Larsson C - Search Results

1

Genetic analysis of lithium-associated parathyroid tumors.

Dwight T, Kytölä S, Teh BT, Theodosopoulos G, Richardson AL, Philips J, Twigg S, Delbridge L, Marsh DJ, Nelson AE, Larsson C, Robinson BG. Dwight T, et al. Among authors: larsson c. Eur J Endocrinol. 2002 May;146(5):619-27. doi: 10.1530/eje.0.1460619. Eur J Endocrinol. 2002. PMID: 11980616

2

Predictive testing for multiple endocrine neoplasia type 1 using DNA polymorphisms.

Larsson C, Shepherd J, Nakamura Y, Blomberg C, Weber G, Werelius B, Hayward N, Teh B, Tokino T, Seizinger B. Larsson C, et al. J Clin Invest. 1992 Apr;89(4):1344-9. doi: 10.1172/JCI115720. J Clin Invest. 1992. PMID: 1348254 Free PMC article.

3

Multiple endocrine neoplasia type I: clinical syndrome to molecular genetics.

Teh BT, Grimmond S, Shepherd J, Larsson C, Hayward N. Teh BT, et al. Among authors: larsson c. Aust N Z J Surg. 1995 Oct;65(10):708-13. doi: 10.1111/j.1445-2197.1995.tb00541.x. Aust N Z J Surg. 1995. PMID: 7487708 Review. No abstract available.

4

Exclusion of the 13-kDa rapamycin binding protein gene (FKBP2) as a candidate gene for multiple endocrine neoplasia type 1.

Grimmond S, Weber G, Larsson C, Walters M, Teh B, Shepherd J, Nordenskjold M, Hayward N. Grimmond S, et al. Among authors: larsson c. Hum Genet. 1995 Apr;95(4):455-8. doi: 10.1007/BF00208976. Hum Genet. 1995. PMID: 7535744

5

Molecular tools for presymptomatic testing in multiple endocrine neoplasia type 1.

Larsson C, Calender A, Grimmond S, Giraud S, Hayward NK, Teh B, Farnebo F. Larsson C, et al. J Intern Med. 1995 Sep;238(3):239-44. doi: 10.1111/j.1365-2796.1995.tb00929.x. J Intern Med. 1995. PMID: 7673853

6

Genetic mapping of the multiple endocrine neoplasia type 1 locus at 11q13.

Teh BT, Cardinal J, Shepherd J, Hayward NK, Weber G, Cameron D, Larsson C. Teh BT, et al. Among authors: larsson c. J Intern Med. 1995 Sep;238(3):249-53. doi: 10.1111/j.1365-2796.1995.tb00931.x. J Intern Med. 1995. PMID: 7673855

7

Familial isolated hyperparathyroidism: a distinct genetic entity with an increased risk of parathyroid cancer.

Wassif WS, Moniz CF, Friedman E, Wong S, Weber G, Nordenskjöld M, Peters TJ, Larsson C. Wassif WS, et al. Among authors: larsson c. J Clin Endocrinol Metab. 1993 Dec;77(6):1485-9. doi: 10.1210/jcem.77.6.7903311. J Clin Endocrinol Metab. 1993. PMID: 7903311

8

Genetic studies of thymic carcinoids in multiple endocrine neoplasia type 1.

Teh BT, Hayward NK, Walters MK, Shepherd JJ, Wilkinson S, Nordenskjold M, Larsson C. Teh BT, et al. Among authors: larsson c. J Med Genet. 1994 Mar;31(3):261-2. doi: 10.1136/jmg.31.3.261. J Med Genet. 1994. PMID: 7912288 Free PMC article. No abstract available.

9

Genetics of multiple endocrine neoplasia type 1.

Larsson C, Weber G, Teh BT, Lagercrantz J. Larsson C, et al. Ann N Y Acad Sci. 1994 Sep 15;733:453-63. doi: 10.1111/j.1749-6632.1994.tb17295.x. Ann N Y Acad Sci. 1994. PMID: 7978894 Review. No abstract available.

10

Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domains.

Heath H 3rd, Odelberg S, Jackson CE, Teh BT, Hayward N, Larsson C, Buist NR, Krapcho KJ, Hung BC, Capuano IV, Garrett JE, Leppert MF. Heath H 3rd, et al. Among authors: larsson c. J Clin Endocrinol Metab. 1996 Apr;81(4):1312-7. doi: 10.1210/jcem.81.4.8636323. J Clin Endocrinol Metab. 1996. PMID: 8636323

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