The fellowship in Pediatric Endocrinology is a three-year ACGME-accredited program providing comprehensive training in clinical patient management and guidance in the development of research skills. The fellowship is at the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) and based at the National Institutes of Health (NIH) Clinical Center, in Bethesda, Maryland (NIH-CC). The NICHD program is based at one of the largest and most sophisticated research institutions in the United States. The clinical center maintains clinical research protocols investigating the treatment of adrenal and pituitary tumors, congenital adrenal hyperplasia, precocious puberty, idiopathic juvenile osteoporosis, Cushings syndrome, obesity, and others. The fellow gains critical skills in the construction and execution of clinical research projects while learning about some of the more rare pediatric endocrine disorders. Participating institutions include Johns Hopkins University (JHU) Department of Pediatrics, Division of Pediatric Endocrinology, The Childrens National Medical Center (CNMC) Division of Pediatric Endocrinology, and Georgetown University (GU) Department of Pediatrics. GU, JHU, and CNMC, serve as primary care facilities, and the NIH-CC houses a large tertiary care referral and research center. These facilities make available to our fellows pediatric endocrine, diabetes, oncology, metabolic, bone disorders, and other pediatric subspecialty clinics and consult services, and general pediatric inpatient and intensive care units. Pediatric Endocrine fellows maintain a weekly continuity clinic with a variety of patients at the NIH-CC and also have a continuity clinics at Children's National medical Center The NICHD fellowship program in Pediatric Endocrinology is among the largest and most prestigious in the world. More information is at the NIH training site: www.training.nih.gov/
| Tirosh, Amit; Valdés, Nuria; Stratakis, Constantine A (2018) Genetics of micronodular adrenal hyperplasia and Carney complex. Presse Med 47:e127-e137 |
| Makri, Angeliki; Bonella, Maria Belen; Keil, Margaret F et al. (2018) Children with MEN1 gene mutations may present first (and at a young age) with Cushing disease. Clin Endocrinol (Oxf) 89:437-443 |
| Makri, Angeliki; Boyce, Alison M; Stratakis, Constantine A et al. (2018) Irreversible Primary Amenorrhea Secondary to Uterine Damage and Premature Ovarian Failure in 2 Patients with Ewing Sarcoma. J Pediatr Adolesc Gynecol : |
| Jha, Abhishek; Ling, Alexander; Millo, Corina et al. (2018) Superiority of 68Ga-DOTATATE over 18F-FDG and anatomic imaging in the detection of succinate dehydrogenase mutation (SDHx )-related pheochromocytoma and paraganglioma in the pediatric population. Eur J Nucl Med Mol Imaging 45:787-797 |
| Hannah-Shmouni, Fady; Moraitis, Andreas G; Romero, Vladimir Valera et al. (2018) Successful Treatment of Estrogen Excess in Primary Bilateral Macronodular Adrenocortical Hyperplasia with Leuprolide Acetate. Horm Metab Res 50:124-132 |
| Chatain, Grégoire P; Patronas, Nicholas; Smirniotopoulos, James G et al. (2018) Potential utility of FLAIR in MRI-negative Cushing's disease. J Neurosurg 129:620-628 |
| Lodish, Maya B; Keil, Margaret F; Stratakis, Constantine A (2018) Cushing's Syndrome in Pediatrics: An Update. Endocrinol Metab Clin North Am 47:451-462 |
| Ironside, Natasha; Chatain, Gregoire; Asuzu, David et al. (2018) Earlier post-operative hypocortisolemia may predict durable remission from Cushing's disease. Eur J Endocrinol 178:255-263 |
| Tatsi, Christina; Stratakis, Constantine A (2018) Neonatal Cushing Syndrome: A Rare but Potentially Devastating Disease. Clin Perinatol 45:103-118 |
| Tirosh, Amit; Auerbach, Adi; Bonella, Belen et al. (2018) Failure to Thrive in the Context of Carney Complex. Horm Res Paediatr 89:38-46 |
Showing the most recent 10 out of 18 publications
