Gretar Gudmundsson
Overview
Explore the profile of Gretar Gudmundsson including associated specialties, affiliations and a list of published articles.
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6
Citations
220
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Recent Articles
1.
Ingre C, Pinto S, Birve A, Press R, Danielsson O, de Carvalho M, et al.
Amyotroph Lateral Scler Frontotemporal Degener
. 2013 Aug;
14(7-8):620-7.
PMID: 23971766
Linkage analysis in Brazilian families with amyotrophic lateral sclerosis (ALS) revealed that a missense mutation p.Pro56Ser in a conserved gene VAMP-associated protein type B and C (VAPB) cosegregates with disease....
2.
Bjornsdottir A, Gudmundsson G, Blondal H, Olafsson E
J Neurol Neurosurg Psychiatry
. 2012 Nov;
84(2):136-40.
PMID: 23192520
Background: Multiple system atrophy (MSA) is a neurodegenerative disorder characterised by autonomic dysfunction with parkinsonism (MSAp) or cerebellar (MSAc) symptoms. At autopsy, α-synuclein inclusions in glial cells of the brain...
3.
Torsdottir G, Kristinsson J, Snaedal J, Sveinbjornsdottir S, Gudmundsson G, Hreidarsson S, et al.
J Neurol Sci
. 2010 Sep;
299(1-2):51-4.
PMID: 20851426
This short review describes a series of case-control studies on the concentration and oxidative activity of ceruloplasmin (CP) in serum and the activity of superoxide dismutase (SOD1) in erythrocytes in...
4.
Anttila V, Stefansson H, Kallela M, Todt U, Terwindt G, Calafato M, et al.
Nat Genet
. 2010 Aug;
42(10):869-73.
PMID: 20802479
Migraine is a common episodic neurological disorder, typically presenting with recurrent attacks of severe headache and autonomic dysfunction. Apart from rare monogenic subtypes, no genetic or molecular markers for migraine...
5.
Torsdottir G, Gudmundsson G, Kristinsson J, Snaedal J, Johannesson T
Neuropsychiatr Dis Treat
. 2009 Jun;
5:55-9.
PMID: 19557100
At the time of this study, there were five known patients with Wilson disease (WD) in Iceland. The mutation, a 7-bp deletion in exon 7 on chromosome 13 for WD,...
6.
Bjornsson A, Gudmundsson G, Gudfinnsson E, Hrafnsdottir M, Benedikz J, Skuladottir S, et al.
Am J Hum Genet
. 2003 Sep;
73(5):986-93.
PMID: 14513409
Migraine is a common form of headache and has a significant genetic component. Here, we report linkage results from a study in Iceland of migraine without aura (MO). The study...