Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness. [electronic resource]
Producer: 20011101Description: E5 p. digitalISSN:- 1098-4275
- Adolescent
- Anti-Inflammatory Agents, Non-Steroidal -- therapeutic use
- Bartter Syndrome -- genetics
- Child
- Child, Preschool
- Chromosomes, Human, Pair 1 -- genetics
- Consanguinity
- Creatinine -- blood
- Cyclooxygenase Inhibitors -- therapeutic use
- Deafness -- genetics
- Dinoprostone -- metabolism
- Diuresis
- Female
- Genetic Linkage
- Growth Disorders -- genetics
- Haplotypes
- Humans
- Hypokalemia -- drug therapy
- Indomethacin -- therapeutic use
- Infant
- Kidney -- diagnostic imaging
- Kidney Failure, Chronic -- diagnosis
- Lebanon
- Male
- Pedigree
- Phenotype
- Renal Tubular Transport, Inborn Errors -- diagnosis
- Retrospective Studies
- Syndrome
- Treatment Outcome
- Turkey
- Ultrasonography
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.