Results 221 to 230 of about 3,553,850 (264)
Coexisting mild autonomous cortisol secretion and isolated adrenocorticotropic hormone deficiency in a patient with an adrenal incidentaloma. [PDF]
JCEM Case RepIkeda K +5 more
europepmc +1 more source
Pituitary magnetic resonance imaging abnormalities and 1-year growth response in children with idiopathic growth hormone deficiency. [PDF]
Ann Pediatr Endocrinol MetabChoe J, Lee J, Kim J.
europepmc +1 more source
Progression From Isolated Growth Hormone Deficiency to Combined Pituitary Hormone Deficiency [PDF]
Growth Hormone and IGF Research, 2017 Growth hormone deficiency (GHD) can present at any time of life from the neonatal period to adulthood, as a result of congenital or acquired insults. It can present as an isolated problem (IGHD) or in combination with other pituitary hormone deficiencies (CPHD). Pituitary deficits can evolve at any time from GHD diagnosis.
Mehul T Dattani
exaly +7 more sources
Multiple Cutaneous Hemangiomas in a Patient With Combined Pituitary Hormone Deficiency
Journal of Pediatric Endocrinology and Metabolism, 2014 Combined pituitary hormone deficiency (CPHD) refers to a rare heterogeneous group of conditions in which there is a deficiency in at least two anterior pituitary hormones. Patients with POU1F1 mutations show a combined pituitary deficiency with low or absent levels of growth hormone, prolactin, and thyroid-stimulating hormone.
Samim Özen +2 more
exaly +5 more sources
Molecular Basis of Combined Pituitary Hormone Deficiencies [PDF]
Endocrine Reviews, 2002 Pituitary gland commitment from oral ectoderm occurs in response to inductive signals from the neuroepithelium of the ventral diencephalon. Invagination of the oral ectoderm leads to the creation of Rathke's pouch. Intensified cell proliferation within Rathke's pouch results in formation of the anterior pituitary lobe.
Laurie E. Cohen, Sally Radovick
exaly +3 more sources