A family-based study of metabolic phenotypes in calcium urolithiasis

Kidney International

Volumn 60, Issue 3, 2001, Pages 1141-1147

  Tessier, Josée ^a   Petrucci, Martin ^a   Trouvé, Marie Lucie ^a   Valiquette, Luc ^a   Guay, Gérald ^a   Ouimet, Denis ^a   Bonnardeaux, Alain ^a  

^a MAISONNEUVE ROSEMONT HOSPITAL   (Canada)

Author keywords

Genetics; Hypercalciuria; Kidney stone; Linkage study; Oxalate; Renal stone formers; Sib pairs; Urinary calcium excretion

Indexed keywords

AMMONIA; CALCIUM; CITRIC ACID; CREATININE; MAGNESIUM; OXALIC ACID; PHOSPHATE; SODIUM; URATE;

ADULT; ARTICLE; BODY MASS; CALCIUM STONE; CONTROLLED STUDY; FAMILY HISTORY; FAMILY STUDY; FEMALE; HUMAN; KIDNEY METABOLISM; MAJOR CLINICAL STUDY; MALE; ONSET AGE; PHENOTYPE; PRIORITY JOURNAL; RISK FACTOR; URINARY EXCRETION; URINE LEVEL; URINE VOLUME;

EID: 0035723349     PISSN: 00852538     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1523-1755.2001.0600031141.x     Document Type: Article

References (42)

1. Heredity in renal stone disease
2. Genetic predisposition to formation of calcium oxalate renal calculi
3. Family history of renal stones in a population study of stone formers and healthy subjects
4. Studies on the prevalence and epidemiology of urinary stone disease in men in Leeds
5. Familial aggregation of renal calcium stone disease
6. Family history and risk of kidney stones
7. Solution chemistry of supersaturation
8. Urinary excretion of calcium and magnesium in patients with calcium-containing renal stones
9. Activity products in stone-forming and non-stone-forming urine
10. Relations between oxalic acid, calcium, magnesium and creatinine excretion in normal men and male patients with calcium oxalate kidney stones
11. Risk factors in calcium stone disease of the urinary tract
12. A biochemical basis for grouping of patients with urolithiasis
13. Prevention of calcium stones with thiazides
14. Composition of renal stones and their frequency in a stone clinic: Relationship to parameters of mineral metabolism in serum and urine
15. Metabolic and clinical disturbances in patients with calcium urolithiasis
16. Urine saturation with calcium salts in normal subjects and idiopathic calcium stone-formers estimated by an improved computer model system
17. A critical evaluation of the urinary inhibiting activity in idiopathic calcium oxalate nephrolithiasis
18. A urinary calcium-citrate index for the evaluation of nephrolithiasis
19. Case-control study of risk factors for idiopathic calcium nephrolithiasis
20. Urinary biochemical profile of patients with ureteric calculi in Jodhpur region (north western India)
21. Low urine citrate excretion as main risk factor for recurrent calcium oxalate nephrolithiasis in males
22. The evaluation of risk factors in male stone-formers attending a general hospital out-patient clinic
23. Familial idiopathic hypercalciuria
24. Autosomal dominant inheritance of hypercalciuria
25. Familial absorptive hypercalciuria in a large kindred
26. Family pattern of idiopathic hypercalciuria and its subtypes
27. Idiopathic calcium urolithiasis: Genetic aspects
28. 3 levels in patients with idiopathic hypercalciuria and in normal subjects
29. Idiopathic hypercalciuria: The contribution of Dr Jacob Lemann, Jr.
30. Renal and absorptive hypercalciuria: A metabolic disturbance with varying and interchanging modes of expression
31. Diet-dependent hypercalciuria in transgenic mice with reduced CLC5 chloride channel expression
32. A prospective study of dietary calcium and other nutrients and the risk of symptomatic kidney stones
33. A common molecular basis for three inherited kidney stone diseases
34. Mechanism of hypercalciuria in genetic hypercalciuric rats. Inherited defect in intestinal calcium transport
35. Hyperoxaluria in idiopathic calcium nephrolithiasis: What are the limits?
36. Reliability of a single 24-hour urine testing for the detection of abnormal stone-forming risk factors
37. Urinary volume, water and recurrences in idiopathic calcium nephrolithiasis: A 5-year randomized prospective study
38. Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis
39. +-ATPase cause renal tubular acidosis with sensorineural deafness
40. Body size and risk of kidney stones
41. Mapping a gene defect in absorptive hypercalciuria to chromosome 1q23.3-q24
42. Linkage strategies for genetically complex traits. II. The power of the affected relative pairs