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Author/Creator Adalsteinsdottir, Berglind

1. A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta. (24th March 2018)

Authors:
Bjornsson, Thorsteinn; Thorolfsdottir, Rosa B; Sveinbjornsson, Gardar; Sulem, Patrick; Norddahl, Gudmundur L; Helgadottir, Anna; Gretarsdottir, Solveig; Magnusdottir, Audur; Danielsen, Ragnar; Sigurdsson, Emil L; Adalsteinsdottir, Berglind; Gunnarsson, Sverrir I; Jonsdottir, Ingileif; Arnar, Davi...
Journal:
European heart journal
Issue:
Volume 39:Number 34(2018)
Page Start:
3243
Record Type:
Journal Article
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2. Fabry Disease in Families With Hypertrophic Cardiomyopathy: Clinical Manifestations in the Classic and Later-Onset Phenotypes. (August 2017)

Authors:
Adalsteinsdottir, Berglind; Palsson, Runolfur; Desnick, Robert J.; Gardarsdottir, Marianna; Teekakirikul, Polakit; Maron, Martin; Appelbaum, Evan; Neisius, Ulf; Maron, Barry J.; Burke, Michael A.; Chen, Brenden; Pagant, Silvere; Madsen, Christoffer V.; Danielsen, Ragnar; Arngrimsson, Reynir; Feld...
Journal:
Circulation
Issue:
Volume 10:Number 4(2017)
Page Start:
Record Type:
Journal Article
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3. Hypertrophic cardiomyopathy in myosin-binding protein C (MYBPC3) Icelandic founder mutation carriers. Issue 1 (5th April 2020)

Authors:
Adalsteinsdottir, Berglind; Burke, Michael; Maron, Barry J; Danielsen, Ragnar; Lopez, Begoña; Diez, Javier; Jarolim, Petr; Seidman, Jonathan; Seidman, Christine E.; Ho, Carolyn Y; Gunnarsson, Gunnar Th
Journal:
Open heart
Issue:
Volume 7:Issue 1(2020)
Page Start:
Record Type:
Journal Article
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