Wolf, Matthias T F <br/><br/>
Follow-up of five patients with FHHNC due to mutations in the Paracellin-1 gene.  [electronic resource] 

 -  Pediatric nephrology (Berlin, Germany)  Aug 2002 
 - 602-8 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0931-041X 
<br/><br/><label>Standard No.: </label>10.1007/s00467-002-0884-4  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Calcium--urine<br/>Child<br/>Child, Preschool<br/>Claudins<br/>Diuretics<br/>Female<br/>Follow-Up Studies<br/>Growth--physiology<br/>Humans<br/>Hydrochlorothiazide--therapeutic use<br/>Kidney Function Tests<br/>Magnesium--blood<br/>Male<br/>Membrane Proteins--genetics<br/>Metal Metabolism, Inborn Errors--blood<br/>Mutation--genetics<br/>Nephrocalcinosis--blood<br/>Puberty--physiology<br/>Retrospective Studies<br/>Sodium Chloride Symporter Inhibitors--therapeutic use