M Babey, P Kopp… - Nature Reviews Endocrinology, 2011 - nature.com Over the past two decades, the genetic and molecular basis of familial forms of diabetes insipidus has been elucidated. Diabetes insipidus is a clinical syndrome characterized by the excretion of abnormally large volumes of diluted urine (polyuria) and increased fluid intake ... All 3 versions
[HTML] from eje.orgM de Fost, ASP van Trotsenburg… - European Journal of …, 2011 - EFES Case A thirty-four-year-old woman and her three-year-old son were evaluated because of polyuria and polydipsia since the age of 1.5 years onwards. Both patients were subjected to a water deprivation test confirming the diagnosis of central DI. Magnetic resonance imaging of the brain of the ... Related articles - All 5 versions
S Kumar, D Burrows, S Dang… - Endocrine Practice, 2011 - AACE Objective: To add to the current scant literature on rare clinical presentations of Sheehan syndrome. Methods: We describe the study patient's clinical, laboratory, and imaging findings and review the literature for publications regarding varied clinical presentations of ... Cited by 1 - Related articles - All 2 versions
BM Christensen, AM Zuber, J Loffing… - Journal of the …, 2011 - Am Soc Nephrol Lithium-induced nephrogenic diabetes insipidus (NDI) is accompanied by polyuria, downregulation of aquaporin 2 (AQP2), and cellular remodeling of the collecting duct (CD). The amiloride-sensitive epithelial sodium channel (ENaC) is a likely candidate for lithium entry. Here, we ... Cited by 1 - Related articles - All 5 versions
[HTML] from nih.govBT Layden, S Dubner, DJ Toft, P Kopp, S Grimm… - Pituitary, 2011 - Springer Abstract We present an unusual case of primary central nervous system (CNS) lymphoma presenting with bilateral symmetric hypothalamic lesions causing diabetes insipidus and hypopituitarism. A 50-year-old male presented initially with mental status changes, ... Cited by 2 - Related articles - All 5 versions
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