Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Andrea E. Balazs"'
Autor:
Nadia Merchant MD, Johanna M. Viau-Colindres MD, Kelly A. Hicks MD, Andrea E. Balazs MD, David E. Wesson MD, Monica E. Lopez MD, Lefkothea Karaviti MD, PhD
Publikováno v:
Global Pediatric Health, Vol 6 (2019)
Background . McCune-Albright syndrome (MAS) is characterized by hyperpigmented macules, endocrinopathies, and fibrous dysplasia. Hyperthyroidism is the second most common endocrinopathy in MAS and its management is challenging, particularly among inf
Externí odkaz:
https://doaj.org/article/8496dc38fa794bb69ac967106035ed38
Publikováno v:
Journal of the Endocrine Society
Catecholamine-secreting tumors are rare among the pediatric population but are increasingly being reported in children with sustained hypoxia secondary to cyanotic congenital heart disease (CCHD). With this review, we report the clinical characterist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e52e4ca0cdc00d3905d97324dc7a1b1
https://doi.org/10.1210/js.2019-00226
https://doi.org/10.1210/js.2019-00226
Publikováno v:
Journal of the Endocrine Society
Background: The etiology of hyperandrogenism in adolescent females includes polycystic ovarian syndrome, non-classical congenital adrenal hyperplasia (CAH), Cushing’s syndrome, androgen-secreting tumors (adrenal or ovarian) or exogenous use. Ovaria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f4a584ebe9cfde36e371775d59f511f
https://doi.org/10.1210/js.2019-sat-289
https://doi.org/10.1210/js.2019-sat-289
Publikováno v:
Journal of the Endocrine Society
Background: Pheochromocytomas and paragangliomas (PHEO/PGL) are catecholamine producing tumors of the autonomous nervous system that arise from the chromaffin cells in the adrenal medulla or extra-adrenal paraganglionic tissue. About 40% of these tum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5da9f373a9f047d24dd7203c7198a30
https://doi.org/10.1210/js.2019-sat-311
https://doi.org/10.1210/js.2019-sat-311
Autor:
Juliana Biro, Lefkothea P. Karaviti, Nicholas J. Patronas, Georgios Z. Papadakis, Mouhammad R. Alwazeer, Maria Merino, Maya Lodish, Electron Kebebew, Andrea E. Balazs, David S. Schrump, Martha Quezado, Meg Keil, Constantine A. Stratakis, Charalampos Lyssikatos, Maya K. Hunter, Alexander S. Karageorgiadis
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 100:141-148
Ectopic ACTH/CRH syndrome is a rare cause of Cushing syndrome (CS), especially in children. The localization, work-up, and management of ACTH/CRH-secreting tumors are discussed.A retrospective study was conducted of patients under 21 years of age eva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::805f9601b0bda375764050ac0ef96864
https://doi.org/10.1210/jc.2014-2945
https://doi.org/10.1210/jc.2014-2945
Autor:
Kelly A. Hicks, Lefkothea P. Karaviti, David E. Wesson, Johanna M. Viau-Colindres, Nadia Merchant, Monica E. Lopez, Andrea E. Balazs
Publikováno v:
Global Pediatric Health, Vol 6 (2019)
Global Pediatric Health
Global Pediatric Health
Background. McCune-Albright syndrome (MAS) is characterized by hyperpigmented macules, endocrinopathies, and fibrous dysplasia. Hyperthyroidism is the second most common endocrinopathy in MAS and its management is challenging, particularly among infa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10c1e51ada30f98c82867b53ea3bd5a5
https://doi.org/10.1177/2333794x19875153
https://doi.org/10.1177/2333794x19875153
Autor:
Yaping Yang, Christine M. Eng, Meenal Mendiratta, Lefkothea P. Karaviti, Alecia Willis, Andrea E. Balazs, Lorraine Potocki
Publikováno v:
International Journal of Pediatric Endocrinology, Vol 2011, Iss 1, p 5 (2011)
International Journal of Pediatric Endocrinology
International Journal of Pediatric Endocrinology
Isolated hypocortisolism due to ACTH deficiency is a rare condition that can be caused by homozygous or compound heterozygous mutations in the gene encoding proopiomelanocortin (POMC). Loss of function mutations of POMC gene typically results in adre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e10c14d9143aa11a12c049c3c296c273
http://www.ijpeonline.com/content/2011/1/5
http://www.ijpeonline.com/content/2011/1/5
Publikováno v:
Clinical pediatrics. 47(3)
We report a 5-year-old girl who presented to our emergency room with respiratory arrest and limb deformities and was subsequently diagnosed with X-linked hypophosphatemic rickets. On normalization of the serum phosphorus concentration, her respirator
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6ce664897778594472fa7a9cff1b933
https://pubmed.ncbi.nlm.nih.gov/18057152
https://pubmed.ncbi.nlm.nih.gov/18057152
Autor:
Andrea E, Balazs, Ioanna, Athanassaki, Sheila K, Gunn, Nina, Tatevian, Stephen A, Huang, Morey W, Haymond, Lefkothea P, Karaviti
Publikováno v:
Annals of clinical and laboratory science. 37(3)
We report a unique case of a 3-mo-old female with consumptive hypothyroidism and liver hemangioendothelioma who required pharmacological doses of thyroid hormones and was cured following liver transplantation. Liver hemangioendotheliomas are capable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1f45b4a03e3adf18ca43b2f982d093f9
https://pubmed.ncbi.nlm.nih.gov/17709695
https://pubmed.ncbi.nlm.nih.gov/17709695