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Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP).
J Neurol. 2024 Jan;271(1):263-273. doi: 10.1007/s00415-023-11968-9. Epub 2023 Sep 9.
J Neurol. 2024.
PMID: 37689591
Exome Sequencing and Multigene Panel Testing in 1,411 Patients With Adult-Onset Neurologic Disorders.
Schuermans N, Verdin H, Ghijsels J, Hellemans M, Debackere E, Bogaert E, Symoens S, Naesens L, Lecomte E, Crosiers D, Bergmans B, Verhoeven K, Poppe B, Laureys G, Herdewyn S, Van Langenhove T, Santens P, De Bleecker JL, Hemelsoet D, Dermaut B; for Program for Undiagnosed Rare Diseases (UD-PrOZA).
Schuermans N, et al. Among authors: ghijsels j.
Neurol Genet. 2023 Apr 26;9(3):e200071. doi: 10.1212/NXG.0000000000200071. eCollection 2023 Jun.
Neurol Genet. 2023.
PMID: 37152446
Free PMC article.
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Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA).
Schuermans N, Hemelsoet D, Terryn W, Steyaert S, Van Coster R, Coucke PJ, Steyaert W, Callewaert B, Bogaert E, Verloo P, Vanlander AV, Debackere E, Ghijsels J, LeBlanc P, Verdin H, Naesens L, Haerynck F, Callens S, Dermaut B, Poppe B; for UD-PrOZA.
Schuermans N, et al. Among authors: ghijsels j.
Orphanet J Rare Dis. 2022 May 23;17(1):210. doi: 10.1186/s13023-022-02365-y.
Orphanet J Rare Dis. 2022.
PMID: 35606766
Free PMC article.
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Radiostrontium in biological material: a precipitation and extraction procedure eliminating the use of fuming nitric acid.
Fourie HO, Ghijsels JP.
Fourie HO, et al. Among authors: ghijsels jp.
Health Phys. 1969 Nov;17(5):685-9. doi: 10.1097/00004032-196911000-00005.
Health Phys. 1969.
PMID: 5394706
No abstract available.
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