-
1
-
-
9144231813
-
Most osteomalacia-associated mesenchymal tumors are a single histopathology entity: An analysis of 32 cases and a comprehensive review of the literature
-
A.L. Folpe, J.C. Fanburg-Smith, S.D. Billings, M. Bisceglia, F. Bertoni, and J.Y. Cho Most osteomalacia-associated mesenchymal tumors are a single histopathology entity: an analysis of 32 cases and a comprehensive review of the literature Am. Surg. Pathol. 28 2004 1 30
-
(2004)
Am. Surg. Pathol.
, vol.28
, pp. 1-30
-
-
Folpe, A.L.1
Fanburg-Smith, J.C.2
Billings, S.D.3
Bisceglia, M.4
Bertoni, F.5
Cho, J.Y.6
-
2
-
-
0347362503
-
The phosphatonin pathway: New insights in phosphate homeostasis
-
S.C. SchiavI, and R. Kumar The phosphatonin pathway: new insights in phosphate homeostasis Kidney Int. 65 2004 1 14
-
(2004)
Kidney Int.
, vol.65
, pp. 1-14
-
-
SchiavI, S.C.1
Kumar, R.2
-
3
-
-
0037464509
-
Oncogenic osteomalacia. A complex dance of factors
-
T.O. Carpenter Oncogenic osteomalacia. A complex dance of factors New Engl. J. Med. 348 2003 1705 1708
-
(2003)
New Engl. J. Med.
, vol.348
, pp. 1705-1708
-
-
Carpenter, T.O.1
-
4
-
-
20244368616
-
Fibroblast Growth Factor in oncogenic osteomalacia and X-linked hypophosphatemia
-
K.B. Jonsson, R. Zahradnik, T. Larsson, K.E. White, T. Sugimoto, and Y. Imahishy Fibroblast Growth Factor in oncogenic osteomalacia and X-linked hypophosphatemia New Engl. J. Med. 348 2003 1655 1663
-
(2003)
New Engl. J. Med.
, vol.348
, pp. 1655-1663
-
-
Jonsson, K.B.1
Zahradnik, R.2
Larsson, T.3
White, K.E.4
Sugimoto, T.5
Imahishy, Y.6
-
5
-
-
14344279878
-
Cloning and characterisation of FGF-23 as a causative factor of tumor-induced osteomalacia
-
T. Shimada, S. Mizutani, T. Muto, T. Yoneya, R. Hino, and S. Takeda Cloning and characterisation of FGF-23 as a causative factor of tumor-induced osteomalacia Proc. Natl. Acad. Sci. USA 98 2001 6500 6505
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 6500-6505
-
-
Shimada, T.1
Mizutani, S.2
Muto, T.3
Yoneya, T.4
Hino, R.5
Takeda, S.6
-
6
-
-
0141525564
-
Serum FGF-23 levels in normal and disordered phosphorus homeostasis
-
T.J. Weber, S. Liu, O. Indridason, and L.D. Quarles Serum FGF-23 levels in normal and disordered phosphorus homeostasis J. Bone Miner. Res. 18 2003 1227 1234
-
(2003)
J. Bone Miner. Res.
, vol.18
, pp. 1227-1234
-
-
Weber, T.J.1
Liu, S.2
Indridason, O.3
Quarles, L.D.4
-
7
-
-
0032916730
-
111 pentetreotide scintigraphy of mesenchymal tumor with oncogenic osteomalacia
-
111 pentetreotide scintigraphy of mesenchymal tumor with oncogenic osteomalacia Clin. Nucl. Med. 24 1999 130 131
-
(1999)
Clin. Nucl. Med.
, vol.24
, pp. 130-131
-
-
Nguyen, B.D.1
Wang, E.A.2
-
8
-
-
0042700023
-
A case of oncogenic osteomalacia detected by 111 IN-pentetreotide total body scan
-
J. Casari, V. Rossi, M. Varenna, M. Gasparini, A. Parafioriti, and A. Failoni A case of oncogenic osteomalacia detected by 111 IN-pentetreotide total body scan Clin. Exp. Rheumatol. 21 2003 493 496
-
(2003)
Clin. Exp. Rheumatol.
, vol.21
, pp. 493-496
-
-
Casari, J.1
Rossi, V.2
Varenna, M.3
Gasparini, M.4
Parafioriti, A.5
Failoni, A.6
-
9
-
-
1642602714
-
Acquisition protocol considerations for combined PET/CT imaging
-
T. Beyer, G. Antoch, S. Muller, T. Egelhof, L.S. Freudenberg, and J. Debatin Acquisition protocol considerations for combined PET/CT imaging J. Nucl. Med. 45 suppl 1 2004 25S 35S
-
(2004)
J. Nucl. Med.
, vol.45
, Issue.1 SUPPL.
-
-
Beyer, T.1
Antoch, G.2
Muller, S.3
Egelhof, T.4
Freudenberg, L.S.5
Debatin, J.6
-
12
-
-
0021991454
-
Oncogenic osteomalacia: Strange tumor in strange places
-
D. Weiss, R.S. Bar, N. Weidner, M. Wener, and F. Lee Oncogenic osteomalacia: strange tumor in strange places Post-Graduate Med. J. 61 1985 349 355
-
(1985)
Post-Graduate Med. J.
, vol.61
, pp. 349-355
-
-
Weiss, D.1
Bar, R.S.2
Weidner, N.3
Wener, M.4
Lee, F.5
-
14
-
-
0023118664
-
Phosphaturic mesenchymal tumors:: A polymorphous group causing osteomalacia or rickets
-
N. Weidner, and D. Santa Cruz Phosphaturic mesenchymal tumors:: a polymorphous group causing osteomalacia or rickets Cancer 59 1987 1442 1454
-
(1987)
Cancer
, vol.59
, pp. 1442-1454
-
-
Weidner, N.1
Santa Cruz, D.2
-
15
-
-
85047693146
-
Secreted frizzled-related protein 4 is a potent tumor-derived phosphaturic agent
-
T. Berndt, T.A. Craig, A.E. Bowe, J. Vassiliadis, D. Reczek, and R. Finnegan Secreted frizzled-related protein 4 is a potent tumor-derived phosphaturic agent J. Clin. Invest. 112 2003 785 794
-
(2003)
J. Clin. Invest.
, vol.112
, pp. 785-794
-
-
Berndt, T.1
Craig, T.A.2
Bowe, A.E.3
Vassiliadis, J.4
Reczek, D.5
Finnegan, R.6
-
16
-
-
10744226781
-
MEPE has the properties of an osteoblastic phosphatonin and minhibin
-
P.S.N. Rowe, Y. Kumagai, G. Gutierrez, I.R. Garret, R. Blacher, and D. Rosen MEPE has the properties of an osteoblastic phosphatonin and minhibin Bone 34 2004 303 319
-
(2004)
Bone
, vol.34
, pp. 303-319
-
-
Rowe, P.S.N.1
Kumagai, Y.2
Gutierrez, G.3
Garret, I.R.4
Blacher, R.5
Rosen, D.6
-
17
-
-
17744395066
-
The autosomal dominant hypophosphatemic rickets (ADHR) gene is a secreted polypeptide overexpressed by tumors that cause phosphate wasting
-
K.E. White, K.B. Jonsson, G. Carn, G. Hampson, T.D. Spector, and M. Mannstadt The autosomal dominant hypophosphatemic rickets (ADHR) gene is a secreted polypeptide overexpressed by tumors that cause phosphate wasting J. Clin. Endocrinol. Metab. 86 2001 497 500
-
(2001)
J. Clin. Endocrinol. Metab.
, vol.86
, pp. 497-500
-
-
White, K.E.1
Jonsson, K.B.2
Carn, G.3
Hampson, G.4
Spector, T.D.5
Mannstadt, M.6
-
18
-
-
2342648890
-
Resolution of severe, adolescent-onset hypophosphatemic rickets following resection of an FGF-23 producing tumor of the distal ulna
-
L.M. Ward, F. Raunch, K.E. White, G. Filler, M.A. Matzinger, and M. Letts Resolution of severe, adolescent-onset hypophosphatemic rickets following resection of an FGF-23 producing tumor of the distal ulna Bone 34 2004 905 911
-
(2004)
Bone
, vol.34
, pp. 905-911
-
-
Ward, L.M.1
Raunch, F.2
White, K.E.3
Filler, G.4
Matzinger, M.A.5
Letts, M.6
-
19
-
-
18744371012
-
Increased circulatory level of biologically active full-length FGF-23 in patients with hypophosphoremic rickets-osteomalacia
-
Y. Yamazaki, R. Okazaki, M. Shibata, Y. Hasegawa, K. Satoh, and T. Tajima Increased circulatory level of biologically active full-length FGF-23 in patients with hypophosphoremic rickets-osteomalacia J. Clin. Endocrinol. Metab. 87 2002 4957 4960
-
(2002)
J. Clin. Endocrinol. Metab.
, vol.87
, pp. 4957-4960
-
-
Yamazaki, Y.1
Okazaki, R.2
Shibata, M.3
Hasegawa, Y.4
Satoh, K.5
Tajima, T.6
-
20
-
-
4043052503
-
Venous sampling for Fibroblast Growth Factor 23 confims preoperative diagnosis of tumor-induced osteomalacia
-
Y. Takeuchy, H. Suzuki, S. Ogura, R. Imai, Y. Yamashita, and T. Yamashita Venous sampling for Fibroblast Growth Factor 23 confims preoperative diagnosis of tumor-induced osteomalacia J. Clin. Endocrinol. Metab. 89 2004 3979 3982
-
(2004)
J. Clin. Endocrinol. Metab.
, vol.89
, pp. 3979-3982
-
-
Takeuchy, Y.1
Suzuki, H.2
Ogura, S.3
Imai, R.4
Yamashita, Y.5
Yamashita, T.6
-
21
-
-
0034805353
-
FGF-23 inhibits renal tubular phosphate transport and is a PHEX substrate
-
A.E. Bowe, R. Finnegan, S.M. Jan de beur, J. Cho, M.A. Levine, and R. Kumar FGF-23 inhibits renal tubular phosphate transport and is a PHEX substrate Biochem. Biophys. Res. Commun. 284 2001 977 981
-
(2001)
Biochem. Biophys. Res. Commun.
, vol.284
, pp. 977-981
-
-
Bowe, A.E.1
Finnegan, R.2
Jan de beur, S.M.3
Cho, J.4
Levine, M.A.5
Kumar, R.6
-
22
-
-
18444375871
-
Mutant FGF-23 responsible for autosomal dominant hypophosphatemia is resistant to proteolytic cleavage and causes hypophosphatemia in vivo
-
T. Shimida, T. Muto, T. Urukawa, T. Yoneya, Y. Yamazaki, and K. Okawa Mutant FGF-23 responsible for autosomal dominant hypophosphatemia is resistant to proteolytic cleavage and causes hypophosphatemia in vivo Endocrinology 143 2002 3179 3182
-
(2002)
Endocrinology
, vol.143
, pp. 3179-3182
-
-
Shimida, T.1
Muto, T.2
Urukawa, T.3
Yoneya, T.4
Yamazaki, Y.5
Okawa, K.6
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