Found: 48
Select item for more details and to access through your institution.
Elevated serum creatine kinase level in diabetic patients with nephrotic syndrome: a role of fluid retention.
- Published in:
- 1987
- By:
- Publication type:
- journal article
T Cell Immunity to Glutamic Acid Decarboxylase in Fulminant Type 1 Diabetes without Significant Elevation of Serum Amylase.
- Published in:
- Annals of the New York Academy of Sciences, 2006, v. 1079, n. 1, p. 181, doi. 10.1196/annals.1375.028
- By:
- Publication type:
- Article
Multiple SNPs in Intron 41 of Thyroglobulin Gene Are Associated with Autoimmune Thyroid Disease in the Japanese Population.
- Published in:
- PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0037501
- By:
- Publication type:
- Article
Subtle 17α-hydroxylase/17,20-lyase deficiency with homozygous Y201N mutation in an infertile woman.
- Published in:
- 2005
- By:
- Publication type:
- journal article
Vitamin D Receptor Gene Polymorphism Is Associated with Graves’ Disease in the Japanese Population.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 12, p. 4639, doi. 10.1210/jcem.85.12.7038
- By:
- Publication type:
- Article
An Unusual Kindred of the Multiple Endocrine Neoplasia Type 1 (MEN1 ) in Japanese.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 3, p. 1327, doi. 10.1210/jcem.85.3.6478
- By:
- Publication type:
- Article
Elevation of circulating proadrenomedullin-N terminal 20-peptide in thyrotoxicosis.
- Published in:
- Clinical Endocrinology, 1997, v. 46, n. 3, p. 271, doi. 10.1046/j.1365-2265.1997.1220934.x
- By:
- Publication type:
- Article
Adult Thyroid Outcomes of Congenital Hypothyroidism.
- Published in:
- Thyroid, 2023, v. 33, n. 5, p. 556, doi. 10.1089/thy.2022.0481
- By:
- Publication type:
- Article
A Filipino patient with fulminant type 1 diabetes.
- Published in:
- 2004
- By:
- Publication type:
- Case Study
Multiple tumors in mitochondrial diabetes associated with tRNALeu(UUR) mutation at position 3264.
- Published in:
- 2003
- By:
- Publication type:
- Case Study
Multiple cranial mononeuropathies with acetylcholine receptor antibody in mitochondrial diabetes.
- Published in:
- 2003
- By:
- Publication type:
- Case Study
Mitochondrial tRNA Mutation at Position 3243 and Symptomatic Polyneuropathy in Type 2 Diabetes.
- Published in:
- 2003
- By:
- Publication type:
- Letter
Influence of alcohol intake and aldehyde dehydrogenase 2 phenotype on peripheral neuropathy of diabetes.
- Published in:
- 2003
- By:
- Publication type:
- Letter
Diabetic vasculopathy and alcohol tolerance trait in type 2 diabetes.
- Published in:
- 2003
- By:
- Publication type:
- Letter
GAD antibody in mitochondrial diabetes associated with tRNA(UUR) mutation at position 3271.
- Published in:
- 2002
- By:
- Publication type:
- Case Study
Lipoma and sensory neuropathy in mitochondrial diabetes associated with tRNA mutation at position 3271.
- Published in:
- 2002
- By:
- Publication type:
- Letter
Absence of Antibodies to ICA512/IA-2 in NIDDM Patients With the Mitochondrial DNA bp 3243 Mutation.
- Published in:
- Diabetes Care, 1997, v. 20, n. 5, p. 903
- By:
- Publication type:
- Article
Mitochondrial aldehyde dehydrogenase in diabetes associated with mitochondrial tRNA(Leu(UUR)) mutation at position 3243.
- Published in:
- 1996
- By:
- Publication type:
- journal article
Diabetes with the 3243 mitochondrial tRNALeu(UUR) mutation. Characteristic neuroimaging findings.
- Published in:
- 1996
- By:
- Publication type:
- journal article
Unpleasant alcohol effect in diabetes associated with 3243 bp mitochondrial tRNALeu(UUR) mutation.
- Published in:
- 1995
- By:
- Publication type:
- Letter
Cellular localization of prolactin-releasing peptide receptors in the human pituitary.
- Published in:
- Acta Neuropathologica, 2003, v. 106, n. 5, p. 495, doi. 10.1007/s00401-003-0753-7
- By:
- Publication type:
- Article
Occurrence of Type 1 Diabetes in Graves' Disease PatientsWho Are Positive for Antiglutamic Acid Decarboxylase Antibodies: An 8-Year Followup Study.
- Published in:
- Journal of Thyroid Research, 2011, p. 1, doi. 10.4061/2011/306487
- By:
- Publication type:
- Article
Early Palliation of Oculomotor Nerve Palsy following Gamma Knife Radiosurgery for Pituitary Adenoma.
- Published in:
- European Neurology, 2002, v. 47, n. 1, p. 61, doi. 10.1159/000047951
- By:
- Publication type:
- Article
Clinical Pictures Associated with Borderline Heteroplasmy Rate of 3243 Mitochondrial tRNA<sup>Leu(UUR)</sup> Mutation in Type 2 Diabetes.
- Published in:
- Diabetes, 2007, v. 56, p. A292
- By:
- Publication type:
- Article
Genetic variation in the gene encoding adiponectin is associated with an increased risk of type 2 diabetes in the Japanese population.
- Published in:
- 2002
- By:
- Publication type:
- journal article
Comparison of Efficacy and Adverse Effects Between Methimazole 15 mg+Inorganic Iodine 38 mg/Day and Methimazole 30 mg/Day as Initial Therapy for Graves' Disease Patients with Moderate to Severe Hyperthyroidism.
- Published in:
- Thyroid, 2015, v. 25, n. 1, p. 43, doi. 10.1089/thy.2014.0084
- By:
- Publication type:
- Article
Thyroid Profiles in a Patient with Resistance to Thyroid Hormone and Episodes of Thyrotoxicosis, Including Repeated Painless Thyroiditis.
- Published in:
- Thyroid, 2013, v. 23, n. 7, p. 898, doi. 10.1089/thy.2012.0004
- By:
- Publication type:
- Article
Association of the Protein Tyrosine Phosphatase Nonreceptor 22 Haplotypes with Autoimmune Thyroid Disease in the Japanese Population.
- Published in:
- Thyroid, 2010, v. 20, n. 8, p. 893, doi. 10.1089/thy.2010.0104
- By:
- Publication type:
- Article
Association of a C/T Single-Nucleotide Polymorphism in the 5' Untranslated Region of the CD40 Gene with Graves' Disease in Japanese.
- Published in:
- Thyroid, 2006, v. 16, n. 5, p. 443
- By:
- Publication type:
- Article
The Codon 620 Single Nucleotide Polymorphismof the Protein Tyrosine Phosphatase-22 GeneDoes not Contribute to Autoimmune Thyroid DiseaseSusceptibility in the Japanese.
- Published in:
- Thyroid, 2005, v. 15, n. 10, p. 1115
- By:
- Publication type:
- Article
Vitamin D Receptor Gene Polymorphisms in Hashimoto's Thyroiditis.
- Published in:
- Thyroid, 2001, v. 11, n. 6, p. 607, doi. 10.1089/105072501750302967
- By:
- Publication type:
- Article
SEL1L Microsatellite Polymorphism in Japanese Patients with Autoimmune Thyroid Diseases.
- Published in:
- Thyroid, 2001, v. 11, n. 4, p. 335, doi. 10.1089/10507250152039064
- By:
- Publication type:
- Article
Vitamin D Receptor Initiation Codon Polymorphism in Japanese Patients with Graves' Disease.
- Published in:
- Thyroid, 2000, v. 10, n. 5, p. 375, doi. 10.1089/thy.2000.10.375
- By:
- Publication type:
- Article
Vitamin D Receptor Initiation Codon Polymorphism in Japanese Patients with Graves' Disease.
- Published in:
- Thyroid, 2000, v. 10, n. 6, p. 475, doi. 10.1089/thy.2000.10.475
- By:
- Publication type:
- Article
CTLA4 Gene Polymorphism Confers Susceptibility to Graves' Disease in Japanese.
- Published in:
- Thyroid, 1997, v. 7, n. 6, p. 843, doi. 10.1089/thy.1997.7.843
- By:
- Publication type:
- Article
Urinary Cortisol Metabolites in the Assessment of Peripheral Thyroid Hormone Action: Application for Diagnosis of Resistance to Thyroid Hormone.
- Published in:
- Thyroid, 1993, v. 3, n. 3, p. 229, doi. 10.1089/thy.1993.3.229
- By:
- Publication type:
- Article
Biallelic PROKR2 variants and congenital hypogonadotropic hypogonadism: a case report and a literature review.
- Published in:
- Endocrine Journal, 2022, v. 69, n. 7, p. 831, doi. 10.1507/endocrj.ej21-0779
- By:
- Publication type:
- Article
Homozygous DUOXA2 mutation (p.Tyr138*) in a girl with congenital hypothyroidism and her apparently unaffected brother: Case report and review of the literature.
- Published in:
- Endocrine Journal, 2017, v. 64, n. 8, p. 807, doi. 10.1507/endocrj.ej16-0564
- By:
- Publication type:
- Article
Genetics of Congenital Isolated TSH Deficiency: Mutation Screening of the Known Causative Genes and a Literature Review.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Identification of compound heterozygous TSHR mutations (R109Q and R450H) in a patient with nonclassic TSH resistance and functional characterization of the mutant receptors.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 3, p. 123, doi. 10.1297/cpe.27.123
- By:
- Publication type:
- Article
Decrease in Serum Adiponectin Level Due to Obesity and Visceral Fat Accumulation in Children.
- Published in:
- Obesity (19307381), 2003, v. 11, n. 9, p. 1072, doi. 10.1038/oby.2003.147
- By:
- Publication type:
- Article
Hepatotoxicity and cutaneous reactions after antithyroid drug administration.
- Published in:
- Clinical Endocrinology, 2012, v. 77, n. 2, p. 310, doi. 10.1111/j.1365-2265.2012.04365.x
- By:
- Publication type:
- Article
Association of a thyroglobulin gene polymorphism with Hashimoto's thyroiditis in the Japanese population.
- Published in:
- Clinical Endocrinology, 2004, v. 61, n. 2, p. 263, doi. 10.1111/j.1365-2265.2004.02096.x
- By:
- Publication type:
- Article
Toxic multinodular goitre in a patient with generalized resistance to thyroid hormone who harbours the R429Q mutation in the thyroid hormone receptor β gene.
- Published in:
- Clinical Endocrinology, 2001, v. 54, n. 1, p. 121, doi. 10.1046/j.1365-2265.2001.01033.x
- By:
- Publication type:
- Article
SNP analysis of the inter-alpha-trypsin inhibitor family heavy chain-related protein (IHRP) gene by a fluorescence-adapted SSCP method.
- Published in:
- BMC Medical Genetics, 2002, v. 3, p. 6, doi. 10.1186/1471-2350-3-6
- By:
- Publication type:
- Article
Vitamin D receptor initiation codon polymorphism influences genetic susceptibility to type 1 diabetes mellitus in the Japanese population.
- Published in:
- BMC Medical Genetics, 2001, v. 2, p. 7, doi. 10.1186/1471-2350-2-7
- By:
- Publication type:
- Article
Estrogen receptor alpha dinucleotide repeat polymorphism in Japanese patients with autoimmune thyroid diseases.
- Published in:
- 2000
- By:
- Publication type:
- Case Study
Lack of association between estrogen receptor β dinucleotide repeat polymorphism and autoimmune thyroid diseases in Japanese patients.
- Published in:
- 2001
- By:
- Publication type:
- Case Study