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Malin Olsson
Kontakt
E-post
malin.olsson@umu.se
Telefon
090-785 16 21
Verksam vid
Anknytning
Första forskningsingenjör vid
Institutionen för folkhälsa och klinisk medicin
Enhet: Avdelningen för medicin
Plats
6M, Norrlands Universitetssjukhus, 5032
Umeå universitet, by1a, B41, NUS, 901 85 Umeå
Publikationer
Publikationer
Forskning
Forskning
2021
New data on the genetic profile and penetrance of hereditary Val30Met transthyretin amyloidosis in Sweden
Amyloid: Journal of Protein Folding Disorders
, Taylor & Francis 2021, Vol. 28, (2) : 84-90
Gorram, Farida; Olsson, Malin; Alarcon, Flora; et al.
2021
Metabolomics analysis for diagnosis and biomarker discovery of transthyretin amyloidosis
Amyloid: Journal of Protein Folding Disorders
, Taylor & Francis Group 2021, Vol. 28, (4) : 234-242
Olsson, Malin; Hellman, Urban; Wixner, Jonas; et al.
2019
Transthyretin Glu54Leu - an unknown mutation within the Swedish population associated with amyloid cardiomyopathy and a unique fibril type
Scandinavian Journal of Clinical and Laboratory Investigation
, Taylor & Francis 2019, Vol. 79, (6) : 372-376
Hellman, Urban; Lång, Kenneth; Ihse, Elisabet; et al.
2018
Non-parametric estimation of survival in age-dependent genetic disease and application to the transthyretin-related hereditary amyloidosis
PLOS ONE
, Public Library Science 2018, Vol. 13, (9)
Alarcon, Flora; Plante-Bordeneuve, Violaine; Olsson, Malin; et al.
2018
Variation of Penetrance estimates in a wide spectrum of TTR-FAP families: implication for management of carriers
Neurology
, Lippincott Williams & Wilkins 2018, Vol. 90
Gorram, Farida; Olsson, Malin; Alarcon, Flora; et al.
2017
Effect of doxycycline and ursodeoxycholic acid on transthyretin amyloidosis
Amyloid: Journal of Protein Folding Disorders
, Vol. 24, (1) : 78-79
Wixner, Jonas; Pilebro, Bjorn; Lundgren, Hans-Erik; et al.
2014
Gene expression profile in hereditary transthyretin amyloidosis: differences in targeted and source organs
Amyloid: Journal of Protein Folding Disorders
, Vol. 21, (2) : 113-119
Norgren, Nina; Olsson, Malin; Nyström, Hanna; et al.
2014
Frequency of the transthyretin Val30Met mutation in the northern Swedish population
Amyloid: Journal of Protein Folding Disorders
, Vol. 21, (1) : 18-20
Olsson, Malin; Jonasson, Jenni; Cederquist, Kristina; et al.
2012
Allele specific expression of the transthyretin gene in Swedish patients with hereditary transthyretin amyloidosis (ATTR V30M) is similar between the two alleles
PLOS ONE
, Vol. 7, (11) : e49981-
Norgren, Nina; Hellman, Urban; Ericzon, Bo Göran; et al.
2010
TTR familial amyloid polyneuropathy: does a mitochondrial polymorphism entirely explain the parent-of-origin difference in penetrance?
European Journal of Human Genetics
Bonaïti, Bernard; Olsson, Malin; Hellman, Urban; et al.
2010
Familial amyloidosis with polyneuropathy: studies of genetic factors modifying the phenotype of the disease
Umeå University medical dissertations
, 1351
Olsson, Malin
2010
A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers
BMC Medical Genetics
, Vol. 11 : 130-
Olsson, Malin; Norgren, Nina; Obayashi, Konen; et al.
2009
Mitochondrial haplogroup is associated with the phenotype of familial amyloidosis with polyneuropathy in Swedish and French patients
Clinical Genetics
, Vol. 75, (2) : 163-168
Olsson, Malin; Hellman, Urban; Planté-Bordeneuve, V; et al.
2009
Report of five rare or previously unknown amyloidogenic transthyretin mutations disclosed in Sweden.
Amyloid: Journal of Protein Folding Disorders
, Vol. 16, (4) : 208-214
Suhr, Ole B; Andersen, Oluf; Aronsson, Thomas; et al.
2008
Impact of serotonin transporter and catechol-O-methyl transferase genes polymorphism on gastrointestinal dysfunction in Swedish and Japanese familial amyloidotic polyneuropathy patients.
Clinica Chimica Acta
, Vol. 398, (1-2) : 10-4
Obayashi, Konen; Olsson, Malin; Anan, Intissar; et al.
Genealogic studies of the Swedish hereditary transthyretin amyloidosis (ATTR V30M) population: differences in age at onset within the population
Norgren, Nina; Andersson Escher, Stefan; Lundgren, Hans-Erik; et al.
Distribution of mitochondrial DNA haplogroups in Portuguese familial amyloidosis with polyneuropathy (FAP) patients
Olsson, Malin; Norgren, Nina; Saraiva, Maria J; et al.
Visa publikationer i DiVA
Forskargrupper
Gruppmedlem
Amyloidoscentrum
Forskningsprojekt
1 januari 2019
Patogenes, diagnostik och behandling av transtyretinamyloidos
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