در حال جستجو در محتوی

ﺑﺎﺯﮔﺸﺖ ﺑﻪ ﺻﻔﺤﻪ ﻗﺒﻠﯽ
خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده: 4 مورد
نسخه الکترونیک
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Adrenal hyperandrogenism
Premature adrenarche
Causes of primary adrenal insufficiency (Addison disease)
Causes of secondary and tertiary adrenal insufficiency in adults
Clinical manifestations of adrenal insufficiency in adults
Determining the etiology of adrenal insufficiency in adults
Diagnosis of adrenal insufficiency in adults
Hyponatremia and hyperkalemia in adrenal insufficiency
Insulin-induced hypoglycemia test protocol
Measurement of ACTH, CRH, and other hypothalamic and pituitary peptides
Metyrapone stimulation tests
Pathogenesis of autoimmune adrenal insufficiency
Pituitary and adrenal gland dysfunction in patients with HIV
Thyroid gland dysfunction in the patient with HIV
Treatment of adrenal insufficiency in adults
Clinical presentation and evaluation of adrenocortical tumors
Evaluation and management of the adrenal incidentaloma
Treatment of adrenocortical carcinoma
Adrenal steroid biosynthesis
Assays of the renin-angiotensin-aldosterone system in adrenal disease
Basic principles in the laboratory evaluation of adrenocortical function
Measurement of ACTH, CRH, and other hypothalamic and pituitary peptides
Overview of the renin-angiotensin system
Physiology and clinical manifestations of normal adrenarche
Adrenal steroid biosynthesis
Clinical manifestations and diagnosis of classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency in infants and children
Diagnosis and treatment of nonclassic (late-onset) congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Genetics and clinical manifestations of classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Genetics and clinical presentation of nonclassic (late-onset) congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Premature adrenarche
Treatment of classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency in adults
Uncommon congenital adrenal hyperplasias
Causes and pathophysiology of Cushing syndrome
Cushing's syndrome due to primary bilateral macronodular adrenal hyperplasia
Cushing's syndrome due to primary pigmented nodular adrenocortical disease
Desmopressin (DDAVP) stimulation test
Dexamethasone suppression tests
Diagnosis and management of Cushing's syndrome during pregnancy
Epidemiology and clinical manifestations of Cushing syndrome
Establishing the cause of Cushing syndrome
Establishing the diagnosis of Cushing syndrome
Measurement of ACTH, CRH, and other hypothalamic and pituitary peptides
Measurement of cortisol in serum and saliva
Measurement of urinary excretion of endogenous and exogenous glucocorticoids
Medical therapy of hypercortisolism (Cushing's syndrome)
Metyrapone stimulation tests
Overview of the treatment of Cushing syndrome
Persistent or recurrent Cushing disease: Surgical adrenalectomy
Primary therapy of Cushing's disease: Transsphenoidal surgery and pituitary irradiation
Determinants of glucocorticoid dosing
Glucocorticoid effects on the immune system
Glucocorticoid withdrawal
Major side effects of inhaled glucocorticoids
Major side effects of systemic glucocorticoids
Pharmacologic use of glucocorticoids
The management of the surgical patient taking glucocorticoids
Apparent mineralocorticoid excess syndromes (including chronic licorice ingestion)
Assays of the renin-angiotensin-aldosterone system in adrenal disease
Diagnosis of primary aldosteronism
Familial hyperaldosteronism
Pathophysiology and clinical features of primary aldosteronism
Treatment of primary aldosteronism
Assays of the renin-angiotensin-aldosterone system in adrenal disease
Etiology, diagnosis, and treatment of hypoaldosteronism (type 4 RTA)
Pituitary and adrenal gland dysfunction in patients with HIV
Thyroid gland dysfunction in the patient with HIV
Multiple endocrine neoplasia type 1: Genetics
Clinical presentation and diagnosis of pheochromocytoma
Pheochromocytoma in genetic disorders
Treatment of pheochromocytoma in adults

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