Found: 29
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Diagnostic Accuracy of Methods for Detection of Antibodies against Type I Interferons in Patients with Endocrine Disorders.
- Published in:
- Journal of Personalized Medicine, 2022, v. 12, n. 12, p. 1948, doi. 10.3390/jpm12121948
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- Publication type:
- Article
Circulating Plasma MicroRNA in Patients With Active Acromegaly.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 2, p. 500, doi. 10.1210/clinem/dgab695
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- Publication type:
- Article
Application of Clinical Blood Metabogram to Type 2 Diabetes Mellitus.
- Published in:
- Metabolites (2218-1989), 2024, v. 14, n. 3, p. 168, doi. 10.3390/metabo14030168
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- Publication type:
- Article
Expanding the Phenotypic and Genotypic Landscape of Autoimmune Polyendocrine Syndrome Type 1.
- Published in:
- 2017
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- Publication type:
- journal article
A case of severe hyperaldosteronism caused by a de novo mutation affecting a critical salt bridge Kir3.4 residue.
- Published in:
- 2015
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- Publication type:
- journal article
Circulating Plasma microRNA to Differentiate Cushing's Disease From Ectopic ACTH Syndrome.
- Published in:
- Frontiers in Endocrinology, 2020, v. 11, p. 1, doi. 10.3389/fendo.2020.00331
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- Publication type:
- Article
Body Weight Reduction Associated with the Sibutramine Treatment: Overall Results of the PRIMAVERA Primary Health Care Trial.
- Published in:
- Obesity Facts: The European Journal of Obesity, 2018, v. 11, n. 4, p. 335, doi. 10.1159/000488880
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- Publication type:
- Article
Diagnosing Impaired Glucose Tolerance Using Direct Infusion Mass Spectrometry of Blood Plasma.
- Published in:
- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0105343
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- Publication type:
- Article
A Potential Rearrangement between CYP19 and TRPM7 Genes on Chromosome 15q21.2 as a Cause of Aromatase Excess Syndrome.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 7, p. 4184, doi. 10.1210/jc.2004-2176
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- Publication type:
- Article
A Novel C-Terminal Growth Hormone Receptor (GHR) Mutation Results in Impaired GHR-STAT5 But Normal STAT-3 Signaling.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 1, p. 542, doi. 10.1210/jc.2003-2133
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- Publication type:
- Article
A Novel IVS2 −2A>T Splicing Mutation in the GH-1 Gene in Familial Isolated Growth Hormone Deficiency Type II in the Spectrum of Other Splicing Mutations in the Russian Population.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 2, p. 820, doi. 10.1210/jc.2002-020269
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- Publication type:
- Article
Prediction of recurrence and remission within 3 years in patients with Cushing disease after successful transnasal adenomectomy.
- Published in:
- Pituitary, 2019, v. 22, n. 6, p. 574, doi. 10.1007/s11102-019-00985-5
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- Publication type:
- Article
A Mutational Hot Spot in the Prop-1 Gene in Russian Children with Combined Pituitary Hormone Deficiency.
- Published in:
- Pituitary, 1998, v. 1, n. 1, p. 45, doi. 10.1023/A:1009918924945
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- Publication type:
- Article
The Russian registry of primary hyperparathyroidism, latest update.
- Published in:
- Frontiers in Endocrinology, 2023, p. 1, doi. 10.3389/fendo.2023.1203437
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- Publication type:
- Article
Effects of active acromegaly on bone mRNA and microRNA expression patterns.
- Published in:
- European Journal of Endocrinology, 2018, v. 178, n. 4, p. 353, doi. 10.1530/EJE-17-0772
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- Publication type:
- Article
Partial deficiency of 17γ-hydroxylase/17,20-lyase caused by a novel missense mutation in the canonical cytochrome heme-interacting motif.
- Published in:
- European Journal of Endocrinology, 2015, v. 172, n. 5, p. K19, doi. 10.1530/EJE-14-0834
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- Publication type:
- Article
Flexible meal-related dosing with repaglinide facilitates glycemic control in therapy-naive type 2 diabetes.
- Published in:
- 2001
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- Publication type:
- journal article
Lack of Association between Genetic Markers on Chromosome 16q22-Q24 and Type 1 Diabetes in Russian Affected Families.
- Published in:
- Croatian Medical Journal, 2005, v. 46, n. 4, p. 670
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- Publication type:
- Article
A Novel Mutation in the Critical P-Box Residue of Steroidogenic Factor-1 Presenting with XY Sex Reversal and Transient Adrenal Failure.
- Published in:
- Hormone Research in Paediatrics, 2018, v. 89, n. 6, p. 450, doi. 10.1159/000481776
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- Publication type:
- Article
Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations.
- Published in:
- Hormone Research in Paediatrics, 2010, v. 73, n. 6, p. 449, doi. 10.1159/000313585
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- Publication type:
- Article
Efficacy and Safety of Biphasic Insulin Aspart 30 in Russian Patients with Type 2 Diabetes: Results of a Multi-Centre, Clinical Experience Study.
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- Diabetes, 2007, v. 56, p. A536
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- Publication type:
- Article
Clinical course and outcome of patients with ACTH-dependent Cushing's syndrome infected with novel coronavirus disease-19 (COVID-19): case presentations.
- Published in:
- Endocrine (1355008X), 2021, v. 72, n. 1, p. 12, doi. 10.1007/s12020-021-02674-5
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- Publication type:
- Article
A summary of the Russian clinical guidelines on the diagnosis and treatment of osteoporosis.
- Published in:
- Osteoporosis International, 2023, v. 34, n. 3, p. 429, doi. 10.1007/s00198-022-06667-6
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- Publication type:
- Article
Three-year progress report of Bone Health TeleECHO Moscow: a strategy to improve the care of patients with osteoporosis and other metabolic skeletal diseases in underserved communities of Russia.
- Published in:
- Osteoporosis International, 2022, v. 33, n. 9, p. 2035, doi. 10.1007/s00198-022-06431-w
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- Publication type:
- Article
Genetic and Epigenetic Aspects of Type 1 Diabetes Mellitus: Modern View on the Problem.
- Published in:
- Biomedicines, 2024, v. 12, n. 2, p. 399, doi. 10.3390/biomedicines12020399
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- Publication type:
- Article
The risk factors for fractures and trabecular bone-score value in patients with endogenous Cushing's syndrome.
- Published in:
- Archives of Osteoporosis, 2015, v. 10, n. 1, p. 1, doi. 10.1007/s11657-015-0244-1
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- Publication type:
- Article
High frequency of mutations in 'dyshormonogenesis genes' in severe congenital hypothyroidism.
- Published in:
- PLoS ONE, 2018, v. 13, n. 9, p. 1, doi. 10.1371/journal.pone.0204323
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- Publication type:
- Article
Diagnostic performance of late-night salivary cortisol measured by automated electrochemiluminescence immunoassay in obese and overweight patients referred to exclude Cushing's syndrome.
- Published in:
- Endocrine (1355008X), 2012, v. 41, n. 3, p. 494, doi. 10.1007/s12020-012-9658-3
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- Publication type:
- Article
A glucokinase gene mutation in a young boy with diabetes mellitus, hyperinsulinemia, and insulin resistance.
- Published in:
- 2017
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- Publication type:
- Case Study