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Results: 1 to 20 of 115

1.

Hyperparathyroidism-jaw tumor syndrome: a case report.

Rekik N, Ben Naceur B, Mnif M, Mnif F, Mnif H, Boudawara T, Abid M.

Ann Endocrinol (Paris). 2010 Mar;71(2):121-6. doi: 10.1016/j.ando.2009.09.004. Epub 2009 Nov 25.

PMID:
19942209
[PubMed - indexed for MEDLINE]
2.

[Hyperparathyroidism-jaw tumor syndrome. A hereditary form of primary hyperparathyroidism with parathyroid carcinoma].

Raue F, Haag Ch, Frank-Raue K.

Dtsch Med Wochenschr. 2007 Jul 29;132(27):1459-62. German.

PMID:
17583828
[PubMed - indexed for MEDLINE]
3.

A case of hyperparathyroidism-jaw tumour syndrome found in the treatment of an ossifying fibroma in the maxillary bone.

Yamashita Y, Akiyama T, Mizusawa N, Yoshimoto K, Goto M.

Int J Oral Maxillofac Surg. 2007 Apr;36(4):365-9. Epub 2006 Oct 18.

PMID:
17052894
[PubMed - indexed for MEDLINE]
4.

Clinical, genetic, and histopathologic investigation of CDC73-related familial hyperparathyroidism.

Masi G, Barzon L, Iacobone M, Viel G, Porzionato A, Macchi V, De Caro R, Favia G, Palù G.

Endocr Relat Cancer. 2008 Dec;15(4):1115-26. doi: 10.1677/ERC-08-0066. Epub 2008 Aug 28.

PMID:
18755853
[PubMed - indexed for MEDLINE]
Free Article
5.

Hyperparathyroidism-jaw tumor syndrome: a report of three large kindred.

Iacobone M, Masi G, Barzon L, Porzionato A, Macchi V, Ciarleglio FA, Palù G, De Caro R, Viel G, Favia G.

Langenbecks Arch Surg. 2009 Sep;394(5):817-25. doi: 10.1007/s00423-009-0511-y. Epub 2009 Jun 16.

PMID:
19529956
[PubMed - indexed for MEDLINE]
6.

Genetic analyses in patients with familial isolated hyperparathyroidism and hyperparathyroidism-jaw tumour syndrome.

Mizusawa N, Uchino S, Iwata T, Tsuyuguchi M, Suzuki Y, Mizukoshi T, Yamashita Y, Sakurai A, Suzuki S, Beniko M, Tahara H, Fujisawa M, Kamata N, Fujisawa K, Yashiro T, Nagao D, Golam HM, Sano T, Noguchi S, Yoshimoto K.

Clin Endocrinol (Oxf). 2006 Jul;65(1):9-16.

PMID:
16817812
[PubMed - indexed for MEDLINE]
7.

Frequent large germline HRPT2 deletions in a French National cohort of patients with primary hyperparathyroidism.

Bricaire L, Odou MF, Cardot-Bauters C, Delemer B, North MO, Salenave S, Vezzosi D, Kuhn JM, Murat A, Caron P, Sadoul JL, Silve C, Chanson P, Barlier A, Clauser E, Porchet N, Groussin L; GTE Group.

J Clin Endocrinol Metab. 2013 Feb;98(2):E403-8. doi: 10.1210/jc.2012-2789. Epub 2013 Jan 4. Erratum in: J Clin Endocrinol Metab. 2013 Apr;98(4):1766.

PMID:
23293331
[PubMed - indexed for MEDLINE]
8.

Surveillance for early detection of aggressive parathyroid disease: carcinoma and atypical adenoma in familial isolated hyperparathyroidism associated with a germline HRPT2 mutation.

Kelly TG, Shattuck TM, Reyes-Mugica M, Stewart AF, Simonds WF, Udelsman R, Arnold A, Carpenter TO.

J Bone Miner Res. 2006 Oct;21(10):1666-71.

PMID:
16995822
[PubMed - indexed for MEDLINE]
9.

[An uncommon cause of hypercalcemia: synchronous carcinoma of two parathyroids in the context of hyperparathyroidism-jaw tumor syndrome].

Veiguela B, Isidro ML, Jorge S, Ruano B.

Endocrinol Nutr. 2010 Oct;57(8):391-3. doi: 10.1016/j.endonu.2010.04.002. Epub 2010 May 18. Spanish. No abstract available.

PMID:
20483674
[PubMed - indexed for MEDLINE]
10.

Primary hyperparathyroidism and jaw tumor syndrome: a novel mutation of the HRPT2 gene.

Carlson AL, Smith CL.

Endocr Pract. 2008 Sep;14(6):743-7.

PMID:
18996796
[PubMed - indexed for MEDLINE]
11.

Dental findings in a family with hyperparathyroidism-jaw tumor syndrome and a novel HRPT2 gene mutation.

Aldred MJ, Talacko AA, Savarirayan R, Murdolo V, Mills AE, Radden BG, Alimov A, Villablanca A, Larsson C.

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2006 Feb;101(2):212-8. Epub 2005 Oct 12.

PMID:
16448924
[PubMed - indexed for MEDLINE]
12.

HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome.

Carpten JD, Robbins CM, Villablanca A, Forsberg L, Presciuttini S, Bailey-Wilson J, Simonds WF, Gillanders EM, Kennedy AM, Chen JD, Agarwal SK, Sood R, Jones MP, Moses TY, Haven C, Petillo D, Leotlela PD, Harding B, Cameron D, Pannett AA, Höög A, Heath H 3rd, James-Newton LA, Robinson B, Zarbo RJ, Cavaco BM, Wassif W, Perrier ND, Rosen IB, Kristoffersson U, Turnpenny PD, Farnebo LO, Besser GM, Jackson CE, Morreau H, Trent JM, Thakker RV, Marx SJ, Teh BT, Larsson C, Hobbs MR.

Nat Genet. 2002 Dec;32(4):676-80. Epub 2002 Nov 18.

PMID:
12434154
[PubMed - indexed for MEDLINE]
13.

Genetic analysis of the MEN1 gene and HPRT2 locus in two Italian kindreds with familial isolated hyperparathyroidism.

Cetani F, Pardi E, Giovannetti A, Vignali E, Borsari S, Golia F, Cianferotti L, Viacava P, Miccoli P, Gasperi M, Pinchera A, Marcocci C.

Clin Endocrinol (Oxf). 2002 Apr;56(4):457-64.

PMID:
11966738
[PubMed - indexed for MEDLINE]
14.

Loss of nuclear expression of parafibromin distinguishes parathyroid carcinomas and hyperparathyroidism-jaw tumor (HPT-JT) syndrome-related adenomas from sporadic parathyroid adenomas and hyperplasias.

Gill AJ, Clarkson A, Gimm O, Keil J, Dralle H, Howell VM, Marsh DJ.

Am J Surg Pathol. 2006 Sep;30(9):1140-9.

PMID:
16931959
[PubMed - indexed for MEDLINE]
15.

[Prophylactic parathyroidectomy for familial parathyroid carcinoma].

Gimm O, Lorenz K, Nguyen Thanh P, Schneyer U, Bloching M, Howell VM, Marsh DJ, Teh BT, Krause U, Dralle H.

Chirurg. 2006 Jan;77(1):15-24. German.

PMID:
16418876
[PubMed - indexed for MEDLINE]
16.

Genetic analyses in familial isolated hyperparathyroidism: implication for clinical assessment and surgical management.

Cetani F, Pardi E, Ambrogini E, Lemmi M, Borsari S, Cianferotti L, Vignali E, Viacava P, Berti P, Mariotti S, Pinchera A, Marcocci C.

Clin Endocrinol (Oxf). 2006 Feb;64(2):146-52.

PMID:
16430712
[PubMed - indexed for MEDLINE]
17.

Hyperparathyroidism-jaw tumor syndrome.

Kutcher MR, Rigby MH, Bullock M, Trites J, Taylor SM, Hart RD.

Head Neck. 2013 Jun;35(6):E175-7. doi: 10.1002/hed.22918. Epub 2012 Feb 2.

PMID:
22302605
[PubMed - indexed for MEDLINE]
18.

Identification of de novo germline mutations in the HRPT2 gene in two apparently sporadic cases with challenging parathyroid tumor diagnoses.

Cavaco BM, Santos R, Félix A, Carvalho D, Lopes JM, Domingues R, Sirgado M, Rei N, Fonseca F, Santos JR, Sobrinho L, Leite V.

Endocr Pathol. 2011 Mar;22(1):44-52. doi: 10.1007/s12022-011-9151-1.

PMID:
21360064
[PubMed - indexed for MEDLINE]
19.

CDC73-Related Disorders.

Rich TA, Hu MI, Martin JW, Perrier ND, Waguespack SG.

In: Pagon RA, Adam MP, Ardinger HH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2014.
2008 Dec 31 [updated 2012 May 24].

PMID:
20301744
[PubMed]
Books & Documents
20.

Detection of the first gross CDC73 germline deletion in an HPT-JT syndrome family.

Cascón A, Huarte-Mendicoa CV, Javier Leandro-García L, Letón R, Suela J, Santana A, Costa MB, Comino-Méndez I, Landa I, Sánchez L, Rodríguez-Antona C, Cigudosa JC, Robledo M.

Genes Chromosomes Cancer. 2011 Nov;50(11):922-9. doi: 10.1002/gcc.20911. Epub 2011 Aug 11.

PMID:
21837707
[PubMed - indexed for MEDLINE]

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