Larsson C - Search Results

1

Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophy.

Silburn PA, Nicholson GA, Teh BT, Blair IP, Pollard JD, Nolan PJ, Larsson C, Boyle RS. Silburn PA, et al. Among authors: larsson c. Neurology. 1998 Apr;50(4):1067-73. doi: 10.1212/wnl.50.4.1067. Neurology. 1998. PMID: 9566396

2

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy.

Sullivan AA, Teh BT, Jeavons S, Schalling M, Silburn P, Larsson C, Boyle R. Sullivan AA, et al. Among authors: larsson c. J Clin Neurosci. 1997 Apr;4(2):176-80. doi: 10.1016/s0967-5868(97)90070-9. J Clin Neurosci. 1997. PMID: 18638952

3

Bilateral multiple renal oncocytomas and cysts associated with a constitutional translocation (8;9)(q24.1;q34.3) and a rare constitutional VHL missense substitution.

Teh BT, Blennow E, Giraud S, Sahlén S, Hii SI, Brookwell R, Brauch H, Nordenskjöld M, Larsson C, Nicol D. Teh BT, et al. Among authors: larsson c. Genes Chromosomes Cancer. 1998 Mar;21(3):260-4. doi: 10.1002/(sici)1098-2264(199803)21:3<260::aid-gcc12>3.0.co;2-t. Genes Chromosomes Cancer. 1998. PMID: 9523203

4

Familial periodic cerebellar ataxia without myokymia maps to a 19-cM region on 19p13.

Teh BT, Silburn P, Lindblad K, Betz R, Boyle R, Schalling M, Larsson C. Teh BT, et al. Among authors: larsson c. Am J Hum Genet. 1995 Jun;56(6):1443-9. Am J Hum Genet. 1995. PMID: 7762567 Free PMC article.

5

Characterization of the mouse Men1 gene and its expression during development.

Stewart C, Parente F, Piehl F, Farnebo F, Quincey D, Silins G, Bergman L, Carle GF, Lemmens I, Grimmond S, Xian CZ, Khodei S, Teh BT, Lagercrantz J, Siggers P, Calender A, Van de Vem V, Kas K, Weber G, Hayward N, Gaudray P, Larsson C. Stewart C, et al. Among authors: larsson c. Oncogene. 1998 Nov 12;17(19):2485-93. doi: 10.1038/sj.onc.1202164. Oncogene. 1998. PMID: 9824159

6

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.

7

Phenotype and phenocopy: the relationship between genotype and clinical phenotype in a single large family with multiple endocrine neoplasia type 1 (MEN 1).

Burgess JR, Nord B, David R, Greenaway TM, Parameswaran V, Larsson C, Shepherd JJ, Teh BT. Burgess JR, et al. Among authors: larsson c. Clin Endocrinol (Oxf). 2000 Aug;53(2):205-11. doi: 10.1046/j.1365-2265.2000.01032.x. Clin Endocrinol (Oxf). 2000. PMID: 10931102

8

Genetic studies of a family with hereditary hyperparathyroidism-jaw tumour syndrome.

Wassif WS, Farnebo F, Teh BT, Moniz CF, Li FY, Harrison JD, Peters TJ, Larsson C, Harris P. Wassif WS, et al. Among authors: larsson c. Clin Endocrinol (Oxf). 1999 Feb;50(2):191-6. doi: 10.1046/j.1365-2265.1999.00633.x. Clin Endocrinol (Oxf). 1999. PMID: 10396361

9

Loss of heterozygosity in sporadic parathyroid tumours: involvement of chromosome 1 and the MEN1 gene locus in 11q13.

Dwight T, Twigg S, Delbridge L, Wong FK, Farnebo F, Richardson AL, Nelson A, Zedenius J, Philips J, Larsson C, Teh BT, Robinson B. Dwight T, et al. Among authors: larsson c. Clin Endocrinol (Oxf). 2000 Jul;53(1):85-92. doi: 10.1046/j.1365-2265.2000.01010.x. Clin Endocrinol (Oxf). 2000. PMID: 10931084

10

Clinical and genetic studies of Van der Woude syndrome in Sweden.

Wong FK, Karsten A, Larson O, Huggare J, Hagberg C, Larsson C, Teh BT, Linder-Aronson S. Wong FK, et al. Among authors: larsson c. Acta Odontol Scand. 1999 Apr;57(2):72-6. doi: 10.1080/000163599428931. Acta Odontol Scand. 1999. PMID: 10445358

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