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Page 1
Complement Activation in 22q11.2 Deletion Syndrome.
Grinde D, Øverland T, Lima K, Schjalm C, Mollnes TE, Abrahamsen TG. Grinde D, et al. Among authors: abrahamsen tg. J Clin Immunol. 2020 Apr;40(3):515-523. doi: 10.1007/s10875-020-00766-x. Epub 2020 Mar 9. J Clin Immunol. 2020. PMID: 32152940 Free PMC article.
T-cell Receptor Excision Circles in Newborns with Heart Defects.
Gul KA, Strand J, Pettersen RD, Brun H, Abrahamsen TG. Gul KA, et al. Among authors: abrahamsen tg. Pediatr Cardiol. 2020 Apr;41(4):809-815. doi: 10.1007/s00246-020-02317-y. Epub 2020 Mar 13. Pediatr Cardiol. 2020. PMID: 32166410 Free PMC article.
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.
Stray-Pedersen A, Sorte HS, Samarakoon P, Gambin T, Chinn IK, Coban Akdemir ZH, Erichsen HC, Forbes LR, Gu S, Yuan B, Jhangiani SN, Muzny DM, Rødningen OK, Sheng Y, Nicholas SK, Noroski LM, Seeborg FO, Davis CM, Canter DL, Mace EM, Vece TJ, Allen CE, Abhyankar HA, Boone PM, Beck CR, Wiszniewski W, Fevang B, Aukrust P, Tjønnfjord GE, Gedde-Dahl T, Hjorth-Hansen H, Dybedal I, Nordøy I, Jørgensen SF, Abrahamsen TG, Øverland T, Bechensteen AG, Skogen V, Osnes LTN, Kulseth MA, Prescott TE, Rustad CF, Heimdal KR, Belmont JW, Rider NL, Chinen J, Cao TN, Smith EA, Caldirola MS, Bezrodnik L, Lugo Reyes SO, Espinosa Rosales FJ, Guerrero-Cursaru ND, Pedroza LA, Poli CM, Franco JL, Trujillo Vargas CM, Aldave Becerra JC, Wright N, Issekutz TB, Issekutz AC, Abbott J, Caldwell JW, Bayer DK, Chan AY, Aiuti A, Cancrini C, Holmberg E, West C, Burstedt M, Karaca E, Yesil G, Artac H, Bayram Y, Atik MM, Eldomery MK, Ehlayel MS, Jolles S, Flatø B, Bertuch AA, Hanson IC, Zhang VW, Wong LJ, Hu J, Walkiewicz M, Yang Y, Eng CM, Boerwinkle E, Gibbs RA, Shearer WT, Lyle R, Orange JS, Lupski JR. Stray-Pedersen A, et al. Among authors: abrahamsen tg. J Allergy Clin Immunol. 2017 Jan;139(1):232-245. doi: 10.1016/j.jaci.2016.05.042. Epub 2016 Jul 16. J Allergy Clin Immunol. 2017. PMID: 27577878 Free PMC article.
Second-Tier Next Generation Sequencing Integrated in Nationwide Newborn Screening Provides Rapid Molecular Diagnostics of Severe Combined Immunodeficiency.
Strand J, Gul KA, Erichsen HC, Lundman E, Berge MC, Trømborg AK, Sørgjerd LK, Ytre-Arne M, Hogner S, Halsne R, Gaup HJ, Osnes LT, Kro GAB, Sorte HS, Mørkrid L, Rowe AD, Tangeraas T, Jørgensen JV, Alme C, Bjørndalen TEH, Rønnestad AE, Lang AM, Rootwelt T, Buechner J, Øverland T, Abrahamsen TG, Pettersen RD, Stray-Pedersen A. Strand J, et al. Among authors: abrahamsen tg. Front Immunol. 2020 Jul 9;11:1417. doi: 10.3389/fimmu.2020.01417. eCollection 2020. Front Immunol. 2020. PMID: 32754152 Free PMC article.
Hypoparathyroidism and autoimmunity in the 22q11.2 deletion syndrome.
Lima K, Abrahamsen TG, Wolff AB, Husebye E, Alimohammadi M, Kämpe O, Følling I. Lima K, et al. Among authors: abrahamsen tg. Eur J Endocrinol. 2011 Aug;165(2):345-52. doi: 10.1530/EJE-10-1206. Epub 2011 May 23. Eur J Endocrinol. 2011. PMID: 21606191
124 results