Found: 21
Select item for more details and to access through your institution.
Thyroid volume is the key predictor of hyperthyroidism remission after radioactive iodine therapy in pediatric patients.
- Published in:
- European Journal of Pediatrics, 2023, v. 182, n. 11, p. 4931, doi. 10.1007/s00431-023-05153-3
- By:
- Publication type:
- Article
Association between Characteristics at Birth, Breastfeeding and Obesity in 22 Countries: The WHO European Childhood Obesity Surveillance Initiative – COSI 2015/2017.
- Published in:
- Obesity Facts: The European Journal of Obesity, 2019, v. 12, n. 2, p. 226, doi. 10.1159/000500425
- By:
- Publication type:
- Article
Expanding the Phenotypic and Genotypic Landscape of Autoimmune Polyendocrine Syndrome Type 1.
- Published in:
- 2017
- By:
- Publication type:
- journal article
A Randomized Phase 2 Study of Long-Acting TransCon GH vs Daily GH in Childhood GH Deficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2017, p. 1673, doi. 10.1210/jc.2016-3776
- By:
- Publication type:
- Article
A glucokinase gene mutation in a young boy with diabetes mellitus, hyperinsulinemia, and insulin resistance.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
A Randomized Phase 2 Study of Long-Acting TransCon GH vs Daily GH in Childhood GH Deficiency.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Long-Acting C-Terminal Peptide-Modified hGH (MOD-4023): Results of a Safety and Dose-Finding Study in GHD Children.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Development of Insulin Detemir/Insulin Aspart Cross-Reacting Antibodies Following Treatment with Insulin Detemir: 104-week Study in Children and Adolescents with Type 1 Diabetes Aged 2-16 Years.
- Published in:
- Diabetes Therapy, 2016, v. 7, n. 4, p. 713, doi. 10.1007/s13300-016-0196-5
- By:
- Publication type:
- Article
GH deficiency status combined with GH receptor polymorphism affects response to GH in children.
- Published in:
- European Journal of Endocrinology, 2015, v. 173, n. 6, p. 777, doi. 10.1530/EJE-15-0474
- By:
- Publication type:
- Article
24-Month Use of Once-Weekly GH, LB03002, in Prepubertal Children With GH Deficiency.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Mutations and Pituitary Morphology in a Series of 82 Patients with PROP1 Gene Defects.
- Published in:
- Hormone Research in Paediatrics, 2011, v. 76, n. 5, p. 348, doi. 10.1159/000332693
- By:
- Publication type:
- Article
Treatment with insulin detemir or NPH insulin in children aged 2-5 yr with type 1 diabetes mellitus.
- Published in:
- Pediatric Diabetes, 2011, v. 12, n. 7, p. 632, doi. 10.1111/j.1399-5448.2010.00750.x
- By:
- Publication type:
- Article
The carriage of the type 1 diabetes-associated R262W variant of human LNK correlates with increased proliferation of peripheral blood monocytes in diabetic patients.
- Published in:
- Pediatric Diabetes, 2011, v. 12, n. 2, p. 127, doi. 10.1111/j.1399-5448.2010.00656.x
- By:
- 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
- By:
- Publication type:
- Article
A Familial Insulin-Like Growth Factor-I Receptor Mutant Leads to Short Stature: Clinical and Biochemical Characterization.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 4, p. 1542, doi. 10.1210/jc.2006-2354
- By:
- Publication type:
- Article
Four novel missense mutations in the CYP21A2 gene detected in Russian patients suffering from the classical form of congenital adrenal hyperplasia: identification, functional characterization, and structural analysis.
- Published in:
- 2006
- By:
- Publication type:
- journal 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
- By:
- 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
- By:
- 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
- By:
- Publication type:
- Article
Growth Hormone Insensitivity (Laron Syndrome) in a Russian Girl of Slavic Origin Caused by a Common Mutation of the GH Receptor Gene.
- Published in:
- International Journal on Disability & Human Development (De Gruyter), 1999, v. 1, n. 2, p. 95, doi. 10.1515/ijdhd.1999.1.2.95
- By:
- 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
- By:
- Publication type:
- Article