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Construction of arginine vasopressin receptor 2-deficient rats by the rGONAD method

Clinical and Experimental Nephrology
Congenital nephrogenic diabetes insipidus (NDI) is a hereditary disease characterized by a reduced response to arginine vasopressin in the renal collecting duct. NDI is primarily caused by mutations in the arginine vasopressin receptor 2 (AVPR2). Several animal models have been developed for congenital NDI; however, the appropriate models are limited ...
Ayaka Kamada   +12 more
openaire   +2 more sources

Management of Arginine Vasopressin Deficiency (Central Diabetes Insipidus) in Neonates and Infants

Hormone Research in Paediatrics
Background: Arginine vasopressin deficiency (AVP-D), previously called central diabetes insipidus (central DI), is the inability to concentrate urine despite elevated serum osmolality (i.e., volume depletion) related to inadequate production of the posterior pituitary hormone vasopressin.
Hannah, Pearlstein   +6 more
openaire   +2 more sources

Insulin-Induced Copeptin Response in Children and Adolescents to Diagnose Arginine Vasopressin Deficiency

Hormone Research in Paediatrics
Introduction: The diagnosis of arginine vasopressin deficiency (AVD, formerly central diabetes insipidus) remains a challenge. In recent years, stimulated copeptin has emerged as a promising tool to diagnose AVD. Methods: In this single centre retrospective study, we identified paediatric patients with suspected pituitary insufficiency who underwent ...
Sebastian, Gippert   +3 more
openaire   +2 more sources

Isolated arginine vasopressin deficiency

Endocrine Abstracts
Lydia Grixti, Earn Gan
openaire   +1 more source

Sellar Xanthogranuloma and Arginine Vasopressin Deficiency

Journal of Modern Medicine
Vitorino Modesto dos Santos   +2 more
openaire   +1 more source

Acute severe hyponatraemia in arginine vasopressin deficiency

Endocrine Abstracts
Sultana Azam   +2 more
openaire   +1 more source

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