Glucocorticoid deficiency

Electrolyte Abnormalities
Cynthia Seitz MD
ElectrolyteAbnormalities.ppt

Clinical Manifestations of Adrenal Insufficiency
adrenal_insufficiency.ppt

Hormones Released from the Anterior Pituitary or Adenohypophysis
Endocrine System.ppt

Fluids and Electrolytes
Charles Hobson MD MHA
Electrolytes_Hobson.ppt

Adrenal Physiology & Steroid Pharmacology
Gary D. Hammer, M.D., Ph.D
AdrenalLectures08.ppt

Lab Assessment a Method of Monitoring
Electrolytes Renal Urinalysis
Renal_electrolytes_ua.ppt

Primary Adrenal Disease
Briana Patterson, M.D.
Primary Adrenal Disease.ppt

Solving Puzzles of Laboratory Data Interpretation
Laboratory Data Interpretation.ppt

Hypothalamic & Pituitary hormones
Eric Lazartigues, Ph.D.
Hypothalamic & Pituitary hormones.ppt

Hyponatremia
Rozina Mithani
Hyponatremia.ppt

Corticosteroids
Corticosteroids.ppt
20 Free scholarly articles

1. Familial glucocorticoid deficiency presenting with generalized hyperpigmentation in an Egyptian child : a case report.
2. Neonatal presentation of familial glucocorticoid deficiency resulting from a novel splice mutation in the melanocortin 2 receptor accessory protein.
3. Arginine vasopressin-independent mechanism of impaired water excretion in a patient with sarcoidosis complicated by central diabetes insipidus and glucocorticoid deficiency.
4. Familial glucocorticoid deficiency type 2: a case report.
5. Missense mutations in the melanocortin 2 receptor accessory protein that lead to late onset familial glucocorticoid deficiency type 2.
6. Isolated Addison's disease is unlikely to be caused by mutations in MC2R, MRAP or STAR, three genes responsible for familial glucocorticoid deficiency.
7. Familial glucocorticoid deficiency with a point mutation in the ACTH receptor: a case report.
8. Nonclassic lipoid congenital adrenal hyperplasia masquerading as familial glucocorticoid deficiency.
9. Phenotypic characteristics of familial glucocorticoid deficiency FGD type 1 and 2.
10. A corticotroph pituitary adenoma as the initial presentation of familial glucocorticoid deficiency.
11. Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency FGD are not associated with long-term mineralocorticoid deficiency.
12. Hypophagia induced by glucocorticoid deficiency is associated with an increased activation of satiety-related responses.
13. The majority of adrenocorticotropin receptor melanocortin 2 receptor mutations found in familial glucocorticoid deficiency type 1 lead to defective trafficking of the receptor to the cell surface.
14. A novel adrenocorticotropin receptor mutation alters its structure and function, causing familial glucocorticoid deficiency.
15. A novel variant of familial glucocorticoid deficiency prevalent among the Irish Traveler population.
16. Clinical and biological phenotype of a patient with familial glucocorticoid deficiency type 2 caused by a mutation of melanocortin 2 receptor accessory protein.
    
17. Familial glucocorticoid deficiency.
18. Unusual presentation of familial glucocorticoid deficiency with a novel MRAP mutation.
19. Molecular analysis of impaired urinary diluting capacity in glucocorticoid deficiency.
20. Combined corticotropin-releasing hormone and glucocorticoid deficiency does not enhance counterregulatory responses after recurrent hypoglycemia in mice.