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Volumn 77, Issue 1, 2006, Pages 15-24

Prophylactic parathyroidectomy for familial parathyroid carcinoma;Das familiäre nebenschilddrüsenkarzinom. Indikation zur prophylaktischen parathyreoidektomie?

Author keywords

Familial; Hereditary; Parathyroid carcinoma; Parathyroidectomy

Indexed keywords

GENETIC SCREENING; GENETICS; HUMAN; NUCLEOTIDE SEQUENCE; PARATHYROID GLAND; PARATHYROID TUMOR; PARATHYROIDECTOMY; PATHOLOGY; PRIMARY HYPERPARATHYROIDISM; REVIEW; RISK ASSESSMENT; SYNDROME;

EID: 31144476152     PISSN: 00094722     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00104-005-1110-2     Document Type: Review
Times cited : (13)

References (64)
  • 1
    • 0036839719 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 12
    • 10744228769 scopus 로고    scopus 로고
    • 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
  • 14
    • 0036326960 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 24
    • 17744379773 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 38
    • 0033292592 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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
  • 47
    • 15144343501 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 51
    • 0842291514 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.