APOE-ε4 Is Associated With Reduced Verbal Memory Performance and Higher Emotional, Cognitive, and Everyday Executive Function Symptoms Two Months After Mild Traumatic Brain Injury von Hellstrøm, Torgeir, Andelic, Nada, Holthe, Øyvor Øistensen, Helseth, Eirik, Server, Andres, Eiklid, Kristin, Sigurdardottir, Solrun

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Whole exome sequencing of sporadic patients with Currarino Syndrome: A report of three trios von Holm, Ingunn, Spildrejorde, Mari, Stadheim, Barbro, Eiklid, Kristin L., Samarakoon, Pubudu S.

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SLC9A6 Mutations Cause X-Linked Mental Retardation, Microcephaly, Epilepsy, and Ataxia, a Phenotype Mimicking Angelman Syndrome von Gilfillan, Gregor D., Selmer, Kaja K., Roxrud, Ingrid, Smith, Raffaella, Kyllerman, Mårten, Eiklid, Kristin, Kroken, Mette, Mattingsdal, Morten, Egeland, Thore, Stenmark, Harald, Sjøholm, Hans, Server, Andres, Samuelsson, Lena, Christianson, Arnold, Tarpey, Patrick, Whibley, Annabel, Stratton, Michael R., Futreal, P. Andrew, Teague, Jon, Edkins, Sarah, Gecz, Jozef, Turner, Gillian, Raymond, F. Lucy, Schwartz, Charles, Stevenson, Roger E., Undlien, Dag E., Strømme, Petter

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Apolipoprotein e4 Status and Brain Structure 12 Months after Mild Traumatic Injury: Brain Age Prediction Using Brain Morphometry and Diffusion Tensor Imaging von Hellstrom, Torgeir, Andelic, Nada, de Lange, Ann-Marie G., Helseth, Eirik, Eiklid, Kristin, Westlye, Lars T.

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Two new Rett syndrome families and review of the literature: expanding the knowledge of MECP2 frameshift mutations von Ravn, Kirstine, Roende, Gitte, Duno, Morten, Fuglsang, Kathrine, Eiklid, Kristin L, Tümer, Zeynep, Nielsen, Jytte B, Skjeldal, Ola H

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A 5.8kb deletion removing the entire MNX1 gene in a Norwegian family with Currarino syndrome von Holm, Ingunn, Monclair, Tom, Lundar, Tryggve, Stadheim, Barbro, Prescott, Trine E., Eiklid, Kristin L.

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CCBE1 mutation in two siblings, one manifesting lymphedema-cholestasis syndrome, and the other, fetal hydrops von Shah, Sohela, Conlin, Laura K, Gomez, Luis, Aagenaes, Øystein, Eiklid, Kristin, Knisely, A S, Mennuti, Michael T, Matthews, Randolph P, Spinner, Nancy B, Bull, Laura N

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A 5.8 kb deletion removing the entire MNX1 gene in a Norwegian family with Currarino syndrome von Holm, Ingunn, Monclair, Tom, Lundar, Tryggve, Stadheim, Barbro, Prescott, Trine E, Eiklid, Kristin L

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Cognitive impairment and the role of the ApoE ε4-allele after stroke-a 13 months follow-up study von Wagle, Jørgen, Farner, Lasse, Flekkøy, Kjell, Wyller, Torgeir B., Sandvik, Leiv, Eiklid, Kristin L., Fure, Brynjar, Stensrød, Brynhild, Engedal, Knut

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Age-dependent clinical problems in a Norwegian national survey of patients with the 22q11.2 deletion syndrome von Lima, Kari, Følling, Ivar, Eiklid, Kristin L., Natvig, Solveig, Abrahamsen, Tore G.

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Familial globotriaosylceramide-associated cardiomyopathy mimicking Fabry disease von Apelland, Turid, Gude, Einar, Strøm, Erik H, Gullestad, Lars, Eiklid, Kristin L, Månsson, Jan-Eric, Reinholt, Finn P, Houge, Gunnar, Dahl, Christen P, Almaas, Vibeke M, Heiberg, Arvid

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Association between ApoE ε4 and Cognitive Impairment after Stroke von Wagle, Jørgen, Farner, Lasse, Flekkøy, Kjell, Wyller, Torgeir Bruun, Sandvik, Leiv, Eiklid, Kristin L., Fure, Brynjar, Stensrød, Brynhild, Engedal, Knut

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Association between ApoE epsilon 4 and Cognitive Impairment after Stroke von Wagle, Joergen, Farner, Lasse, Flekkoey, Kjell, Wyller, Torgeir Bruun, Sandvik, Leiv, Eiklid, Kristin L, Fure, Brynjar, Stensroed, Brynhild, Engedal, Knut

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Copy number variation findings among 50 children and adolescents with autism spectrum disorder von Sorte, Hanne S, Gjevik, Elen, Sponheim, Eili, Eiklid, Kristin L, Rødningen, Olaug K

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A novel BMPR2 gene mutation associated with exercise-induced pulmonary hypertension in septal defects von Möller, Thomas, Leren, Trond P., Eiklid, Kristin L., Holmstrøm, Henrik, Fredriksen, Per Morten, Thaulow, Erik

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Aagenaes syndrome/lymphedema cholestasis syndrome 1 is caused by a founder variant in the 5’-untranslated region of UNC45A von Almaas, Runar, Atneosen-Åsegg, Monica, Ytre-Arne, Mari Eknes, Melheim, Maria, Sorte, Hanne Sørmo, Cízková, Dana, Reims, Henrik Mikael, Bezrouk, Aleš, Harrison, Sean Philip, Strand, Janne, Hermansen, Johanne Uthus, Andersen, Sofie Strøm, Eiklid, Kristin Louise, Mokrý, Jaroslav, Sullivan, Gareth John, Stray-Pedersen, Asbjørg

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Cognitive impairment and the role of the ApoE ε 4‐allele after stroke—a 13 months follow‐up study von Wagle, Jørgen, Farner, Lasse, Flekkøy, Kjell, Wyller, Torgeir B., Sandvik, Leiv, Eiklid, Kristin L., Fure, Brynjar, Stensrød, Brynhild, Engedal, Knut

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Characterization of a Norwegian cherubism cohort; molecular genetic findings, oral manifestations and quality of life von Prescott, Trine, Redfors, Maria, Rustad, Cecilie Fremstad, Eiklid, Kristin Louise, Geirdal, Amy Østertun, Storhaug, Kari, Jensen, Janicke Liaaen

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ABCB4 sequence variations in young adults with cholesterol gallstone disease von Nakken, Karl Esten, Labori, Knut Jørgen, Rødningen, Olaug K., Nakken, Sigve, Berge, Knut E., Eiklid, Kristin, Ræder, Morten G.

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Cognitive impairment and the role of the ApoE [epsilon]4-allele after stroke - a 13 months follow-up study von Wagle, Jørgen, Farner, Lasse, Flekkøy, Kjell, Wyller, Torgeir B, Sandvik, Leiv, Eiklid, Kristin L, Fure, Brynjar, Stensrød, Brynhild, Engedal, Knut

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