Larsson C - Search Results

1

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

2

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

3

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.

4

Oculopharyngeal muscular dystrophy (OPMD)--report and genetic studies of an Australian kindred.

Teh BT, Sullivan AA, Farnebo F, Zander C, Li FY, Strachan N, Schalling M, Larsson C, Sandstrom P. Teh BT, et al. Among authors: larsson c. Clin Genet. 1997 Jan;51(1):52-5. doi: 10.1111/j.1399-0004.1997.tb02415.x. Clin Genet. 1997. PMID: 9084936

5

Gene identification in autosomal dominant disorders.

Teh BT, Lagercrantz J, Weber G, Larsson C. Teh BT, et al. Among authors: larsson c. AJNR Am J Neuroradiol. 1997 May;18(5):991-2. AJNR Am J Neuroradiol. 1997. PMID: 9159384 Free PMC article. No abstract available.

6

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

7

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.

8

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

9

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

10

Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas.

Teh BT, Farnebo F, Kristoffersson U, Sundelin B, Cardinal J, Axelson R, Yap A, Epstein M, Heath H 3rd, Cameron D, Larsson C. Teh BT, et al. Among authors: larsson c. J Clin Endocrinol Metab. 1996 Dec;81(12):4204-11. doi: 10.1210/jcem.81.12.8954016. J Clin Endocrinol Metab. 1996. PMID: 8954016

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