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Fletta eftir efnisorði "Magnetic resonance imaging"

Fletta eftir efnisorði "Magnetic resonance imaging"

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    Brain ventricle parcellation using a deep neural network: Application to patients with ventriculomegaly 
    Shao, Muhan; Han, Shuo; Carass, Aaron; Li, Xiang; Blitz, Ari M.; Shin, Jaehoon; Prince, Jerry L.; Ellingsen, Lotta María (Elsevier BV, 2019)
    Numerous brain disorders are associated with ventriculomegaly, including both neuro-degenerative diseases and cerebrospinal fluid disorders. Detailed evaluation of the ventricular system is important for these conditions to help understand the pathogenesis ...
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    Genetics of neurodevelopmental disorders: Effects of rare sequence variants on brain structure and function 
    Walters, Guðmundur Bragi (University of Iceland, School of Health Sciences, Faculty of Medicine, 2023-06)
    Introduction and aims: Development of the nervous system is a complex and highly regulated process that, when impaired, can result in a multitude of disorders of varying behavioural, cognitive, and functional severity. Variation in brain structure and ...
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    Intraocular pressure decrease does not affect blood flow rate of ophthalmic artery in ocular hypertension 
    Jóhannesson, Gauti; Qvarlander, Sara; Wåhlin, Anders; Ambarki, Khalid; Hallberg, Per; Eklund, Anders; Lindén, Christina (2020-10)
    PURPOSE. To investigate if decrease of IOP affects the volumetric blood flow rate in the ophthalmic artery (OA) in patients with previously untreated ocular hypertension. METHODS. Subjects with untreated ocular hypertension (n = 30; mean age 67 ± 8 ...
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    MAP1B mutations cause intellectual disability and extensive white matter deficit 
    Walters, G. Bragi; Gústafsson, Ómar; Sveinbjornsson, Gardar; Eiriksdottir, Valgerdur Kristin; Ágústsdóttir, Arna B.; Jónsdóttir, Guðrún A.; Steinberg, Stacy; Gunnarsson, Árni F.; Magnússon, Magnús I.; Unnsteinsdóttir, Unnur; Lee, Amy L.; Jónasdóttir, Aðalbjörg; Sigurðsson, Ásgeir; Jónasdóttir, Áslaug; Skúladóttir, Ástrós; Jonsson, Lina; Nawaz, Muhammad S.; sulem, patrick; Frigge, Mike; Ingason, Andrés; Love, Askell; Norðdahl, Guðmundur L.; Zervas, Mark; Gudbjartsson, Daniel; Ulfarsson, Magnus; Sæmundsen, Evald E.; Stefansson, Hreinn; Stefansson, Kari (Springer Science and Business Media LLC, 2018-08-27)
    Discovery of coding variants in genes that confer risk of neurodevelopmental disorders is an important step towards understanding the pathophysiology of these disorders. Wholegenome sequencing of 31,463 Icelanders uncovers a frameshift variant ...