Found: 11
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Short Stature Homeobox-Containing Haploinsufficiency in Seven Siblings with Short Stature.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
Metastatic Medullary Thyroid Cancer in a Pediatric Patient with MEN 2B: Emphasis on the Need for Early Recognition of Extrathyroidal Clinical Findings Associated with MEN 2B.
- Published in:
- Clinical Pediatrics, 2006, v. 45, n. 5, p. 463, doi. 10.1177/0009922806289625
- By:
- Publication type:
- Article
Decreased Bone Mineral Density and Vertebral Compression Fractures in a Young Adult Male with 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia (CAH): Is CAH an Unrecognized Population at Risk for Glucocorticoid-Induced Osteoporosis?
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2010, v. 23, n. 1/2, p. 179, doi. 10.1515/JPEM.2010.23.1-2.179
- By:
- Publication type:
- Article
Hypophosphatemic Rickets in Opsismodysplasia.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2007, v. 20, n. 1, p. 79
- By:
- Publication type:
- Article
Access to care among patients with osteogenesis imperfecta during the COVID-19 pandemic.
- Published in:
- Archives of Osteoporosis, 2023, v. 18, n. 1, p. 1, doi. 10.1007/s11657-023-01355-2
- By:
- Publication type:
- Article
Dental Implications of Osteogenesis Imperfecta: Treatment with IV Bisphosphonate: Report of a Case.
- Published in:
- 2011
- By:
- Publication type:
- Case Study
Unmasking of Partial Diabetes Insipidus during Stress but Not Maintenance Dosing of Glucocorticoids in an Infant with Septo-Optic Dysplasia.
- Published in:
- 2011
- By:
- Publication type:
- Case Study
Alternative Strategies for the Treatment of Classical Congenital Adrenal Hyperplasia: Pitfalls and Promises.
- Published in:
- International Journal of Pediatric Endocrinology, 2010, p. 1, doi. 10.1155/2010/670960
- By:
- Publication type:
- Article
Cell Cycle-Dependent Localization of Voltage-Dependent Calcium Channels and the Mitotic Apparatus in a Neuroendocrine Cell Line(AtT-20).
- Published in:
- International Journal of Cell Biology, 2009, v. 2009, p. 1, doi. 10.1155/2009/487959
- By:
- Publication type:
- Article
Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical management.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Congenital Hyperinsulinism and Glucose Hypersensitivity in Homozygous and Heterozygous Carriers of Kir6.2 (KCNJ11) Mutation V290M Mutation.
- Published in:
- Diabetes, 2011, v. 60, n. 1, p. 209, doi. 10.2337/db10-0731
- By:
- Publication type:
- Article