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Longer titles found: Glucocorticoid deficiency 1 (view)

searching for Glucocorticoid deficiency 12 found (28 total)

alternate case: glucocorticoid deficiency

ACTH receptor (2,316 words) [view diff] exact match in snippet view article find links to article

cardiovascular disorders. Mutations in this receptor cause familial glucocorticoid deficiency (FGD) type 1, in which patients have high levels of serum ACTH

Steroidogenic acute regulatory protein (2,294 words) [view diff] exact match in snippet view article find links to article

function of StAR result in nonclassic lipoid CAH or familial glucocorticoid deficiency type 3. All known mutations disrupt StAR function by altering

List of causes of hypoglycemia (1,265 words) [view diff] exact match in snippet view article find links to article

Dumping syndrome Elevated vagal tone Ethanol Ethionamide Familial glucocorticoid deficiency Familial hyperinsulinemic hypoglycemia type 3 Familial hyperinsulinemic

List of diseases (G) (846 words) [view diff] exact match in snippet view article

anomalies Glossopharyngeal neuralgia Glossophobia Glucagonoma Glucocorticoid deficiency, familial Glucocorticoid resistance Glucocorticoid sensitive hypertension

Seviteronel (882 words) [view diff] exact match in snippet view article find links to article

must be administered in combination with prednisone to avoid glucocorticoid deficiency and mineralocorticoid excess due to 17α-hydroxylase inhibition)

Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency (1,830 words) [view diff] exact match in snippet view article find links to article

corticosterone have enough weak glucocorticoid activity to prevent glucocorticoid deficiency and adrenal crisis. Genetic females affected by total 17α-hydroxylase

Sheehan's syndrome (2,956 words) [view diff] exact match in snippet view article find links to article

hypothyroidism), adrenal gland (adrenal insufficiency due to glucocorticoid deficiency), sex hormone (gonadotropin deficiency), prolactin (a hormone

Adrenal crisis (4,957 words) [view diff] exact match in snippet view article find links to article

congenital adrenal hyperplasia, adrenoleukodystrophy, familial glucocorticoid deficiency, combined pituitary hormone deficiency, and POMC mutation. Adrenal

MRAP2 (2,212 words) [view diff] exact match in snippet view article find links to article

new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2". Nature Genetics. 37 (2): 166–70. doi:10.1038/ng1501.

Antiandrogen (15,079 words) [view diff] exact match in snippet view article find links to article

are excessive production and levels of adrenal androgens due to glucocorticoid deficiency and hence HPA axis overactivity. In women with insulin resistance

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (20,580 words) [view diff] exact match in snippet view article find links to article

Martin-Grace J, Thompson CJ, Sherlock M (June 2020). "The management of glucocorticoid deficiency: Current and future perspectives". Clinica Chimica Acta; International

List of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article

Glomuvenous malformations; 138000; GLML Glucocorticoid deficiency 2; 607398; MRAP Glucocorticoid deficiency, due to ACTH unresponsiveness; 202200; MC2R