2001
DOI: 10.1016/s0749-0704(05)70149-4
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Syndromes of Excess Antidiuretic Hormone Release

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Cited by 53 publications
(81 citation statements)
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“…In elderly, hyponatremia is multifactorial. It can be due to age related decrease in total body water, diminished thirst mechanism or age related reduction in glomerular filtration rate (fewer glomeruli and a decreased renal blood flow in the elderly), which results in increased passive reabsorption of water in the distal tubule and impaired urinary diluting capacity [2,3]. Syndrome of inappropriate anti diuretic hormone secretion (SIADH) is the commonest cause of chronic hyponatremia and in most of the cases the etiology remains unclear even after routine investigations [4].…”
Section: Introductionmentioning
confidence: 99%
“…In elderly, hyponatremia is multifactorial. It can be due to age related decrease in total body water, diminished thirst mechanism or age related reduction in glomerular filtration rate (fewer glomeruli and a decreased renal blood flow in the elderly), which results in increased passive reabsorption of water in the distal tubule and impaired urinary diluting capacity [2,3]. Syndrome of inappropriate anti diuretic hormone secretion (SIADH) is the commonest cause of chronic hyponatremia and in most of the cases the etiology remains unclear even after routine investigations [4].…”
Section: Introductionmentioning
confidence: 99%
“…Also, a wide range of drugs including antiinflammatory drugs, tricyclic antidepressants, serotonin-selective reuptake inhibitors and some antineoplastic agents, may cause of SIADH [35][36][37]. In contrast to hyponatremia in CHF or liver cirrhosis, hyponatremia in SIADH is typically associated with higher urine sodium concentration (Figure 4).…”
Section: Pathogenesis Of the Syndrome Of Inappropriate Antidiuretic Hmentioning
confidence: 99%
“…As principais mutações associadas ao DI Familiar são Gly-57-Ser e Gly-17-Val, no resíduo da neurofisina II. Uma mutação frame-shift na NPII causa o DI autossômico recessivo em ratos (23,24). Um estudo espanhol demonstrou que a substituição da glicina na posição 23 pela arginina na neurofisina II, no éxon 2 do gene, relaciona-se com o DI familiar (25).…”
Section: Diabetes Insípidus Central Congênitounclassified
“…Um estudo espanhol demonstrou que a substituição da glicina na posição 23 pela arginina na neurofisina II, no éxon 2 do gene, relaciona-se com o DI familiar (25). Diversas outras mutações vêm sendo estudadas e a sua identificação em famílias afetadas permite o rastreamento e o diagnóstico precoces, facilitando o manuseio clínico e o planejamento familiar (24).…”
Section: Diabetes Insípidus Central Congênitounclassified
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