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Parental experiences with behavioural problems in Smith-Magenis syndrome: The need for syndrome-specific competence.
J Intellect Disabil. 2019 Sep;23(3):359-372. doi: 10.1177/1744629519847375. Epub 2019 May 2.
J Intellect Disabil. 2019.
PMID: 31046579
Free PMC article.
A structured assessment of motor function and behavior in patients with Kleefstra syndrome.
Schmidt S, Nag HE, Hunn BS, Houge G, Hoxmark LB.
Schmidt S, et al. Among authors: hoxmark lb.
Eur J Med Genet. 2016 Apr;59(4):240-8. doi: 10.1016/j.ejmg.2016.01.004. Epub 2016 Jan 22.
Eur J Med Genet. 2016.
PMID: 26808425
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A structured assessment of motor function, behavior, and communication in patients with Wolf-Hirschhorn syndrome.
Nag HE, Bergsaker DK, Hunn BS, Schmidt S, Hoxmark LB.
Nag HE, et al. Among authors: hoxmark lb.
Eur J Med Genet. 2017 Nov;60(11):610-617. doi: 10.1016/j.ejmg.2017.08.013. Epub 2017 Aug 14.
Eur J Med Genet. 2017.
PMID: 28818479
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Health service experiences among adults with hereditary spastic paraparesis or neurofibromatosis type 1.
Fjermestad KW, Kanavin Ø, Nyhus L, Hoxmark LB.
Fjermestad KW, et al. Among authors: hoxmark lb.
Mol Genet Genomic Med. 2020 Oct;8(10):e1399. doi: 10.1002/mgg3.1399. Epub 2020 Sep 14.
Mol Genet Genomic Med. 2020.
PMID: 32924306
Free PMC article.
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Health Survey of Adults with Neurofibromatosis 1 Compared to Population Study Controls.
Fjermestad KW, Nyhus L, Kanavin ØJ, Heiberg A, Hoxmark LB.
Fjermestad KW, et al. Among authors: hoxmark lb.
J Genet Couns. 2018 Sep;27(5):1102-1110. doi: 10.1007/s10897-018-0229-5. Epub 2018 Feb 10.
J Genet Couns. 2018.
PMID: 29429039
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Health survey of adults with hereditary spastic paraparesis compared to population study controls.
Fjermestad KW, Kanavin ØJ, Næss EE, Hoxmark LB, Hummelvoll G.
Fjermestad KW, et al. Among authors: hoxmark lb.
Orphanet J Rare Dis. 2016 Jul 13;11(1):98. doi: 10.1186/s13023-016-0469-0.
Orphanet J Rare Dis. 2016.
PMID: 27412159
Free PMC article.
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