Zoekresultaten - Reynir Arngrı́msson

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  1. 1
    C-Reactive Protein Is Elevated 30 Years After Eclamptic Pregnancy

    C-Reactive Protein Is Elevated 30 Years After Eclamptic Pregnancy door Carl A. Hubel, Robert W. Powers, Sunna Snaedal, Hilary S. Gammill, Roberta B. Ness, James M. Roberts, Reynir Arngrı́msson

    Gepubliceerd in 2008
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  2. 2
    MODY in Iceland is associated with mutations in HNF -1? and a novel mutation in NeuroD1

    MODY in Iceland is associated with mutations in HNF -1? and a novel mutation in NeuroD1 door S. Y. Kristinsson, Bente A. Talseth‐Palmer, Eirı́kur Steingrı́msson, A. V. Thorsson, T. Helgason, Á. B. Hreidarsson, Eirny Tholl Thorolfsdottir, Reynir Arngrı́msson

    Gepubliceerd in 2001
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  3. 3
    Evidence for a Familial Pregnancy-Induced Hypertension Locus in the eNOS-Gene Region

    Evidence for a Familial Pregnancy-Induced Hypertension Locus in the eNOS-Gene Region door Reynir Arngrı́msson, Caroline Hayward, Sophie Nadaud, Ásdís Baldursdóttir, James J. Walker, Wang A. Liston, Ragnheiür I. Bjarnadóttir, D. J. H. Brock, Reynir Tómas Geirsson, James Connor, Florent Soubrier

    Gepubliceerd in 1997
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  4. 4
    A genome-wide scan for preeclampsia in the Netherlands

    A genome-wide scan for preeclampsia in the Netherlands door Augusta MA Lachmeijer, Reynir Arngrı́msson, Esther J. Bastiaans, Michael L. Frigge, Gerard Pals, Sigrún Sigurðardóttir, Hreinn Stefánsson, Bernhard Ø. Palsson, Dan L. Nicolae, Augustin Kong, Jan G. Aarnoudse, Jeff R Gulcher, Guustaaf A. Dekker, Leo P. ten Kate, Kāri Stefánsson

    Gepubliceerd in 2001
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  5. 5
    Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters

    Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters door Gudny A. Arnadottir, Brynjar Ö. Jensson, S Marelsson, Gerald Sulem, Ásmundur Oddsson, Ragnar P. Kristjansson, Stefania Benónísdóttir, Sigurjón A. Guðjónsson, Gísli Másson, Guðmundur Á. Þórisson, Jona Saemundsdottir, Ólafur Þ. Magnússon, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Ásgeir Sigurðsson, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Reynir Arngrı́msson, Patrick Sulem, Kāri Stefánsson

    Gepubliceerd in 2017
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  6. 6
    COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

    COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA door Brynjar Ö. Jensson, Sif Hansdóttir, Gudny A. Arnadottir, Gerald Sulem, Ragnar P. Kristjansson, Ásmundur Oddsson, Stefania Benónísdóttir, Hákon Jónsson, Agnar Helgason, Jona Saemundsdottir, Ólafur Þ. Magnússon, Gísli Másson, Guðmundur Á. Þórisson, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Ásgeir Sigurðsson, Ingileif Jónsdóttir, Vigdís Pétursdóttir, Jón R. Kristinsson, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Reynir Arngrı́msson, Patrick Sulem, Gunnar Guðmundsson, Hreinn Stefánsson

    Gepubliceerd in 2017
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  7. 7
    Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2

    Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2 door Sigurdís Haraldsdóttir, Þórunn Rafnar, Wendy L. Frankel, Sylvia Einarsdottir, Ásgeir Sigurðsson, Heather Hampel, Pétur Snæbjörnsson, Gísli Másson, Daniel Weng, Reynir Arngrı́msson, Birte Kehr, Ahmet Yılmaz, Stefán Haraldsson, Patrick Sulem, Tryggvi Stefánsson, Peter G. Shields, Fridbjörn Sigurdsson, Tanios Bekaii‐Saab, Páll Helgi Möller, Margrét Steinarsdóttir, Kristín Alexíusdóttir, Megan P. Hitchins, Colin C. Pritchard, Albert de la Chapelle, Jón G. Jónasson, Richard M. Goldberg, Kāri Stefánsson

    Gepubliceerd in 2017
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  8. 8
    Recommendations for initiation and cessation of enzyme replacement therapy in patients with Fabry disease: the European Fabry Working Group consensus document

    Recommendations for initiation and cessation of enzyme replacement therapy in patients with Fabry disease: the European Fabry Working Group consensus document door Marieke Biegstraaten, Reynir Arngrı́msson, Frédéric Barbey, Lut Boks, Franco Cecchi, Patrick Deegan, Ulla Feldt‐Rasmussen, Tarekegn Geberhiwot, Dominique P. Germain, Christian J. Hendriksz, Derralynn Hughes, Ilkka Kantola, Nesrin Karabul, Christine Lavery, Gabor E. Linthorst, Atul Mehta, Erica van de Mheen, João Paulo Oliveira, Rossella Parini, Uma Ramaswami, Michael Rudnicki, Andreas L. Serra, Claudia Sommer, Gere Sunder‐Plassmann, Einar Svarstad, Annelies Sweeb, Wim Terryn, Anna Tylki‐Szymańska, Camilla Tøndel, Bojan Vujkovac, Frank Weidemann, Frits A. Wijburg, Peter Woolfson, Carla E. M. Hollak

    Gepubliceerd in 2015
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  9. 9
    A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease

    A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease door Gudny A. Arnadottir, Gudmundur L. Norddahl, Steinunn Guðmundsdóttir, Arna B. Agustsdottir, Snævar Sigurðsson, Brynjar Ö. Jensson, Kristbjörg Bjarnadóttir, Fannar Theódórs, Stefania Benónísdóttir, Erna V. Ivarsdottir, Ásmundur Oddsson, Ragnar P. Kristjansson, Gerald Sulem, Kristjan F. Alexandersson, Thorhildur Juliusdottir, Kjartan R. Guðmundsson, Jona Saemundsdottir, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Ásgeir Sigurðsson, Paolo Manzanillo, Sigurjón A. Guðjónsson, Guðmundur Á. Þórisson, Ólafur Þ. Magnússon, Gísli Másson, Kjartan B. Örvar, Hilma Hólm, Sigurður Björnsson, Reynir Arngrı́msson, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Ingileif Jónsdóttir, Ásgeir Haraldsson, Patrick Sulem, Kāri Stefánsson

    Gepubliceerd in 2018
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