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Clinical Manifestations of Adrenal Insufficiency
Hormones Released from the Anterior Pituitary or Adenohypophysis
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Fluids and Electrolytes
Charles Hobson MD MHA
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Adrenal Physiology & Steroid Pharmacology
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Lab Assessment a Method of Monitoring
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Primary Adrenal Disease
Briana Patterson, M.D.
Primary Adrenal Disease.
Solving Puzzles of Laboratory Data Interpretation
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Hypothalamic & Pituitary hormones
Eric Lazartigues, Ph.D.
Hypothalamic & Pituitary hormones.
Hyponatremia
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20 Free scholarly articles
- Familial glucocorticoid deficiency presenting with generalized hyperpigmentation in an Egyptian child : a case report.
- Neonatal presentation of familial glucocorticoid deficiency resulting from a novel splice mutation in the melanocortin 2 receptor accessory protein.
- Arginine vasopressin-independent mechanism of impaired water excretion in a patient with sarcoidosis complicated by central diabetes insipidus and glucocorticoid deficiency.
- Familial glucocorticoid deficiency type 2: a case report.
- Missense mutations in the melanocortin 2 receptor accessory protein that lead to late onset familial glucocorticoid deficiency type 2.
- Isolated Addison's disease is unlikely to be caused by mutations in MC2R, MRAP or STAR, three genes responsible for familial glucocorticoid deficiency.
- Familial glucocorticoid deficiency with a point mutation in the ACTH receptor: a case report.
- Nonclassic lipoid congenital adrenal hyperplasia masquerading as familial glucocorticoid deficiency.
- Phenotypic characteristics of familial glucocorticoid deficiency FGD type 1 and 2.
- A corticotroph pituitary adenoma as the initial presentation of familial glucocorticoid deficiency.
- Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency FGD are not associated with long-term mineralocorticoid deficiency.
- Hypophagia induced by glucocorticoid deficiency is associated with an increased activation of satiety-related responses.
- 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.
- A novel adrenocorticotropin receptor mutation alters its structure and function, causing familial glucocorticoid deficiency.
- A novel variant of familial glucocorticoid deficiency prevalent among the Irish Traveler population.
- Clinical
and biological phenotype of a patient with familial glucocorticoid deficiency type 2 caused by a mutation of
melanocortin 2 receptor accessory protein.
- Familial glucocorticoid deficiency.
- Unusual presentation of familial glucocorticoid deficiency with a novel MRAP mutation.
- Molecular analysis of impaired urinary diluting capacity in glucocorticoid deficiency.
- Combined corticotropin-releasing hormone and glucocorticoid deficiency does not enhance counterregulatory responses after recurrent hypoglycemia in mice.
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