Laurell T - Search Results

1

Measuring the aesthetic and functional outcome of pollicization.

Torabi F, Laurell T. Torabi F, et al. Among authors: laurell t. J Hand Surg Eur Vol. 2024 Oct;49(9):1160-1162. doi: 10.1177/17531934241247280. Epub 2024 Apr 27. J Hand Surg Eur Vol. 2024. PMID: 38676543

2

[No title available]

Laurell T, Smith GD, Weber DM. Laurell T, et al. J Hand Surg Eur Vol. 2024 Aug 22:17531934241270346. doi: 10.1177/17531934241270346. Online ahead of print. J Hand Surg Eur Vol. 2024. PMID: 39169791 No abstract available.

3

Epidemiology of congenital upper limb anomalies in 562 children born in 1997 to 2007: a total population study from stockholm, sweden.

Ekblom AG, Laurell T, Arner M. Ekblom AG, et al. Among authors: laurell t. J Hand Surg Am. 2010 Nov;35(11):1742-54. doi: 10.1016/j.jhsa.2010.07.007. Epub 2010 Oct 20. J Hand Surg Am. 2010. PMID: 20961708

4

Epidemiology of congenital upper limb anomalies in Stockholm, Sweden, 1997 to 2007: application of the Oberg, Manske, and Tonkin classification.

Ekblom AG, Laurell T, Arner M. Ekblom AG, et al. Among authors: laurell t. J Hand Surg Am. 2014 Feb;39(2):237-48. doi: 10.1016/j.jhsa.2013.11.014. J Hand Surg Am. 2014. PMID: 24480684

5

Functional Assessment of Children and Adolescents with Symbrachydactyly: A Unilateral Hand Malformation.

Goodell PB, Bauer AS, Oishi S, Arner M, Laurell T, Taylor SL, James MA. Goodell PB, et al. Among authors: laurell t. J Bone Joint Surg Am. 2017 Jul 5;99(13):1119-1128. doi: 10.2106/JBJS.16.01283. J Bone Joint Surg Am. 2017. PMID: 28678125 Free PMC article.

6

Detection of germline mosaicism in fathers of children with intellectual disability syndromes caused by de novo variants.

Frisk S, Wachtmeister A, Laurell T, Lindstrand A, Jäntti N, Malmgren H, Lagerstedt-Robinson K, Tesi B, Taylan F, Nordgren A. Frisk S, et al. Among authors: laurell t. Mol Genet Genomic Med. 2022 Apr;10(4):e1880. doi: 10.1002/mgg3.1880. Epub 2022 Feb 4. Mol Genet Genomic Med. 2022. PMID: 35118825 Free PMC article.

7

Cancer risk in individuals with polydactyly: a Swedish population-based cohort study.

Wachtmeister A, Tettamanti G, Nordgren I, Norrby C, Laurell T, Lu Y, Skarin Nordenvall A, Nordgren A. Wachtmeister A, et al. Among authors: laurell t. Br J Cancer. 2024 Sep;131(4):755-762. doi: 10.1038/s41416-024-02770-z. Epub 2024 Jun 29. Br J Cancer. 2024. PMID: 38951698 Free PMC article.

8

Goltz syndrome in males: A clinical report of a male patient carrying a novel PORCN variant and a review of the literature.

Frisk S, Grandpeix-Guyodo C, Popovic Silwerfeldt K, Hjartarson HT, Chatzianastassiou D, Magnusson I, Laurell T, Nordgren A. Frisk S, et al. Among authors: laurell t. Clin Case Rep. 2018 Sep 21;6(11):2103-2110. doi: 10.1002/ccr3.1783. eCollection 2018 Nov. Clin Case Rep. 2018. PMID: 30455901 Free PMC article.

9

Molecular and clinical delineation of the 17q22 microdeletion phenotype.

Laurell T, Lundin J, Anderlid BM, Gorski JL, Grigelioniene G, Knight SJ, Krepischi AC, Nordenskjöld A, Price SM, Rosenberg C, Turnpenny PD, Vianna-Morgante AM, Nordgren A. Laurell T, et al. Eur J Hum Genet. 2013 Oct;21(10):1085-92. doi: 10.1038/ejhg.2012.306. Epub 2013 Jan 30. Eur J Hum Genet. 2013. PMID: 23361222 Free PMC article.

10

A novel 13 base pair insertion in the sonic hedgehog ZRS limb enhancer (ZRS/LMBR1) causes preaxial polydactyly with triphalangeal thumb.

Laurell T, Vandermeer JE, Wenger AM, Grigelioniene G, Nordenskjöld A, Arner M, Ekblom AG, Bejerano G, Ahituv N, Nordgren A. Laurell T, et al. Hum Mutat. 2012 Jul;33(7):1063-6. doi: 10.1002/humu.22097. Epub 2012 May 11. Hum Mutat. 2012. PMID: 22495965 Free PMC article.

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