Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Amita Adhikari"'
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 34:267-271
Objectives Activating germline mutations of the thyroid-stimulating hormone receptor (TSHR) are responsible for a rare form of neonatal nonautoimmune hyperthyroidism (NAH). We report the first case of familial neonatal neonatal nonautoimmune associat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4336718e0a37922ab46849d49d984d7
https://doi.org/10.1515/jpem-2020-0291
https://doi.org/10.1515/jpem-2020-0291
Autor:
Marwan Zidan, Hanaa Zidan, Chandra Edwin, Dania Abushanab, Amita Adhikari, Colleen Buggs-Saxton, Nidhi Gupta, Aida N. Lteif, Kathleen Moltz
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Objective: While there is general agreement that patient education is essential for compliance, no objective tools exist to assess knowledge in children and parents of children with endocrine disorders. We aimed to design and validate a Pediatric End
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a334f2c1f4cdea9730426ae90402194
https://doi.org/10.4274/jcrpe.3171
https://doi.org/10.4274/jcrpe.3171
Publikováno v:
Journal of the Endocrine Society
Introduction Mutations in the SRY gene presenting as sex reversal is rare and not associated with problems in other organ systems. We report a case of a 46 XY adolescent with history of cleft lip and palate, phenotypically female, diagnosed with a mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c58e3b5986153cae76166e74c5f4cc5
http://europepmc.org/articles/PMC6552224
http://europepmc.org/articles/PMC6552224
Publikováno v:
Journal of the Endocrine Society
Introduction The Histrelin acetate implant (50 mg) has been used widely in the treatment of central precocious puberty (CPP). The implant is inserted subcutaneously and provides continuous release of gonadotropin releasing hormone analog (GnRHa) Hist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::539f7b6ee9cb77adc037190a8ca828cb
https://doi.org/10.1210/js.2019-sat-298
https://doi.org/10.1210/js.2019-sat-298
Publikováno v:
Journal of the Endocrine Society
Activating germline mutations of the TSH receptor are responsible for a rare form of non-autoimmune hyperthyroidism transmitted as an autosomal dominant trait. We describe the case of a patient and her mother presenting with neonatal non-autoimmune h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7b9acba09d9c5f090e2f3c2f70a7e78
https://doi.org/10.1210/js.2019-mon-264
https://doi.org/10.1210/js.2019-mon-264
Publikováno v:
American Journal of Human Biology. 23:325-332
Context The Mountain Ok (Mt Ok) people of Telefomin, who live at the interior of Papua New Guinea (PNG), were documented over 25 years ago to be one of the shortest populations on record, with average adult height below the fifth percentile (US). Ser
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e20b3b85f613ad1895f812b36f939a4
https://doi.org/10.1002/ajhb.21134
https://doi.org/10.1002/ajhb.21134
Autor:
Stefan S. Fajans, Joyce M. Lee, Inas H. Thomas, Ram K. Menon, Amita Adhikari, Ming Chen, Delia M. Vazquez, Josephine Z. Kasa-Vubu, Natinder Saini
Publikováno v:
Pediatric Diabetes. 10:492-496
Permanent neonatal diabetes mellitus is a rare disorder known to be caused by activating mutations in KCNJ11 or ABCC8, inactivating mutations in INS, or very rarely in GCK or insulin promotor factor-1 (IPF-1) genes. We report a patient with permanent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ffd596642a50c3abc37af05c417d760
https://doi.org/10.1111/j.1399-5448.2009.00526.x
https://doi.org/10.1111/j.1399-5448.2009.00526.x
Autor:
Steven Buck, Tania T. Sarker, Manisha Gadgeel, Yaddanapudi Ravindranath, Bülent Özgönenel, Amita Adhikari
An eighteen-year-old female with Graves thyrotoxicosis presented with methimazole-induced agranulocytosis and total myeloid aplasia. The bone marrow at presentation showed complete absence of myeloid precursors and striking plasmacytosis. 16 days lat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c320a0bbe154c97a1e09accb8ba01aa
https://europepmc.org/articles/PMC4925526/
https://europepmc.org/articles/PMC4925526/
Autor:
Colleen Buggs-Saxton, Chandra Edwin, Amita Adhikari, Nidhi Gupta, Kathleen Moltz, Dania Abushanab, Aida N. Lteif, Marwan Zidan, Hanaa Zidan
Publikováno v:
Pediatrics. 137:57A-57A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e989acc583178d80fa461874077c3213
https://doi.org/10.1542/peds.137.supplement_3.57a
https://doi.org/10.1542/peds.137.supplement_3.57a