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Glucagon-stimulated copeptin measurements in the differential diagnosis of diabetes insipidus: a double-blind randomized placebo-controlled study.

European Journal of Endocrinology, 2022
BACKGROUND The differential diagnosis of diabetes insipidus is challenging. The most reliable approaches are copeptin measurements after hypertonic saline infusion or arginine, which is a known growth hormone secretagogue but has recently also been shown
Cihan Atila   +5 more
semanticscholar   +1 more source

Diagnosis and management of diabetes insipidus for the internist: an update

Journal of Internal Medicine, 2021
Diabetes insipidus is a disorder characterized by excretion of large amounts of hypotonic urine. Four entities have to be differentiated: central diabetes insipidus resulting from a deficiency of the hormone arginine vasopressin (AVP) in the pituitary ...
M. Christ-Crain, B. Winzeler, J. Refardt
semanticscholar   +1 more source

Diabetes Insipidus After Endoscopic Transsphenoidal Surgery.

Neurosurgery, 2020
BACKGROUND Diabetes insipidus (DI) is a recognized transient or permanent complication following transsphenoidal surgery (TSS) for pituitary tumors. OBJECTIVE To describe significant experience with the incidence of DI after TSS, identifying predictive
William T. Burke   +5 more
semanticscholar   +1 more source

Diabetes insipidus

Critical Care Medicine, 1992
To review the pathophysiology, diagnosis, and treatment of the syndromes of diabetes insipidus with an emphasis on those situations likely to be encountered in the critical care setting.Extensive clinical experience and relevant publications from the English literature identified via MEDLINE search, citation in reviews, publications of original data ...
L S, Blevins, G S, Wand
openaire   +2 more sources

Diabetes insipidus

Annales d'Endocrinologie, 2013
Diabetes insipidus (DI) is characterized by hypotonic polyuria greater than 3 liters/24 hours in adults and persisting even during water deprivation. It is mostly due to a defect in arginin-vasopressin (AVP) synthesis (central DI); other causes are: AVP resistance (nephrogenic DI), abnormal thirst regulation (primary polydipsia) or early destruction of
Clara, Leroy   +6 more
openaire   +2 more sources

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