Bartter syndrome type 3: An unusual cause of nephrolithiasis [4]

Nephrology Dialysis Transplantation

Volumn 17, Issue 3, 2002, Pages 521-523

  Colussi, Giacomo ^a   De Ferrari, Maria Elisabetta ^a   Tedeschi, Silvana ^b   Prandoni, Silvia ^b   Syrén, Marie Louise ^b   Civati, Giovanni ^a  

^a OSPEDALE NIGUARDA CA GRANDA   (Italy)

^b ICP Hospital   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ALDOSTERONE; BICARBONATE; BUMETANIDE; CHLORIDE CHANNEL; CHLORIDE ION; CITRIC ACID; CYSTEINE; DESMOPRESSIN; DIURETIC AGENT; DNA FRAGMENT; FUROSEMIDE; HYDROCHLOROTHIAZIDE; MAGNESIUM; OXALIC ACID; POTASSIUM ION; RENIN; SODIUM ION; STRUVITE; URIC ACID; WATER;

ADULT; BARTTER SYNDROME; CASE REPORT; CLINICAL PROTOCOL; DIURESIS; DNA SEQUENCE; ECHOGRAPHY; GENE MUTATION; GENETIC SCREENING; HENLE LOOP; HUMAN; HYPOKALEMIA; ION TRANSPORT; KIDNEY CALCIFICATION; KIDNEY FUNCTION; LABORATORY TEST; LETTER; MALE; METABOLIC ACIDOSIS; NEPHROLITHIASIS; POLYMERASE CHAIN REACTION; POTASSIUM DEPLETION; PRIORITY JOURNAL; RISK FACTOR; SODIUM EXCRETION;

EID: 0036197906     PISSN: 09310509     EISSN: None     Source Type: Journal    
DOI: 10.1093/ndt/17.3.521     Document Type: Letter

References (8)

1. Genotype-phenotype correlations in normotensive patients with primary renal tubular hypokalemic metabolic alkalosis
2. Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
3. Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome
4. Abnormal reabsorption of Na/Cl by the thiazide-inhibitable transporter of the distal convoluted tubule in Gitelman's syndrome
5. Uric acid and calcium oxalate nephrolithiasis
6. Pathogenesis and clinical course of mixed calcium oxalate and uric acid nephrolithiasis
7. Citrate and renal calculi
8. Citrate excretion: A window on renal metabolism