-
1
-
-
0011859792
-
Genetics of urolithiasis
-
FB Stapleton DP Jones Genetics of urolithiasis A Spitzer ED Avner Inheritance of kidney and urinary tract diseases 1990 Kluwer Academic Publishers Boston 293 315
-
(1990)
, pp. 293-315
-
-
Stapleton, FB1
Jones, DP2
-
2
-
-
85119813480
-
Clinical and laboratory studies of 207 consecutive patients in a kidney stone clinic
-
RA Melnick PH Henneman Clinical and laboratory studies of 207 consecutive patients in a kidney stone clinic N Engl J Med 259 1958 370 374
-
(1958)
N Engl J Med
, vol.259
, pp. 370-374
-
-
Melnick, RA1
Henneman, PH2
-
3
-
-
18344417824
-
Urolithiasis in children: the role of hypercalciuria
-
FB Stapleton CP McKay HN Noe Urolithiasis in children: the role of hypercalciuria Pediatr Ann 16 1987 980 992
-
(1987)
Pediatr Ann
, vol.16
, pp. 980-992
-
-
Stapleton, FB1
McKay, CP2
Noe, HN3
-
4
-
-
0018644610
-
Physiological basis for absorptive and renal hypercalciuria
-
CYC Pak Physiological basis for absorptive and renal hypercalciuria Am J Physiol 237 1979 F415 F423
-
(1979)
Am J Physiol
, vol.237
, pp. F415-F423
-
-
Pak, CYC1
-
7
-
-
0031748292
-
X-linked recessive nephrolithiasis: presentation and diagnosis in children
-
SJ Schurman AGW Norden SJ Scheinman X-linked recessive nephrolithiasis: presentation and diagnosis in children J Pediatr 132 1998 859 862
-
(1998)
J Pediatr
, vol.132
, pp. 859-862
-
-
Schurman, SJ1
Norden, AGW2
Scheinman, SJ3
-
8
-
-
8544254724
-
Characterization of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stone) disorders
-
SE Lloyd W Günther SHS Pearce A Thomson ML Bianchi M Bosio Characterization of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stone) disorders Hum Mol Genet 6 1997 1233 1239
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1233-1239
-
-
Lloyd, SE1
Günther, W2
Pearce, SHS3
Thomson, A4
Bianchi, ML5
Bosio, M6
-
9
-
-
0028038212
-
Dent's disease: a familial proximal renal tubular syndrome with low molecular weight proteinuria, hypercalciuria, nephrocalcinosis, metabolic bone disease, progressive renal failure and a marked male predominance
-
OM Wrong AGW Norden TG. Feest Dent's disease: a familial proximal renal tubular syndrome with low molecular weight proteinuria, hypercalciuria, nephrocalcinosis, metabolic bone disease, progressive renal failure and a marked male predominance Q J Med 87 1994 473 493
-
(1994)
Q J Med
, vol.87
, pp. 473-493
-
-
Wrong, OM1
Norden, AGW2
Feest, TG.3
-
10
-
-
0028957547
-
Hypercalciuria and nephrocalcinosis in patients with idiopathic low molecular weight proteinuria in Japan
-
T Igarashi H Hayakawa H Shiraga H Kawato K Yan H Kawaguchi Hypercalciuria and nephrocalcinosis in patients with idiopathic low molecular weight proteinuria in Japan Nephron 69 1995 242 247
-
(1995)
Nephron
, vol.69
, pp. 242-247
-
-
Igarashi, T1
Hayakawa, H2
Shiraga, H3
Kawato, H4
Yan, K5
Kawaguchi, H6
-
12
-
-
0030075382
-
Crystal clear chloride channels
-
SC Hebert Crystal clear chloride channels Nature 379 1996 398 399
-
(1996)
Nature
, vol.379
, pp. 398-399
-
-
Hebert, SC1
-
13
-
-
0029015415
-
Characterization of carrier females and affected males with X-linked recessive nephrolithiasis
-
SC Reinhart AGW Norden M Lapsley RV Thakker J Pang AM Moses Characterization of carrier females and affected males with X-linked recessive nephrolithiasis J Am Soc Nephrol 5 1995 1451 1461
-
(1995)
J Am Soc Nephrol
, vol.5
, pp. 1451-1461
-
-
Reinhart, SC1
Norden, AGW2
Lapsley, M3
Thakker, RV4
Pang, J5
Moses, AM6
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