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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 1
2009 2
2010 1
2011 2
2013 2
2014 1
2016 2
2017 3
2018 4
2019 4
2020 3
2021 5
2022 3
2023 3

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29 results

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Page 1
Pycnodysostosis in children and adults.
Hald JD, Beck-Nielsen S, Gregersen PA, Gjørup H, Langdahl B. Hald JD, et al. Among authors: gjorup h. Bone. 2023 Apr;169:116674. doi: 10.1016/j.bone.2023.116674. Epub 2023 Jan 13. Bone. 2023. PMID: 36646263 No abstract available.
[Diagnosis, monitoring and treatment of tuberous sclerosis complex].
Reinhard M, Sunde L, Madsen MG, Andersen BN, Bendstrup E, Sommerlund M, Gjørup H, Larsen DA, Møller HU, Nielsen DG, Mortensen UM, Handrup MM, Aagaard NKM, Cortnum S, Khatir DS, Bayat M, Andersen G, Stausbøl-Grøn B, Christensen J. Reinhard M, et al. Among authors: gjorup h. Ugeskr Laeger. 2019 Nov 4;181(45):V05190293. Ugeskr Laeger. 2019. PMID: 31791451 Free article. Review. Danish.
B3GAT3-related linkeropathy and an in-frame homozygous deletion in an adult patient.
Bolund ACS, Langdahl B, Laurberg TB, Hellfritzsch MB, Gjørup H, Møller-Madsen B, Nielsen TØ, Farholt S, Gregersen PA. Bolund ACS, et al. Among authors: gjorup h. Eur J Med Genet. 2021 Dec;64(12):104342. doi: 10.1016/j.ejmg.2021.104342. Epub 2021 Sep 16. Eur J Med Genet. 2021. PMID: 34537402 Free article. Review.
Moebius sequence -a multidisciplinary clinical approach.
Pedersen LK, Maimburg RD, Hertz JM, Gjørup H, Pedersen TK, Møller-Madsen B, Østergaard JR. Pedersen LK, et al. Among authors: gjorup h. Orphanet J Rare Dis. 2017 Jan 6;12(1):4. doi: 10.1186/s13023-016-0559-z. Orphanet J Rare Dis. 2017. PMID: 28061881 Free PMC article.
29 results