Results 141 to 150 of about 4,644 (193)

Erdheim-Chester disease mimicking Wilms tumor in a child: a diagnostic challenge. [PDF]

BMC Pediatr
Khalak S, Nakonechnyi A.
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Lithium-induced kidney injury and fibrosis: A versatile model to explore cellular pathways of injury and repair. [PDF]

Physiol Rep
Mehta P, Slatter T, Walker R.
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Endocrine and Metabolic Challenges of Long-Term Lithium Therapy: Diagnostic and Management Considerations. [PDF]

Cureus
Kopanos S, Feldkamp J.
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Sodium and Water Homeostasis in Children: Pathogenesis, Diagnosis, and Treatment. [PDF]

J Clin Med
Dąbek M, Szyszka M, Skrzypczyk P.
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Hyperosmolar hyperglycemic state with severe hypernatremia coexisting with central diabetes insipidus: A case report and literature review. [PDF]

Open Life Sci
Yao C, Zhu L, Shou S, Jin H, Zhang Y.
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Nephrogenic Diabetes Insipidus

Advances in Chronic Kidney Disease, 1998
Nephrogenic diabetes insipidus (NDI), which can be inherited or acquired, is characterized by an inability to concentrate urine despite normal or elevated plasma concentrations of the antidiuretic hormone arginine vasopressin (AVP). Polyuria, with hyposthenuria, and polydipsia are the cardinal clinical manifestations of the disease.
S E, DICKER, M G, EGGLETON
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Nephrogenic Diabetes Insipidus

Pediatrics In Review, 1996
Nephrogenic diabetes insipidus (NDI) is a disorder, either congenital or acquired, in which antidiuretic hormone (ADH) secretion is normal, but the ability to concentrate urine is reduced because of insensitivity of the collecting tubule to ADH. The antidiuretic action of arginine vasopressin requires binding of the hormone to the renal type V2 ...
J, FABIAN, V, DUFEK
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