Search Results - "Asbjornsdottir, Birna"

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    Zonulin-Dependent Intestinal Permeability in Children Diagnosed with Mental Disorders: A Systematic Review and Meta-Analysis by Asbjornsdottir, Birna, Snorradottir, Heiddis, Andresdottir, Edda, Fasano, Alessio, Lauth, Bertrand, Gudmundsson, Larus S, Gottfredsson, Magnus, Halldorsson, Thorhallur Ingi, Birgisdottir, Bryndis Eva

    Published in Nutrients (03-07-2020)
    “…Worldwide, up to 20% of children and adolescents experience mental disorders, which are the leading cause of disability in young people. Research shows that…”
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    Episodic ataxia type 2 (EA2) with interictal myokymia and focal dystonia by Nielsen, Emilie Neerup, Ásbjörnsdóttir, Birna, Møller, Lisbeth Birk, Nielsen, Jørgen Erik, Lindquist, Suzanne Granhøj

    Published in Cold Spring Harbor molecular case studies (01-10-2022)
    “…Episodic ataxia type 1 and 2 (EA1 and EA2) are the most well-described of the episodic ataxias. They are autosomal dominantly inherited early-onset diseases…”
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    Meals, Microbiota and Mental Health in Children and Adolescents by Asbjornsdottir, Birna, Lauth, Bertrand, Fasano, Alessio, Thorsdottir, Inga, Karlsdottir, Ingibjorg, Gudmundsson, Larus S, Gottfredsson, Magnus, Smarason, Orri, Sigurdardottir, Sigurveig, Halldorsson, Thorhallur I, Marteinsson, Viggo Thor, Gudmundsdottir, Valborg, Birgisdottir, Bryndis Eva

    Published in PloS one (01-09-2022)
    “…Recent studies indicate that the interplay between diet, intestinal microbiota composition, and intestinal permeability can impact mental health. More than 10%…”
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    D15 The blood-brain barrier integrity and frequency of CSF Th17.1 cells in Huntington´s disease by Ásbjörnsdóttir, Birna, Musaeus, Christian Sandøe, Hellem, Marie NN, Vinther-Jensen, Tua, Hjermind, Lena E, Simonsen, Anja Hviid, von Essen, Marina R, Sellebjerg, Finn, Nielsen, Jørgen Erik

    “…BackgroundThe role of blood-brain barrier (BBB) in the pathogenesis of Huntington´s disease (HD) is not well understood. We recently found increased frequency…”
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    Widening the spectrum of spinocerebellar ataxia autosomal recessive type 10 (SCAR10) by Ásbjörnsdóttir, Birna, Henriksen, Otto Mølby, Lindquist, Suzanne, Møller, Lisbeth Birk, Sidaros, Annette, Nielsen, Jørgen Erik

    Published in BMJ case reports (07-03-2022)
    “…Biallelic pathogenic variants in the gene cause spinocerebellar ataxia recessive type 10. We report two patients, both compound heterozygous for variants,…”
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