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Results: 1 to 20 of 115

Similar articles for PubMed (Select 11807402)

1.

Familial isolated hyperparathyroidism: clinical and genetic characteristics of 36 kindreds.

Simonds WF, James-Newton LA, Agarwal SK, Yang B, Skarulis MC, Hendy GN, Marx SJ.

Medicine (Baltimore). 2002 Jan;81(1):1-26. Review. No abstract available.

PMID:
11807402
2.

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
3.

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
4.

Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP).

Villablanca A, Calender A, Forsberg L, Höög A, Cheng JD, Petillo D, Bauters C, Kahnoski K, Ebeling T, Salmela P, Richardson AL, Delbridge L, Meyrier A, Proye C, Carpten JD, Teh BT, Robinson BG, Larsson C.

J Med Genet. 2004 Mar;41(3):e32. No abstract available.

5.

[Familial hyperparathyroidism].

Suzuki S.

Nihon Rinsho. 2006 Jun 28;Suppl 2:16-9. Review. Japanese. No abstract available.

PMID:
16817340
6.

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, Grandell U, Farnebo F, Nordenskjöld M, Pearce CJ, Carmichael D, Larsson C, Harris PE.

Am J Hum Genet. 1998 Nov;63(5):1544-9. No abstract available.

7.

Genetic screening for MEN1 mutations in families presenting with familial primary hyperparathyroidism.

Perrier ND, Villablanca A, Larsson C, Wong M, Ituarte P, Teh BT, Clark OH.

World J Surg. 2002 Aug;26(8):907-13. Epub 2002 May 21.

PMID:
12016470
8.

Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism.

Pannett AA, Kennedy AM, Turner JJ, Forbes SA, Cavaco BM, Bassett JH, Cianferotti L, Harding B, Shine B, Flinter F, Maidment CG, Trembath R, Thakker RV.

Clin Endocrinol (Oxf). 2003 May;58(5):639-46.

PMID:
12699448
9.

Multiple Endocrine Neoplasia type 1.

Piecha G, Chudek J, Wiecek A.

Eur J Intern Med. 2008 Mar;19(2):99-103. doi: 10.1016/j.ejim.2007.08.004. Epub 2007 Nov 7. Review.

PMID:
18249304
10.

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
11.

Hyperparathyroidism of multiple endocrine neoplasia type 1: candidate gene and parathyroid calcium sensing protein expression.

Carling T, Rastad J, Ridefelt P, Gobl A, Hellman P, Oberg K, Rask L, Larsson C, Juhlin C, Akerström G, et al.

Surgery. 1995 Dec;118(6):924-30; discussion 930-1.

PMID:
7491535
12.

Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications.

Warner J, Epstein M, Sweet A, Singh D, Burgess J, Stranks S, Hill P, Perry-Keene D, Learoyd D, Robinson B, Birdsey P, Mackenzie E, Teh BT, Prins JB, Cardinal J.

J Med Genet. 2004 Mar;41(3):155-60.

13.

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.

J Clin Endocrinol Metab. 2004 Jan;89(1):96-102.

PMID:
14715834
14.

Involvement of the MEN1 gene locus in familial isolated hyperparathyroidism.

Villablanca A, Wassif WS, Smith T, Höög A, Vierimaa O, Kassem M, Dwight T, Forsberg L, Du Q, Learoyd D, Jones K, Stranks S, Juhlin C, Teh BT, Carling T, Robinson B, Larsson C.

Eur J Endocrinol. 2002 Sep;147(3):313-22.

15.

Genetic alterations in primary and secondary hyperparathyroidism.

Shan L, Nakamura Y, Nakamura M, Yokoi T, Kakudo K.

Pathol Int. 1998 Aug;48(8):569-74. Review.

PMID:
9736402
16.

A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome.

Haven CJ, Wong FK, van Dam EW, van der Juijt R, van Asperen C, Jansen J, Rosenberg C, de Wit M, Roijers J, Hoppener J, Lips CJ, Larsson C, Teh BT, Morreau H.

J Clin Endocrinol Metab. 2000 Apr;85(4):1449-54.

PMID:
10770180
17.

Mutational and gross deletion study of the MEN1 gene and correlation with clinical features in Spanish patients.

Cebrián A, Ruiz-Llorente S, Cascón A, Pollán M, Díez JJ, Picó A, Tellería D, Benítez J, Robledo M.

J Med Genet. 2003 May;40(5):e72. No abstract available.

18.

Multiple endocrine neoplasia type 1 (MEN1) in Austria.

Weinhäusel A, Kaserer K, Vierhapper H, Niederle B, Haas OA; Study Group of Multiple Endocrine Neoplasia Austria.

Wien Klin Wochenschr. 2002 Apr 15;114(7):252-7.

PMID:
12089860
19.

Genotype-phenotype analysis in multiple endocrine neoplasia type 1.

Kouvaraki MA, Lee JE, Shapiro SE, Gagel RF, Sherman SI, Sellin RV, Cote GJ, Evans DB.

Arch Surg. 2002 Jun;137(6):641-7.

PMID:
12049533
20.

Isolated familial hyperparathyroidism with a novel mutation of the MEN1 gene.

Dwarakanathan AA, Zwart S, Oathus RC.

Endocr Pract. 2000 May-Jun;6(3):268-70.

PMID:
11421544
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