Dunø M - Search Results

1

Cell-free fetal DNA for genetic evaluation in Copenhagen Pregnancy Loss Study (COPL): a prospective cohort study.

Schlaikjær Hartwig T, Ambye L, Gruhn JR, Petersen JF, Wrønding T, Amato L, Chi-Ho Chan A, Ji B, Bro-Jørgensen MH, Werge L, Petersen MMBS, Brinkmann C, Petersen JB, Dunø M, Bache I, Herrgård MJ, Jørgensen FS, Hoffmann ER, Nielsen HS; COPL consortium. Schlaikjær Hartwig T, et al. Among authors: duno m. Lancet. 2023 Mar 4;401(10378):762-771. doi: 10.1016/S0140-6736(22)02610-1. Epub 2023 Feb 2. Lancet. 2023. PMID: 36739882

2

Crouzon syndrome associated with acanthosis nigricans: prenatal 2D and 3D ultrasound findings and postnatal 3D CT findings.

Nørgaard P, Hagen CP, Hove H, Dunø M, Nissen KR, Kreiborg S, Jørgensen FS. Nørgaard P, et al. Among authors: duno m. Acta Radiol Short Rep. 2012 May 17;1(4):arsr.2012.110017. doi: 10.1258/arsr.2012.110017. eCollection 2012. Acta Radiol Short Rep. 2012. PMID: 23986840 Free PMC article.

3

[Harlequin ichthyosis with a diaphragmatic hernia and a new mutation].

Andersen LHJ, Kelstrup L, Olsen TE, Dunø M, Jørgensen FS. Andersen LHJ, et al. Among authors: duno m. Ugeskr Laeger. 2018 Sep 3;180(36):V01180078. Ugeskr Laeger. 2018. PMID: 30187851 Free article. Danish.

4

Lecocytes mutation load declines with age in carriers of the m.3243A>G mutation: A 10-year Prospective Cohort.

Langdahl JH, Larsen M, Frost M, Andersen PH, Yderstraede KB, Vissing J, Dunø M, Thomassen M, Frederiksen AL. Langdahl JH, et al. Among authors: duno m. Clin Genet. 2018 Apr;93(4):925-928. doi: 10.1111/cge.13201. Clin Genet. 2018. PMID: 29266179

5

SCA28: Novel Mutation in the AFG3L2 Proteolytic Domain Causes a Mild Cerebellar Syndrome with Selective Type-1 Muscle Fiber Atrophy.

Svenstrup K, Nielsen TT, Aidt F, Rostgaard N, Duno M, Wibrand F, Vinther-Jensen T, Law I, Vissing J, Roos P, Hjermind LE, Nielsen JE. Svenstrup K, et al. Among authors: duno m. Cerebellum. 2017 Feb;16(1):62-67. doi: 10.1007/s12311-016-0765-1. Cerebellum. 2017. PMID: 26868664

6

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: duno m. BMC Pediatr. 2023 Oct 30;23(1):544. doi: 10.1186/s12887-023-04312-7. BMC Pediatr. 2023. PMID: 37899466 Free PMC article.

7

Cardiac involvement in myotonic dystrophy: a nationwide cohort study.

Lund M, Diaz LJ, Ranthe MF, Petri H, Duno M, Juncker I, Eiberg H, Vissing J, Bundgaard H, Wohlfahrt J, Melbye M. Lund M, et al. Among authors: duno m. Eur Heart J. 2014 Aug 21;35(32):2158-64. doi: 10.1093/eurheartj/ehu157. Epub 2014 Apr 16. Eur Heart J. 2014. PMID: 24742887

8

Open source non-invasive prenatal testing platform and its performance in a public health laboratory.

Johansen P, Richter SR, Balslev-Harder M, Miltoft CB, Tabor A, Duno M, Kjaergaard S. Johansen P, et al. Among authors: duno m. Prenat Diagn. 2016 Jun;36(6):530-6. doi: 10.1002/pd.4819. Epub 2016 Apr 24. Prenat Diagn. 2016. PMID: 27027563

9

Hydroxylated Long-Chain Acylcarnitines are Biomarkers of Mitochondrial Myopathy.

Vissing CR, Dunø M, Wibrand F, Christensen M, Vissing J. Vissing CR, et al. Among authors: duno m. J Clin Endocrinol Metab. 2019 Dec 1;104(12):5968-5976. doi: 10.1210/jc.2019-00721. J Clin Endocrinol Metab. 2019. PMID: 31294795

10

Genetic analysis of Charcot-Marie-Tooth disease in Denmark and the implementation of a next generation sequencing platform.

Vaeth S, Christensen R, Dunø M, Lildballe DL, Thorsen K, Vissing J, Svenstrup K, Hertz JM, Andersen H, Jensen UB. Vaeth S, et al. Among authors: duno m. Eur J Med Genet. 2019 Jan;62(1):1-8. doi: 10.1016/j.ejmg.2018.04.003. Epub 2018 Apr 11. Eur J Med Genet. 2019. PMID: 29653220

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