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Genetics and diagnosis of central diabetes insipidus
Annales d'Endocrinologie, 2012Most of the central diabetes insipidus cases seen in general practice are acquired but the rare cases of hereditary autosomal dominant or recessive neurohypophyseal diabetes insipidus have provided further cellular understanding of the mechanisms responsible for pre-hormone folding, maturation and release.
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Current Perspective on the Pathogenesis of Central Diabetes Insipidus
Journal of Pediatric Endocrinology and Metabolism, 2005Diabetes insipidus is a heterogeneous condition characterised by polyuria and polydipsia caused by a lack of secretion of vasopressin, its physiological suppression following excessive water intake, or kidney resistance to its action. The clinical and laboratory diagnosis is confirmed by standard tests, but recent advances in molecular biology and ...
GHIRARDELLO S +3 more
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Central diabetes insipidus: beware of Langerhans cell histiocytosis!
The Netherlands journal of medicine, 2018Langerhans cell histiocytosis (LCH) is a rare disorder, characterised by a monoclonal proliferation of aberrant histiocytes that accumulate in and infiltrate into different organs. When the hypothalamic-pituitary axis is involved, central diabetes insipidus (CDI) can be its first manifestation.
Brys, A D H +4 more
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Familial central diabetes insipidus
Medicina Clínica (English Edition), 2020M. Pilar Bahíllo-Curieses +2 more
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