-
1
-
-
0029796174
-
The calcium-sensing receptor: a window into the physiology and pathophysiology of mineral ion metabolism
-
Chattopadhyay N., Mithal A., and Brown E. The calcium-sensing receptor: a window into the physiology and pathophysiology of mineral ion metabolism. Endocr Rev 17 (1996) 289-307
-
(1996)
Endocr Rev
, vol.17
, pp. 289-307
-
-
Chattopadhyay, N.1
Mithal, A.2
Brown, E.3
-
2
-
-
0035138842
-
Extracellular calcium sensing and intracellular calcium signaling
-
Brown E.M., and MacLeod R.J. Extracellular calcium sensing and intracellular calcium signaling. Physiol Rev 81 (2001) 240-297
-
(2001)
Physiol Rev
, vol.81
, pp. 240-297
-
-
Brown, E.M.1
MacLeod, R.J.2
-
3
-
-
0029951194
-
Extracellular calcium-sensing receptor: implications for calcium and magnesium handling in the kidney
-
Hebert S.C. Extracellular calcium-sensing receptor: implications for calcium and magnesium handling in the kidney. Kidney Int 50 (1996) 2129-2139
-
(1996)
Kidney Int
, vol.50
, pp. 2129-2139
-
-
Hebert, S.C.1
-
5
-
-
0019788427
-
The hypocalciuric or benign variant of familial hypercalcemia: clinical, and biochemical features in fifteen kindreds
-
Marx S.J., Attie M.F., Levine M.A., Spiegel A.M., Downs Jr. R.W., and Lasker R.D. The hypocalciuric or benign variant of familial hypercalcemia: clinical, and biochemical features in fifteen kindreds. Medicine 60 (1981) 397-412
-
(1981)
Medicine
, vol.60
, pp. 397-412
-
-
Marx, S.J.1
Attie, M.F.2
Levine, M.A.3
Spiegel, A.M.4
Downs Jr., R.W.5
Lasker, R.D.6
-
6
-
-
0021052251
-
Familial benign hypercalcaemia
-
Menko F.H., Bijvoet O.L.M., Fronen J.L.H.H., Sandler L.M., Adami S., O'Riordan J.L.H., et al. Familial benign hypercalcaemia. Q J Med 52 (1983) 120-140
-
(1983)
Q J Med
, vol.52
, pp. 120-140
-
-
Menko, F.H.1
Bijvoet, O.L.M.2
Fronen, J.L.H.H.3
Sandler, L.M.4
Adami, S.5
O'Riordan, J.L.H.6
-
7
-
-
0020516783
-
Urinary calcium excretion in familial hypocalciuric hypercalcemia
-
Attie M.F., Gill J.R., Stock J.L., Spiegel A.M., Downs R.W., Levine M.A., et al. Urinary calcium excretion in familial hypocalciuric hypercalcemia. J Clin Invest 72 (1983) 667-676
-
(1983)
J Clin Invest
, vol.72
, pp. 667-676
-
-
Attie, M.F.1
Gill, J.R.2
Stock, J.L.3
Spiegel, A.M.4
Downs, R.W.5
Levine, M.A.6
-
8
-
-
0017328913
-
Neonatal primary hyperparathyroidism with autosomal dominant inheritance
-
Spiegel A.M., Harrison H.E., Marx S.J., Brown E.M., and Aurbach G.D. Neonatal primary hyperparathyroidism with autosomal dominant inheritance. J Pediatr 90 (1977) 269-272
-
(1977)
J Pediatr
, vol.90
, pp. 269-272
-
-
Spiegel, A.M.1
Harrison, H.E.2
Marx, S.J.3
Brown, E.M.4
Aurbach, G.D.5
-
9
-
-
0020075824
-
An association between neonatal severe primary hyperparathyroidism and familial hypocalciuric hypercalcemia in three kindreds
-
Marx S.J., Attie M.F., Speigel A.M., Levine M.A., Lasker R.D., and Fox M. An association between neonatal severe primary hyperparathyroidism and familial hypocalciuric hypercalcemia in three kindreds. N Engl J Med 306 (1982) 257-264
-
(1982)
N Engl J Med
, vol.306
, pp. 257-264
-
-
Marx, S.J.1
Attie, M.F.2
Speigel, A.M.3
Levine, M.A.4
Lasker, R.D.5
Fox, M.6
-
10
-
-
0019990596
-
Neonatal primary hyperparathyroidism in familial hypocalciuric hypercalcemia
-
Matsuo M., Okita K., Takemine H., and Fujita T. Neonatal primary hyperparathyroidism in familial hypocalciuric hypercalcemia. Am J Dis Child 136 (1982) 728-731
-
(1982)
Am J Dis Child
, vol.136
, pp. 728-731
-
-
Matsuo, M.1
Okita, K.2
Takemine, H.3
Fujita, T.4
-
11
-
-
0022537970
-
Severe primary hyperparathyroidism in a neonate with two hypercalcemic parents: management with parathyroidectomy and heterotopic autotransplantation
-
Cooper L., Wertheimer J., Levey R., Brown E., Leboff M., Wilkinson R., et al. Severe primary hyperparathyroidism in a neonate with two hypercalcemic parents: management with parathyroidectomy and heterotopic autotransplantation. Pediatrics 78 (1986) 263-268
-
(1986)
Pediatrics
, vol.78
, pp. 263-268
-
-
Cooper, L.1
Wertheimer, J.2
Levey, R.3
Brown, E.4
Leboff, M.5
Wilkinson, R.6
-
12
-
-
0021966594
-
Familial hypocalciuric hypercalcemia. Mild expression of the gene in heterozygotes and severe expression in homozygotes
-
Marx S.J., Fraser D., and Rapoport A. Familial hypocalciuric hypercalcemia. Mild expression of the gene in heterozygotes and severe expression in homozygotes. Am J Med 78 (1985) 15-22
-
(1985)
Am J Med
, vol.78
, pp. 15-22
-
-
Marx, S.J.1
Fraser, D.2
Rapoport, A.3
-
14
-
-
0028848215
-
Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism
-
Pearce S.H.S., Trump D., Wooding C., Besser G.M., Chew S.L., Grant D.B., et al. Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism. J Clin Invest 96 (1995) 2683-2692
-
(1995)
J Clin Invest
, vol.96
, pp. 2683-2692
-
-
Pearce, S.H.S.1
Trump, D.2
Wooding, C.3
Besser, G.M.4
Chew, S.L.5
Grant, D.B.6
-
15
-
-
0028220464
-
Familial hypocalciuiric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype
-
Pollak M.R., Chou Y.-H.W., Marx S.J., Steinman B., Cole D.E.C., Brandi M.L., et al. Familial hypocalciuiric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype. J Clin Invest 93 (1994) 1108-1112
-
(1994)
J Clin Invest
, vol.93
, pp. 1108-1112
-
-
Pollak, M.R.1
Chou, Y.-H.W.2
Marx, S.J.3
Steinman, B.4
Cole, D.E.C.5
Brandi, M.L.6
-
16
-
-
0019990596
-
Neonatal primary hyperparathyroidism in familial hypocalciuric hypercalcemia
-
Matsuo M., Okita K., Takemine H., and Fujita T. Neonatal primary hyperparathyroidism in familial hypocalciuric hypercalcemia. Am J Dis Child 136 (1982) 728-731
-
(1982)
Am J Dis Child
, vol.136
, pp. 728-731
-
-
Matsuo, M.1
Okita, K.2
Takemine, H.3
Fujita, T.4
-
17
-
-
14044254270
-
Mutant extracellular calcium-sensing receptors and severity of disease [editorial]
-
Brown E.M. Mutant extracellular calcium-sensing receptors and severity of disease [editorial]. J Clin Endocrinol Metab 90 (2005) 1246-1248
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 1246-1248
-
-
Brown, E.M.1
-
18
-
-
0028037143
-
Autosomal dominant hypocalcemia cause by a Ca2+-sensing receptor gene mutation
-
Pollak M.R., Brown E.M., Estep H.L., McLaine P.N., Kifor O., Park J., et al. Autosomal dominant hypocalcemia cause by a Ca2+-sensing receptor gene mutation. Nat Genet 8 (1994) 303-307
-
(1994)
Nat Genet
, vol.8
, pp. 303-307
-
-
Pollak, M.R.1
Brown, E.M.2
Estep, H.L.3
McLaine, P.N.4
Kifor, O.5
Park, J.6
-
19
-
-
10144256536
-
A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor
-
Pearce S.H.S., Williamson C., Kifor O., Bai M., Coulthard M.G., Davies M., et al. A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor. N Engl J Med 335 (1996) 1115-1122
-
(1996)
N Engl J Med
, vol.335
, pp. 1115-1122
-
-
Pearce, S.H.S.1
Williamson, C.2
Kifor, O.3
Bai, M.4
Coulthard, M.G.5
Davies, M.6
-
20
-
-
0037206034
-
Association between activating mutations of calcium-sensing receptor and Bartter's syndrome
-
Watanabe S., Fukumoto S., Chang H., Takeuchi Y., Hasgawa Y., Okazaki R., et al. Association between activating mutations of calcium-sensing receptor and Bartter's syndrome. Lancet 360 (2002) 692-694
-
(2002)
Lancet
, vol.360
, pp. 692-694
-
-
Watanabe, S.1
Fukumoto, S.2
Chang, H.3
Takeuchi, Y.4
Hasgawa, Y.5
Okazaki, R.6
-
21
-
-
67650119128
-
The calcium-sensing receptor
-
Alpern R.J., and Hebert S.C. (Eds), Elsevier Saunders, Philadelphia
-
Hebert S.C., Riccardi D., and Geibel J.P. The calcium-sensing receptor. In: Alpern R.J., and Hebert S.C. (Eds). Seldin and Giebisch's the kidney. 3rd ed. Vol 2 (2008), Elsevier Saunders, Philadelphia 1785-1802
-
(2008)
Seldin and Giebisch's the kidney. 3rd ed.
, vol.2
, pp. 1785-1802
-
-
Hebert, S.C.1
Riccardi, D.2
Geibel, J.P.3
-
22
-
-
12144285037
-
The calcium-sensing receptor: a key factor in the pathogenesis of secondary hyperparathyroidism
-
Rodriguez M., Nemeth E., and Martin D. The calcium-sensing receptor: a key factor in the pathogenesis of secondary hyperparathyroidism. Am J Physiol Renal Physiol 288 (2005) F253-F264
-
(2005)
Am J Physiol Renal Physiol
, vol.288
-
-
Rodriguez, M.1
Nemeth, E.2
Martin, D.3
-
23
-
-
0031727116
-
Calcium-sensing by parathyroid glands in secondary hyperparathyroidism
-
Goodman W.G., Veldhuis J.D., Belin T.R., Van Herle A.J., Juppner H., and Salusky I.B. Calcium-sensing by parathyroid glands in secondary hyperparathyroidism. J Clin Endocrinal Metab 83 (1998) 2765-2772
-
(1998)
J Clin Endocrinal Metab
, vol.83
, pp. 2765-2772
-
-
Goodman, W.G.1
Veldhuis, J.D.2
Belin, T.R.3
Van Herle, A.J.4
Juppner, H.5
Salusky, I.B.6
-
24
-
-
29144431716
-
Effects of the calcimimetic cinacalcet HCl on cardiovascular disease, fracture, and health-related quality of life in secondary hyperparathyroidism
-
Cunningham J., Danese M., Olson K., Klassen P., and Chertow G.M. Effects of the calcimimetic cinacalcet HCl on cardiovascular disease, fracture, and health-related quality of life in secondary hyperparathyroidism. Kidney Int 68 (2005) 1793-1800
-
(2005)
Kidney Int
, vol.68
, pp. 1793-1800
-
-
Cunningham, J.1
Danese, M.2
Olson, K.3
Klassen, P.4
Chertow, G.M.5
-
25
-
-
47349115283
-
Calcimimetics in chronic kidney disease: evidence, opportunities and challenges
-
Evennpoel P. Calcimimetics in chronic kidney disease: evidence, opportunities and challenges. Kidney Int 74 (2008) 265-275
-
(2008)
Kidney Int
, vol.74
, pp. 265-275
-
-
Evennpoel, P.1
-
26
-
-
44649135371
-
Calcimimetics as an adjunctive treatment for familial hypophosphatemic rickets
-
Alon U., Levy-Olomucki R., Moore W.V., Stubbs J., Liu S., and Quarles L.D. Calcimimetics as an adjunctive treatment for familial hypophosphatemic rickets. Clin J Am Soc Nephrol 3 (2008) 658-664
-
(2008)
Clin J Am Soc Nephrol
, vol.3
, pp. 658-664
-
-
Alon, U.1
Levy-Olomucki, R.2
Moore, W.V.3
Stubbs, J.4
Liu, S.5
Quarles, L.D.6
-
27
-
-
51549114722
-
Cinacalcet is efficacious in pediatric dialysis patients
-
Silverstein D., Kher K.K., Moudgil A., Khurana M., Wilcox J., and Moylan K. Cinacalcet is efficacious in pediatric dialysis patients. Pediatr Nephrol 23 (2008) 1817-1822
-
(2008)
Pediatr Nephrol
, vol.23
, pp. 1817-1822
-
-
Silverstein, D.1
Kher, K.K.2
Moudgil, A.3
Khurana, M.4
Wilcox, J.5
Moylan, K.6
-
28
-
-
51549087339
-
Cinacalcet for secondary hyperparathyroidism in children with end-stage renal disease
-
Muscheites J., Wigger M., Druekler E., Fischer D.-C., Kundt G., and Haffner D. Cinacalcet for secondary hyperparathyroidism in children with end-stage renal disease. Pediatr Nephrol 23 (2008) 1823-1829
-
(2008)
Pediatr Nephrol
, vol.23
, pp. 1823-1829
-
-
Muscheites, J.1
Wigger, M.2
Druekler, E.3
Fischer, D.-C.4
Kundt, G.5
Haffner, D.6
-
29
-
-
0033775213
-
Proximal tubular phosphate reabsorption: molecular mechanisms
-
Murer H., Hernando N., Forster I., and Biber J. Proximal tubular phosphate reabsorption: molecular mechanisms. Physiol Rev 80 (2000) 1373-1409
-
(2000)
Physiol Rev
, vol.80
, pp. 1373-1409
-
-
Murer, H.1
Hernando, N.2
Forster, I.3
Biber, J.4
-
30
-
-
0033763097
-
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
-
The ADHR Consortium
-
The ADHR Consortium. Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23. Nat Genet 26 (2000) 345-348
-
(2000)
Nat Genet
, vol.26
, pp. 345-348
-
-
-
31
-
-
33845631059
-
Klotho converts canonical FGF receptor into a specific receptor for FGF23
-
Urakawa I., Yamazaki Y., Shimada T., Iijima K., Hasegawa H., Okawa K., et al. Klotho converts canonical FGF receptor into a specific receptor for FGF23. Nature 444 (2006) 770-774
-
(2006)
Nature
, vol.444
, pp. 770-774
-
-
Urakawa, I.1
Yamazaki, Y.2
Shimada, T.3
Iijima, K.4
Hasegawa, H.5
Okawa, K.6
-
32
-
-
14344279878
-
Cloning and characterization of FGF23 as a causative factor of tumor-induced osteomalacia
-
Shimada T., Mizutani S., Muto T., Yoneya T., Hino R., Takeda S., et al. Cloning and characterization of FGF23 as a causative factor of tumor-induced osteomalacia. Proc Natl Acad Sci U S A 98 (2001) 6500-6505
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 6500-6505
-
-
Shimada, T.1
Mizutani, S.2
Muto, T.3
Yoneya, T.4
Hino, R.5
Takeda, S.6
-
33
-
-
0029160578
-
A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets
-
The HYP Consortium
-
The HYP Consortium. A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. Nat Genet 11 (1995) 130-136
-
(1995)
Nat Genet
, vol.11
, pp. 130-136
-
-
-
34
-
-
20244368616
-
Fibroblast growth factor 23 in oncogenic osteomalacia and X-linked hypophosphatemia
-
Jonsson K.B., Zahradnik R., Larsson T., White K.E., Sugimoto T., Imanishi Y., et al. Fibroblast growth factor 23 in oncogenic osteomalacia and X-linked hypophosphatemia. N Engl J Med 348 (2003) 1656-1663
-
(2003)
N Engl J Med
, vol.348
, pp. 1656-1663
-
-
Jonsson, K.B.1
Zahradnik, R.2
Larsson, T.3
White, K.E.4
Sugimoto, T.5
Imanishi, Y.6
-
35
-
-
27844501565
-
Dietary and serum phosphorus regulate fibroblast growth factor 23 expression and 1,25-dihydroxyvitamin D metabolism in mice
-
Perwad F., Azam N., Zhang M.Y., Yamashita T., Tenenhouse H.S., and Portale A.A. Dietary and serum phosphorus regulate fibroblast growth factor 23 expression and 1,25-dihydroxyvitamin D metabolism in mice. Endocrinology 146 (2005) 5358-5364
-
(2005)
Endocrinology
, vol.146
, pp. 5358-5364
-
-
Perwad, F.1
Azam, N.2
Zhang, M.Y.3
Yamashita, T.4
Tenenhouse, H.S.5
Portale, A.A.6
-
36
-
-
0031035615
-
Autosomal dominant hypophosphatemic rickets/osteomalacia: clinical characterization of a novel renal phosphate-wasting disorder
-
Econs M.J., and McEnery P.T. Autosomal dominant hypophosphatemic rickets/osteomalacia: clinical characterization of a novel renal phosphate-wasting disorder. J Clin Endocrinol Metab 82 (1997) 674-681
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 674-681
-
-
Econs, M.J.1
McEnery, P.T.2
-
37
-
-
34249664523
-
FGF23 concentrations vary with disease status in autosomal dominant hypophosphatemic rickets
-
Imel E.A., Hui S.L., and Econs M.J. FGF23 concentrations vary with disease status in autosomal dominant hypophosphatemic rickets. J Bone Miner Res 22 (2007) 520-526
-
(2007)
J Bone Miner Res
, vol.22
, pp. 520-526
-
-
Imel, E.A.1
Hui, S.L.2
Econs, M.J.3
-
38
-
-
0035703765
-
Loss of renal phosphate wasting in a child with autosomal dominant hypophosphatemic rickets caused by a FGF23 mutation
-
Kruse K., Woelfel D., Strom T.M., and Storm T.M. Loss of renal phosphate wasting in a child with autosomal dominant hypophosphatemic rickets caused by a FGF23 mutation. Horm Res 55 (2001) 305-308
-
(2001)
Horm Res
, vol.55
, pp. 305-308
-
-
Kruse, K.1
Woelfel, D.2
Strom, T.M.3
Storm, T.M.4
-
39
-
-
0035186837
-
Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23
-
White K.E., Carn G., Lorenz-Depiereux B., Benet-Pages A., Strom T.M., and Econs M.J. Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23. Kidney Int 60 (2001) 2079-2086
-
(2001)
Kidney Int
, vol.60
, pp. 2079-2086
-
-
White, K.E.1
Carn, G.2
Lorenz-Depiereux, B.3
Benet-Pages, A.4
Strom, T.M.5
Econs, M.J.6
-
40
-
-
0019430590
-
Autosomal hypophosphataemic bone disease responds to 1,25-(OH)2D3
-
Scriver C.R., Reade T., Halal F., Costa T., and Cole D.E. Autosomal hypophosphataemic bone disease responds to 1,25-(OH)2D3. Arch Dis Child 56 (1981) 203-207
-
(1981)
Arch Dis Child
, vol.56
, pp. 203-207
-
-
Scriver, C.R.1
Reade, T.2
Halal, F.3
Costa, T.4
Cole, D.E.5
-
41
-
-
33750427897
-
DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis
-
Lorenz-Depiereux B., Bastepe M., et-Pages A., Amyere M., Wagenstaller J., Muller-Barth U., et al. DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis. Nat Genet 38 (2006) 1248-1250
-
(2006)
Nat Genet
, vol.38
, pp. 1248-1250
-
-
Lorenz-Depiereux, B.1
Bastepe, M.2
et-Pages, A.3
Amyere, M.4
Wagenstaller, J.5
Muller-Barth, U.6
-
42
-
-
33750454816
-
Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism
-
Feng J.Q., Ward L.M., Liu S., Lu Y., Xie Y., Yuan B., et al. Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism. Nat Genet 38 (2006) 1310-1315
-
(2006)
Nat Genet
, vol.38
, pp. 1310-1315
-
-
Feng, J.Q.1
Ward, L.M.2
Liu, S.3
Lu, Y.4
Xie, Y.5
Yuan, B.6
-
43
-
-
20044383563
-
Dmp1-deficient mice display severe defects in cartilage formation responsible for a chondrodysplasia-like phenotype
-
Ye L., Mishina Y., Chen D., Huang H., Dallas S.L., Dallas M.R., et al. Dmp1-deficient mice display severe defects in cartilage formation responsible for a chondrodysplasia-like phenotype. J Biol Chem 280 (2005) 6197-6203
-
(2005)
J Biol Chem
, vol.280
, pp. 6197-6203
-
-
Ye, L.1
Mishina, Y.2
Chen, D.3
Huang, H.4
Dallas, S.L.5
Dallas, M.R.6
-
44
-
-
0022002364
-
Hereditary hypophosphatemic rickets with hypercalciuria
-
Tieder M., Modai D., Samuel R., Arie R., Halabe A., Bab I., et al. Hereditary hypophosphatemic rickets with hypercalciuria. N Engl J Med 312 (1985) 611-617
-
(1985)
N Engl J Med
, vol.312
, pp. 611-617
-
-
Tieder, M.1
Modai, D.2
Samuel, R.3
Arie, R.4
Halabe, A.5
Bab, I.6
-
45
-
-
31544460435
-
Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3
-
Lorenz-Depiereux B., et-Pages A., Eckstein G., Tenenbaum-Rakover Y., Wagenstaller J., Tiosano D., et al. Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3. Am J Hum Genet 78 (2006) 193-201
-
(2006)
Am J Hum Genet
, vol.78
, pp. 193-201
-
-
Lorenz-Depiereux, B.1
et-Pages, A.2
Eckstein, G.3
Tenenbaum-Rakover, Y.4
Wagenstaller, J.5
Tiosano, D.6
-
46
-
-
0028363099
-
Tumor-induced osteomalacia-unveiling a new hormone
-
Econs M.J., and Drezner M.K. Tumor-induced osteomalacia-unveiling a new hormone. N Engl J Med 330 (1994) 1679-1681
-
(1994)
N Engl J Med
, vol.330
, pp. 1679-1681
-
-
Econs, M.J.1
Drezner, M.K.2
-
47
-
-
33845964211
-
Oncogenic osteomalacia: exact tumor localization by co-registration of positron emission and computed tomography
-
Hesse E., Moessinger E., Rosenthal H., Laenger F., Brabant G., Petrich T., et al. Oncogenic osteomalacia: exact tumor localization by co-registration of positron emission and computed tomography. J Bone Miner Res 22 (2007) 158-162
-
(2007)
J Bone Miner Res
, vol.22
, pp. 158-162
-
-
Hesse, E.1
Moessinger, E.2
Rosenthal, H.3
Laenger, F.4
Brabant, G.5
Petrich, T.6
-
48
-
-
2642546399
-
Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis
-
Topaz O., Shurman D.L., Bergman R., Indelman M., Ratajczak P., Mizrachi M., et al. Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis. Nat Genet 36 (2004) 579-581
-
(2004)
Nat Genet
, vol.36
, pp. 579-581
-
-
Topaz, O.1
Shurman, D.L.2
Bergman, R.3
Indelman, M.4
Ratajczak, P.5
Mizrachi, M.6
-
49
-
-
3242656464
-
FGF23 is processed by proprotein convertases but not by PHEX
-
Benet-Pages A., Lorenz-Depiereux B., Zischka H., White K.E., Econs M.J., and Strom T.M. FGF23 is processed by proprotein convertases but not by PHEX. Bone 35 (2004) 455-462
-
(2004)
Bone
, vol.35
, pp. 455-462
-
-
Benet-Pages, A.1
Lorenz-Depiereux, B.2
Zischka, H.3
White, K.E.4
Econs, M.J.5
Strom, T.M.6
-
50
-
-
23844457598
-
Fibroblast growth factor-23 mutants causing familial tumoral calcinosis are differentially processed
-
Larsson T., Davis S.I., Garringer H.J., Mooney S.D., Draman M.S., Cullen M.J., et al. Fibroblast growth factor-23 mutants causing familial tumoral calcinosis are differentially processed. Endocrinology 146 (2005) 3883-3891
-
(2005)
Endocrinology
, vol.146
, pp. 3883-3891
-
-
Larsson, T.1
Davis, S.I.2
Garringer, H.J.3
Mooney, S.D.4
Draman, M.S.5
Cullen, M.J.6
-
51
-
-
43749088566
-
A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis
-
Ichikawa S., Imel E.A., Kreiter M.L., Yu X., Mackenzie D.S., Sorenson A.H., et al. A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis. J Musculoskelet Neuronal Interact 7 (2007) 318-319
-
(2007)
J Musculoskelet Neuronal Interact
, vol.7
, pp. 318-319
-
-
Ichikawa, S.1
Imel, E.A.2
Kreiter, M.L.3
Yu, X.4
Mackenzie, D.S.5
Sorenson, A.H.6
-
52
-
-
34250649644
-
The emerging role of the fibroblast growth factor-23-klotho axis in renal regulation of phosphate homeostasis
-
Razzaque M.S., and Lanske B. The emerging role of the fibroblast growth factor-23-klotho axis in renal regulation of phosphate homeostasis. J Endocrinol 194 (2007) 1-10
-
(2007)
J Endocrinol
, vol.194
, pp. 1-10
-
-
Razzaque, M.S.1
Lanske, B.2
-
53
-
-
0344945402
-
Circulating concentration of FGF-23 increases as renal function declines in patients with chronic kidney disease, but does not change in response to variation in phosphate intake in healthy volunteers
-
Larsson T., Nisbeth U., Ljunggren O., Juppner H., and Jonsson K.B. Circulating concentration of FGF-23 increases as renal function declines in patients with chronic kidney disease, but does not change in response to variation in phosphate intake in healthy volunteers. Kidney Int 64 (2003) 2272-2279
-
(2003)
Kidney Int
, vol.64
, pp. 2272-2279
-
-
Larsson, T.1
Nisbeth, U.2
Ljunggren, O.3
Juppner, H.4
Jonsson, K.B.5
-
54
-
-
2342481131
-
FGF-23 in patients with end-stage renal disease on hemodialysis
-
Imanishi Y., Inaba M., Nakatsuka K., Nagasue K., Okuno S., Yoshihara A., et al. FGF-23 in patients with end-stage renal disease on hemodialysis. Kidney Int 65 (2004) 1943-1946
-
(2004)
Kidney Int
, vol.65
, pp. 1943-1946
-
-
Imanishi, Y.1
Inaba, M.2
Nakatsuka, K.3
Nagasue, K.4
Okuno, S.5
Yoshihara, A.6
-
55
-
-
49249104701
-
Fibroblast growth factor 23 and mortality among patients undergoing hemodialysis
-
Gutierrez O.M., Mannstadt M., Isakova T., Rauh-Hain J.A., Tamez H., Shah A., et al. Fibroblast growth factor 23 and mortality among patients undergoing hemodialysis. N Engl J Med 359 (2008) 584-592
-
(2008)
N Engl J Med
, vol.359
, pp. 584-592
-
-
Gutierrez, O.M.1
Mannstadt, M.2
Isakova, T.3
Rauh-Hain, J.A.4
Tamez, H.5
Shah, A.6
-
56
-
-
34548497123
-
Fibroblast growth factor 23 (FGF23) predicts progression of chronic kidney disease: the Mild to Moderate Kidney Disease (MMKD) Study
-
Fliser D., Kollerits B., Neyer U., Ankerst D.P., Lhotta K., Lingenhel A., et al. Fibroblast growth factor 23 (FGF23) predicts progression of chronic kidney disease: the Mild to Moderate Kidney Disease (MMKD) Study. J Am Soc Nephrol 18 (2007) 2600-2608
-
(2007)
J Am Soc Nephrol
, vol.18
, pp. 2600-2608
-
-
Fliser, D.1
Kollerits, B.2
Neyer, U.3
Ankerst, D.P.4
Lhotta, K.5
Lingenhel, A.6
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