Two children with diabetes insipidus secondary to a chronic inflammatory infiltrate of the infundibulum – infundibuloneurohypophysitis – are presented. Features unique to these cases are contrasted with prior case reports. The differential diagnoses of diabetes insipidus and inflammatory pituitary disorders are discussed. Rec-ommendations for diagnosis and treatment are pro-posed
Objective. To identify the causes of central diabetes insipidus (CDI) by evaluating the values of ma...
Summary: We present the cases of two children with presumed idiopathic central diabetes insipidus wh...
Central Diabetes Insipidus (CDI) is mainly associated with structural pathologies of the hypothalami...
We report on a 15-year-old girl who had presented with acute onset central diabetes insipidus at the...
Infundibuloneurohypophysitis is a rare disorder which involves inflammation of the pituitary stalk a...
Objective: Despite lymphocytic or autoimmune infundibuloneurohypophysitis (INH) is an increasingly r...
Central diabetes insipidus (CDI) is a complex disorder in which large volumes of dilute urine are ex...
Diabetes insipidus of central origin usually results from lesions in the hypothalamic neurohypophyse...
Lymphocytic hypophysitis is a neuroendocrine disorder characterized by autoimmune infiammation of th...
The syndrome of diabetes insipidus may arise from many different lesions of the hypothalamo-hypophys...
Objective. In pediatric central diabetes insipidus (CDI), etiology diagnosis and pituitary function ...
PubMedID: 1391802Diabetes insipidus (DI) is a disorder characterized by polyuria, polydipsia and inc...
Diabetes insipidus (DI) is rare in childhood and has a wide-ranging aetiology including the involvem...
WOS: A1992JK96300013PubMed ID: 1391802Diabetes insipidus (DI) is a disorder characterized by polyuri...
Contains fulltext : 49351.pdf (publisher's version ) (Closed access)Central diabet...
Objective. To identify the causes of central diabetes insipidus (CDI) by evaluating the values of ma...
Summary: We present the cases of two children with presumed idiopathic central diabetes insipidus wh...
Central Diabetes Insipidus (CDI) is mainly associated with structural pathologies of the hypothalami...
We report on a 15-year-old girl who had presented with acute onset central diabetes insipidus at the...
Infundibuloneurohypophysitis is a rare disorder which involves inflammation of the pituitary stalk a...
Objective: Despite lymphocytic or autoimmune infundibuloneurohypophysitis (INH) is an increasingly r...
Central diabetes insipidus (CDI) is a complex disorder in which large volumes of dilute urine are ex...
Diabetes insipidus of central origin usually results from lesions in the hypothalamic neurohypophyse...
Lymphocytic hypophysitis is a neuroendocrine disorder characterized by autoimmune infiammation of th...
The syndrome of diabetes insipidus may arise from many different lesions of the hypothalamo-hypophys...
Objective. In pediatric central diabetes insipidus (CDI), etiology diagnosis and pituitary function ...
PubMedID: 1391802Diabetes insipidus (DI) is a disorder characterized by polyuria, polydipsia and inc...
Diabetes insipidus (DI) is rare in childhood and has a wide-ranging aetiology including the involvem...
WOS: A1992JK96300013PubMed ID: 1391802Diabetes insipidus (DI) is a disorder characterized by polyuri...
Contains fulltext : 49351.pdf (publisher's version ) (Closed access)Central diabet...
Objective. To identify the causes of central diabetes insipidus (CDI) by evaluating the values of ma...
Summary: We present the cases of two children with presumed idiopathic central diabetes insipidus wh...
Central Diabetes Insipidus (CDI) is mainly associated with structural pathologies of the hypothalami...