severe
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:
- severe
-
1. Causing distress and especially physical discomfort or pain.
2. Hard to endure.
3. Serious.
Used in 49 Article abstracts
Used in 49 Article abstracts
- A Novel Deletion Mutation in the Arginine Vasopressin Receptor 2 Gene and Skewed X Chromosome Inactivation in a Female Patient with Congenital Nephrogenic Diabetes Insipidus
- A novel splicing mutation in the V2 vasopressin receptor.
- ARC Syndrome: An Expanding Range of Phenotypes
- ARDS Following Acute Lithium Carbonate Intoxication
- Altered Expression of Renal AQPs and Na+ Transporters in Rats with Lithium-Induced NDI
- Aquaporin Molecular Biology and Clinical Abnormalities of the Water Transport Channels
- Aquaporins in the Kidney: From Molecules to Medicine
- Bladder Function Impairment in Aquaporin-2 Defective Nephrogenic Diabetes Insipidus
- Causes of Reversible Nephrogenic Diabetes Insipidus: A Systematic Review
- Changes in Cellular Composition of Kidney Collecting Duct Cells in Rats with Lithium-Induced NDI
- Changes of Rat Kidney AQP2 and Na,K-ATPase mRNA Expression in Lithium-Induced Nephrogenic Diabetes Insipidus
- Characterization of an Aquaporin-2 Water Channel Gene Mutation Causing Partial Nephrogenic Diabetes Insipidus in a Mexican Family: Evidence of Increased Frequency of the Mutation in the Town of Origin
- Clinical Presentation and Follow-Up of 30 Patients with Congenital Nephrogenic Diabetes Insipidus
- Concentrating Defect in Experimental Nephrotic Syndrome: Altered Expression of Aquaporins and Thick Ascending Limb Na+ Transporters
- Congestive Heart Failure in Rats is Associated with Increased Expression and Targeting of Aquaporin-2 Water Channel in Collecting Duct
- Development of Water Transport in the Collecting Duct
- Diabetes Insipidus in Uricase-Deficient Mice: A Model for Evaluating Therapy with Poly(Ethylene Glycol)-Modified Uricase
- Diversity of Nephrogenic Diabetes Insipidus Mutations and Importance of Early Recognition and Treatment
- Downregulation of Renal Aquaporins in Response to Unilateral Ureteral Obstruction
- Evaluation and Management of Diabetes Insipidus
- Hypokalemia-Induced Downregulation of Aquaporin-2 Water Channel Expression in Rat Kidney Medulla and Cortex
- Hypokalemic Nephropathy and Nephrogenic Diabetes Insipidus Due to Excessive Consumption of a Soft Drink
- Hyponatremia and Hypernatremia
- Intrafamilial Phenotype Variability in Nephrogenic Diabetes Insipidus
- Lithium Nephrotoxicity: A Progressive Combined Glomerular and Tubulointerstitial Nephropathy
- Lithium-induced Down regulation of Aquaporin-2 Water Channel Expression in Rat Kidney Medulla
- Lithium-induced nephrogenic diabetes insipidus in older people.
- Lithium-induced nephrogenic diabetes insipidus.
- Mesalazine Associated Nephrogenic Diabetes Insipidus Presenting as Weight Loss
- Mutations in the Vasopressin V2 Receptor Gene in Two Families with Nephrogenic Diabetes Insipidus
- Neonatal Mortality in an Aquaporin-2 Knock-in Mouse Model of Recessive Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus (Bichet - November 1998)
- Nephrogenic Diabetes Insipidus in a Lethargic Lithium-Treated Patient
- Pemetrexed-Induced Acute Renal Failure, Nephrogenic Diabetes Insipidus, and Renal Tubular Acidosis in a Patient with Non-Small Cell Lung Cancer
- Physiological Importance of Aquaporin Water Channels
- Primary Hyperparathyroidism and Coexisting Nephrogenic Diabetes Insipidus: Rapid Postoperative Correction
- Risk Factors for Ifosfamide Nephrotoxicity in Children
- Role of Aquaporin Water Channels in Kidney and Lung
- Segment Specific ENaC Downregulation in Kidney of Rats with Lithium-Induced NDI
- Severe Lactic Acidosis and Renal Involvement in a Patient with Relapsed Burkitt's Lymphoma
- Successful Treatment with Hydrochlorothiazide and Amiloride in an Infant with Congenital Nephrogenic Diabetes Insipidus
- Tenofovir-Related Nephrotoxicity in Human Immunodeficiency Virus-Infected Patients: Three Cases of Renal Failure, Fanconi Syndrome, and Nephrogenic Diabetes Insipidus
- The V2 vasopressin receptor mutations and fluid homeostasis.
- The valve bladder syndrome: 20 years later.
- Three-point Linkage Analysis using Multiple DNA Polymorphic Markers in Families with X-linked Nephrogenic Diabetes Insipidus
- Treatment of Congenital Nephrogenic Diabetes Insipidus by Hydrochlorothiazide and Cyclooxygenase-2 Inhibitor
- Treatment of Nephrogenic Diabetes Insipidus with Hydrochlorothiazide and Amiloride
- Very Severe Self-Poisoning Lithium Carbonate Intoxication Causing a Myocardial Infarction
- [Two Cases of Hypercalcemic Nephropathy Associated with Primary Hyperparathyroidism] (Japanese)
Used in 17 Article bodies
Used in 17 Article bodies
- A Congenital Renal Tubular Defect
- Analysis of Vasopressin Receptor Type II (V2R) Gene in Three Japanese Pedigrees with Congenital Nephrogenic Diabetes Insipidus: Identification of a Family with Complete Deletion of the V2R Gene
- Hereditary Vasopressin Resistance in Man and Mouse
- Hyperosmolar Coma and Lithium-induced Diabetes Insipidus
- Inborn Errors of Signal Transduction: Mutations in G Proteins and G Protein-coupled Receptors as a Cause of Disease
- Index of Suspicion. Case 2. Nephrogenic Diabetes Insipidus
- Lithium-Induced Nephrogenic Diabetes Insipidus Treated with Indomethacin
- Molecular Analysis of X-Linked Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus Secondary to Lithium Therapy in the Postoperative Patient: A Case Report
- Nephrogenic Diabetes Insipidus in North America. The Hopewell Hypothesis
- Nephrogenic Diabetes Insipidus: A Cause of Severe Nonobstructive Urinary Tract Dilatation
- Nephrogenic Diabetes Insipidus: Transmitted by Females and Appearing During Infancy in Males
- Persistent Nephrogenic Diabetes Insipidus Following Lithium Therapy
- Proposed Cause of Marked Vasopressin Resistance in a Female with an X-Linked Recessive V2 Receptor Abnormality
- Risk Factors for Ifosfamide Nephrotoxicity in Children
- Role of Aquaporin-2 Water Channels in Urinary Concentration and Dilution Defects
Used in 63 Article translations
Used in 63 Article translations
- A Family Case of Nephrogenic Diabetes Insipidus
- A Novel Deletion Mutation in the Arginine Vasopressin Receptor 2 Gene and Skewed X Chromosome Inactivation in a Female Patient with Congenital Nephrogenic Diabetes Insipidus
- A Null Mutation in the Vasopressin V2 Receptor Gene (AVPR2) Associated with Nephrogenic Diabetes Insipidus in the Hopewell Kindred
- A Variant of Nephrogenic Diabetes Insipidus: V2 Receptor Abnormality Restricted to the Kidney
- Amphotericin B-induced Nephrogenic Diabetes Insipidus in a Case of Cryptococcemia
- Aquaporin-2 Water Channel Mutations and Nephrogenic Diabetes Insipidus: New Variations on a Theme
- 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
- Cerebral Defects and Nephrogenic Diabetes Insipidus with the ARC Syndrome: Additional Findings or a New Syndrome (ARCC-NDI)?
- Changes of Rat Kidney AQP2 and Na,K-ATPase mRNA Expression in Lithium-Induced Nephrogenic Diabetes Insipidus
- Characterization of an Aquaporin-2 Water Channel Gene Mutation Causing Partial Nephrogenic Diabetes Insipidus in a Mexican Family: Evidence of Increased Frequency of the Mutation in the Town of Origin
- Clinical Utility of Direct Mutation Testing for Congenital Nephrogenic Diabetes Insipidus in Families
- Congestive Heart Failure in Rats is Associated with Increased Expression and Targeting of Aquaporin-2 Water Channel in Collecting Duct
- Defects of G Protein-Coupled Signal Transduction in Human Disease
- Detection of Skewed X-Inactivation in Two Female Carriers of Vasopressin Type 2 Receptor Gene Mutation
- Diabetes Insipidus (Hendy, Bichet)
- Diabetes Insipidus (Robertson)
- Diabetes Insipidus [Bell]
- Disordered Water Channel Expression and Distribution in Acquired Nephrogenic Diabetes Insipidus
- Emergency Treatment of Lithium-Induced Diabetes Insipidus with Nonsteroidal Anti-Inflammatory Drugs
- Evaluation and Management of Diabetes Insipidus
- Hereditary Nephrogenic Diabetes Insipidus
- Hyperuricemia as a Clue for Central Diabetes Insipidus (Lack of V1 Effect) in the Differential Diagnosis of Polydipsia
- Hyponatremia and Hypernatremia
- Index of Suspicion. Case 2. Nephrogenic Diabetes Insipidus
- Intracanial Calcifications and Nephrogenic Diabetes Insipidus
- Intracranial Calcification in Siblings with Nephrogenic Diabetes Insipidus: CT and MRI
- Intrafamilial Phenotype Variability in Nephrogenic Diabetes Insipidus
- Lithium-induced Down regulation of Aquaporin-2 Water Channel Expression in Rat Kidney Medulla
- Misfolding of Mutant Aquaporin-2 Water Channels in Nephrogenic Diabetes Insipidus
- Molecular Analysis of X-Linked 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 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
- Nephrogenic Diabetes Insipidus: Transmitted by Females and Appearing During Infancy in Males
- Notes on Some Cases of Diabetes Insipidus with Marked Family and Hereditary Tendencies
- On Hereditary Diabetes Insipidus With Special Regard to a Sex-Linked Form
- Pathogenesis and Treatment of Autosomal-Dominant Nephrogenic Diabetes Insipidus Caused by an Aquaporin 2 Mutation
- Pathophysiology of Aquaporin-2 in Water Balance Disorders
- Pemetrexed-Induced Acute Renal Failure, Nephrogenic Diabetes Insipidus, and Renal Tubular Acidosis in a Patient with Non-Small Cell Lung Cancer
- Pharmacologic Chaperones as a Potential Treatment for X-linked Nephrogenic Diabetes Insipidus
- 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]
- Primary Hyperparathyroidism and Coexisting Nephrogenic Diabetes Insipidus: Rapid Postoperative Correction
- Recurrent Dehydration in a Young Girl
- Risk Factors for Ifosfamide Nephrotoxicity in Children
- Severe Lactic Acidosis and Renal Involvement in a Patient with Relapsed Burkitt's Lymphoma
- Severely Impaired Urinary Concentrating Ability in Transgenic Mice Lacking Aquaporin-1 Water Channels
- Severely Impaired Urine-Concentrating Ability in Mice Lacking the CLC-K1 Chloride Channel
- The Aquaporin Family of Water Channel Proteins in Clinical Medicine
- 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
- Upregulation of Urea Transporter UT-A2 and Water Channels AQP2 and AQP3 in Mice Lacking Urea Transporter UT-B
- Vasopressin Type-2 Receptor and Aquaporin-2 Water Channel Mutants in Nephrogenic Diabetes Insipidus
- Very Severe Self-Poisoning Lithium Carbonate Intoxication Causing a Myocardial Infarction
Used in 11 Faq answers
Used in 11 Faq answers
- How can a girl have NDI? I thought only boys had it.
- How does someone get NDI from taking Lithium?
- In NDI patients with hypernatremia, is the hypernatremia due to the inability of the patient to drink the huge volumes of water needed to maintain fluid balance or the blunting of thirst?
- Is NDI life-threatening, and what symptoms should be watched for?
- Is it possible to control the symptoms of NDI without medication--through diet and fluid intake alone?
- 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
- Should females with NDI be medicated differently than males?
- What are the consequences of a serum sodium level being either too high or too low?
- What are the long-term side effects of the medications?
- What can be done to manage the enlarged bladder problem and kidney damage?
- What is the life expectancy of an NDI child?
Used in 14 Proceeding abstracts
Used in 14 Proceeding abstracts
- A Novel dominant mutation of the aquaporin-2 gene resulting in partial nephrogenic diabetes insipidus
- Analysis of molecular mechanisms causing V2 vasopressin receptor dysfunction in four patients with X-linked nephrogenic diabetes insipidus
- Bartter syndrome with sensorineural deafness: molecular genetics
- Congenital (present a birth) severe diabetes insipidus. Most patients have nephrogenic diabetes insipidus (NDI), but some patients have autosomal recessive central (neurogenic) diabetes insipidus
- Decreased Aquaporin-2 Water Channel Expression in Acquired Nephrogenic Diabetes Insipidus
- Diversity of Nephrogenic Diabetes Insipidus Mutations and Importance of Early Recognition and Treatment
- Generation of Germ Line Heterozygous Mice for Aquaporin-2 Conditional Knock-Out and Knock-In Models of NDI
- High proportion of ROMK processing defects underlying hyperprostaglandin E syndrome/antenatal Bartter syndrome
- Nephrogenic Diabetes Insipidus in a Palestine Sibship
- Osmolality and solute composition regulate aquaporin-2 expression in primary cultured renal principal cells
- Pitfalls in the Differential Diagnosis of Nephrogenic Diabetes Insipidus.
- Rediscovery of Swedish Kindred with X-linked 'Vasopressin-Responsive' Diabetes Insipidus: Validation and Explanation of the Unusual Clinical Phenotype
- Variations in clinical phenotype associated with different mutations of the V2 receptor gene in X-linked recessive congenital nephrogenic DI (xCNDI)
- Vasopressin-V2-receptor dependent and independent regulation of collecting duct aquaporin-2 expression and trafficking
Used in 7 Proceeding translations
Used in 7 Proceeding translations
- Decreased Aquaporin-2 Water Channel Expression in Acquired Nephrogenic Diabetes Insipidus
- Diversity of Nephrogenic Diabetes Insipidus Mutations and Importance of Early Recognition and Treatment
- Gene Mutation Analysis of NDI patients in Japan
- Generation of Germ Line Heterozygous Mice for Aquaporin-2 Conditional Knock-Out and Knock-In Models of NDI
- Recycling of the V2 Vasopressin Receptor
- Rediscovery of Swedish Kindred with X-linked 'Vasopressin-Responsive' Diabetes Insipidus: Validation and Explanation of the Unusual Clinical Phenotype
- Variations in clinical phenotype associated with different mutations of the V2 receptor gene in X-linked recessive congenital nephrogenic DI (xCNDI)
Used in 64 Term definitions
Used in 64 Term definitions
- Duchenne's muscular dystrophy
- NDI Abstract of Article: 510
- Niemann-Pick disease
- Vibrio
- Vibrio cholerae
- acute
- acute bronchitis
- acute tubular necrosis
- acutely
- agony
- alcohol dependence
- anaphylactic hypersensitivity
- bone marrow transplant
- cancer
- cardiogenic shock
- cholera
- cholera toxin
- congenital lactose intolerance
- cytomegalic inclusion disease
- diphtheria
- dysthymia
- dysthymic disorder
- epididymo-orchitis
- extreme
- flat smallpox
- fulminant
- gout
- harsh
- hemolytic-uremic syndrome
- hemorrhagic smallpox
- hepatic encephalopathy
- histiocytosis X
- histoplasmosis
- hydrocephalus
- hydrocortisone
- hypomanic episode
- hypophosphatasia
- hypoplasia
- hypothyroidism
- influenza
- keen
- lactic acid
- malaria
- mental deficiency
- mental retardation
- modified smallpox
- ophthalmia
- phenylketonuria
- pheochromocytoma
- porphyric neuropathy
- porphyric polyneuropathy
- progression
- proximal renal tubular acidosis
- renal biopsy
- respiratory syncytial viruses
- rubella
- secondary or progressive coccidioidomycosis
- sickle cell anemia
- spleen
- status asthmaticus
- toxic
- type 1 diabetes mellitus
- tyrosinase-negative (ty-neg) oculocutaneous albinism
- von Willebrand's disease



