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

Autor: Hellstrøm, Torgeir, Andelic, Nada, Holthe, Øyvor, Helseth, Eirik, Server, Andrés, Eiklid, Kristin Louise, Sigurdardottir, Solrun

Publikováno v: Hellstrøm, Torgeir Andelic, Nada Holthe, Øyvor Helseth, Eirik Server, Andrés Eiklid, Kristin Louise Sigurdardottir, Solrun . 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. Frontiers in Neurology. 2022, 13, 1-9
Frontiers in Neurology

Externí odkaz: http://hdl.handle.net/10852/97895

Apolipoprotein ɛ4 Status and Brain Structure 12 Months after Mild Traumatic Injury: Brain Age Prediction Using Brain Morphometry and Diffusion Tensor Imaging

Autor: Hellstrøm, Torgeir, Andelic, Nada, de Lange, Ann-Marie Glasø, Helseth, Eirik, Eiklid, Kristin Louise, Westlye, Lars Tjelta

Publikováno v: Hellstrøm, Torgeir Andelic, Nada de Lange, Ann-Marie Glasø Helseth, Eirik Eiklid, Kristin Louise Westlye, Lars Tjelta . Apolipoprotein ɛ4 Status and Brain Structure 12 Months after Mild Traumatic Injury: Brain Age Prediction Using Brain Morphometry and Diffusion Tensor Imaging. Jo
Jo

Externí odkaz: http://hdl.handle.net/10852/86394
https://www.duo.uio.no/bitstream/handle/10852/86394/2/Apolipoprotein%2B%25C9%259B4%2BStatus%2Band%2BBrain%2BStructure%2B12%2BMonths%2Bafter%2BMild%2BTraumatic%2BInjury%253B%2BBrain%2BAge%2BPrediction%2BUsing%2BBrain%2BMorphometry%2Band%2BDiffusion%2BTensor%2BImaging.pdf

CFTR gene mutations and asthma in the Norwegian Environment and Childhood Asthma study

Autor: Munthe-Kaas, Monica Cheng, Lødrup Carlsen, Karin C., Carlsen, Kai-Håkon, Skinningsrud, Beate, Håland, Geir, Devulapalli, Chandra Sekhar, Pettersen, Morten, Eiklid, Kristin

Publikováno v: In Respiratory Medicine 2006 100(12):2121-2128

Two new Rett syndrome families and review of the literature: expanding the knowledge of MECP2 frameshift mutations

Autor: Eiklid Kristin L, Fuglsang Kathrine, Duno Morten, Roende Gitte, Ravn Kirstine, Tümer Zeynep, Nielsen Jytte B, Skjeldal Ola H

Publikováno v: Orphanet Journal of Rare Diseases, Vol 6, Iss 1, p 58 (2011)

Abstract Background Rett syndrome (RTT) is an X-linked dominant neurodevelopmental disorder, which is usually caused by de novo mutations in the MECP2 gene. More than 70% of the disease causing MECP2 mutations are eight recurrent C to T transitions,

Externí odkaz: https://doaj.org/article/4c1c2f0aeaed41d2bef23f9cf21ab891

Characterization of a Norwegian cherubism cohort; molecular genetic findings, oral manifestations and quality of life

Autor: Prescott, Trine, Redfors, Maria, Rustad, Cecilie Fremstad, Eiklid, Kristin Louise, Geirdal, Amy Østertun, Storhaug, Kari, Jensen, Janicke Liaaen

Publikováno v: In European Journal of Medical Genetics March 2013 56(3):131-137