-
1
-
-
0036839719
-
Epidemiology of primary hyperparathyroidism in Europe
-
Adami S, Marcocci C, Gatti D (2002) Epidemiology of primary hyperparathyroidism in Europe. J Bone Miner Res 17 Suppl 2: N18-23
-
(2002)
J Bone Miner Res
, vol.17
, Issue.2 SUPPL.
-
-
Adami, S.1
Marcocci, C.2
Gatti, D.3
-
2
-
-
2342469843
-
Genetics of primary hyperparathyroidism
-
Brandi ML, Falchetti A (2004) Genetics of primary hyperparathyroidism. Urol Int 72 Suppl 1:11-16
-
(2004)
Urol Int
, vol.72
, Issue.1 SUPPL.
, pp. 11-16
-
-
Brandi, M.L.1
Falchetti, A.2
-
3
-
-
85047682409
-
Guidelines for diagnosis and therapy of MEN type 1 and type 2
-
Brandi ML, Gagel RF, Angeli A et al. (2001) Guidelines for diagnosis and therapy of MEN type 1 and type 2. J Clin Endocrinol Metab 86:5658-5671
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 5658-5671
-
-
Brandi, M.L.1
Gagel, R.F.2
Angeli, A.3
-
4
-
-
17744369268
-
Familial hypercalcemia and hypercalciuria caused by a novel mutation in the cytoplasmic tail of the calcium receptor
-
Carling T, Szabo E, Bai M et al. (2000) Familial hypercalcemia and hypercalciuria caused by a novel mutation in the cytoplasmic tail of the calcium receptor. J Clin Endocrinol Metab 85:2042-2047
-
(2000)
J Clin Endocrinol Metab
, vol.85
, pp. 2042-2047
-
-
Carling, T.1
Szabo, E.2
Bai, M.3
-
5
-
-
12344296364
-
Parathyroid surgery in familial hyperparathyroid disorders
-
Carling T, Udelsman R (2005) Parathyroid surgery in familial hyperparathyroid disorders. J Intern Med 257:27-37
-
(2005)
J Intern Med
, vol.257
, pp. 27-37
-
-
Carling, T.1
Udelsman, R.2
-
6
-
-
18744385803
-
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome
-
Carpten JD, Robbins CM, Villablanca A et al. (2002) HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome. Nat Genet 32:676-680
-
(2002)
Nat Genet
, vol.32
, pp. 676-680
-
-
Carpten, J.D.1
Robbins, C.M.2
Villablanca, A.3
-
7
-
-
11144355570
-
Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 gene
-
Cavaco BM, Guerra L, Bradley KJ et al. (2004) Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 gene. J Clin Endocrinol Metab 89:1747-1752
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 1747-1752
-
-
Cavaco, B.M.1
Guerra, L.2
Bradley, K.J.3
-
8
-
-
8744299920
-
Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: Germline and somatic mutations in familial and sporadic parathyroid tumors
-
Cetani F, Pardi E, Borsari S et al. (2004) Genetic analyses 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)
J Clin Endocrinol Metab
, vol.89
, pp. 5583-5591
-
-
Cetani, F.1
Pardi, E.2
Borsari, S.3
-
9
-
-
0036228986
-
Genetic analysis of the MEN1 gene and HPRT2 locus in two Italian kindreds with familial isolated hyperparathyroidism
-
Oxf
-
Cetani F, Pardi E, Giovannetti A et al. (2002) Genetic analysis of the MEN1 gene and HPRT2 locus in two Italian kindreds with familial isolated hyperparathyroidism. Clin Endocrinol (Oxf) 56:457-454
-
(2002)
Clin Endocrinol
, vol.56
, pp. 457-1454
-
-
Cetani, F.1
Pardi, E.2
Giovannetti, A.3
-
10
-
-
0030963446
-
Positional cloning of the gene for multiple endocrine neoplasia-type 1
-
Chandrasekharappa SC, Guru SC, Manickam P et al. (1997) Positional cloning of the gene for multiple endocrine neoplasia-type 1. Science 276:404-407
-
(1997)
Science
, vol.276
, pp. 404-407
-
-
Chandrasekharappa, S.C.1
Guru, S.C.2
Manickam, P.3
-
11
-
-
0038695145
-
Hyperparathyroidism-jaw tumour syndrome
-
Chen JD, Morrison C, Zhang C, Kahnoski K, Carpten JD, Teh BT (2003) Hyperparathyroidism-jaw tumour syndrome. J Intern Med 253:634-642
-
(2003)
J Intern Med
, vol.253
, pp. 634-642
-
-
Chen, J.D.1
Morrison, C.2
Zhang, C.3
Kahnoski, K.4
Carpten, J.D.5
Teh, B.T.6
-
12
-
-
10744228769
-
Trial to predict malignancy of affected parathyroid glands in primary hyperparathyroidism
-
Chen Q, Kaji H, Nomura R, Sowa H et al. (2003) Trial to predict malignancy of affected parathyroid glands in primary hyperparathyroidism. Endocr J 50:527-534
-
(2003)
Endocr J
, vol.50
, pp. 527-534
-
-
Chen, Q.1
Kaji, H.2
Nomura, R.3
Sowa, H.4
-
13
-
-
0017762328
-
Parathyroid carcinoma in familial hyperparathyroidism
-
Dinnen JS, Greenwoood RH, Jones JH, Walker DA, Williams ED (1977) Parathyroid carcinoma in familial hyperparathyroidism. J Clin Pathol 30:966-975
-
(1977)
J Clin Pathol
, vol.30
, pp. 966-975
-
-
Dinnen, J.S.1
Greenwoood, R.H.2
Jones, J.H.3
Walker, D.A.4
Williams, E.D.5
-
14
-
-
0036326960
-
Concurrent parathyroid adenomas and carcinoma in the setting of multiple endocrine neoplasia type 1: Presentation as hypercalcemic crisis
-
Dionisi S, Minisola S, Pepe J, De Geronimo S, Paglia F, Memeo L, Fitzpatrick LA (2002) Concurrent parathyroid adenomas and carcinoma in the setting of multiple endocrine neoplasia type 1: presentation as hypercalcemic crisis. Mayo Clin Proc 77:866-869
-
(2002)
Mayo Clin Proc
, vol.77
, pp. 866-869
-
-
Dionisi, S.1
Minisola, S.2
Pepe, J.3
De Geronimo, S.4
Paglia, F.5
Memeo, L.6
Fitzpatrick, L.A.7
-
15
-
-
0027303248
-
Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC
-
Donis-Keller H, Dou S, Chi D et al. (1993) Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC. Hum Mol Genet 2:851-856
-
(1993)
Hum Mol Genet
, vol.2
, pp. 851-856
-
-
Donis-Keller, H.1
Dou, S.2
Chi, D.3
-
16
-
-
10644256728
-
Risk factors of paralysis and functional outcome after recurrent laryngeal nerve monitoring in thyroid surgery
-
Dralle H, Sekulla C, Haerting J et al. (2004) Risk factors of paralysis and functional outcome after recurrent laryngeal nerve monitoring in thyroid surgery. Surgery 136:1310-1322
-
(2004)
Surgery
, vol.136
, pp. 1310-1322
-
-
Dralle, H.1
Sekulla, C.2
Haerting, J.3
-
17
-
-
4644256817
-
The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis
-
Eng C, Clayton D, Schuffenecker I et al. (1996) The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis. JAMA 276:1575-1579
-
(1996)
JAMA
, vol.276
, pp. 1575-1579
-
-
Eng, C.1
Clayton, D.2
Schuffenecker, I.3
-
18
-
-
0031810011
-
Familial isolated hyperparathyroidism due to multiple adenomas associated with ossifying jaw fibroma and multiple uterine adenomyomatous polyps
-
Fujikawa M, Okamura K, Sato K, Mizokami T, Tamaki K, Yanagida T, Fujishima M (1998) Familial isolated hyperparathyroidism due to multiple adenomas associated with ossifying jaw fibroma and multiple uterine adenomyomatous polyps. Eur J Endocrinol 138:557-561
-
(1998)
Eur J Endocrinol
, vol.138
, pp. 557-561
-
-
Fujikawa, M.1
Okamura, K.2
Sato, K.3
Mizokami, T.4
Tamaki, K.5
Yanagida, T.6
Fujishima, M.7
-
19
-
-
0036839828
-
Familial benign hypocalciuric hypercalcemia
-
Fuleihan Gel H (2002) Familial benign hypocalciuric hypercalcemia. J Bone Miner Res 17 Suppl 2: N51-56
-
(2002)
J Bone Miner Res
, vol.17
, Issue.2 SUPPL.
-
-
Fuleihan Gel, H.1
-
21
-
-
1642535326
-
Multiple endocrine neoplasia type 1 and Zollinger-Ellison syndrome: A prospective study of 107 cases and comparison with 1009 cases from the literature
-
Baltimore
-
Gibril F, Schumann M, Pace A, Jensen RT (2004) Multiple endocrine neoplasia type 1 and Zollinger-Ellison syndrome: a prospective study of 107 cases and comparison with 1009 cases from the literature. Medicine (Baltimore) 83:43-83
-
(2004)
Medicine
, vol.83
, pp. 43-83
-
-
Gibril, F.1
Schumann, M.2
Pace, A.3
Jensen, R.T.4
-
22
-
-
0035223922
-
Multiple endocrine neoplasia type 2: Clinical aspects
-
Gimm O (2001) Multiple endocrine neoplasia type 2: clinical aspects. Front Horm Res 28:103-130
-
(2001)
Front Horm Res
, vol.28
, pp. 103-130
-
-
Gimm, O.1
-
23
-
-
0036271297
-
Familial parathyroid carcinoma in a child
-
Hamill J, Maoate K, Beasley SW, Corbett R, Evans J (2002) Familial parathyroid carcinoma in a child. J Paediatr Child Health 38:314-317
-
(2002)
J Paediatr Child Health
, vol.38
, pp. 314-317
-
-
Hamill, J.1
Maoate, K.2
Beasley, S.W.3
Corbett, R.4
Evans, J.5
-
24
-
-
17744379773
-
A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome
-
Haven CJ, Wong FK, van Dam EW et al. (2000) A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome. J Clin Endocrinol Metab 85:1449-1454
-
(2000)
J Clin Endocrinol Metab
, vol.85
, pp. 1449-1454
-
-
Haven, C.J.1
Wong, F.K.2
Van Dam, E.W.3
-
25
-
-
0034331332
-
Familial hypocalciuric hypercalcemia
-
Heath DA (2000) Familial hypocalciuric hypercalcemia. Rev Endocr Metab Disord 1:291-296
-
(2000)
Rev Endocr Metab Disord
, vol.1
, pp. 291-296
-
-
Heath, D.A.1
-
26
-
-
0034329531
-
Molecular mechanisms of primary hyperparathyroidism
-
Hendy GN (2000) Molecular mechanisms of primary hyperparathyroidism. Rev Endocr Metab Disord 1:297-305
-
(2000)
Rev Endocr Metab Disord
, vol.1
, pp. 297-305
-
-
Hendy, G.N.1
-
27
-
-
0033073851
-
Hyperparathyroidism-jaw tumor syndrome: The HRPT2 locus is within a 0.7-cM region on chromosome 1q
-
Hobbs MR, Pole AR, Pidwirny GN et al. (1999) Hyperparathyroidism-jaw tumor syndrome: the HRPT2 locus is within a 0.7-cM region on chromosome 1q. Am J Hum Genet 64:518-525
-
(1999)
Am J Hum Genet
, vol.64
, pp. 518-525
-
-
Hobbs, M.R.1
Pole, A.R.2
Pidwirny, G.N.3
-
28
-
-
0041328511
-
HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours
-
Howell VM, Haven O, Kahnoski K et al. (2003) HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours. J Med Genet 40:657-663
-
(2003)
J Med Genet
, vol.40
, pp. 657-663
-
-
Howell, V.M.1
Haven, O.2
Kahnoski, K.3
-
29
-
-
5144223335
-
A molecular diagnosis of hyperparathyroidism-jaw tumor syndrome in an adolescent with recurrent kidney stones
-
Howell VM, Zori RT, Stalker HJ et al. (2004) A molecular diagnosis of hyperparathyroidism-jaw tumor syndrome in an adolescent with recurrent kidney stones. J Pediatr 145:567
-
(2004)
J Pediatr
, vol.145
, pp. 567
-
-
Howell, V.M.1
Zori, R.T.2
Stalker, H.J.3
-
30
-
-
0033179565
-
Two hundred eighty-six cases of parathyroid carcinoma treated in the U.S. between 1985-1995: A National Cancer Data Base Report
-
The American College of Surgeons Commission on Cancer and the American Cancer Society
-
Hundahl SA, Fleming ID, Fremgen AM, Menck HR (1999) Two hundred eighty-six cases of parathyroid carcinoma treated in the U.S. between 1985-1995: a National Cancer Data Base Report. The American College of Surgeons Commission on Cancer and the American Cancer Society. Cancer 86:538-544
-
(1999)
Cancer
, vol.86
, pp. 538-544
-
-
Hundahl, S.A.1
Fleming, I.D.2
Fremgen, A.M.3
Menck, H.R.4
-
31
-
-
10044292986
-
Up-to-date on parathyroid carcinoma: Analysis of an experience of 19 cases
-
Iacobone M, Lumachi F, Favia G (2004) Up-to-date on parathyroid carcinoma: analysis of an experience of 19 cases. J Surg Oncol 88:223-228
-
(2004)
J Surg Oncol
, vol.88
, pp. 223-228
-
-
Iacobone, M.1
Lumachi, F.2
Favia, G.3
-
32
-
-
0025642521
-
Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: A clinically and genetically distinct syndrome
-
Jackson CE, Norum RA, Boyd SB, Talpos GB, Wilson SD, Taggart RT, Mallette LE (1990) Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: a clinically and genetically distinct syndrome. Surgery 108:1006-1012; discussion 1012-1003
-
(1990)
Surgery
, vol.108
, pp. 1006-1012
-
-
Jackson, C.E.1
Norum, R.A.2
Boyd, S.B.3
Talpos, G.B.4
Wilson, S.D.5
Taggart, R.T.6
Mallette, L.E.7
-
33
-
-
6844254551
-
Metastatic parathyroid carcinoma in the MEN2A syndrome
-
Oxf
-
Jenkins PJ, Satta MA, Simmgen M et al. (1997) Metastatic parathyroid carcinoma in the MEN2A syndrome. Clin Endocrinol (Oxf) 47:747-751
-
(1997)
Clin Endocrinol
, vol.47
, pp. 747-751
-
-
Jenkins, P.J.1
Satta, M.A.2
Simmgen, M.3
-
34
-
-
0033671351
-
Primary hyperparathyroidism detected in a health screening. The Tromso study
-
Jorde R, Bonaa KH, Sundsfjord J (2000) Primary hyperparathyroidism detected in a health screening. The Tromso study. J Clin Epidemiol 53:1164-1169
-
(2000)
J Clin Epidemiol
, vol.53
, pp. 1164-1169
-
-
Jorde, R.1
Bonaa, K.H.2
Sundsfjord, J.3
-
35
-
-
0028376125
-
Familial primary hyperparathyroidism complicated with Wilms' tumor
-
Kakinuma A, Morimoto I, Nakano Y et al. (1994) Familial primary hyperparathyroidism complicated with Wilms' tumor. Intern Med 33:123-126
-
(1994)
Intern Med
, vol.33
, pp. 123-126
-
-
Kakinuma, A.1
Morimoto, I.2
Nakano, Y.3
-
36
-
-
0034457762
-
Familial isolated hyperparathyroidism as a variant of multiple endocrine neoplasia type 1 in a large Danish pedigree
-
Kassem M, Kruse TA, Wong FK, Larsson C, Teh BT (2000) Familial isolated hyperparathyroidism as a variant of multiple endocrine neoplasia type 1 in a large Danish pedigree. J Clin Endocrinol Metab 85:165-167
-
(2000)
J Clin Endocrinol Metab
, vol.85
, pp. 165-167
-
-
Kassem, M.1
Kruse, T.A.2
Wong, F.K.3
Larsson, C.4
Teh, B.T.5
-
37
-
-
17644391034
-
Is parathyroid carcinoma indeed a lethal disease?
-
Kleinpeter KP, Lovato JF, Clark PB, Wooldridge T, Norman ES, Bergman S, Perrier ND (2005) Is parathyroid carcinoma indeed a lethal disease? Ann Surg Oncol 12:260-266
-
(2005)
Ann Surg Oncol
, vol.12
, pp. 260-266
-
-
Kp, K.1
Lovato, J.F.2
Clark, P.B.3
Wooldridge, T.4
Norman, E.S.5
Bergman, S.6
Perrier, N.D.7
-
38
-
-
0033292592
-
Parathyroid cancer: Biology and management
-
Koea JB, Shaw JH (1999) Parathyroid cancer: biology and management. Surg Oncol 8:155-165
-
(1999)
Surg Oncol
, vol.8
, pp. 155-165
-
-
Koea, J.B.1
Shaw, J.H.2
-
39
-
-
0023179798
-
Parathyroid carcinoma versus parathyroid adenoma in patients with profound hypercalcemia
-
Levin KE, Galante M, Clark OH (1987) Parathyroid carcinoma versus parathyroid adenoma in patients with profound hypercalcemia. Surgery 101:649-660
-
(1987)
Surgery
, vol.101
, pp. 649-660
-
-
Levin, K.E.1
Galante, M.2
Clark, O.H.3
-
40
-
-
20044362410
-
A Novel IVS2-1G>A mutation causes aberrant splicing of the HRPT2 gene in a family with hyperparathyroidism-jaw tumor syndrome
-
Moon SD, Park JH, Kim EM et al. (2005) A Novel IVS2-1G>A mutation causes aberrant splicing of the HRPT2 gene in a family with hyperparathyroidism- jaw tumor syndrome. J Clin Endocrinol Metab 90:878-883
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 878-883
-
-
Moon, S.D.1
Park, J.H.2
Kim, E.M.3
-
41
-
-
0027231568
-
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
-
Mulligan LM, Kwok JBJ, Healey CS et al. (1993) Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Nature 363:458-460
-
(1993)
Nature
, vol.363
, pp. 458-460
-
-
Mulligan, L.M.1
Kwok, J.B.J.2
Healey, C.S.3
-
42
-
-
0026340710
-
Diagnosis and treatment of patients with parathyroid carcinoma: An update and review
-
Obara T, Fujimoto Y (1991) Diagnosis and treatment of patients with parathyroid carcinoma: an update and review. World J Surg 15:738-744
-
(1991)
World J Surg
, vol.15
, pp. 738-744
-
-
Obara, T.1
Fujimoto, Y.2
-
43
-
-
0037427562
-
Menin interacting proteins as clues toward the understanding of multiple endocrine neoplasia type 1
-
Poisson A, Zablewska B, Gaudray P (2003) Menin interacting proteins as clues toward the understanding of multiple endocrine neoplasia type 1. Cancer Lett 189:1-10
-
(2003)
Cancer Lett
, vol.189
, pp. 1-10
-
-
Poisson, A.1
Zablewska, B.2
Gaudray, P.3
-
44
-
-
0019415931
-
Fibroosseous tumors of the facial skeleton in association with primary hyperparathyroidism: An endocrine syndrome or coincidence?
-
Rosen IB, Palmer JA (1981) Fibroosseous tumors of the facial skeleton in association with primary hyperparathyroidism: an endocrine syndrome or coincidence? Am J Surg 142:494-498
-
(1981)
Am J Surg
, vol.142
, pp. 494-498
-
-
Rosen, I.B.1
Palmer, J.A.2
-
46
-
-
0026761009
-
Prognostic factors in parathyroid cancer: A review of 95 cases
-
Sandelin K, Auer G, Bondeson L, Grimelius L, Farnebo LO (1992) Prognostic factors in parathyroid cancer: a review of 95 cases. World J Surg 16:724-731
-
(1992)
World J Surg
, vol.16
, pp. 724-731
-
-
Sandelin, K.1
Auer, G.2
Bondeson, L.3
Grimelius, L.4
Farnebo, L.O.5
-
47
-
-
15144343501
-
Risk and penetrance of primary hyperparathyroidism in multiple endocrine neoplasia type 2A families with mutations at codon 634 of the RET proto-oncogene
-
Groupe D'étude des Tumeurs a Calcitonine
-
Schuffenecker I, Virally-Monod M, Brohet R et al. (1998) Risk and penetrance of primary hyperparathyroidism in multiple endocrine neoplasia type 2A families with mutations at codon 634 of the RET proto-oncogene. Groupe D'étude des Tumeurs a Calcitonine. J Clin Endocrinol Metab 83:487-491
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 487-491
-
-
Schuffenecker, I.1
Virally-Monod, M.2
Brohet, R.3
-
48
-
-
0142213734
-
Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma
-
Shattuck TM, Valimaki S, Obara T et al. (2003) Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma. N Engl J Med 349:1722-1729
-
(2003)
N Engl J Med
, vol.349
, pp. 1722-1729
-
-
Shattuck, T.M.1
Valimaki, S.2
Obara, T.3
-
49
-
-
0029889612
-
Evaluation and management of primary hyperparathyroidism
-
Silverberg SJ, Bilezikian JP (1996) Evaluation and management of primary hyperparathyroidism. J Clin Endocrinol Metab 81:2036-2040
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 2036-2040
-
-
Silverberg, S.J.1
Bilezikian, J.P.2
-
50
-
-
0036141731
-
Familial isolated hyperparathyroidism: Clinical and genetic characteristics of 36 kindreds
-
Baltimore
-
Simonds WF, James-Newton LA, Agarwal SK, Yang B, Skarulis MC, Hendy GN, Marx SJ (2002) Familial isolated hyperparathyroidism: clinical and genetic characteristics of 36 kindreds. Medicine (Baltimore) 81:1-26
-
(2002)
Medicine
, vol.81
, pp. 1-26
-
-
Simonds, W.F.1
James-Newton, L.A.2
Agarwal, S.K.3
Yang, B.4
Skarulis, M.C.5
Hendy, G.N.6
Marx, S.J.7
-
51
-
-
0842291514
-
Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome
-
Simonds WF, Robbins CM, Agarwal SK, Hendy GN, Carpten JD, Marx SJ (2004) Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome. J Clin Endocrinol Metab 89:96-102
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 96-102
-
-
Simonds, W.F.1
Robbins, C.M.2
Agarwal, S.K.3
Hendy, G.N.4
Carpten, J.D.5
Marx, S.J.6
-
53
-
-
0032231883
-
A family with isolated hyperparathyroidism segregating a missense MEN1 mutation and showing loss of the wild-type alleles in the parathyroid tumors
-
Teh BT, Esapa CT, Houlston R et al. (1998) A family with isolated hyperparathyroidism segregating a missense MEN1 mutation and showing loss of the wild-type alleles in the parathyroid tumors. Am J Hum Genet 63:1544-1549
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1544-1549
-
-
Teh, B.T.1
Esapa, C.T.2
Houlston, R.3
-
54
-
-
1842403802
-
Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: Linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas
-
Teh BT, Farnebo F, Kristoffersson U et al. (1996) Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas. J Clin Endocrinol Metab 81:4204-4211
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 4204-4211
-
-
Teh, B.T.1
Farnebo, F.2
Kristoffersson, U.3
-
55
-
-
15144343105
-
Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families
-
Teh BT, Farnebo F, Twigg S et al. (1998) Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families. J Clin Endocrinol Metab 83:2114-2120
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 2114-2120
-
-
Teh, B.T.1
Farnebo, F.2
Twigg, S.3
-
56
-
-
2942513691
-
Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP)
-
Villablanca A, Calender A, Forsberg L et al. (2004) Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP). J Med Genet 41: e32
-
(2004)
J Med Genet
, vol.41
-
-
Villablanca, A.1
Calender, A.2
Forsberg, L.3
-
57
-
-
12144288720
-
Genetic testing in familial isolated hyperparathyroidism: Unexpected results and their implications
-
Warner J, Epstein M, Sweet A et al. (2004) Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications. J Med Genet 41:155-160
-
(2004)
J Med Genet
, vol.41
, pp. 155-160
-
-
Warner, J.1
Epstein, M.2
Sweet, A.3
-
58
-
-
0005470070
-
Genetic studies of a family with hereditary hyperparathyroidism-jaw tumour syndrome
-
Oxf
-
Wassif WS, Farnebo F, Teh BT et al. (1999) Genetic studies of a family with hereditary hyperparathyroidism-jaw tumour syndrome. Clin Endocrinol (Oxf) 50:191-196
-
(1999)
Clin Endocrinol
, vol.50
, pp. 191-196
-
-
Wassif, W.S.1
Farnebo, F.2
Teh, B.T.3
-
59
-
-
0027140277
-
Familial isolated hyperparathyroidism: A distinct genetic entity with an increased risk of parathyroid cancer
-
Wassif WS, Moniz CF, Friedman E et al. (1993) Familial isolated hyperparathyroidism: a distinct genetic entity with an increased risk of parathyroid cancer. J Clin Endocrinol Metab 77:1485-1489
-
(1993)
J Clin Endocrinol Metab
, vol.77
, pp. 1485-1489
-
-
Wassif, W.S.1
Moniz, C.F.2
Friedman, E.3
-
60
-
-
0142213741
-
HRPT2, a marker of parathyroid cancer
-
Weinstein LS, Simonds WF (2003) HRPT2, a marker of parathyroid cancer. N Engl J Med 349:1691-1692
-
(2003)
N Engl J Med
, vol.349
, pp. 1691-1692
-
-
Weinstein, L.S.1
Simonds, W.F.2
-
61
-
-
14644397229
-
Parafibromin, product of the hyperparathyroidism-jaw tumor syndrome gene HRPT2, regulates cyclin D1/PRAD1 expression
-
Woodard GE, Lin L, Zhang JH, Agarwal SK, Marx SJ, Simonds WF (2005) Parafibromin, product of the hyperparathyroidism-jaw tumor syndrome gene HRPT2, regulates cyclin D1/PRAD1 expression. Oncogene 24:1272-1276
-
(2005)
Oncogene
, vol.24
, pp. 1272-1276
-
-
Woodard, G.E.1
Lin, L.2
Zhang, J.H.3
Agarwal, S.K.4
Marx, S.J.5
Simonds, W.F.6
-
62
-
-
0026764932
-
Parathyroid carcinoma: Clinical and pathologic features in 43 patients
-
Baltimore
-
Wynne AG, van Heerden J, Carney JA, Fitzpatrick LA (1992) Parathyroid carcinoma: clinical and pathologic features in 43 patients. Medicine (Baltimore) 71:197-205
-
(1992)
Medicine
, vol.71
, pp. 197-205
-
-
Wynne, A.G.1
Van Heerden, J.2
Carney, J.A.3
Fitzpatrick, L.A.4
-
63
-
-
0034873353
-
A case of familial isolated hyperparathyroidism with ectopic parathyroid cancer
-
Yamashita K, Suzuki S, Yumita W et al. (2001) A case of familial isolated hyperparathyroidism with ectopic parathyroid cancer. Endocr J 48:453-458
-
(2001)
Endocr J
, vol.48
, pp. 453-458
-
-
Yamashita, K.1
Suzuki, S.2
Yumita, W.3
-
64
-
-
0031938392
-
Familial isolated primary hyperparathyroidism with parathyroid carcinomas: Clinical and molecular features
-
Oxf
-
Yoshimoto K, Endo H, Tsuyuguchi M et al. (1998) Familial isolated primary hyperparathyroidism with parathyroid carcinomas: clinical and molecular features. Clin Endocrinol (Oxf) 48:67-72
-
(1998)
Clin Endocrinol
, vol.48
, pp. 67-72
-
-
Yoshimoto, K.1
Endo, H.2
Tsuyuguchi, M.3
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