{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,7,12]],"date-time":"2024-07-12T17:16:29Z","timestamp":1720804589383},"reference-count":30,"publisher":"Springer Science and Business Media LLC","issue":"6","license":[{"start":{"date-parts":[[2002,6,1]],"date-time":"2002-06-01T00:00:00Z","timestamp":1022889600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Endocrinol Invest"],"published-print":{"date-parts":[[2002,6]]},"DOI":"10.1007\/bf03345492","type":"journal-article","created":{"date-parts":[[2014,3,21]],"date-time":"2014-03-21T18:19:39Z","timestamp":1395425979000},"page":"508-512","source":"Crossref","is-referenced-by-count":8,"title":["MEN1 gene alterations do not correlate with the phenotype of sporadic primary hyperparathyroidism"],"prefix":"10.1007","volume":"25","author":[{"given":"F.","family":"Cetani","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.","family":"Pardi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.","family":"Vignali","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S.","family":"Borsari","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Picone","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L.","family":"Cianferotti","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.","family":"Ambrogini","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P.","family":"Miccoli","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Pinchera","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Marcocci","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2014,3,22]]},"reference":[{"key":"BF03345492_CR1","doi-asserted-by":"crossref","first-page":"189","DOI":"10.1056\/NEJM198001243020402","volume":"302","author":"H Heath 3rd","year":"1980","unstructured":"Heath H. 3rd, Hodgson S.F., Kennedy M.A. Primary hyperparathyroidism: incidence, morbidity, and potential economic impact in a community. N. Engl. J. Med. 1980, 302: 189\u2013193.","journal-title":"N. Engl. J. Med."},{"key":"BF03345492_CR2","first-page":"1544","volume":"18","author":"BT Teh","year":"1998","unstructured":"Teh B.T., Esapa C., Houlston R., Grandell U., Farnebo F., Nordenskjod M. Familial isolated hyperparathyroidism associated with a constitutional MEN1 mutations. Am. J. Hum. Genet. 1998, 18: 1544\u20131549.","journal-title":"Am. J. Hum. Genet."},{"key":"BF03345492_CR3","first-page":"2114","volume":"83","author":"BT Teh","year":"1998","unstructured":"Teh B.T., Farnebo F., Twigg S., et al. Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21\u2013q32 in a subset of families. J. Clin. Endocrinol. Metab. 1998, 83: 2114\u20132120.","journal-title":"J. Clin. Endocrinol. Metab."},{"key":"BF03345492_CR4","doi-asserted-by":"crossref","first-page":"349","DOI":"10.1007\/BF03343872","volume":"5","author":"C Bergwitz","year":"2001","unstructured":"Bergwitz C., Bremer B., Soudah B., Mayr B., Brabant G., Familial isolated parathyroid adenoma in a consanguineous family. J. Endocrinol. Invest. 2001, 5: 349\u2013355.","journal-title":"J. Endocrinol. Invest."},{"key":"BF03345492_CR5","first-page":"457","volume-title":"The parathyroids: Basic and clinical concepts","author":"JP Bilezikian","year":"1994","unstructured":"Bilezikian J.P., Silverberg S., Gartenberg F., et al. Clinical presentation of primary hyperparathyroidism. In: Bilezikian J.P., Marcus R., Levine M.A. (Eds.), The parathyroids: Basic and clinical concepts. Raven Press, New York, 1994, p. 457."},{"key":"BF03345492_CR6","doi-asserted-by":"crossref","first-page":"93","DOI":"10.1016\/S0889-8529(18)30118-X","volume":"23","author":"A Arnold","year":"1994","unstructured":"Arnold A. Molecular mechanisms of parathyroid neoplasia. Endocrinol. Metab. Clin. North Am. 1994, 23: 93\u2013107.","journal-title":"Metab. Clin. North Am."},{"key":"BF03345492_CR7","first-page":"3775","volume":"84","author":"F Farnebo","year":"1999","unstructured":"Farnebo F., Kytola S., Teh B.T., et al. Alternative genetic pathways in parathyroid tumorigenesis. J. Clin. Endocrinol. Metab. 1999, 84: 3775\u20133780.","journal-title":"J. Clin. Endocrinol. Metab."},{"key":"BF03345492_CR8","first-page":"599","volume":"56","author":"H Tahara","year":"1996","unstructured":"Tahara H., Smith A., Gaz R., Cryns V., Arnold A. Genomic localization of novel candidate tumor suppressor gene loci in human parathyroid adenomas. Cancer Res. 1996, 56: 599\u2013605.","journal-title":"Cancer Res."},{"key":"BF03345492_CR9","doi-asserted-by":"crossref","first-page":"370","DOI":"10.1007\/BF03343875","volume":"5","author":"CA Stratakis","year":"2001","unstructured":"Stratakis C.A. Clinical genetics of multiple endocrine neoplasias, Carney complex and related syndromes. J. Endocrinol. Invest. 2001, 5: 370\u2013383.","journal-title":"J. Endocrinol. Invest."},{"key":"BF03345492_CR10","doi-asserted-by":"crossref","first-page":"404","DOI":"10.1126\/science.276.5311.404","volume":"276","author":"S Chandrasekharappa","year":"1997","unstructured":"Chandrasekharappa S., Guru S., Manickam P., et al. Positional cloning of the gene for multiple endocrine neoplasia type 1. Science 1997, 276: 404\u2013407.","journal-title":"Science"},{"key":"BF03345492_CR11","doi-asserted-by":"crossref","unstructured":"European Consortium on MEN1 Identification of the multiple endocrine neoplasia type 1. Hum. Mol. Genet. 1997, 6: 1177\u20131183.","DOI":"10.1093\/hmg\/6.7.1177"},{"key":"BF03345492_CR12","doi-asserted-by":"crossref","first-page":"429","DOI":"10.1530\/eje.0.1400429","volume":"140","author":"F Cetani","year":"1999","unstructured":"Cetani F., Pardi E., Cianferotti L., et al. A new mutation of the MEN1 gene in an Italian kindred with multiple endocrine neoplasia type 1. Eur. J. Endocrinol. 1999, 140: 429\u2013433.","journal-title":"Eur. J. Endocrinol."},{"key":"BF03345492_CR13","doi-asserted-by":"crossref","first-page":"1968","DOI":"10.1073\/pnas.87.5.1968","volume":"87","author":"C Bystrom","year":"1992","unstructured":"Bystrom C., Larsson C., Blomberg C., et al. Localization of the gene for multiple endocrine neoplasia type 1 to a small region within chromosome 11q13 by deletion mapping in tumors. Proc. Natl. Acad. Sci. USA 1992, 87: 1968\u20131972.","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"BF03345492_CR14","first-page":"1223","volume":"2","author":"MR Toliat","year":"1997","unstructured":"Toliat M.R., Berger W., Ropers H.H., Neuhaus P., Wieddenmann B. Mutations in the MEN1 gene in sporadic neuroendocrine tumors of gastroenteropatic system. Lancet 1997, 2: 1223.","journal-title":"Lancet"},{"key":"BF03345492_CR15","first-page":"5446","volume":"57","author":"Z Zhuang","year":"1997","unstructured":"Zhuang Z., Ezzat S.Z., Vortmeyer A.O., et al. Mutations of the MEN1 tumor suppressor gene in pituitary tumors. Cancer Res. 1997, 57: 5446\u20135451.","journal-title":"Cancer Res."},{"key":"BF03345492_CR16","doi-asserted-by":"crossref","first-page":"375","DOI":"10.1038\/ng0897-375","volume":"16","author":"C Heppner","year":"1997","unstructured":"Heppner C., Kester M.B., Agarwal S.K., et al. Somatic mutation of the MEN1 gene in parathyroid tumors. Nature Genetics 1997, 16: 375\u2013378.","journal-title":"Nature Genetics"},{"key":"BF03345492_CR17","first-page":"2960","volume":"83","author":"T Carling","year":"1998","unstructured":"Carling T., Correa P., Hessman O., Hedberg J., Skogseid B., Lindberg D. Parathyroid MEN1 gene mutations in relation to clinical characteristics of nonfamilial primary hyperparathyroidism. J. Clin. Endocrinol. Metab. 1998, 83: 2960\u20132963.","journal-title":"J. Clin. Endocrinol. Metab."},{"key":"BF03345492_CR18","first-page":"2627","volume":"83","author":"F Farnebo","year":"1998","unstructured":"Farnebo F., Teh B.T., Kytola S., Svensson A., Phelan C., Sandelin K. Alterations of the MEN1 gene in sporadic parathyroid tumors. J. Clin. Endocrinol. Metab. 1998, 83: 2627\u20132630.","journal-title":"J. Clin. Endocrinol. Metab."},{"key":"BF03345492_CR19","doi-asserted-by":"crossref","first-page":"S9","DOI":"10.1002\/jbmr.5650061406","volume":"6","author":"JT Potts","year":"1991","unstructured":"Potts J.T. NIH Consensus Development Conference Statement on Primary Hyperparathyroidism. J. Bone. Miner. Res. 1991, 6: S9\u2013S13.","journal-title":"J. Bone. Miner. Res."},{"key":"BF03345492_CR20","first-page":"1.21","volume-title":"Molecular Cloning: A laboratory manual","author":"J Sambrook","year":"1989","unstructured":"Sambrook J., Fitsch E.F., Maniatis T. Molecular Cloning: A laboratory manual, 2nd ed., Vol. 1 and 2. Cold Spring Harbor Laboratory, Cold Spring Harbor, 1989, 1.21\u20131.24."},{"key":"BF03345492_CR21","first-page":"1039","volume":"57","author":"LV Debelenko","year":"1997","unstructured":"Debelenko L.V., Emmert-Buck M.R., Manickam P., et al. Haplotype analysis defines a minimal interval for the multiple endocrine neoplasia type 1 (MEN1) gene. Cancer Res. 1997, 57: 1039\u20131042.","journal-title":"Cancer Res."},{"key":"BF03345492_CR22","doi-asserted-by":"crossref","first-page":"445","DOI":"10.1002\/1098-1004(200011)16:5<445::AID-HUMU12>3.0.CO;2-6","volume":"16","author":"F Cetani","year":"2000","unstructured":"Cetani F., Pardi E., Giovannetti A., et al. Six novel MEN1 gene mutations in sporadic parathyroid tumors. Hum. Mutat. 2000, 16: 445\u2013448.","journal-title":"Hum. Mutat."},{"key":"BF03345492_CR23","doi-asserted-by":"crossref","first-page":"9","DOI":"10.1002\/gcc.2870130103","volume":"13","author":"VL Cryns","year":"1995","unstructured":"Cryns V.L., Yi S.M., Tabara H., Gaz R.D., Arnold A. Frequent loss of chromosome 1p DNA in parathyroid adenomas. Genes Chromosom. Cancer 1995, 13: 9\u201313.","journal-title":"Genes Chromosom. Cancer"},{"key":"BF03345492_CR24","first-page":"818","volume":"78","author":"C Marcocci","year":"1994","unstructured":"Marcocci C., Golia F., Bruno-Bossio G., Vignali E., Pinchera A. Carefully monitored levothyroxine therapy is not associated with bone loss in premenopausal women. J. Clin. Endocrinol. Metab. 1994, 78: 818\u2013823.","journal-title":"J. Clin. Endocrinol. Metab."},{"key":"BF03345492_CR25","doi-asserted-by":"crossref","first-page":"2034","DOI":"10.1172\/JCI114114","volume":"83","author":"A Arnold","year":"1989","unstructured":"Arnold A., Kim H.G., Eddy R.L., et al. Molecular cloning and chromosomal mapping of DNA rearranged with the parathyroid hormone gene in a parathyroid adenoma. J. Clin. Invest. 1989, 83: 2034\u20132040.","journal-title":"J. Clin. Invest."},{"key":"BF03345492_CR26","doi-asserted-by":"crossref","first-page":"878","DOI":"10.1359\/jbmr.1999.14.6.878","volume":"14","author":"F Cetani","year":"1999","unstructured":"Cetani F., Pinchera A., Pardi E., et al. No evidence for mutations in the calcium-sensing receptor gene in sporadic parathyroid adenomas. J. Bone. Miner. Res. 1999, 14: 878\u2013882.","journal-title":"J. Bone. Miner. Res."},{"key":"BF03345492_CR27","doi-asserted-by":"crossref","first-page":"403","DOI":"10.1046\/j.1365-2265.1999.00779.x","volume":"51","author":"T Carling","year":"1999","unstructured":"Carling T., Imanishi Y., Gaz R.D., Arnold A. RAD51 as a candidate parathyroid tumor suppressor gene on chromosome 15q: absence of somatic mutations. Clin. Endocrinol. 1999, 51: 403\u2013407.","journal-title":"Clin. Endocrinol."},{"key":"BF03345492_CR28","doi-asserted-by":"crossref","first-page":"757","DOI":"10.1056\/NEJM199403173301105","volume":"330","author":"VL Cryns","year":"1994","unstructured":"Cryns V.L., Thor A., Xu H.J., Hu S.X., Wierman M.E., Arnold A. Loss of the retinoblastoma tumor-suppressor gene in parathyroid carcinoma. N. Engl. J. Med. 1994, 330: 757\u2013761.","journal-title":"N. Engl. J. Med."},{"key":"BF03345492_CR29","first-page":"6804","volume":"15","author":"E Friedman","year":"1992","unstructured":"Friedman E., De Marco L., Gejman P.V., et al. Allelic loss from chromosome 11 in parathyroid tumors. Cancer Res. 1992, 15: 6804\u20136809.","journal-title":"Cancer Res."},{"key":"BF03345492_CR30","first-page":"2615","volume":"85","author":"MMR Bhuiyan","year":"2000","unstructured":"Bhuiyan M.M.R., Sato M., Murao K., Imachi H., Namihira H., Takahara J. Expression of menin in parathyroid tumors. J. Clin: Endocrinol. Metab. 2000, 85: 2615\u20132619.","journal-title":"J. Clin: Endocrinol. Metab."}],"container-title":["Journal of Endocrinological Investigation"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF03345492.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF03345492\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF03345492","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,5,25]],"date-time":"2024-05-25T07:34:50Z","timestamp":1716622490000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF03345492"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2002,6]]},"references-count":30,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2002,6]]}},"alternative-id":["BF03345492"],"URL":"https:\/\/doi.org\/10.1007\/bf03345492","relation":{},"ISSN":["0391-4097","1720-8386"],"issn-type":[{"value":"0391-4097","type":"print"},{"value":"1720-8386","type":"electronic"}],"subject":[],"published":{"date-parts":[[2002,6]]}}}