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Moderate‐carbohydrate diet without caloric or lipid restriction for Japanese adult patients with nonalcoholic fatty liver disease: A prospective cohort study.
- Published in:
- Hepatology Research, 2023, v. 53, n. 12, p. 1185, doi. 10.1111/hepr.13954
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- Publication type:
- Article
Bilateral atrophy of the extensor digitorum brevis muscle might be a useful sign for diagnosing diabetic polyneuropathy in Japanese men who do not sit in the traditional "seiza" style.
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- Journal of Diabetes Investigation, 2021, v. 12, n. 3, p. 398, doi. 10.1111/jdi.13367
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- Publication type:
- Article
Clinical polyneuropathy does not increase with prediabetes or metabolic syndrome in the Japanese general population.
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- Journal of Diabetes Investigation, 2019, v. 10, n. 6, p. 1565, doi. 10.1111/jdi.13058
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- Publication type:
- Article
Difference in normal limit values of nerve conduction parameters between Westerners and Japanese people might need to be considered when diagnosing diabetic polyneuropathy using a Point‐of‐Care Sural Nerve Conduction Device (NC‐stat®/DPNCheck™)
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- Journal of Diabetes Investigation, 2018, v. 9, n. 5, p. 1173, doi. 10.1111/jdi.12818
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- Publication type:
- Article
Familial Young-Onset Diabetes, Pre-Diabetes and Cardiovascular Disease Are Associated with Genetic Variants of <i>DACH1</i> in Chinese.
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- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0084770
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- Article
Polymorphisms in the IDE-KIF11-HHEX gene locus are reproducibly associated with type 2 diabetes in a Japanese population.
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- 2008
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- Publication type:
- journal article
PAX4 mutations in Thais with maturity onset diabetes of the young.
- Published in:
- 2007
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- Publication type:
- journal article
Nonsense and Missense Mutations in the Human Hepatocyte Nuclear Factor-1β Gene (TCF2) and Their Relation to Type 2 Diabetes in Japanese.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 8, p. 3859, doi. 10.1210/jcem.87.8.8776
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- Publication type:
- Article
A Case of Albright’s Hereditary Osteodystrophy-Like Syndrome Complicated by Several Endocrinopathies: Normal Gsα Gene and Chromosome 2q37.
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- Journal of Clinical Endocrinology & Metabolism, 1998, v. 83, n. 5, p. 1563, doi. 10.1210/jc.83.5.1563
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- Publication type:
- Article
A polymorphic marker in the leptin gene associated with Japanese morbid obesity.
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- Journal of Molecular Medicine, 2000, v. 78, n. 9, p. 516, doi. 10.1007/s001090000143
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- Publication type:
- Article
Chronic Kidney Disease Has a More Powerful Impact on Peripheral Arterial Disease Than Metabolic Syndrome in Japanese Type 2 Diabetic Patients.
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- Metabolic Syndrome & Related Disorders, 2009, v. 7, n. 4, p. 323, doi. 10.1089/met.2008.0074
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- Publication type:
- Article
Uncoupling Protein 2 Promoter Polymorphism -866G/A Affects Peripheral Nerve Dysfunction in Japanese Type 2 Diabetic Patients.
- Published in:
- Diabetes Care, 2006, v. 29, n. 4, p. 888, doi. 10.2337/diacare.29.04.06.dc05-1984
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- Publication type:
- Article
Negative pressure suction during blood sampling may reduce the difference in self-monitoring of blood glucose results between fingertip pricking and forearm pricking.
- Published in:
- 2004
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- Publication type:
- journal article
Lessons learned from molecular biology of insulin-gene mutations.
- Published in:
- 1990
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- Publication type:
- journal article
A novel mutation, Ser159Pro in the NeuroD1/BETA2 gene contributes to the development of diabetes in a Chinese potential MODY family.
- Published in:
- Molecular & Cellular Biochemistry, 2007, v. 303, n. 1/2, p. 115, doi. 10.1007/s11010-007-9463-0
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- Publication type:
- Article
Clinical and functional characterization of the Pro1198 Leu ABCC8 gene mutation associated with permanent neonatal diabetes mellitus.
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- Journal of Diabetes Investigation, 2013, v. 4, n. 3, p. 269, doi. 10.1111/jdi.12049
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- Publication type:
- Article
Increased arterial stiffness is closely associated with hyperglycemia and improved by glycemic control in diabetic patients.
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- Journal of Diabetes Investigation, 2013, v. 4, n. 1, p. 82, doi. 10.1111/j.2040-1124.2012.00229.x
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- Publication type:
- Article
Expression of wild-type and mutant S20G hIAPP in physiologic knock-in mouse models fails to induce islet amyloid formation, but induces mild glucose intolerance.
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- Journal of Diabetes Investigation, 2012, v. 3, n. 2, p. 138, doi. 10.1111/j.2040-1124.2011.00166.x
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- Publication type:
- Article
Pro198Leu missense polymorphism of the glutathione peroxidase 1 gene might be a common genetic predisposition of distal symmetric polyneuropathy and macrovascular disease in Japanese type 2 diabetic patients.
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- Journal of Diabetes Investigation, 2011, v. 2, n. 6, p. 474, doi. 10.1111/j.2040-1124.2011.00127.x
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- Publication type:
- Article
Numbness and paresthesia in bilateral toes and soles, and disproportional sweating restricted to face and trunk are suitable symptoms useful for the diagnosis of diabetic symmetric polyneuropathy.
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- Journal of Diabetes Investigation, 2011, v. 2, n. 6, p. 464, doi. 10.1111/j.2040-1124.2011.00124.x
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- Publication type:
- Article
Insulin gene mutations and diabetes.
- Published in:
- Journal of Diabetes Investigation, 2011, v. 2, n. 2, p. 92, doi. 10.1111/j.2040-1124.2011.00100.x
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- Publication type:
- Article
Effect of anti-oxidants, Ricetrienol and α-tocopherol, on adipocytokine abnormalities and fatty liver in Otsuka Long-Evans Tokushima Fatty diabetic rats.
- Published in:
- Journal of Diabetes Investigation, 2011, v. 2, n. 3, p. 186, doi. 10.1111/j.2040-1124.2010.00090.x
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- Publication type:
- Article
Report of the Committee on the Classification and Diagnostic Criteria of Diabetes Mellitus.
- Published in:
- Journal of Diabetes Investigation, 2010, v. 1, n. 5, p. 212, doi. 10.1111/j.2040-1124.2010.00074.x
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- Publication type:
- Article
Pro198Leu Missense Polymorphism of Glutathione Peroxidase 1 Gene Affects Impaired Vibratory Perception in Toe and the Painful Leg Cramp in Japanese Type 2 Diabetic Patients.
- Published in:
- Diabetes, 2007, v. 56, p. A610
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- Publication type:
- Article
Diabetes Phenotype in Wild-Type and S20G Mutant Human IAPP Knock-In Mice Without Simultaneous Intraislet Amyloid.
- Published in:
- Diabetes, 2007, v. 56, p. A375
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- Publication type:
- Article
Common Variant in the Transcription Factor7-Like2 (TCF7L2) Gene Is Associated with Impaired Insulin Secretion in Japanese Type 2 Diabetic Patients.
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- Diabetes, 2007, v. 56, p. A297
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- Publication type:
- Article
Increased Fluctuations in Blood Glucose and Systolic Blood Pressure Are Risk Factors of the Diabetic Retinopathy.
- Published in:
- Diabetes, 2007, v. 56, p. A218
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- Publication type:
- Article
Association Studies of Variants in the Genes Involved in Pancreatic β-Cell Function in Type 2 Diabetes in Japanese Subjects.
- Published in:
- Diabetes, 2006, v. 55, n. 8, p. 2379, doi. 10.2337/db05-1203
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- Publication type:
- Article
A functional variant in the human betacellulin gene promoter is associated with type 2 diabetes.
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- 2005
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- Publication type:
- journal article
Functional variants in the glutathione peroxidase-1 (GPx-1) gene are associated with increased intima-media thickness of carotid arteries and risk of macrovascular diseases in japanese type 2 diabetic patients.
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- 2004
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- Publication type:
- journal article
Uncoupling protein 2 promoter polymorphism -866G/A affects its expression in beta-cells and modulates clinical profiles of Japanese type 2 diabetic patients.
- Published in:
- 2004
- By:
- Publication type:
- journal article
A missense mutation of Pax4 gene (R121W) is associated with type 2 diabetes in Japanese.
- Published in:
- 2001
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- Publication type:
- journal article
The Pro[sup 12]...Ala Substitution in PPAR-gamma Is Associated With Resistance to Development of...
- Published in:
- Diabetes, 2001, v. 50, n. 4, p. 891, doi. 10.2337/diabetes.50.4.891
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- Publication type:
- Article
Nonsense mutation of islet-1 gene (Q310X) found in a type 2 diabetic patient with a strong family history.
- Published in:
- 2000
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- Publication type:
- journal article
Expression of naturally occurring variants in the muscle glycogen synthase gene.
- Published in:
- 1999
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- Publication type:
- journal article
Missense mutation of amylin gene (S20G) in Japanese NIDDM patients.
- Published in:
- 1996
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- Publication type:
- journal article
Human Prohormone Convertase 3 Gene.
- Published in:
- Diabetes, 1996, v. 45, n. 7, p. 897, doi. 10.2337/diab.45.7.897
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- Publication type:
- Article
Association of the prohormone convertase 2 gene (PCSK2) on chromosome 20 with NIDDM in Japanese subjects.
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- 1995
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- Publication type:
- journal article
Serum type IV collagen concentrations in diabetic patients with microangiopathy as determined by enzyme immunoassay with monoclonal antibodies.
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- 1990
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- Publication type:
- journal article
Use of in vitro DNA amplification to screen family members for an insulin gene mutation.
- Published in:
- 1988
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- Publication type:
- journal article
Ghrelin inhibits insulin secretion through the AMPK–UCP2 pathway in β cells
- Published in:
- FEBS Letters, 2010, v. 584, n. 8, p. 1503, doi. 10.1016/j.febslet.2010.02.069
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- Publication type:
- Article
A fast placement technique for covered tracheobronchial stents in patients with complicated esophagorespiratory fistulas.
- Published in:
- 2005
- By:
- Publication type:
- journal article
Truncal Pruritus of Unknown Origin May Be a Symptom of Diabetic Polyneuropathy.
- Published in:
- Diabetes Care, 2010, v. 33, n. 1, p. 150, doi. 10.2337/dc09-0632
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- Publication type:
- Article
568-P: Pain Threshold of Intraepidermal Nerve Terminal Reflects Small Nerve Fiber Function and Rises in Early Phase of Diabetes.
- Published in:
- Diabetes, 2019, v. 68, p. N.PAG, doi. 10.2337/db19-568-P
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- Publication type:
- Article