Found: 16
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p.Gln318X and p.Val281Leu as the Major Variants of CYP21A2 Gene in Children with Idiopathic Premature Pubarche.
- Published in:
- International Journal of Endocrinology, 2020, p. 1, doi. 10.1155/2020/4329791
- By:
- Publication type:
- Article
p.Gln318X and p.Val281Leu as the Major Variants of CYP21A2 Gene in Children with Idiopathic Premature Pubarche.
- Published in:
- International Journal of Endocrinology, 2020, p. 1, doi. 10.1155/2020/4329791
- By:
- Publication type:
- Article
p.Gln318X and p.Val281Leu as the Major Variants of CYP21A2 Gene in Children with Idiopathic Premature Pubarche.
- Published in:
- International Journal of Endocrinology, 2020, p. 1, doi. 10.1155/2020/4329791
- By:
- Publication type:
- Article
The Effect of Metformin as an Adjunct Therapy in Adolescents with Type 1 Diabetes.
- Published in:
- Journal of Clinical & Diagnostic Research, 2017, v. 11, n. 4, p. 1, doi. 10.7860/JCDR/2017/24901.9725
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- Publication type:
- Article
Genetic variant profiling of neonatal diabetes mellitus in Iranian patients: Unveiling 58 distinct variants in 14 genes.
- Published in:
- Journal of Diabetes Investigation, 2024, v. 15, n. 10, p. 1390, doi. 10.1111/jdi.14254
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- Publication type:
- Article
Assessment of Vitamin D Status and Response to Vitamin D3 in Obese and Non-Obese Iranian Children.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Global perspective on pediatric growth hormone registries: a systematic review.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 6, p. 709, doi. 10.1515/jpem-2022-0045
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- Publication type:
- Article
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy: report of three cases from Iran.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 8, p. 979, doi. 10.1515/jpem-2016-0017
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- Publication type:
- Article
Molecular and clinical characterization of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) in Iranian non-Jewish patients: report of two novel AIRE gene pathogenic variants.
- Published in:
- Orphanet Journal of Rare Diseases, 2022, v. 17, n. 1, p. 1, doi. 10.1186/s13023-021-02170-z
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- Publication type:
- Article
Acute infantile liver failure syndrome type 2 in a 2.5‐year‐old boy: A case report.
- Published in:
- 2023
- By:
- Publication type:
- Case Study
Pediatric Glioblastoma Multiforme in Association with Turner's Syndrome: A Case Report.
- Published in:
- Pediatric Neurosurgery, 2015, v. 50, n. 1, p. 38, doi. 10.1159/000368804
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- Publication type:
- Article
Evaluation of Effects of the COVID-19 Crisis on Disease Management in Children with Type 1 Diabete.
- Published in:
- Immunology & Genetics Journal, 2023, v. 6, n. 3, p. 103, doi. 10.18502/igj.v6i3.16574
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- Publication type:
- Article
Hypothyroidism among pediatric patients with type 1 diabetes mellitus, from patients' characteristics to disease severity.
- Published in:
- Clinical Pediatric Endocrinology, 2017, v. 26, n. 2, p. 73, doi. 10.1297/cpe.26.73
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- Publication type:
- Article
Mucopolysaccharidosis Type I in Children, a Forgotten Diagnosis Responsible for Undiagnosed Musculoskeletal Complaints: Report of Two Cases.
- Published in:
- Acta Medica, 2019, v. 62, n. 4, p. 161, doi. 10.14712/18059694.2020.6
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- Publication type:
- Article
Evaluation of serum IgA levels in Iranian patients with type 1 diabetes mellitus.
- Published in:
- Acta Diabetologica, 2012, v. 49, n. 2, p. 131, doi. 10.1007/s00592-010-0183-7
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- Publication type:
- Article
Proptosis, Micrognathia, Low Set Ear and Chest Deformity in a Patient with Extra Marker Chromosome 22.
- Published in:
- Acta Medica Iranica, 2015, v. 53, n. 12, p. 782
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- Publication type:
- Article