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British Journal of Haematology|February 22, 2011
Renal dysfunction in patients with thalassaemiaCharles T Quinn, Valerie L Johnson, Hae-Young Kim, et al.
The Journal of Clinical Endocrinology and Metabolism|June 27, 2020
A Phase 2, Multicenter Study of Nevanimibe for the Treatment of Congenital Adrenal HyperplasiaDiala El-Maouche, Deborah P Merke, Maria G Vogiatzi, et al.
The Journal of Clinical Endocrinology and Metabolism|May 22, 2023
Crinecerfont, a CRF1 Receptor Antagonist, Lowers Adrenal Androgens in Adolescents With Congenital Adrenal HyperplasiaRon S Newfield, Kyriakie Sarafoglou, Patricia Y Fechner, et al.
Blood|June 18, 2010
Bone loss caused by iron overload in a murine model: importance of oxidative stressJaime Tsay, Zheiwei Yang, F Patrick Ross, et al.
Epilepsy Research|June 23, 2018
PCDH19-related epilepsy in a male with Klinefelter syndrome: Additional evidence supporting PCDH19 cellular interference disease mechanismEdward J Romasko, Elizabeth T DeChene, Jorune Balciuniene, et al.
American Journal of Medical Genetics. Part A|February 16, 2023
Expanding the reproductive organ phenotype of CHD7-spectrum disorderTomoki T Nomakuchi, Melinda Danowitz, Blythe Stewart, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 29, 2008
Bone disease in thalassemia: a frequent and still unresolved problemMaria G Vogiatzi, Eric A Macklin, Ellen B Fung, et al.
British Journal of Haematology|July 17, 2009
Differences in the prevalence of growth, endocrine and vitamin D abnormalities among the various thalassaemia syndromes in North AmericaMaria G Vogiatzi, Eric A Macklin, Felicia L Trachtenberg, et al.
Pediatrics|November 6, 2025
Reference Growth Charts for Children With 47,XXY/Klinefelter SyndromeShanlee M Davis, Taylor E Marshall, Karli S Swenson, et al.
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