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Page 1
Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants.
Hum Genet. 2022 Nov;141(11):1723-1738. doi: 10.1007/s00439-022-02441-0. Epub 2022 Feb 28.
Hum Genet. 2022.
PMID: 35226187
Free PMC article.
Genotype and Phenotype Analyses of a Novel WFS1 Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38.
Velde HM, Huizenga XJJ, Yntema HG, Haer-Wigman L, Beynon AJ, Oostrik J, Pegge SAH, Kremer H, Lanting CP, Pennings RJE.
Velde HM, et al.
Genes (Basel). 2023 Feb 10;14(2):457. doi: 10.3390/genes14020457.
Genes (Basel). 2023.
PMID: 36833385
Free PMC article.
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Spin in Published Reports of Tinnitus Randomized Controlled Trials: Evidence of Overinterpretation of Results.
Velde HM, van Heteren JAA, Smit AL, Stegeman I.
Velde HM, et al.
Front Neurol. 2021 Jul 16;12:693937. doi: 10.3389/fneur.2021.693937. eCollection 2021.
Front Neurol. 2021.
PMID: 34335451
Free PMC article.
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Evaluation of Sleep Quality and Fatigue in Patients with Usher Syndrome Type 2a.
Hendricks JM, Metz JR, Velde HM, Weeda J, Hartgers F, Yzer S, Hoyng CB, Pennings RJE, Collin RWJ, Boss MHM, de Vrieze E, van Wijk E.
Hendricks JM, et al. Among authors: velde hm.
Ophthalmol Sci. 2023 May 5;3(4):100323. doi: 10.1016/j.xops.2023.100323. eCollection 2023 Dec.
Ophthalmol Sci. 2023.
PMID: 37334034
Free PMC article.
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Long-Term Outcome of Symptomatic Patients Undergoing Hybrid Revascularisation for Extracranial Carotid Artery Tandem Stenosis.
Meershoek AJA, Velde HM, Toorop RJ, Hazenberg SCEVB, de Borst GJ.
Meershoek AJA, et al. Among authors: velde hm.
Eur J Vasc Endovasc Surg. 2019 May;57(5):627-631. doi: 10.1016/j.ejvs.2018.11.016. Epub 2019 Apr 12.
Eur J Vasc Endovasc Surg. 2019.
PMID: 30987818
Free article.
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Analysis of Rotterdam Study cohorts confirms a previously identified RIPOR2 in-frame deletion as a prevalent genetic factor in phenotypically variable adult-onset hearing loss (DFNA21) in the Netherlands.
Velde HM, Homans NC, Goedegebure A, Lanting CP, Pennings RJE, Kremer H.
Velde HM, et al.
J Med Genet. 2023 Nov;60(11):1061-1066. doi: 10.1136/jmg-2023-109146. Epub 2023 May 10.
J Med Genet. 2023.
PMID: 37164627
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