-
1
-
-
0034700450
-
Hyperparathyroid and hypoparathyroid disorders
-
S.J. Marx, Hyperparathyroid and hypoparathyroid disorders. N. Engl. J. Med. 343, 1863-1865 (2000)
-
(2000)
N. Engl. J. Med.
, vol.343
, pp. 1863-1865
-
-
Marx, S.J.1
-
3
-
-
56749107613
-
Parathyroid carcinoma
-
C. Marcocci, F. Cetani, M.R. Rubin, S.J. Silverberg, A. Pinchera, J.P. Bilezikian, Parathyroid carcinoma. J. Bone Miner. Res. 23, 1869-1880 (2008)
-
(2008)
J. Bone Miner. Res.
, vol.23
, pp. 1869-1880
-
-
Marcocci, C.1
Cetani, F.2
Rubin, M.R.3
Silverberg, S.J.4
Pinchera, A.5
Bilezikian, J.P.6
-
5
-
-
0015590315
-
Parathyroid carcinoma. A study of 70 cases
-
B. Schantz, B. Castleman, Parathyroid carcinoma. A study of 70 cases. Cancer 31, 600-605 (1973)
-
(1973)
Cancer
, vol.31
, pp. 600-605
-
-
Schantz, B.1
Castleman, B.2
-
6
-
-
24344493254
-
Parathyroid carcinoma in pathology and genetics of tumours of endocrine organs
-
Ed. By R.A. DeLellis R.V. Lloyd P.U. Heitz C. Eng (IARC Press Lyon 2004
-
L. Bondeson, L. Grimelius, R.A. DeLellis, R. Lloyd, G. Akerstrom, C. Larsson, A. Arnold, C. Eng, E. Shane, J.P. Bilezikian, Parathyroid carcinoma, in Pathology and genetics of tumours of endocrine organs. WHO classification of tumours, ed. by R.A. DeLellis, R.V. Lloyd, P.U. Heitz, C. Eng (IARC Press, Lyon, 2004), pp. 124-127
-
WHO Classification Of Tumours
, pp. 124-127
-
-
Bondeson, L.1
Grimelius, L.2
DeLellis, R.A.3
Lloyd, R.4
Akerstrom, G.5
Larsson, C.6
Arnold, A.7
Eng, C.8
Shane, E.9
Bilezikian, J.P.10
-
7
-
-
60749129611
-
Challenging lesions in the differential diagnosis of endocrine tumors: Parathyroid carcinoma
-
R.A. DeLellis, Challenging lesions in the differential diagnosis of endocrine tumors: Parathyroid carcinoma. Endocr. Pathol. 19, 221-225 (2008)
-
(2008)
Endocr. Pathol.
, vol.19
, pp. 221-225
-
-
DeLellis, R.A.1
-
8
-
-
18744385803
-
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome
-
J.D. Carpten, C.M. Robbins, A. Villablanca, L. Forsberg, S. Presciuttini, J. Bailey-Wilson, W.F. Simonds, E.M. Gillanders, A.M. Kennedy, J.D. Chen, S.K. Agarwal, R. Sood, M.P. Jones, T.Y. Moses, C. Haven, D. Petillo, P.D. Leotlela, B. Harding, D. Cameron, A.A. Pannett, A. Höög, H. Heath 3rd, L.A. James-Newton, B. Robinson, R.J. Zarbo, B.M. Cavaco, W. Wassif, N.D. Perrier, I.B. Rosen, U. Kristoffersson, P.D. Turnpenny, L.O. Farnebo, G.M. Besser, C.E. Jackson, H. Morreau, J.M. Trent, R.V. Thakker, S.J. Marx, B.T. Teh, C. Larsson, M.R. Hobbs, HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome. Nat. Genet. 32, 676-680 (2002)
-
(2002)
Nat. Genet.
, vol.32
, pp. 676-680
-
-
Carpten, J.D.1
Robbins, C.M.2
Villablanca, A.3
Forsberg, L.4
Presciuttini, S.5
Bailey-Wilson, J.6
Simonds, W.F.7
Gillanders, E.M.8
Kennedy, A.M.9
Chen, J.D.10
Agarwal, S.K.11
Sood, R.12
Jones, M.P.13
Moses, T.Y.14
Haven, C.15
Petillo, D.16
Leotlela, P.D.17
Harding, B.18
Cameron, D.19
Pannett, A.A.20
Höög, A.21
Heath III, H.22
James-Newton, L.A.23
Robinson, B.24
Zarbo, R.J.25
Cavaco, B.M.26
Wassif, W.27
Perrier, N.D.28
Rosen, I.B.29
Kristoffersson, U.30
Turnpenny, P.D.31
Farnebo, L.O.32
Besser, G.M.33
Jackson, C.E.34
Morreau, H.35
Trent, J.M.36
Thakker, R.V.37
Marx, S.J.38
Teh, B.T.39
Larsson, C.40
Hobbs, M.R.41
more..
-
9
-
-
77149133985
-
Cell division cycle protein 73 homolog (CDC73) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors
-
P.J. Newey, M.R. Bowl, T. Cranston, R.V. Thakker, Cell division cycle protein 73 homolog (CDC73) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors. Hum. Mutat. 31, 295-307 (2010)
-
(2010)
Hum. Mutat.
, vol.31
, pp. 295-307
-
-
Newey, P.J.1
Bowl, M.R.2
Cranston, T.3
Thakker, R.V.4
-
10
-
-
0142213734
-
Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma
-
T.M. Shattuck, S. Valimäki, T. Obara, R.D. Gaz, O.H. Clark, D. Shoback, M.E. Wierman, K. Tojo, C.M. Robbins, J.D. Carpten, L.O. Farnebo, C. Larsson, A. Arnold, Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma. N. Engl. J. Med. 349, 1722-1729 (2003)
-
(2003)
N. Engl. J. Med.
, vol.349
, pp. 1722-1729
-
-
Shattuck, T.M.1
Valimäki, S.2
Obara, T.3
Gaz, R.D.4
Clark, O.H.5
Shoback, D.6
Wierman, M.E.7
Tojo, K.8
Robbins, C.M.9
Carpten, J.D.10
Farnebo, L.O.11
Larsson, C.12
Arnold, A.13
-
11
-
-
34547812591
-
Parafibromin immunoreactivity: Its use as an additional diagnostic marker for parathyroid tumor classification
-
C.C. Juhlin, A. Villablanca, K. Sandelin, F. Haglund, J. Nordenstrom, L. Forsberg, L. Branstrom, T. Obara, A. Arnold, C. Larsson, A. Höög, Parafibromin immunoreactivity: Its use as an additional diagnostic marker for parathyroid tumor classification. Endocr. Relat. Cancer 14, 501-512 (2007)
-
(2007)
Endocr. Relat. Cancer
, vol.14
, pp. 501-512
-
-
Juhlin, C.C.1
Villablanca, A.2
Sandelin, K.3
Haglund, F.4
Nordenstrom, J.5
Forsberg, L.6
Branstrom, L.7
Obara, T.8
Arnold, A.9
Larsson, C.10
Höög, A.11
-
12
-
-
34249041993
-
Should parafibromin staining replace HRPT2 gene analysis as an additional tool for histologic diagnosis of parathyroid carcinoma?
-
F. Cetani, E. Ambrogini, P. Viacava, E. Pardi, G. Fanelli, A.G. Naccarato, S. Borsari, M. Lemmi, P. Berti, P. Miccoli, A. Pinchera, C. Marcocci, Should parafibromin staining replace HRPT2 gene analysis as an additional tool for histologic diagnosis of parathyroid carcinoma? Eur. J. Endocrinol. 156, 547-554 (2007)
-
(2007)
Eur. J. Endocrinol.
, vol.156
, pp. 547-554
-
-
Cetani, F.1
Ambrogini, E.2
Viacava, P.3
Pardi, E.4
Fanelli, G.5
Naccarato, A.G.6
Borsari, S.7
Lemmi, M.8
Berti, P.9
Miccoli, P.10
Pinchera, A.11
Marcocci, C.12
-
13
-
-
0041328511
-
HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours
-
V.M. Howell, C.J. Haven, K. Kahnoski, S.K. Khoo, D. Petillo, J. Chen, G.J. Fleuren, B.G. Robinson, L.W. Delbridge, J. Philips, A.E. Nelson, U. Krause, K. Hammje, H. Dralle, C. Hoang-Vu, O. Gimm, D.J. Marsh, H. Morreau, B.T. Teh, HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours. J. Med. Genet. 40, 657-663 (2003)
-
(2003)
J. Med. Genet.
, vol.40
, pp. 657-663
-
-
Howell, V.M.1
Haven, C.J.2
Kahnoski, K.3
Khoo, S.K.4
Petillo, D.5
Chen, J.6
Fleuren, G.J.7
Robinson, B.G.8
Delbridge, L.W.9
Philips, J.10
Nelson, A.E.11
Krause, U.12
Hammje, K.13
Dralle, H.14
Hoang-Vu, C.15
Gimm, O.16
Marsh, D.J.17
Morreau, H.18
Teh, B.T.19
-
14
-
-
59749089671
-
Accuracy of combined protein gene product 9.5 and parafibromin markers for immunohistochemical diagnosis of parathyroid carcinoma
-
V.M. Howell, A. Gill, A. Clarkson, A.E. Nelson, R. Dunne, L.W. Delbridge, B.G. Robinson, B.T. Teh, O. Gimm, D.J. Marsh, Accuracy of combined protein gene product 9.5 and parafibromin markers for immunohistochemical diagnosis of parathyroid carcinoma. J. Clin. Endocrinol. Metab. 94, 434-441 (2009)
-
(2009)
J. Clin. Endocrinol. Metab.
, vol.94
, pp. 434-441
-
-
Howell, V.M.1
Gill, A.2
Clarkson, A.3
Nelson, A.E.4
Dunne, R.5
Delbridge, L.W.6
Robinson, B.G.7
Teh, B.T.8
Gimm, O.9
Marsh, D.J.10
-
15
-
-
24344498667
-
HRPT2 mutational analysis of typical sporadic parathyroid adenomas
-
L.J. Krebs, T.M. Shattuck, A. Arnold, HRPT2 mutational analysis of typical sporadic parathyroid adenomas. J. Clin. Endocrinol. Metab. 90, 5505-5507 (2005)
-
(2005)
J. Clin. Endocrinol. Metab.
, vol.90
, pp. 5505-5507
-
-
Krebs, L.J.1
Shattuck, T.M.2
Arnold, A.3
-
16
-
-
8744299920
-
Genetic analysis of the HRPT2 gene in primary hyperparathyroidism: Germline and somatic mutations in familial and sporadic parathyroid tumors
-
F. Cetani, E. Pardi, S. Borsari, P. Viacava, G. Dipollina, L. Cianferotti, E. Ambrogini, E. Gazzerro, G. Colussi, P. Berti, P. Miccoli, A. Pinchera, C. Marcocci, Genetic analysis of the HRPT2 gene in primary hyperparathyroidism: Germline and somatic mutations in familial and sporadic parathyroid tumors. J. Clin. Endocrinol. Metab. 89, 5583-5591 (2004)
-
(2004)
J. Clin. Endocrinol. Metab.
, vol.89
, pp. 5583-5591
-
-
Cetani, F.1
Pardi, E.2
Borsari, S.3
Viacava, P.4
Dipollina, G.5
Cianferotti, L.6
Ambrogini, E.7
Gazzerro, E.8
Colussi, G.9
Berti, P.10
Miccoli, P.11
Pinchera, A.12
Marcocci, C.13
-
17
-
-
5144220874
-
Loss of parafibromin immunoreactivity is a distinguishing feature of parathyroid carcinoma
-
M.H. Tan, C. Morrison, P. Wang, X. Yang, C.J. Haven, C. Zhang, P. Zhao, M.S. Tretiakova, E. Korpi-Hyovalti, J.R. Burgess, K.C. Soo, W.K. Cheah, B. Cao, J. Resau, H. Morreau, B.T. Teh, Loss of parafibromin immunoreactivity is a distinguishing feature of parathyroid carcinoma. Clin. Cancer Res. 10, 6629-6637 (2004)
-
(2004)
Clin. Cancer Res.
, vol.10
, pp. 6629-6637
-
-
Tan, M.H.1
Morrison, C.2
Wang, P.3
Yang, X.4
Haven, C.J.5
Zhang, C.6
Zhao, P.7
Tretiakova, M.S.8
Korpi-Hyovalti, E.9
Burgess, J.R.10
Soo, K.C.11
Cheah, W.K.12
Cao, B.13
Resau, J.14
Morreau, H.15
Teh, B.T.16
-
18
-
-
33748058806
-
Loss of nuclear expression of parafibromin distinguishes parathyroid carcinomas and hyperparathyroidism-jaw tumor (HPT-JT) syndrome-related adenomas from sporadic parathyroid adenomas and hyperplasias
-
A.J. Gill, A. Clarkson, O. Gimm, J. Keil, H. Dralle, V.M. Howell, D.J. Marsh, Loss of nuclear expression of parafibromin distinguishes parathyroid carcinomas and hyperparathyroidism-jaw tumor (HPT-JT) syndrome-related adenomas from sporadic parathyroid adenomas and hyperplasias. Am. J. Surg. Pathol. 30, 1140-1149 (2006)
-
(2006)
Am. J. Surg. Pathol.
, vol.30
, pp. 1140-1149
-
-
Gill, A.J.1
Clarkson, A.2
Gimm, O.3
Keil, J.4
Dralle, H.5
Howell, V.M.6
Marsh, D.J.7
-
19
-
-
77956460947
-
Parafibromin and APC as screening markers for malignant potential in atypical parathyroid adenomas
-
C.C. Juhlin, I.-L. Nilsson, K. Johansson, F. Haglund, A. Villablanca, A. Höög, C. Larsson, Parafibromin and APC as screening markers for malignant potential in atypical parathyroid adenomas. Endocr. Pathol. 21, 166-177 (2010)
-
(2010)
Endocr. Pathol.
, vol.21
, pp. 166-177
-
-
Juhlin, C.C.1
Nilsson, I.-L.2
Johansson, K.3
Haglund, F.4
Villablanca, A.5
Höög, A.6
Larsson, C.7
-
20
-
-
67749122986
-
Immunohistochemical expression of parafibromin is of limited value in distinguishing parathyroid carcinoma from adenoma
-
abstract
-
S. Mangray, K.C. Kurek, E. Sabo, R.A. DeLellis, Immunohistochemical expression of parafibromin is of limited value in distinguishing parathyroid carcinoma from adenoma. Mod. Pathol. 21, 108A (2008). abstract
-
(2008)
Mod. Pathol.
, vol.21
-
-
Mangray, S.1
Kurek, K.C.2
Sabo, E.3
DeLellis, R.A.4
-
21
-
-
59449099285
-
Defining a molecular phenotype for benign and malignant parathyroid tumors
-
G.G. Fernandez-Ranvier, E. Khanafshar, D. Tacha, M. Wong, E. Kebebew, Q.Y. Duh, O.H. Clark, Defining a molecular phenotype for benign and malignant parathyroid tumors. Cancer 115, 334-344 (2009)
-
(2009)
Cancer
, vol.115
, pp. 334-344
-
-
Fernandez-Ranvier, G.G.1
Khanafshar, E.2
Tacha, D.3
Wong, M.4
Kebebew, E.5
Duh, Q.Y.6
Clark, O.H.7
-
22
-
-
33745066836
-
Loss of parafibromin expression in a subset of parathyroid adenomas
-
C.C. Juhlin, C. Larsson, T. Yakoleva, I. Leibiger, B. Leibiger, A. Alimov, G. Weber, A. Hoog, A. Villablanca, Loss of parafibromin expression in a subset of parathyroid adenomas. Endocr. Relat. Cancer 13, 509-523 (2006)
-
(2006)
Endocr. Relat. Cancer
, vol.13
, pp. 509-523
-
-
Juhlin, C.C.1
Larsson, C.2
Yakoleva, T.3
Leibiger, I.4
Leibiger, B.5
Alimov, A.6
Weber, G.7
Hoog, A.8
Villablanca, A.9
-
23
-
-
34548034205
-
Identification of MEN1 and HRPT2 somatic mutations in paraffin-embedded (sporadic) parathyroid carcinomas
-
C.J. Haven, M. van Puijenbroek, M.H. Tan, B.T. Teh, G.J. Fleuren, T. van Wezel, H. Morreau, Identification of MEN1 and HRPT2 somatic mutations in paraffin-embedded (sporadic) parathyroid carcinomas. Clin. Endocrinol. 67, 370-376 (2007)
-
(2007)
Clin. Endocrinol.
, vol.67
, pp. 370-376
-
-
Haven, C.J.1
Van Puijenbroek, M.2
Tan, M.H.3
Teh, B.T.4
Fleuren, G.J.5
Van Wezel, T.6
Morreau, H.7
-
24
-
-
77951648285
-
Calcium-sensing receptor (CASR) mutations in hypercalcemic states: Studies from a single endocrine clinic over three years
-
V. Guarnieri, L. Canaff, F.H.J. Yun, A. Scillitani, C. Battista, L.A. Muscarella, B.Y.L. Wong, A. Notarangelo, L. D'Agruma, M. Sacco, D.E.C. Cole, G.N. Hendy, Calcium-sensing receptor (CASR) mutations in hypercalcemic states: Studies from a single endocrine clinic over three years. J. Clin. Endocrinol. Metab. 95, 1819-1829 (2010)
-
(2010)
J. Clin. Endocrinol. Metab.
, vol.95
, pp. 1819-1829
-
-
Guarnieri, V.1
Canaff, L.2
Yun, F.H.J.3
Scillitani, A.4
Battista, C.5
Muscarella, L.A.6
Wong, B.Y.L.7
Notarangelo, A.8
D'Agruma, L.9
Sacco, M.10
Cole, D.E.C.11
Hendy, G.N.12
-
25
-
-
33747668789
-
Diagnosis of parathyroid tumors in familial isolated hyperparathyroidism with HRPT2 mutation: Implications for cancer surveillance
-
V. Guarnieri, A. Scillitani, L.A. Muscarella, C. Battista, N. Bonfitto, M. Bisceglia, S. Minisola, M.L. Mascia, L. D'Agruma, D.E.C. Cole, Diagnosis of parathyroid tumors in familial isolated hyperparathyroidism with HRPT2 mutation: Implications for cancer surveillance. J. Clin. Endocrinol. Metab. 91, 2827-2832 (2006)
-
(2006)
J. Clin. Endocrinol. Metab.
, vol.91
, pp. 2827-2832
-
-
Guarnieri, V.1
Scillitani, A.2
Muscarella, L.A.3
Battista, C.4
Bonfitto, N.5
Bisceglia, M.6
Minisola, S.7
Mascia, M.L.8
D'Agruma, L.9
Cole, D.E.C.10
-
26
-
-
53949123368
-
Re: Familial hyperparathyroidism: Surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutations
-
V. Guarnieri, M. Bisceglia, N. Bonfitto, F. Cetani, C. Marcocci, S. Minisola, C. Battista, I. Chiodini, D.E.C. Cole, A. Scillitani, Re: Familial hyperparathyroidism: Surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutations. Surgery 144, 839-840 (2008)
-
(2008)
Surgery
, vol.144
, pp. 839-840
-
-
Guarnieri, V.1
Bisceglia, M.2
Bonfitto, N.3
Cetani, F.4
Marcocci, C.5
Minisola, S.6
Battista, C.7
Chiodini, I.8
Cole, D.E.C.9
Scillitani, A.10
-
27
-
-
34249009427
-
Parathyroid adenoma
-
WHO Classification Of Tumours Ed. By R.A. DeLellis R.V. Lloyd P.U. Heitz C. Eng (IARC Press Lyon 2004
-
L. Grimelius, R.A. DeLellis, L. Bondeson, G. Akerstrom, A. Arnold, K.O. Frinssila, G.N. Hendy, D. Dupuy, C. Eng, Parathyroid adenoma, in Pathology and genetics of tumours of endocrine organs. WHO classification of tumours, ed. by R.A. DeLellis, R.V. Lloyd, P.U. Heitz, C. Eng (IARC Press, Lyon, 2004), pp. 128-132
-
Pathology And Genetics Of Tumours Of Endocrine Organs
, pp. 128-132
-
-
Grimelius, L.1
DeLellis, R.A.2
Bondeson, L.3
Akerstrom, G.4
Arnold, A.5
Frinssila, K.O.6
Hendy, G.N.7
Dupuy, D.8
Eng, C.9
-
28
-
-
0033168843
-
Allelotype of posterior uveal melanoma: Implications for a bifurcated tumor progression pathway
-
P. Parrella, D. Sidransky, S.L. Merbs, Allelotype of posterior uveal melanoma: Implications for a bifurcated tumor progression pathway. Cancer Res. 59, 3032-3037 (1999)
-
(1999)
Cancer Res.
, vol.59
, pp. 3032-3037
-
-
Parrella, P.1
Sidransky, D.2
Merbs, S.L.3
-
29
-
-
58249097267
-
Clinical, genetic, and histopathologic investigation of CDC73-related familial hyperparathyroidism
-
G. Masi, L. Barzon, M. Iacobone, G. Viel, A. Porzionato, V. Macchi, R. De Caro, G. Favia, G. Palù, Clinical, genetic, and histopathologic investigation of CDC73-related familial hyperparathyroidism. Endocr. Relat. Cancer 15, 1115-1126 (2008)
-
(2008)
Endocr. Relat. Cancer
, vol.15
, pp. 1115-1126
-
-
Masi, G.1
Barzon, L.2
Iacobone, M.3
Viel, G.4
Porzionato, A.5
Macchi, V.6
De Caro, R.7
Favia, G.8
Palù, G.9
-
30
-
-
0035334774
-
Evaluation of loss of heterozygosity/allelic imbalance scoring in tumor DNA
-
R.I. Skotheim, C.B. Diep, S.M. Kraggerud, K.S. Jakobsen, R.A. Lothe, Evaluation of loss of heterozygosity/allelic imbalance scoring in tumor DNA. Cancer Genet. Cytogenet. 127, 64-70 (2001)
-
(2001)
Cancer Genet. Cytogenet.
, vol.127
, pp. 64-70
-
-
Skotheim, R.I.1
Diep, C.B.2
Kraggerud, S.M.3
Jakobsen, K.S.4
Lothe, R.A.5
-
31
-
-
0028106197
-
Clinical course of metastatic parathyroid cancer
-
K. Sandelin, O. Tullgren, L.O. Farnebo, Clinical course of metastatic parathyroid cancer. World J. Surg. 18, 594-599 (1994)
-
(1994)
World J. Surg.
, vol.18
, pp. 594-599
-
-
Sandelin, K.1
Tullgren, O.2
Farnebo, L.O.3
-
32
-
-
83455163973
-
Identification of the first germline HRPT2 wholegene deletion in a patient with primary hyperparathyroidism
-
R. Domingues, R.A. Tomaz, C. Martins, C. Nunes, M.J. Bugalho, B.M. Cavaco, Identification of the first germline HRPT2 wholegene deletion in a patient with primary hyperparathyroidism. Clin. Endocrinol. 76, 33-38 (2012)
-
(2012)
Clin. Endocrinol.
, vol.76
, pp. 33-38
-
-
Domingues, R.1
Tomaz, R.A.2
Martins, C.3
Nunes, C.4
Bugalho, M.J.5
Cavaco, B.M.6
-
33
-
-
84863545280
-
Haploinsufficient gene selection in cancer
-
C.D. Greenman, Haploinsufficient gene selection in cancer. Science 337, 47-48 (2012)
-
(2012)
Science
, vol.337
, pp. 47-48
-
-
Greenman, C.D.1
-
34
-
-
33749257125
-
Surveillance for early detection of aggressive parathyroid disease: Carcinoma and atypical adenoma in familial isolated hyperparathyroidism associated with a germline HRPT2 mutation
-
T.G. Kelly, T.M. Shattuck, M. Reyes-Mugica, A.F. Stewart, W.F. Simonds, R. Udelsman, A. Arnold, T.O. Carpenter, Surveillance for early detection of aggressive parathyroid disease: Carcinoma and atypical adenoma in familial isolated hyperparathyroidism associated with a germline HRPT2 mutation. J. Bone Miner. Res. 21, 1666-1671 (2006)
-
(2006)
J. Bone Miner. Res.
, vol.21
, pp. 1666-1671
-
-
Kelly, T.G.1
Shattuck, T.M.2
Reyes-Mugica, M.3
Stewart, A.F.4
Simonds, W.F.5
Udelsman, R.6
Arnold, A.7
Carpenter, T.O.8
-
35
-
-
79960016936
-
Absence of nucleolar parafibromin immunoreactivity in subsets of parathyroid malignant tumours
-
C.C. Juhlin, F. Haglund, T. Obara, A. Arnold, C. Larsson, A. Höög, Absence of nucleolar parafibromin immunoreactivity in subsets of parathyroid malignant tumours. Virchows Arch. 459, 47-53 (2011)
-
(2011)
Virchows Arch.
, vol.459
, pp. 47-53
-
-
Juhlin, C.C.1
Haglund, F.2
Obara, T.3
Arnold, A.4
Larsson, C.5
Höög, A.6
-
36
-
-
33751179021
-
Rapid mutation screening for HRPT2 and MEN1 mutations associated with familial and sporadic primary hyperparathyroidism
-
V.M. Howell, J.W. Cardinal, A.L. Richardson, O. Gimm, B.G. Robinson, D.J. Marsh, Rapid mutation screening for HRPT2 and MEN1 mutations associated with familial and sporadic primary hyperparathyroidism. J. Mol. Diagn. 8, 559-566 (2006)
-
(2006)
J. Mol. Diagn.
, vol.8
, pp. 559-566
-
-
Howell, V.M.1
Cardinal, J.W.2
Richardson, A.L.3
Gimm, O.4
Robinson, B.G.5
Marsh, D.J.6
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