Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Sheila, Gunn"'
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
Autor:
Paul F. Austin, Elizabeth B. Yerkes, Ilina Rosoklija, Lefkothea P. Karaviti, Deborah L. Jacobson, Anthony D'Oro, Sheila Gunn, Paul Kokorowski, Earl Y. Cheng, Hillary M. Kapa, Diane Chen, Duong Tu, Alyssa C. Messina, Courtney Finlayson, Mimi S. Kim, Leena Nahata, Thomas F. Kolon, Emilie K. Johnson
Publikováno v:
Journal of Urology. 204:835-842
The medical terminology applied to differences/disorders of sex development has been viewed negatively by some affected individuals. A clinical population of patients with differences/disorders of sex development and their caregivers were surveyed re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bed357ff03b07c833dcd9ec31fe0065
https://doi.org/10.1097/ju.0000000000001076
https://doi.org/10.1097/ju.0000000000001076
Publikováno v:
Companion to Primary Care Mental Health ISBN: 9781846198465
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98d59ab5980d98baea900a7b43784718
https://doi.org/10.1201/9781846198465-14
https://doi.org/10.1201/9781846198465-14
Autor:
Bonnie, McCann-Crosby, Frank Xavier, Placencia, Oluyemisi, Adeyemi-Fowode, Jennifer, Dietrich, Rachel, Franciskovich, Sheila, Gunn, Marni, Axelrad, Duong, Tu, David, Mann, Lefkothea, Karaviti, Vernon Reid, Sutton
Publikováno v:
Pediatric endocrinology reviews : PER. 16(1)
Classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency causes elevated androgen levels, which can lead to virilization of female external genitalia. Prenatal dexamethasone treatment has been shown to be effective in preventing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dd7dcdb7f1d7941c2e6c9ff47fee99c6
https://pubmed.ncbi.nlm.nih.gov/30371037
https://pubmed.ncbi.nlm.nih.gov/30371037
Autor:
Johanna Viau, Colindres, Marni, Axelrad, Laurence, McCullough, E O'Brian, Smith, Gene O, Huang, Duong D, Tu, Jennifer L, Bercaw-Pratt, Min-Jye, Cheni, Meenal, Mendiratta, Sheila, Gunn, Reid, Sutton, Charles, Macias, Lefkothea P, Karaviti
Publikováno v:
Pediatric endocrinology reviews : PER. 13(3)
45,X/46,XY gonadal dysgenesis is a disorder of sexual differentiation with a wide clinical presentation, ranging from Turner-like females to individuals with genital ambiguity to azoospermic but otherwise normal-appearing males. Hence, patients can b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bd9d624c1bfc18ec4d2134513559f18b
https://pubmed.ncbi.nlm.nih.gov/27116846
https://pubmed.ncbi.nlm.nih.gov/27116846
Autor:
Min-Jye, Chen, Bach-Mai K, Vu, Marni, Axelrad, Jennifer E, Dietrich, Patricio, Gargollo, Sheila, Gunn, Charles G, Macias, Laurence B, McCullough, David R, Roth, V Reid, Sutton, Lefkothea P, Karaviti
Publikováno v:
Pediatric endocrinology reviews : PER. 12(4)
Androgen insensitivity syndrome (AIS) is an undervirilization syndrome in individuals with 46, XY karyotype. The undervirilization can be complete feminization or incomplete virilization with grades of ambiguity. AIS is caused by mutations in the and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9e42bea0aee36bd886007feac4da6f7f
https://pubmed.ncbi.nlm.nih.gov/26182482
https://pubmed.ncbi.nlm.nih.gov/26182482
Autor:
Bonnie, McCann-Crosby, Min-Jye, Chen, Sarah K, Lyons, Yuezhen, Lin, Marni, Axelrad, Jennifer E, Dietrich, V Reid, Sutton, Charles G, Macias, Sheila, Gunn, Lefkothea, Karaviti
Publikováno v:
Pediatric endocrinology reviews : PER. 12(2)
Nonclassical congenital adrenal hyperplasia (NCCAH) caused by 21-hydroxylase deficiency is a common autosomal recessive condition that can present with a wide range of hyperandrogenemic signs in childhood or adulthood. The management of children with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4498028a2020d56430a06297c01d2024
https://pubmed.ncbi.nlm.nih.gov/25581988
https://pubmed.ncbi.nlm.nih.gov/25581988
Autor:
Min-Jye, Chen, Lefkothea P, Karaviti, Charles G, Macias, David R, Roth, Sheila, Gunn, V Reid, Sutton, Bruce, Schlomer
Publikováno v:
Pediatric endocrinology reviews : PER. 12(1)
Hypospadias is a common congenital malformation in males, the cause of which may be genetic, hormonal, or environmental, although it usually is idiopathic or possibly multifactorial. Determining the optimal diagnostic testing and management remains a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c049025b23b2c7b885c69606065dffd7
https://pubmed.ncbi.nlm.nih.gov/25345085
https://pubmed.ncbi.nlm.nih.gov/25345085
Autor:
Sheila Gunn
In the wake of 2010's historic general election politics commands more column inches and air time than ever before. Yet most political journalists failed to foresee the consequences of a coalition government. And they are still struggling to understa