Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Swashti Agarwal"'
Autor:
Swashti Agarwal MD, Duong D. Tu MD, Paul F. Austin MD, Michael E. Scheurer PhD, Lefkothea P Karaviti MD, PhD
Publikováno v:
Global Pediatric Health, Vol 7 (2020)
Background. Gonadotropin therapy is not typically used for pubertal induction in hypogonadotropic hypogonadism (HH), however, represents a promising alternative to testosterone. It can potentially lead to the maintenance of future fertility in additi
Externí odkaz:
https://doaj.org/article/6a7e4d0fdd9346b7bc40d9fe01f526d2
Publikováno v:
AACE Clinical Case Reports, Vol 5, Iss 3, Pp e187-e191 (2019)
ABSTRACT: Objective: Subcutaneous insulin resistance syndrome (SIRS) is a rare entity, characterized by increased resistance to subcutaneous insulin and normal sensitivity to intravenous insulin, with no increase in circulating insulin antibodies. Li
Externí odkaz:
https://doaj.org/article/5bd9fe7265ff4954becd07cf6fd0bcdc
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:
AACE Clinical Case Reports, Vol 5, Iss 3, Pp e187-e191 (2019)
Objective: Subcutaneous insulin resistance syndrome (SIRS) is a rare entity, characterized by increased resistance to subcutaneous insulin and normal sensitivity to intravenous insulin, with no increase in circulating insulin antibodies. Little is kn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5dd7198eb3fcfdd1c7003ade59eb4a55
https://doi.org/10.4158/accr-2018-0493
https://doi.org/10.4158/accr-2018-0493
Autor:
Dawn Hagerty, Vatcharapan Umpaichitra, Swashti Agarwal, Jamila Cooper, Salvador Castells, Aditi Khokhar, Laura Dunkley, Albara Marwa, Sheila Perez-Colon, Vivian L. Chin
Publikováno v:
Journal of the National Medical Association. 111:37-45
Objective With the rising incidence of Type 1 diabetes (T1DM), it is important to recognize deficiencies in care and areas of improvement to provide better access to resources and education for T1DM patients. The objective of this study was to recogn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1fac0c9bbc92c072751e7d97a98a8c5
https://doi.org/10.1016/j.jnma.2018.05.002
https://doi.org/10.1016/j.jnma.2018.05.002
Publikováno v:
Global Pediatric Health, Vol 7 (2020)
Background. Gonadotropin therapy is not typically used for pubertal induction in hypogonadotropic hypogonadism (HH), however, represents a promising alternative to testosterone. It can potentially lead to the maintenance of future fertility in additi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0788bf0e99a46aacb84a76276c8b9991
https://doaj.org/article/6a7e4d0fdd9346b7bc40d9fe01f526d2
https://doaj.org/article/6a7e4d0fdd9346b7bc40d9fe01f526d2
Publikováno v:
Journal of the Endocrine Society
Background: The use of gonadotropins is a recent strategy for inducing puberty in adolescent males with hypogonadotropic hypogonadism (HH). Testosterone use has been discouraged in patients who desire to preserve fertility. Human chorionic gonadotrop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91a9ea9dce04218a1e565f87052192e5
http://europepmc.org/articles/PMC7208018
http://europepmc.org/articles/PMC7208018
Publikováno v:
Journal of the Endocrine Society
Background: We describe the diagnostic dilemma and treatment challenges faced in a rare case of 1,25-OHD mediated hypercalcemia. Clinical Case: A 13 year old boy was admitted with severe hypercalcemia (calcium 15.5 mg/dl) in the setting of a non-spec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9f59989963dc4c3f6487e92bcbaff3d
http://europepmc.org/articles/PMC7207645
http://europepmc.org/articles/PMC7207645
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
Publikováno v:
Molecular Syndromology. 8:50-54
Williams syndrome is a multisystem disorder caused by contiguous gene deletion in 7q11.23, commonly associated with distinctive facial features, supravalvular aortic stenosis, short stature, idiopathic hypercalcemia, developmental delay, joint laxity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::283f0bd74889fa5a1dd78eaa9459b5a7
https://doi.org/10.1159/000452360
https://doi.org/10.1159/000452360