Found: 12
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De novo Pure Partial Trisomy 6p Associated with Facial Dysmorphism, Developmental Delay, Brain Anomalies, and Primary Congenital Hypothyroidism.
- Published in:
- Molecular Syndromology, 2023, v. 14, n. 1, p. 35, doi. 10.1159/000525393
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- Publication type:
- Article
In response to: "Children with Newly Diagnosed Type 1 Diabetes Before and During the COVID-19 Pandemic".
- Published in:
- 2022
- By:
- Publication type:
- Letter to the Editor
A Long-Term Comparison of Presenting Characteristics of Children with Newly Diagnosed Type 1 Diabetes Before and During the COVID-19 Pandemic.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2022, v. 14, n. 3, p. 267, doi. 10.4274/jcrpe.galenos.2022.2021-10-2
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- Publication type:
- Article
Heart-Type Fatty Acid Binding Protein Level as a Tool in Identification of Early Cardiac Effects of Diabetic Ketoacidosis.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2017, v. 9, n. 2, p. 118, doi. 10.4274/jcrpe.3961
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- Publication type:
- Article
Growth Patterns of Children of Same Geographic Background Reared in Different Environments.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2014, v. 6, n. 4, p. 233, doi. 10.4274/jcrpe.1612
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- Publication type:
- Article
Clinical, sonographical, and pathological findings of pediatric thyroid nodules.
- Published in:
- European Journal of Pediatrics, 2021, v. 180, n. 9, p. 2823, doi. 10.1007/s00431-021-04032-z
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- Publication type:
- Article
Partial remission in children and adolescents with type 1 diabetes: an analysis based on the insulin dose-adjusted hemoglobin A1c.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2021, v. 34, n. 10, p. 1311, doi. 10.1515/jpem-2021-0048
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- Publication type:
- Article
Kocher-Debré-Semelaigne syndrome with rhabdomyolysis and increased creatinine.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2015, v. 28, n. 11/12, p. 1383, doi. 10.1515/jpem-2014-0411
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- Publication type:
- Article
Chondrocalcinosis related to familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2015, v. 28, n. 5/6, p. 713, doi. 10.1515/jpem-2013-0254
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- Publication type:
- Article
Marine-Lenhart syndrome in a young girl.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 1/2, p. 189, doi. 10.1515/jpem-2013-0302
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- Publication type:
- Article
Extremely rare cause of hyperkalemia: ileostomy-induced hyperkalemia in extremely low birth weight infants.
- Published in:
- 2024
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- Publication type:
- Case Study
Intrathyroidal ectopic thymus: an important entity in the differential diagnosis of thyroid nodules.
- Published in:
- Turkish Journal of Pediatrics, 2022, v. 64, n. 5, p. 909, doi. 10.24953/turkjped.2021.4842
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- Publication type:
- Article