Olsson M - Search Results

1

Mitochondrial haplogroup is associated with the phenotype of familial amyloidosis with polyneuropathy in Swedish and French patients.

Olsson M, Hellman U, Planté-Bordeneuve V, Jonasson J, Lång K, Suhr OB. Olsson M, et al. Clin Genet. 2009 Feb;75(2):163-8. doi: 10.1111/j.1399-0004.2008.01097.x. Epub 2008 Nov 1. Clin Genet. 2009. PMID: 19018796

2

Impact of serotonin transporter and catechol-O-methyl transferase genes polymorphism on gastrointestinal dysfunction in Swedish and Japanese familial amyloidotic polyneuropathy patients.

Obayashi K, Olsson M, Anan I, Ueda M, Nakamura M, Okamoto S, Yamashita T, Miida T, Ando Y, Suhr OB. Obayashi K, et al. Among authors: olsson m. Clin Chim Acta. 2008 Dec;398(1-2):10-4. doi: 10.1016/j.cca.2008.07.033. Epub 2008 Aug 5. Clin Chim Acta. 2008. PMID: 18760272

3

Report of five rare or previously unknown amyloidogenic transthyretin mutations disclosed in Sweden.

Suhr OB, Andersen O, Aronsson T, Jonasson J, Kalimo H, Lundahl C, Lundgren HE, Melberg A, Nyberg J, Olsson M, Sandberg A, Westermark P. Suhr OB, et al. Among authors: olsson m. Amyloid. 2009 Dec;16(4):208-14. doi: 10.3109/13506120903421587. Amyloid. 2009. PMID: 19922332

4

TTR familial amyloid polyneuropathy: does a mitochondrial polymorphism entirely explain the parent-of-origin difference in penetrance?

Bonaïti B, Olsson M, Hellman U, Suhr O, Bonaïti-Pellié C, Planté-Bordeneuve V. Bonaïti B, et al. Among authors: olsson m. Eur J Hum Genet. 2010 Aug;18(8):948-52. doi: 10.1038/ejhg.2010.36. Epub 2010 Mar 17. Eur J Hum Genet. 2010. PMID: 20234390 Free PMC article.

5

A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers.

Olsson M, Norgren N, Obayashi K, Plante-Bordeneuve V, Suhr OB, Cederquist K, Jonasson J. Olsson M, et al. BMC Med Genet. 2010 Sep 14;11:130. doi: 10.1186/1471-2350-11-130. BMC Med Genet. 2010. PMID: 20840742 Free PMC article.

6

Allele specific expression of the transthyretin gene in swedish patients with hereditary transthyretin amyloidosis (ATTR V30M) is similar between the two alleles.

Norgren N, Hellman U, Ericzon BG, Olsson M, Suhr OB. Norgren N, et al. Among authors: olsson m. PLoS One. 2012;7(11):e49981. doi: 10.1371/journal.pone.0049981. Epub 2012 Nov 19. PLoS One. 2012. PMID: 23185504 Free PMC article.

7

Frequency of the transthyretin Val30Met mutation in the northern Swedish population.

Olsson M, Jonasson J, Cederquist K, Suhr OB. Olsson M, et al. Amyloid. 2014 Mar;21(1):18-20. doi: 10.3109/13506129.2013.860027. Epub 2014 Feb 6. Amyloid. 2014. PMID: 24555660

8

Gene expression profile in hereditary transthyretin amyloidosis: differences in targeted and source organs.

Norgren N, Olsson M, Nyström H, Ericzon BG, de Tayrac M, Genin E, Planté-Bordeneuve V, Suhr OB. Norgren N, et al. Among authors: olsson m. Amyloid. 2014 Jun;21(2):113-9. doi: 10.3109/13506129.2014.894908. Epub 2014 Mar 7. Amyloid. 2014. PMID: 24601850 Free PMC article.

9

Effect of doxycycline and ursodeoxycholic acid on transthyretin amyloidosis.

Wixner J, Pilebro B, Lundgren HE, Olsson M, Anan I. Wixner J, et al. Among authors: olsson m. Amyloid. 2017 Mar;24(sup1):78-79. doi: 10.1080/13506129.2016.1269739. Epub 2016 Dec 31. Amyloid. 2017. PMID: 28042702 Clinical Trial. No abstract available.

10

Non-parametric estimation of survival in age-dependent genetic disease and application to the transthyretin-related hereditary amyloidosis.

Alarcon F, Planté-Bordeneuve V, Olsson M, Nuel G. Alarcon F, et al. Among authors: olsson m. PLoS One. 2018 Sep 25;13(9):e0203860. doi: 10.1371/journal.pone.0203860. eCollection 2018. PLoS One. 2018. PMID: 30252892 Free PMC article.

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