Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Erica A. Steen"'
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Familial hemophagocytic lymphohistiocytosis (fHLH) encompasses a group of rare inherited immune dysregulation disorders characterized by loss-of-function mutations in one of several genes involved in the assembly, exocytosis, and function of cytotoxi
Externí odkaz:
https://doaj.org/article/8ad0452ff17f4a50b6f610427f750423
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Hemophagocytic lymphohistiocytosis (HLH) is a hyperinflammatory disorder characterized by the inability to properly terminate an immune response. Familial HLH (FHLH) and related immune dysregulation syndromes are associated with mutations in the gene
Externí odkaz:
https://doaj.org/article/a1bf01ecb2e847d28c69fed45a4347ff
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports. 2023
Summary An 11-year-old girl with past medical history of septic shock and multi-organ failure at age 5 presented to her primary care doctor with concern for pallor of the lips. Laboratory studies demonstrated low free thyroxine (T4) and normal thyroi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f7e887cc8ee04387c197448dc8eed92
https://doi.org/10.1530/edm-23-0021
https://doi.org/10.1530/edm-23-0021
Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, Vol 12 (2021)
Frontiers in Immunology, Vol 12 (2021)
Hemophagocytic lymphohistiocytosis (HLH) is a hyperinflammatory disorder characterized by the inability to properly terminate an immune response. Familial HLH (FHLH) and related immune dysregulation syndromes are associated with mutations in the gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56e44956b541b52aa5f61559edab24c1
http://europepmc.org/articles/PMC8635482
http://europepmc.org/articles/PMC8635482
Autor:
Erica A Steen, Susan A Phillips
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2024)
A 6.6-year-old female presented to endocrinology with precocious puberty for evaluation and management. Workup was initiated, and a diagnosis of central precocious puberty was confirmed. A decision was made to initiate pubertal blockade using gonadot
Externí odkaz:
https://doaj.org/article/1da3f1cd4f994344a4a8e74b98201be8