References
- Matin SF, Streem SB. Metabolic risk factors in patients with ureteropelvic junction obstruction and renal calculi. J Urol 2000; 163: 1676–8
- Husmann DA, Milliner DS, Segura JW. Ureteropelvic junction obstruction with concurrent renal pelvic calculi in the pediatric patient: a long-term followup. J Urol 1996; 156: 741–3
- Husmann DA, Milliner DS, Segura JW. Ureteropelvic junction obstruction with a simultaneous renal calculus: long-term followup. J Urol 1995; 153: 1399–402
- Tekin A, Tekgul S, Atsu N, Ergen A, Kendi S. Ureteropelvic junction obstruction and coexisting renal calculi in children: role of metabolic abnormalities. Urology 2001; 57: 542–6
- García-Nieto V, Siverio B, Monge M, Toledo C, Molini N. Urinary calcium excretion in children with vesicoureteral reflux. Nephrol Dial Transplant 2003; 18: 507–11
- Ubalde E, García de Jalón A, Abad A, Loris C. Excreción urinaria de calcio en niños sanos. Estudio colaborativo multicéntrico. Nefrología 1998; 8: 224–30
- Butani L, Kalia A. Idiopathic hypercalciuria in children—how valid are the existing diagnostic criteria?. Pediatr Nephrol 2004; 19: 577–82
- Melián JS, García-Nieto V, Sosa AM. Herencia y prevalencia de hipercalciuria en la población infantil de la isla de La Gomera. Nefrología 2000; 20: 510–6
- García-Nieto V, Monge M, Navarro-González JF, Chahin J, Rodrigo MD, Ferrández C. Differences in renal handling of water between children and adults with idiopathic hypercalciuria. Renal stone disease. Crystallization process, pathophysiology, metabolic disorders and prevention, P Jungers, Daudon. Elsevier, Paris 1997; 106
- Serio A, Fraioli A. Epidemiology of nephrolithiasis. Nephron 1999; 81(Suppl 1)26–30
- Hesse A, Brandle E, Wilbert D, Kohrmann KU, Alken P. Study on the prevalence and incidence of urolithiasis in Germany comparing the years 1979 vs. 2000. Eur Urol 2003; 44: 709–13
- Manz F, Kehrt R, Lausen B, Merkel A. Urinary calcium excretion in healthy children and adolescents. Pediatr Nephrol 1999; 13: 894–9
- Cohen B, Goldman SM, Kopilnick M, Khurana AV, Salik JO. Ureteropelvic junction obstruction: its occurrence in 3 members of a single family. J Urol 1978; 120: 361–4
- Buscemi M, Shanske A, Mallet E, Ozoktay S, Hanna MK. Dominantly inherited ureteropelvic junction obstruction. Urology 1985; 26: 568–71
- Sengar DP, Rashid A, Wolfish NM. Familial urinary tract anomalies: association with the major histocompatibility complex in man. J Urol 1979; 121: 194–7
- Santava A, Utikalova A, Bartova A, Drabek J, Santavy J, Scheinar J. Familial hydronephrosis unlinked to the HLA complex. Am J Med Genet 1997; 70: 118–20
- Izquierdo L, Porteous M, Paramo PG, Connor J.M. Evidence for genetic heterogeneity in hereditary hydronephrosis caused by pelvi-ureteric junction obstruction, with one locus assigned to chromosome 6p. Hum Genet 1992; 89: 557–60
- Mackintosh P, Almarhoos G, Heath DA. HLA linkage with familial vesicoureteral reflux and familial pelvi-ureteric junction obstruction. Tissue Antigens 1989; 34: 185–9
- Parsons V, Munson KW, Thompson P, Packham D, Kennedy L. Renal reflux, scarring, cystometrography and tissue types. Proc Eur Dial Transplant Assoc 1979; 16: 542–50
- Zervas J, Costi-Mantsis E, Constantopoulos C, Dimopoulos C. Human leukocyte antigens and vesicoureteral reflux in Greek children. Eur Urol 1986; 12: 230–1
- Nishimura H, Yerkes E, Hohenfellner K, Miyazaki Y, Ma J, Hunley TE, et al. Role of the angiotensin type 2 receptor gene in congenital anomalies of the kidney and urinary tract, CAKUT, of mice and men. Mol Cell 1999; 3: 1–10
- Molini Menchón N, García-Nieto V. Displasia renal multiquística en la infancia. Trastornos asociados. BCSP Can Ped 2002; 26: 51–7