Found: 25
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Secondary Hypogonadism due to Excessive Ingestion of Isoflavone in a Man.
- Published in:
- Internal Medicine, 2022, v. 61, n. 19, p. 2899, doi. 10.2169/internalmedicine.8578-21
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- Article
Carney Complex Complicated with Primary Pigmented Nodular Adrenocortical Disease without Cushing's Syndrome Recurrence for Five Years after Unilateral Adrenalectomy.
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- Internal Medicine, 2022, v. 61, n. 2, p. 205, doi. 10.2169/internalmedicine.7418-21
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- Article
Clinical Utility of the Adrenocorticotropin Stimulation Test with/without Dexamethasone Suppression for Definitive and Subtype Diagnosis of Primary Aldosteronism.
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- International Journal of Molecular Sciences, 2017, v. 18, n. 5, p. 948, doi. 10.3390/ijms18050948
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- Article
Immunohistochemical Expression of Choline Acetyltransferase and Catecholamine-Synthesizing Enzymes in Head-and-Neck and Thoracoabdominal Paragangliomas and Pheochromocytomas.
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- Endocrine Pathology, 2021, v. 32, n. 4, p. 442, doi. 10.1007/s12022-021-09694-x
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- Article
The Diagnostic Dilemma of GATA3 Immunohistochemistry in Pheochromocytoma and Paraganglioma.
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- Endocrine Pathology, 2020, v. 31, n. 2, p. 95, doi. 10.1007/s12022-020-09618-1
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- Article
Genotype–Phenotype Correlations in 30 Japanese Patients With Congenital Hypothyroidism Attributable to TG Defects.
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- Journal of Clinical Endocrinology & Metabolism, 2024, v. 109, n. 9, p. 2358, doi. 10.1210/clinem/dgae098
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- Article
Inactivation of a Frameshift TSH Receptor Variant Val711Phefs*18 is Due to Acquisition of a Hydrophobic Degron.
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- 2021
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- 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.
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- Clinical Pediatric Endocrinology, 2018, v. 27, n. 3, p. 123, doi. 10.1297/cpe.27.123
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- Article
Glucose Effectiveness Decreases in Relationship to a Subtle Worsening of Metabolic Parameters in Young Japanese with Normal Glucose Tolerance.
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- Metabolic Syndrome & Related Disorders, 2021, v. 19, n. 7, p. 409, doi. 10.1089/met.2021.0017
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- Article
Body Roundness Index Is Better Correlated with Insulin Sensitivity than Body Shape Index in Young and Middle-Aged Japanese Persons.
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- Metabolic Syndrome & Related Disorders, 2024, v. 22, n. 2, p. 151, doi. 10.1089/met.2023.0175
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- Article
Hereditary pheochromocytoma/paraganglioma syndrome with a novel mutation in the succinate dehydrogenase subunit B gene in a Japanese family: two case reports.
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- 2021
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- Publication type:
- journal article
Insulin and Proinsulin Dynamics Progressively Deteriorate From Within the Normal Range Toward Impaired Glucose Tolerance.
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- Journal of the Endocrine Society, 2020, v. 4, n. 7, p. 1, doi. 10.1210/jendso/bvaa066
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- Article
Adult Thyroid Outcomes of Congenital Hypothyroidism.
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- Thyroid, 2023, v. 33, n. 5, p. 556, doi. 10.1089/thy.2022.0481
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- Article
Association between sarcopenia and the severity of diabetic polyneuropathy assessed by nerve conduction studies in Japanese patients with type 2 diabetes mellitus.
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- Journal of Diabetes Investigation, 2022, v. 13, n. 8, p. 1357, doi. 10.1111/jdi.13788
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- Article
Phenotypic Variability in a Family with Carney Complex Accompanied by a Novel Mutation Involving PRKAR1A.
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- Tohoku Journal of Experimental Medicine, 2022, v. 257, n. 4, p. 337, doi. 10.1620/tjem.2022.J051
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- Article
Postloading insulinemia is independently associated with arterial stiffness in young Japanese persons.
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- Hypertension Research, 2021, v. 44, n. 11, p. 1515, doi. 10.1038/s41440-021-00749-4
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- Article
GWAS of thyroid dysgenesis identifies a risk locus at 2q33.3 linked to regulation of Wnt signaling.
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- Human Molecular Genetics, 2022, v. 31, n. 23, p. 3967, doi. 10.1093/hmg/ddac093
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- Article
Genetics of Congenital Isolated TSH Deficiency: Mutation Screening of the Known Causative Genes and a Literature Review.
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- 2019
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- Publication type:
- journal article
Association of ghrelin dynamics with beta cell function in Japanese subjects with normal glucose tolerance.
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- Clinical Endocrinology, 2019, v. 91, n. 5, p. 616, doi. 10.1111/cen.14073
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- Article
Clinical characteristics and efficacy of pioglitazone in a Japanese patient with familial partial lipodystrophy due to peroxisome proliferator-activated receptor γ gene mutation.
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- Endocrine Journal, 2023, v. 70, n. 1, p. 69, doi. 10.1507/endocrj.ej22-0140
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- Article
Biallelic PROKR2 variants and congenital hypogonadotropic hypogonadism: a case report and a literature review.
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- Endocrine Journal, 2022, v. 69, n. 7, p. 831, doi. 10.1507/endocrj.ej21-0779
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- Article
Therapeutic efficacy and limitations of potassium iodide for patients newly diagnosed with Graves' disease.
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- Endocrine Journal, 2020, v. 67, n. 6, p. 631, doi. 10.1507/endocrj.ej19-0379
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- Article
Mild thyroid peroxidase deficiency caused by TPO mutations with residual activity: Correlation between clinical phenotypes and enzymatic activity.
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- Endocrine Journal, 2017, v. 64, n. 11, p. 1087, doi. 10.1507/endocrj.ej17-0194
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- Article
Homozygous DUOXA2 mutation (p.Tyr138*) in a girl with congenital hypothyroidism and her apparently unaffected brother: Case report and review of the literature.
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- Endocrine Journal, 2017, v. 64, n. 8, p. 807, doi. 10.1507/endocrj.ej16-0564
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- Article
Aldosterone excess may inhibit insulin secretion: A comparative study on glucose metabolism pre- and post-adrenalectomy in patients with primary aldosteronism.
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- Endocrine Journal, 2017, v. 64, n. 3, p. 339, doi. 10.1507/endocrj.ej16-0500
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- Article