorphism with maternal inheritance and onset of type 2 diabetes in Japanese patients

Experimental and clinical endocrinology & diabetes, 2001, Vol.109 (7), p.361

2001

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Meta-analysis of three diabetes population studies: association of inactive ALDH2 genotype with maternal inheritance of diabetes

Diabetes research and clinical practice, 2004-12, Vol.66, p.S145-S147

2004

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Decrease in Serum Adiponectin Level Due to Obesity and Visceral Fat Accumulation in Children

Obesity (Silver Spring, Md.), 2003-09, Vol.11 (9), p.1072-1079

2003

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CMOS LSI-based multichip flexible neural stimulation device with embedded bulk Pt electrodes

Electronics letters, 2007, Vol.43 (1), p.10-12

2007

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Acute metabolic cataract as a first manifestation of diabetes mellitus in a 12-year-old girl

Diabetologia, 2004-03, Vol.47 (3), p.592-593

2004

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Toxic multinodular goitre in a patient with generalized resistance to thyroid hormone who harbours the R429Q mutation in the thyroid hormone receptor β gene

Clinical endocrinology (Oxford), 2001-01, Vol.54 (1), p.121-124

2001

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Mitochondrial tRNA(Leu(UUR)) mutation at position 3243 detected in patients with type 1 diabetes

Diabetes research and clinical practice, 2005-01, Vol.67 (1), p.92-94

2005

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Deposition of a-SiC:H thin film from organosilicon material by remote plasma CVD method

Thin solid films, 2000-06, Vol.368 (2), p.181-184

2000

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A case of type 2 diabetes with high levels of plasma and urinary C-peptide

Diabetes research and clinical practice, 2004-12, Vol.66, p.S125-S128

2004

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The Codon 620 Single Nucleotide Polymorphism of the Protein Tyrosine Phosphatase-22 Gene Does not Contribute to Autoimmune Thyroid Disease Susceptibility in the Japanese

Thyroid (New York, N.Y.), 2005-10, Vol.15 (10), p.1115-1118

2005

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Silent mixed corticotroph and somatotroph macroadenomas presenting with pituitary apoplexy

Acta neuropathologica, 2001-11, Vol.102 (5), p.435-440

2001

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Effects of pioglitazone on metabolic parameters, body fat distribution, and serum adiponectin levels in Japanese male patients with type 2 diabetes

Metabolism, clinical and experimental, 2002-03, Vol.51 (3), p.314-317

2002

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SEL1L Microsatellite Polymorphism in Japanese Patients with Autoimmune Thyroid Diseases

Thyroid (New York, N.Y.), 2001-04, Vol.11 (4), p.335-338

2001

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Open-label Compassionate Use One Year-treatment with Pirfenidone to Patients with Chronic Pulmonary Fibrosis

Internal Medicine, 2002, Vol.41(12), pp.1118-1123

2002

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Maternal inheritance of diabetes is associated with inactive ALDH2 genotype in diabetics with renal failure in Japanese

Diabetes research and clinical practice, 2003-05, Vol.60 (2), p.143-145

2003

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PP2 EFFECTIVENESS OF SITAGLIPTIN ON IMPROVING VASCULAR INFLAMMATION WITH PRESERVING BETA-CELL FUNCTION IN JAPANESE TYPE 2 DIABETES – PROSPECTIVE AND OBSERVATIONAL STUDY OF SINGLE-Y

Vitamin D receptor gene polymorphism is associated with Graves' disease in the Japanese population

Laboratory investigation of microelectronics-based stimulators for large-scale suprachoroidal transretinal stimulation (STS)

Genomic polymorphism in the interferon-induced helicase (IFIH1) gene does not confer susceptibility to autoimmune thyroid disease in the Japanese population

Vitamin D Receptor Gene Polymorphisms in Hashimoto's Thyroiditis

Changes in the distribution pattern of gelatin-binding protein of 28 kDa (adiponectin) in myocardial remodelling after ischaemic injury

Genetic Variation in the Gene Encoding Adiponectin Is Associated With an Increased Risk of Type 2 Diabetes in the Japanese Population

Correlation between the adiponectin-leptin ratio and parameters of insulin resistance in patients with type 2 diabetes

Correlation of the adipocyte-derived protein adiponectin with insulin resistance index and serum high-density lipoprotein-cholesterol, independent of body mass index, in the Japanese population

Lipoma and opthalmoplegia in mitochondrial diabetes associated with small heteroplasmy level of 3243 tRNA(Leu(UUR)) mutation

Association of the mitochondrial DNA 5178A/C polymorphism with maternal inheritance and onset of type 2 diabetes in Japanese patients

Meta-analysis of three diabetes population studies: association of inactive ALDH2 genotype with maternal inheritance of diabetes

Decrease in Serum Adiponectin Level Due to Obesity and Visceral Fat Accumulation in Children

CMOS LSI-based multichip flexible neural stimulation device with embedded bulk Pt electrodes

Acute metabolic cataract as a first manifestation of diabetes mellitus in a 12-year-old girl

Toxic multinodular goitre in a patient with generalized resistance to thyroid hormone who harbours the R429Q mutation in the thyroid hormone receptor β gene

Mitochondrial tRNA(Leu(UUR)) mutation at position 3243 detected in patients with type 1 diabetes

Deposition of a-SiC:H thin film from organosilicon material by remote plasma CVD method

A case of type 2 diabetes with high levels of plasma and urinary C-peptide

The Codon 620 Single Nucleotide Polymorphism of the Protein Tyrosine Phosphatase-22 Gene Does not Contribute to Autoimmune Thyroid Disease Susceptibility in the Japanese

Silent mixed corticotroph and somatotroph macroadenomas presenting with pituitary apoplexy

Effects of pioglitazone on metabolic parameters, body fat distribution, and serum adiponectin levels in Japanese male patients with type 2 diabetes

SEL1L Microsatellite Polymorphism in Japanese Patients with Autoimmune Thyroid Diseases

Open-label Compassionate Use One Year-treatment with Pirfenidone to Patients with Chronic Pulmonary Fibrosis

Maternal inheritance of diabetes is associated with inactive ALDH2 genotype in diabetics with renal failure in Japanese

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