dehydration
The definitions used in this glossary of terminology either have been provided by the authors of the articles, or have been extracted wholly or in part, or paraphrased from the following sources: The American Medical Association Encyclopedia of Medicine, Charles B. Clayman, MD, Medical Editor, Random House, New York, 1989; Biotechnology from A to Z, 2d Edition, William Bains, Oxford University Press, New York, New York, 2002; A Dictionary of Genetics, 6th Edition, Robert C. King and William D. Stansfield, Oxford University Press, New York, New York, 2002; Dorland's Illustrated Medical Dictionary, 29th and 30th Editions, W. B. Saunders Company, Philadelphia, 2000, 2003; Genes VII, Benjamin Lewin, Oxford University Press, New York, New York, 2000; The Gale Encyclopedia of Genetic Disorders, Volumes I and II, Stacey L. Blachford, Ed., Thomson Learning, New York, New York, 2002; The Merriam-Webster Dictionary, Merriam-Webster, Inc., Springfield, Massachusetts, 1997; Molecular Biology of the Cell, 3rd Edition, Bruce Alberts, et al., Garland Publishing, 1994; The Random House Dictionary of the English Language, Unabridged Edition, 1966; Webster's Ninth New Collegiate Dictionary, 1991.
DEFINITION:
- dehydration
-
The condition that results from excessive loss of body water.
hypernatremic dehydration - A condition in which electrolyte losses are disproportionately smaller than water losses.
Used in 35 Article abstracts
Used in 35 Article abstracts
- A historical cohort study of kidney damage in long-term lithium patients: continued surveillance needed.
- Altered Expression of COX-1, COX-2, and mPGES in Rats with Nephrogenic and Central Diabetes Insipidus
- Causes of Reversible Nephrogenic Diabetes Insipidus: A Systematic Review
- Clinical Utility of Direct Mutation Testing for Congenital Nephrogenic Diabetes Insipidus in Families
- Cloning of an Aquaporin Homologue Present in Water Channel Containing Endosomes of Toad Urinary Bladder
- Dehydration Reverses Vasopressin Antagonist-Induced Diuresis and Aquaporin-2 Downregulation in Rats
- Development of Urinary Concentrating Capacity: Role of Aquaporin-2
- Diabetes Insipidus [Bell]
- Diabetes Insipidus in Uricase-Deficient Mice: A Model for Evaluating Therapy with Poly(Ethylene Glycol)-Modified Uricase
- Dissociation Between Urine Osmolality and Urinary Excretion of Aquaporin-2 in Healthy Volunteers
- Diversity of Nephrogenic Diabetes Insipidus Mutations and Importance of Early Recognition and Treatment
- Dural Sinus Thrombosis with Severe Hypernatremia Developing in a Patient on Long-Term Lithium Therapy
- Evaluation and Management of Diabetes Insipidus
- Familial Nephrogenic Diabetes Insipidus: Report of Two Families
- Hyperosmolar Nonketotic Coma Precipitated by Lithium-induced Nephrogenic Diabetes Insipidus
- Hyperuricemia as a Clue for Central Diabetes Insipidus (Lack of V1 Effect) in the Differential Diagnosis of Polydipsia
- Identification of Mutations in the Arginine Vasopressin Receptor 2 Gene Causing Nephrogenic Diabetes Insipidus in Chinese Patients
- Isolation of Human aquaporin-CD Gene
- Methyl-β-Cyclodextrin Induces Vasopressin-Independent Apical Accumulation of Aquaporin-2 in the Isolated, Perfused Rat Kidney
- Molecular and Cellular Biology of Vasopressin and Oxytocin Receptors and Action in the Kidney
- Mutations in the Vasopressin V2 Receptor Gene in Two Families with Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus (Bichet - November 1998)
- Pathogenesis and Treatment of Autosomal-Dominant Nephrogenic Diabetes Insipidus Caused by an Aquaporin 2 Mutation
- Reverse Pharmacological Effect of Loop Diuretics and Altered rBSC1 Expression in Rats with Lithium Nephropathy
- The V2 vasopressin receptor mutations and fluid homeostasis.
- Three-point Linkage Analysis using Multiple DNA Polymorphic Markers in Families with X-linked Nephrogenic Diabetes Insipidus
- Treatment of Nephrogenic Diabetes Insipidus with Hydrochlorothiazide and Amiloride
- Urinary Excretion of Aquaporin-2 in Patients with Diabetes Insipidus
- Vasopressin-Independent Renal Urinary Concentration: Increased rBSC1 and Enhanced Countercurrent Multiplication
- X-linked Nephrogenic Diabetes Insipidus: from the Ship Hopewell to RFLP Studies
- [Nephrogenic Diabetes Insipidus] (Hungarian)
- [Non-Lithiasic Hereditary Tubulopathies] (Article in French)
- [Pathological Aspects of Water Transport in the Collecting Ducts] (French)
- [Recent Advances in Vasopressin Receptors and Signal Transduction System] (Japanese)
- cDNA Cloning of a Functional Water Channel From Toad Urinary Bladder Epithelium
Used in 9 Article bodies
Used in 9 Article bodies
- A Congenital Renal Tubular Defect
- Evidence that the Antidiuretic Substance in the Plasma of Children with Nephrogenic Diabetes Insipidus is Antidiuretic Hormone
- Hereditary Vasopressin Resistance in Man and Mouse
- Hyperosmolar Coma and Lithium-induced Diabetes Insipidus
- Index of Suspicion. Case 2. Nephrogenic Diabetes Insipidus
- Molecular Analysis of X-Linked Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus in a Patient Taking Cidofovir
- Nephrogenic Diabetes Insipidus: Transmitted by Females and Appearing During Infancy in Males
Used in 72 Article translations
Used in 72 Article translations
- A Congenital Defect of Water Metabolism
- A Family Case of Nephrogenic Diabetes Insipidus
- A Null Mutation in the Vasopressin V2 Receptor Gene (AVPR2) Associated with Nephrogenic Diabetes Insipidus in the Hopewell Kindred
- Altered Expression of COX-1, COX-2, and mPGES in Rats with Nephrogenic and Central Diabetes Insipidus
- Aquaporins: From Physiology to Nephrogenic Diabetes Insipidus
- Biochemical Basis of Partial Nephrogenic Diabetes Insipidus Phenotypes
- Brief Report: A Molecular Defect in the Vasopressin V2-Receptor Gene Causing Nephrogenic Diabetes Insipidus
- Brief Report: A Mutation in the Vasopressin V2-Receptor Gene in a Kindred with X-Linked Nephrogenic Diabetes Insipidus
- Clinical Utility of Direct Mutation Testing for Congenital Nephrogenic Diabetes Insipidus in Families
- Cloning of an Aquaporin Homologue Present in Water Channel Containing Endosomes of Toad Urinary Bladder
- Cognitive and Psychosocial Functioning of Patients with Congenital Nephrogenic Diabetes Insipidus
- Congenital Nephrogenic Diabetes Insipidus
- Constitutive Nitric Oxide Synthase in Hypothalami of Normal and Hereditary Diabetes Insipidus Rats and Mice: Role of Nitric Oxide in Osmotic Regulation and its Mechanism
- Defects of G Protein-Coupled Signal Transduction in Human Disease
- Dehydration Reverses Vasopressin Antagonist-Induced Diuresis and Aquaporin-2 Downregulation in Rats
- Diabetes Insipidus (Robertson)
- Diabetes Insipidus [Bell]
- Differential Diagnosis and Pathophysiology of Diabetes Insipidus
- Differential Diagnosis of Polyuria
- Disordered Water Channel Expression and Distribution in Acquired Nephrogenic Diabetes Insipidus
- Evaluation and Management of Diabetes Insipidus
- Familial Nephrogenic Diabetes Insipidus: Report of Two Families
- From Vasopressin Receptor to Water Channel: Intracellular Traffic, Constraint and By-pass
- Hemifacial Spasm in Albright's Hereditary Osteodystrophy with Pseudopseudohypoparathyroidism and Nephrogenic Diabetes Insipidus--Case Report
- Hereditary Nephrogenic Diabetes Insipidus
- Hereditary Nephrogenic Diabetes Insipidus and Bilateral Nonobstructive Hydronephrosis
- High Serum Immunoreactive Trypsin Not Caused by Cystic Fibrosis (letter)
- Hypokalemic Nephropathy and Nephrogenic Diabetes Insipidus Due to Excessive Consumption of a Soft Drink
- Hyponatremia and Hypernatremia
- Index of Suspicion. Case 2. Nephrogenic Diabetes Insipidus
- Intracanial Calcifications and Nephrogenic Diabetes Insipidus
- Intracranial Calcification in Nephrogenic Diabetes Insipidus
- Intracranial Calcification in Siblings with Nephrogenic Diabetes Insipidus: CT and MRI
- Intracranial Calcifications Associated with Nephrogenic Diabetes Insipidus
- Intrafamilial Phenotype Variability in Nephrogenic Diabetes Insipidus
- Isolation of Human aquaporin-CD Gene
- Molecular Analysis of X-Linked Nephrogenic Diabetes Insipidus
- Molecular Biology of Diabetes Insipidus
- Molecular Mechanisms for the Regulation of Water Transport in Amphibian Epithelia by Antidiuretic Hormone
- Molecular and Cellular Biology of Vasopressin and Oxytocin Receptors and Action in the Kidney
- Molecular and Cellular Defects in Nephrogenic Diabetes Insipidus
- Mutations in the Vasopressin V2 Receptor and Aquaporin-2 Genes in 12 Families with Congenital Nephrogenic Diabetes Insipidus
- Nature and Recurrence of AVPR2 Mutations in X-Linked Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus (Bichet - November 1998)
- Nephrogenic Diabetes Insipidus (Bichet)
- Nephrogenic Diabetes Insipidus Secondary to Lithium Therapy in the Postoperative Patient: A Case Report
- Nephrogenic Diabetes Insipidus in Sibling Colts
- Nephrogenic Diabetes Insipidus: Causes Revealed
- Nephrogenic Diabetes Insipidus: Clinical Symptoms, Pathogenesis, Genetics and Treatment
- Nephrogenic Diabetes Insipidus: Identification of the Genetic Defect
- Pathogenesis and Treatment of Autosomal-Dominant Nephrogenic Diabetes Insipidus Caused by an Aquaporin 2 Mutation
- Pathophysiology of Aquaporin-2 in Water Balance Disorders
- Phenotypes Developed in Secretin Receptor-Null Mice Indicated a Role for Secretin in Regulating Renal Water Reabsorption
- Physiology and Pathophysiology of the Aquaporin-2 Water Channel
- Polyuria and Polydipsia. Problems Associated with Patient Evaluation
- Polyuria in Childhood
- Prevention of Intracranial Calcifications and Brain Damage Associated with Nephrogenic Diabetes Insipidus [Letter; Comment]
- Recurrent Dehydration in a Young Girl
- Renal Aquaporins
- Successful Treatment with Hydrochlorothiazide and Amiloride in an Infant with Congenital Nephrogenic Diabetes Insipidus
- The Clinical Importance of the Urinary Excretion of Aquaporin-2
- The Management of Diabetes Insipidus in Adults
- Transient Nephrogenic Diabetes Insipidus Accompanied by Possible Psychogenic Polydipsia
- Treatment of Nephrogenic Diabetes Insipidus with Hydrochlorothiazide and Amiloride
- Two Novel Mutations in the Vasopressin V2 Receptor Gene in Unrelated Japanese Kindreds with Nephrogenic Diabetes Insipidus
- Urinary Excretion of Aquaporin-2 in Humans: A Potential Marker of Collecting Duct Responsiveness to Vasopressin
- Urinary Excretion of Aquaporin-2 in Patients with Diabetes Insipidus
- Use of T1-weighted MR Imaging to Differentiate between Primary Polydipsia and Central Diabetes Insipidus
- Vasopressin Receptors in Health and Disease
- Vasopressin-Independent Renal Urinary Concentration: Increased rBSC1 and Enhanced Countercurrent Multiplication
- cDNA Cloning of a Functional Water Channel From Toad Urinary Bladder Epithelium
Used in 8 Faq answers
Used in 8 Faq answers
- Are headaches a symptoms of NDI?
- How does someone get NDI from taking Lithium?
- How is NDI diagnosed?
- Is NDI life-threatening, and what symptoms should be watched for?
- Maxide is a brand-name diuretic to treat high-blood pressure. In my case, however, this diuretic causes my system to require less water intake and therefore less fluid output. Have you heard of this reverse-effect on persons with diabetes insipidus?
- My child has NDI and needs to have dental work done. They want to give him general anesthesia which requires that he has no water four hours prior to the dental work. Is this OK?
- My son's male cousin who is 3 years old was just diagnosed with Diabetes Insipidus. They are trying to find out if there is a genetic link. My son who is 21 years old now, has frequent urination, up at least 7 times throughout the night to void. He states
- What is the life expectancy of an NDI child?
Used in 15 Proceeding abstracts
Used in 15 Proceeding abstracts
- A mouse model for X-linked nephrogenic diabetes insipidus
- Congenital (present a birth) severe diabetes insipidus. Most patients have nephrogenic diabetes insipidus (NDI), but some patients have autosomal recessive central (neurogenic) diabetes insipidus
- Decrease in urine volume and increase in urine osmolality after SR49059 administration in five adult male patients with X-linked nephrogenic diabetes insipidus
- Diversity of Nephrogenic Diabetes Insipidus Mutations and Importance of Early Recognition and Treatment
- Expressional alteration of sodium transporter in the thick ascending limb of Henle and urinary concentration
- Growth in males with (well-managed) nephrogenic diabetes insipidus
- Lack of AVP-induced phosphorylation of the Aquaporin-2 mutants AQP2-R254L and AQP2-R254Q explains dominant Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus Patients in Japan
- Nephrogenic Diabetes Insipidus in a Palestine Sibship
- New insights in water channel physiology revealed by transgenic mouse models
- Nutritional Concerns for Persons with NDI
- Pitfalls in the Differential Diagnosis of Nephrogenic Diabetes Insipidus.
- Prostaglandins as Stimulants of AQP2 Expression: a Possible Future Treatment for NDI?
- Purinergic Control of Medullary Collecting Duct Function: A Novel Vasopressin-independent Regulatory Mechanism
- The Low Sodium Diet for Nephrogenic Diabetes Insipidus
Used in 4 Proceeding translations
Used in 4 Proceeding translations
- Congenital (present a birth) severe diabetes insipidus. Most patients have nephrogenic diabetes insipidus (NDI), but some patients have autosomal recessive central (neurogenic) diabetes insipidus
- Diversity of Nephrogenic Diabetes Insipidus Mutations and Importance of Early Recognition and Treatment
- Growth in males with (well-managed) nephrogenic diabetes insipidus
- Nephrogenic Diabetes Insipidus in a Palestine Sibship



