Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Erin Greenup"'
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
ContextWiedemann-Steiner Syndrome (WSS) is a genetic disorder associated with an array of clinical phenotypes, including advanced bone age and short stature. 11-ketotestosterone (11KT) is a member of the group known as 11-oxygenated C19 androgens tha
Externí odkaz:
https://doaj.org/article/254bc5ed9c5d4065a78ffe4b6f56ca30
Publikováno v:
Endocrinology, Diabetes & Metabolism, Vol 4, Iss 2, Pp n/a-n/a (2021)
Abstract Background Type 2 diabetes (T2DM) in children is considered rare before puberty. Objective Describe the characteristics and outcomes of children with T2DM diagnosed at or before 10 years of age. Methods Retrospective electronic medical recor
Externí odkaz:
https://doaj.org/article/e4a1780dc1e74e97834d0e4603be7944
Publikováno v:
Endocrinology, Diabetes & Metabolism
Endocrinology, Diabetes & Metabolism, Vol 4, Iss 2, Pp n/a-n/a (2021)
Endocrinology, Diabetes & Metabolism, Vol 4, Iss 2, Pp n/a-n/a (2021)
Background Type 2 diabetes (T2DM) in children is considered rare before puberty. Objective Describe the characteristics and outcomes of children with T2DM diagnosed at or before 10 years of age. Methods Retrospective electronic medical record review
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45fcf7f04c6b1c340aadbc914196c87f
https://pubmed.ncbi.nlm.nih.gov/33855201
https://pubmed.ncbi.nlm.nih.gov/33855201
Publikováno v:
Journal of the Endocrine Society
Osteopetrosis is a rare group of bone disorders characterized by defective osteoclast bone resorption causing high bone mineral density. A high bone mineral density in combination with defective skeletal mineralization results in a phenotype of osteo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b783bf02add9095505564e4d6a165407
http://europepmc.org/articles/PMC7255499
http://europepmc.org/articles/PMC7255499