Congenital nephrogenic diabetes insipidus

J Am Soc Nephrol. 1997 Dec;8(12):1951-8. doi: 10.1681/ASN.V8121951.
No abstract available

Publication types

  • Historical Article
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Amino Acid Sequence
  • Aquaporin 2
  • Aquaporin 6
  • Aquaporins*
  • Arginine Vasopressin / physiology
  • Deamino Arginine Vasopressin / pharmacology
  • Dehydration / etiology
  • Diabetes Insipidus, Nephrogenic* / complications
  • Diabetes Insipidus, Nephrogenic* / diagnosis
  • Diabetes Insipidus, Nephrogenic* / epidemiology
  • Diabetes Insipidus, Nephrogenic* / genetics
  • Diabetes Insipidus, Nephrogenic* / history
  • Diabetes Insipidus, Nephrogenic* / physiopathology
  • Drug Resistance
  • Female
  • Founder Effect
  • Genetic Carrier Screening
  • Genetic Heterogeneity
  • History, 17th Century
  • History, 18th Century
  • Humans
  • Incidence
  • Infant
  • Infant, Newborn
  • Intellectual Disability / etiology
  • Ion Channels / deficiency
  • Ion Channels / genetics
  • Ion Channels / physiology
  • Ireland / ethnology
  • Kidney Failure, Chronic / etiology
  • Male
  • Models, Biological
  • Models, Molecular
  • Molecular Sequence Data
  • Mutation
  • Nephrons / physiopathology
  • Nova Scotia / epidemiology
  • Prenatal Diagnosis
  • Prevalence
  • Protein Conformation
  • Receptors, Vasopressin / chemistry
  • Receptors, Vasopressin / deficiency
  • Receptors, Vasopressin / genetics
  • Receptors, Vasopressin / physiology
  • X Chromosome / genetics

Substances

  • AQP2 protein, human
  • Aquaporin 2
  • Aquaporin 6
  • Aquaporins
  • Ion Channels
  • Receptors, Vasopressin
  • Arginine Vasopressin
  • Deamino Arginine Vasopressin