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pro vyhledávání: '"Tina Y Hu"'
Autor:
Andrew J. Bauer, Bethany Auble, Amy L. Clark, Tina Y. Hu, Amber Isaza, Kyle P. McNerney, Daniel L. Metzger, Lindsey Nicol, Samuel R. Pierce, Richard Sidlow
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Monocarboxylate transporter 8 (MCT8) deficiency is a rare, X-linked disorder arising from mutations in the SLC16A2 gene and resulting from dysfunctional thyroid hormone transport. This disorder is characterized by profound neurodevelopmental delay an
Externí odkaz:
https://doaj.org/article/9aa8cd96d30c4def9908a9d3f71c8e2b
Publikováno v:
Pediatric diabetesREFERENCES. 23(4)
Transition from pediatric to adult healthcare systems is a difficult process for young adults with Type 1 Diabetes (T1D) and most patients experience a deterioration in disease control. Mental health (MH) disorders are common in individuals with T1D
Autor:
Katrina Conard, Tina Y Hu, Loren Berman, Tejal Mody, Anthony Gannon, Jeanne M. Franzone, William J. Parkes
Publikováno v:
Journal of the Endocrine Society
BACKGROUND: Parathyroid carcinoma (PC) is exceptionally rare in children and its clinical features are poorly understood. Available reports have identified that very high serum calcium and parathyroid hormone levels would be expected in this disease.