Åström E - Search Results

1

Autosomal dominant brachyolmia in a large Swedish family: phenotypic spectrum and natural course.

Grigelioniene G, Geiberger S, Horemuzova E, Moström E, Jäntti N, Neumeyer L, Åström E, Nordenskjöld M, Nordgren A, Mäkitie O. Grigelioniene G, et al. Among authors: astrom e. Am J Med Genet A. 2014 Jul;164A(7):1635-41. doi: 10.1002/ajmg.a.36502. Epub 2014 Mar 26. Am J Med Genet A. 2014. PMID: 24677493 Review.

2

Novel mutations in the LRP5 gene in patients with Osteoporosis-pseudoglioma syndrome.

Pekkinen M, Grigelioniene G, Akin L, Shah K, Karaer K, Kurtoğlu S, Ekbote A, Aycan Z, Sağsak E, Danda S, Åström E, Mäkitie O. Pekkinen M, et al. Among authors: astrom e. Am J Med Genet A. 2017 Dec;173(12):3132-3135. doi: 10.1002/ajmg.a.38491. Epub 2017 Oct 21. Am J Med Genet A. 2017. PMID: 29055141 No abstract available.

3

Expanding the Clinical Spectrum of Phenotypes Caused by Pathogenic Variants in PLOD2.

Leal GF, Nishimura G, Voss U, Bertola DR, Åström E, Svensson J, Yamamoto GL, Hammarsjö A, Horemuzova E, Papadiogannakis N, Iwarsson E, Grigelioniene G, Tham E. Leal GF, et al. Among authors: astrom e. J Bone Miner Res. 2018 Apr;33(4):753-760. doi: 10.1002/jbmr.3348. Epub 2018 Jan 4. J Bone Miner Res. 2018. PMID: 29178448 Free article.

4

Genetic epidemiology, prevalence, and genotype-phenotype correlations in the Swedish population with osteogenesis imperfecta.

Lindahl K, Åström E, Rubin CJ, Grigelioniene G, Malmgren B, Ljunggren Ö, Kindmark A. Lindahl K, et al. Among authors: astrom e. Eur J Hum Genet. 2015 Aug;23(8):1042-50. doi: 10.1038/ejhg.2015.81. Epub 2015 May 6. Eur J Hum Genet. 2015. PMID: 25944380 Free PMC article.

5

Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta - A retrospective cohort study.

Andersson K, Dahllöf G, Lindahl K, Kindmark A, Grigelioniene G, Åström E, Malmgren B. Andersson K, et al. Among authors: astrom e. PLoS One. 2017 May 12;12(5):e0176466. doi: 10.1371/journal.pone.0176466. eCollection 2017. PLoS One. 2017. PMID: 28498836 Free PMC article.

6

Mutations in COL1A1/A2 and CREB3L1 are associated with oligodontia in osteogenesis imperfecta.

Andersson K, Malmgren B, Åström E, Nordgren A, Taylan F, Dahllöf G. Andersson K, et al. Among authors: astrom e. Orphanet J Rare Dis. 2020 Mar 31;15(1):80. doi: 10.1186/s13023-020-01361-4. Orphanet J Rare Dis. 2020. PMID: 32234057 Free PMC article.

7

Tooth agenesis in osteogenesis imperfecta related to mutations in the collagen type I genes.

Malmgren B, Andersson K, Lindahl K, Kindmark A, Grigelioniene G, Zachariadis V, Dahllöf G, Åström E. Malmgren B, et al. Among authors: astrom e. Oral Dis. 2017 Jan;23(1):42-49. doi: 10.1111/odi.12568. Epub 2016 Sep 13. Oral Dis. 2017. PMID: 27510842

8

Decreased fracture rate, pharmacogenetics and BMD response in 79 Swedish children with osteogenesis imperfecta types I, III and IV treated with Pamidronate.

Lindahl K, Kindmark A, Rubin CJ, Malmgren B, Grigelioniene G, Söderhäll S, Ljunggren Ö, Åström E. Lindahl K, et al. Among authors: astrom e. Bone. 2016 Jun;87:11-8. doi: 10.1016/j.bone.2016.02.015. Epub 2016 Mar 5. Bone. 2016. PMID: 26957348

9

Genetic epidemiology, prevalence, and genotype-phenotype correlations in the Swedish population with osteogenesis imperfecta.

Lindahl K, Åström E, Rubin CJ, Grigelioniene G, Malmgren B, Ljunggren Ö, Kindmark A. Lindahl K, et al. Among authors: astrom e. Eur J Hum Genet. 2015 Aug;23(8):1112. doi: 10.1038/ejhg.2015.129. Eur J Hum Genet. 2015. PMID: 26177859 Free PMC article. No abstract available.

10

Pre- and postnatal transplantation of fetal mesenchymal stem cells in osteogenesis imperfecta: a two-center experience.

Götherström C, Westgren M, Shaw SW, Aström E, Biswas A, Byers PH, Mattar CN, Graham GE, Taslimi J, Ewald U, Fisk NM, Yeoh AE, Lin JL, Cheng PJ, Choolani M, Le Blanc K, Chan JK. Götherström C, et al. Among authors: astrom e. Stem Cells Transl Med. 2014 Feb;3(2):255-64. doi: 10.5966/sctm.2013-0090. Epub 2013 Dec 16. Stem Cells Transl Med. 2014. PMID: 24342908 Free PMC article. Clinical Trial.

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