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  1. Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel missense mutation in AVP gene in a large Italian kindred

    Purpose

    Familial neurohypophysial diabetes insipidus (FNDI), commonly caused by autosomal dominant arginine vasopressin (AVP) mutations, is a rare...

    Carlotta Marzocchi, Silvia Cantara, ... Marco Capezzone in Endocrine
    Article Open access 28 July 2021

  2. Deficiency of WFS1 leads to the impairment of AVP secretion under dehydration in male mice

    Wolfram syndrome (WS) is mainly caused by mutations in the WFS1 gene and characterized by diabetes mellitus, optic atrophy, hearing loss, and central...

    Junki Kurimoto, Hiroshi Takagi, ... Hiroshi Arima in Pituitary
    Article 05 March 2021

  3. Targeting Sigma Receptors for the Treatment of Neurodegenerative and Neurodevelopmental Disorders

    The sigma-1 receptor is a 223 amino acid-long protein with a recently identified structure. The sigma-2 receptor is a genetically unrelated protein...

    Dicson S. Malar, Premrutai Thitilertdecha, ... James M. Brimson in CNS Drugs
    Article 11 May 2023

  4. Identification of an AVP-NPII mutation within the AVP moiety in a family with neurohypophyseal diabetes insipidus: review of the literature

    Familial neurohypophyseal diabetes insipidus (FNDI) is a disorder characterized by excess excretion of diluted urine (polyuria) and increased uptake...

    Costas Koufaris, Angelos Alexandrou, ... Nicos Skordis in Hormones
    Article 01 July 2015

  7. Lymphocytic hypophysitis: Disease spectrum and approach to diagnosis and therapy

    Lymphocytic hypophysitis (LYH) is a neuroendocrine disorder characterized by autoimmune inflammation of the pituitary gland with various degrees of...

    Juan-Andres Rivera in Pituitary
    Article 01 March 2006

  8. The influence of vasopressin deficiency and acute desmopressin administration on melatonin secretion in patients with central diabetes insipidus

    Melatonin secretion is modulated by the light-dark schedule, mainly through a sympathetic input to the pineal gland. Besides this, arginine...

    S. B. Catrina, R. Rotarus, ... K. Brismar in Journal of Endocrinological Investigation
    Article 01 January 2004

  10. A novel splicing mutation in the V2 vasopressin receptor

    In order to elucidate the molecular basis and the clinical characteristics of X-linked recessive nephrogenic diabetes insipidus (CNDI) in a kindred...

    K. Kamperis, C. Siggaard, ... S. Rittig in Pediatric Nephrology
    Article 01 October 2000

  11. Lymphocytic infundibuloneurohypophysitis presenting as diabetes insipidus in a man

    We report a patient with diabetes insipidus, whose sella magnetic resonance imaging revealed a normal hypophysis with a focal nodular thickening of...

    N. Kamel, Şen Dağci Ilgin, ... S. Güllü in Journal of Endocrinological Investigation
    Article 01 September 1998

  12. Diabetes Insipidus

    Cranial diabetes insipidus (DI) arises when release of arginine vasopressin (AVP, antidiuretic hormone) in response to osmotic stimuli is inadequate....

    Jonathan R. Seckl, David B. Dunger in Drugs
    Article 01 August 1992

  13. Growth and Growth Hormone: I. changes in Serum Level of Growth Hormone Following Hypoglycemia in 134 children with Growth Rctardation

    Extract: The change in levels of growth hormone in serum (SGH) following insulin-induced hypoglycemia was evaluated in 134 prepubertal children with...

    S L Kaplan, C A L Abrams, ... M M Grumbach in Pediatric Research
    Article 01 January 1968
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