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Cerebral Palsy - Early Diagnosis and Intervention Trial: protocol for the prospective multicentre CP-EDIT study with focus on diagnosis, prognostic factors, and intervention.
Hoei-Hansen CE, Weber L, Johansen M, Fabricius R, Hansen JK, Viuff AF, Rønde G, Hahn GH, Østergaard E, Duno M, Larsen VA, Madsen CG, Røhder K, Elvrum AG, Laugesen B, Ganz M, Madsen KS, Willerslev-Olsen M, Debes NM, Christensen J, Christensen R, Rackauskaite G. Hoei-Hansen CE, et al. Among authors: ostergaard e. BMC Pediatr. 2023 Oct 30;23(1):544. doi: 10.1186/s12887-023-04312-7. BMC Pediatr. 2023. PMID: 37899466 Free PMC article.
The postgraduate medical educational climate assessed by the Danish Residency Educational Climate Test (DK-RECT): a validation and cross-sectional observational study.
Jacobsen RB, Boor K, Christensen KB, Ung VH, Carlsen J, Kirk O, Hanefeld Dziegiel M, Østergaard E, Rochat P, Albrecht-Beste E, Droogh M, Lapperre TS, Scheele F, Sørensen JL. Jacobsen RB, et al. Among authors: ostergaard e. BMC Med Educ. 2023 Dec 12;23(1):943. doi: 10.1186/s12909-023-04909-7. BMC Med Educ. 2023. PMID: 38087289 Free PMC article.
Variants in ZFX are associated with an X-linked neurodevelopmental disorder with recurrent facial gestalt.
Shepherdson JL, Hutchison K, Don DW, McGillivray G, Choi TI, Allan CA, Amor DJ, Banka S, Basel DG, Buch LD, Carere DA, Carroll R, Clayton-Smith J, Crawford A, Dunø M, Faivre L, Gilfillan CP, Gold NB, Gripp KW, Hobson E, Holtz AM, Innes AM, Isidor B, Jackson A, Katsonis P, Amel Riazat Kesh L; Genomics England Research Consortium; Küry S, Lecoquierre F, Lockhart P, Maraval J, Matsumoto N, McCarrier J, McCarthy J, Miyake N, Moey LH, Németh AH, Østergaard E, Patel R, Pope K, Posey JE, Schnur RE, Shaw M, Stolerman E, Taylor JP, Wadman E, Wakeling E, White SM, Wong LC, Lupski JR, Lichtarge O, Corbett MA, Gecz J, Nicolet CM, Farnham PJ, Kim CH, Shinawi M. Shepherdson JL, et al. Among authors: ostergaard e. Am J Hum Genet. 2024 Mar 7;111(3):487-508. doi: 10.1016/j.ajhg.2024.01.007. Epub 2024 Feb 6. Am J Hum Genet. 2024. PMID: 38325380
Novel Alu insertion in the ZEB2 gene causing Mowat-Wilson syndrome.
Barington M, Bak M, Kjartansdóttir KR, Hansen TVO, Birkedal U, Østergaard E, Hove HB. Barington M, et al. Among authors: ostergaard e. Am J Med Genet A. 2024 Apr 11:e63581. doi: 10.1002/ajmg.a.63581. Online ahead of print. Am J Med Genet A. 2024. PMID: 38600862
Status epilepticus in POLG disease: a large multinational study.
Hikmat O, Naess K, Engvall M, Klingenberg C, Rasmussen M, Brodtkorb E, Ostergaard E, de Coo I, Pias-Peleteiro L, Isohanni P, Uusimaa J, Majamaa K, Kärppä M, Ortigoza-Escobar JD, Tangeraas T, Berland S, Harrison E, Biggs H, Horvath R, Darin N, Rahman S, Bindoff LA. Hikmat O, et al. Among authors: ostergaard e. J Neurol. 2024 Jun 1. doi: 10.1007/s00415-024-12463-5. Online ahead of print. J Neurol. 2024. PMID: 38822839
203 results